Hits from PDB	Structure Title	EC number
1O2U	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O2V	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O2W	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O2X	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O2Y	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O2Z	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O30	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O31	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O32	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O33	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O34	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O35	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O36	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O37	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O38	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O39	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3A	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3B	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3C	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3D	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3E	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3F	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3G	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3H	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3I	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3J	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3K	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3L	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3M	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3N	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3O	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.4
1O3P	ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS	3.4.21.73
1O3W	STRUCTURE OF THE INHIBITOR FREE TRIPLE MUTANT (K53,56,120M) OF PHOSPHOLIPASE A2	3.1.1.4
1O4W	CRYSTAL STRUCTURE OF A PIN (PILT N-TERMINUS) DOMAIN CONTAINING PROTEIN (AF0591) FROM ARCHAEOGLOBUS FULGIDUS AT 1.90 A RESOLUTION	3.1
1O4Y	THE THREE-DIMENSIONAL STRUCTURE OF BETA-AGARASE A FROM ZOBELLIA GALACTANIVORANS	3.2.1.81
1O4Z	THE THREE-DIMENSIONAL STRUCTURE OF BETA-AGARASE B FROM ZOBELLIA GALACTANIVORANS	3.2.1.81
1O59	CRYSTAL STRUCTURE OF ALLANTOICASE (YIR029W) FROM SACCHAROMYCES CEREVISIAE AT 2.40 A RESOLUTION	3.5.3.4
1O5A	DISSECTING AND DESIGNING INHIBITOR SELECTIVITY DETERMINANTS AT THE S1 SITE USING AN ARTIFICIAL ALA190 PROTEASE (ALA190 UPA)	3.4.21.73
1O5B	DISSECTING AND DESIGNING INHIBITOR SELECTIVITY DETERMINANTS AT THE S1 SITE USING AN ARTIFICIAL ALA190 PROTEASE (ALA190 UPA)	3.4.21.73
1O5C	DISSECTING AND DESIGNING INHIBITOR SELECTIVITY DETERMINANTS AT THE S1 SITE USING AN ARTIFICIAL ALA190 PROTEASE (ALA190 UPA)	3.4.21.73
1O5D	DISSECTING AND DESIGNING INHIBITOR SELECTIVITY DETERMINANTS AT THE S1 SITE USING AN ARTIFICIAL ALA190 PROTEASE (ALA190 UPA)	3.4.21.21
1O5E	DISSECTING AND DESIGNING INHIBITOR SELECTIVITY DETERMINANTS AT THE S1 SITE USING AN ARTIFICIAL ALA190 PROTEASE (ALA190 UPA)	3.4.21 3.4.21.106
1O5F	DISSECTING AND DESIGNING INHIBITOR SELECTIVITY DETERMINANTS AT THE S1 SITE USING AN ARTIFICIAL ALA190 PROTEASE (ALA190 UPA)	3.4.21 3.4.21.106
1O5G	DISSECTING AND DESIGNING INHIBITOR SELECTIVITY DETERMINANTS AT THE S1 SITE USING AN ARTIFICIAL ALA190 PROTEASE (ALA190 UPA)	3.4.21.5
1O5R	CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE COMPLEXED WITH A POTENT INHIBITOR	3.5.4.4
1O6E	EPSTEIN-BARR VIRUS PROTEASE	3.4.21.97
1O6F	PROLYL OLIGOPEPTIDASE FROM PORCINE BRAIN, D641A MUTANT WITH BOUND PEPTIDE LIGAND SUC-GLY-PRO	3.4.21.26
1O6G	PROLYL OLIGOPEPTIDASE FROM PORCINE BRAIN, D641N MUTANT WITH BOUND PEPTIDE LIGAND SUC-GLY-PRO	3.4.21.26
1O6I	CHITINASE B FROM SERRATIA MARCESCENS COMPLEXED WITH THE CATALYTIC INTERMEDIATE MIMIC CYCLIC DIPEPTIDE CI4.	3.2.1.14
1O6X	NMR SOLUTION STRUCTURE OF THE ACTIVATION DOMAIN OF HUMAN PROCARBOXYPEPTIDASE A2	3.4.17.15
1O75	TP47, THE 47-KILODALTON LIPOPROTEIN OF TREPONEMA PALLIDUM	3.4
1O77	CRYSTAL STRUCTURE OF THE C713S MUTANT OF THE TIR DOMAIN OF HUMAN TLR2	3.2.2.6
1O7A	HUMAN BETA-HEXOSAMINIDASE B	3.2.1.52
1O7D	THE STRUCTURE OF THE BOVINE LYSOSOMAL A-MANNOSIDASE SUGGESTS A NOVEL MECHANISM FOR LOW PH ACTIVATION	3.2.1.24
1O7E	CRYSTAL STRUCTURE OF THE CLASS A BETA-LACTAMSE L2 FROM STENOTROPHOMONAS MALTOPHILIA AT 1.51 ANGSTROM	3.5.2.6
1O7J	ATOMIC RESOLUTION STRUCTURE OF ERWINIA CHRYSANTHEMI L-ASPARAGINASE	3.5.1.1
1O86	CRYSTAL STRUCTURE OF HUMAN ANGIOTENSIN CONVERTING ENZYME IN COMPLEX WITH LISINOPRIL.	3.4.15.1 3.2.1
1O8A	CRYSTAL STRUCTURE OF HUMAN ANGIOTENSIN CONVERTING ENZYME (NATIVE).	3.4.15.1 3.2.1
1O8P	UNBOUND STRUCTURE OF CSCBM6-3 FROM CLOSTRIDIUM STERCORARIUM	3.2.1.8
1O8S	STRUCTURE OF CSCBM6-3 FROM CLOSTRIDIUM STERCORARIUM IN COMPLEX WITH CELLOBIOSE	3.2.1.8
1O8U	THE 2 ANGSTROM STRUCTURE OF 6-OXO CAMPHOR HYDROLASE: NEW STRUCTURAL DIVERSITY IN THE CROTONASE SUPERFAMILY	3.7.1.18
1OA2	COMPARISON OF FAMILY 12 GLYCOSIDE HYDROLASES AND RECRUITED SUBSTITUTIONS IMPORTANT FOR THERMAL STABILITY	3.2.1.4
1OA3	COMPARISON OF FAMILY 12 GLYCOSIDE HYDROLASES AND RECRUITED SUBSTITUTIONS IMPORTANT FOR THERMAL STABILITY	3.2.1.4
1OA4	COMPARISON OF FAMILY 12 GLYCOSIDE HYDROLASES AND RECRUITED SUBSTITUTIONS IMPORTANT FOR THERMAL STABILITY	3.2.1.4
1OA7	STRUCTURE OF MELANOCARPUS ALBOMYCES ENDOGLUCANASE IN COMPLEX WITH CELLOBIOSE	3.2.1.4
1OA9	STRUCTURE OF MELANOCARPUS ALBOMYCES ENDOGLUCANASE	3.2.1.4
1OAN	CRYSTAL STRUCTURE OF THE DENGUE 2 VIRUS ENVELOPE PROTEIN	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
1OB0	KINETIC STABILIZATION OF BACILLUS LICHENIFORMIS ALPHA-AMYLASE THROUGH INTRODUCTION OF HYDROPHOBIC RESIDUES AT THE SURFACE	3.2.1.1
1OB2	E. COLI ELONGATION FACTOR EF-TU COMPLEXED WITH THE ANTIBIOTIC KIRROMYCIN, A GTP ANALOG, AND PHE-TRNA	3.6.1.48
1OB5	T. AQUATICUS ELONGATION FACTOR EF-TU COMPLEXED WITH THE ANTIBIOTIC ENACYLOXIN IIA, A GTP ANALOG, AND PHE-TRNA	3.6.1.48
1OB8	HOLLIDAY JUNCTION RESOLVING ENZYME	3.1.22.4
1OB9	HOLLIDAY JUNCTION RESOLVING ENZYME	3.1.22.4
1OBA	MULTIMODULAR PNEUMOCOCCAL CELL WALL ENDOLYSIN FROM PHAGE CP-1 COMPLEXED WITH CHOLINE	3.2.1.17
1OBB	ALPHA-GLUCOSIDASE A, AGLA, FROM THERMOTOGA MARITIMA IN COMPLEX WITH MALTOSE AND NAD+	3.2.1.20
1OBR	CARBOXYPEPTIDASE T	3.4.17.18
1OBS	STRUCTURE OF RICIN A CHAIN MUTANT	3.2.2.22
1OBT	STRUCTURE OF RICIN A CHAIN MUTANT, COMPLEX WITH AMP	3.2.2.22
1OBW	STRUCTURE OF INORGANIC PYROPHOSPHATASE	3.6.1.1
1OC5	D405N MUTANT OF THE CELLOBIOHYDROLASE CEL6A FROM HUMICOLA INSOLENS IN COMPLEX WITH METHYL-CELLOBIOSYL-4-DEOXY-4-THIO-BETA-D-CELLOBIOSIDE	3.2.1.91
1OC6	STRUCTURE NATIVE OF THE D405N MUTANT OF THE CELLOBIOHYDROLASE CEL6A FROM HUMICOLA INSOLENS AT 1.5 ANGSTROM RESOLUTION	3.2.1.91
1OC7	D405N MUTANT OF THE CELLOBIOHYDROLASE CEL6A FROM HUMICOLA INSOLENS IN COMPLEX WITH METHYL-TETRATHIO-ALPHA-D-CELLOPENTOSIDE AT 1.1 ANGSTROM RESOLUTION	3.2.1.91
1OCB	STRUCTURE OF THE WILD-TYPE CELLOBIOHYDROLASE CEL6A FROM HUMICOLAS INSOLENS IN COMPLEX WITH A FLUORESCENT SUBSTRATE	3.2.1.91
1OCE	ACETYLCHOLINESTERASE (E.C. 3.1.1.7) COMPLEXED WITH MF268	3.1.1.7
1OCJ	MUTANT D416A OF THE CELLOBIOHYDROLASE CEL6A FROM HUMICOLA INSOLENS IN COMPLEX WITH A THIOPENTASACCHARIDE AT 1.3 ANGSTROM RESOLUTION	3.2.1.91
1OCN	MUTANT D416A OF THE CELLOBIOHYDROLASE CEL6A FROM HUMICOLA INSOLENS IN COMPLEX WITH A CELLOBIO-DERIVED ISOFAGOMINE AT 1.3 ANGSTROM RESOLUTION	3.2.1.91
1OCQ	COMPLEX OF THE ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHEARANS AT 1.08 ANGSTROM RESOLUTION WITH CELLOBIO-DERIVED ISOFAGOMINE	3.2.1.4
1OD0	FAMILY 1 B-GLUCOSIDASE FROM THERMOTOGA MARITIMA	3.2.1.21
1OD1	ENDOTHIAPEPSIN PD135,040 COMPLEX	3.4.23.22
1OD3	STRUCTURE OF CSCBM6-3 FROM CLOSTRIDIUM STERCORARIUM IN COMPLEX WITH LAMINARIBIOSE	3.2.1.8
1OD8	XYLANASE XYN10A FROM STREPTOMYCES LIVIDANS IN COMPLEX WITH XYLOBIO-ISOFAGOMINE LACTAM	3.2.1.8
1ODG	VERY-SHORT-PATCH DNA REPAIR ENDONUCLEASE BOUND TO ITS REACTION PRODUCT SITE	3.1
1ODS	CEPHALOSPORIN C DEACETYLASE FROM BACILLUS SUBTILIS	3.1.1.41 3.1.1.72
1ODT	CEPHALOSPORIN C DEACETYLASE MUTATED, IN COMPLEX WITH ACETATE	3.1.1.41 3.1.1.72
1ODU	CRYSTAL STRUCTURE OF THERMOTOGA MARITIMA ALPHA-FUCOSIDASE IN COMPLEX WITH FUCOSE	3.2.1.51
1ODW	NATIVE HIV-1 PROTEINASE	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1ODX	HIV-1 PROTEINASE MUTANT A71T, V82A	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1ODY	HIV-1 PROTEASE COMPLEXED WITH AN INHIBITOR LP-130	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1ODZ	EXPANSION OF THE GLYCOSYNTHASE REPERTOIRE TO PRODUCE DEFINED MANNO-OLIGOSACCHARIDES	3.2.1.78
1OE4	XENOPUS SMUG1, AN ANTI-MUTATOR URACIL-DNA GLYCOSYLASE	3.2.2
1OE5	XENOPUS SMUG1, AN ANTI-MUTATOR URACIL-DNA GLYCOSYLASE	3.2.2
1OE6	XENOPUS SMUG1, AN ANTI-MUTATOR URACIL-DNA GLYCOSYLASE	3.2.2
1OEM	PTP1B WITH THE CATALYTIC CYSTEINE OXIDIZED TO A SULFENYL-AMIDE BOND	3.1.3.48
1OEO	PTP1B WITH THE CATALYTIC CYSTEINE OXIDIZED TO SULFONIC ACID	3.1.3.48
1OES	OXIDATION STATE OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
1OET	OXIDATION STATE OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
1OEU	OXIDATION STATE OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
1OEV	OXIDATION STATE OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
1OEW	ATOMIC RESOLUTION STRUCTURE OF NATIVE ENDOTHIAPEPSIN	3.4.23.22
1OEX	ATOMIC RESOLUTION STRUCTURE OF ENDOTHIAPEPSIN IN COMPLEX WITH A HYDROXYETHYLENE TRANSITION STATE ANALOGUE INHIBITOR H261	3.4.23.22
1OFC	NUCLEOSOME RECOGNITION MODULE OF ISWI ATPASE	3.6.4
1OG1	CRYSTAL STRUCTURE OF THE EUCARYOTIC MONO-ADP-RIBOSYLTRANSFERASE ART2.2 IN COMPLEX WITH TAD	2.4.2.31 3.2.2.5
1OG3	CRYSTAL STRUCTURE OF THE EUKARYOTIC MONO-ADP-RIBOSYLTRANSFERASE ART2.2 MUTANT E189I IN COMPLEX WITH NAD	2.4.2.31 3.2.2.5
1OG4	CRYSTAL STRUCTURE OF THE EUCARYOTIC MONO-ADP-RIBOSYLTRANSFERASE ART2.2 MUTANT E189A IN COMPLEX WITH NADH	2.4.2.31 3.2.2.5
1OGB	CHITINASE B FROM SERRATIA MARCESCENS MUTANT D142N	3.2.1.14
1OGG	CHITINASE B FROM SERRATIA MARCESCENS MUTANT D142N IN COMPLEX WITH INHIBITOR ALLOSAMIDIN	3.2.1.14
1OGH	STRUCTURE OF THE BIFUNCTIONAL DCTP DEAMINASE-DUTPASE FROM METHANOCALDOCOCCUS JANNASCHII	3.5.4.13 3.6.1.23 3.5.4.30
1OGK	THE CRYSTAL STRUCTURE OF TRYPANOSOMA CRUZI DUTPASE IN COMPLEX WITH DUDP	3.6.1.23
1OGL	THE CRYSTAL STRUCTURE OF NATIVE TRYPANOSOMA CRUZI DUTPASE	3.6.1.23
1OGM	DEX49A FROM PENICILLIUM MINIOLUTEUM	3.2.1.11
1OGO	DEX49A FROM PENICILLIUM MINIOLUTEUM COMPLEX WITH ISOMALTOSE	3.2.1.11
1OGS	HUMAN ACID-BETA-GLUCOSIDASE	3.2.1.45 2.4.1 3.2.1.104 3.2.1
1OHC	STRUCTURE OF THE PROLINE DIRECTED PHOSPHATASE CDC14	3.1.3.16 3.1.3.48
1OHD	STRUCTURE OF CDC14 IN COMPLEX WITH TUNGSTATE	3.1.3.16 3.1.3.48
1OHE	STRUCTURE OF CDC14B PHOSPHATASE WITH A PEPTIDE LIGAND	3.1.3.16 3.1.3.48
1OHT	PEPTIDOGLYCAN RECOGNITION PROTEIN LB	3.5.1.28
1OI4	CRYSTAL STRUCTURE OF YHBO FROM ESCHERICHIA COLI	3.1.2 3.5.1 3.5.1.124
1OI8	5'-NUCLEOTIDASE (E. COLI) WITH AN ENGINEERED DISULFIDE BRIDGE (P90C, L424C)	3.1.3.5 3.6.1.45
1OIE	5'-NUCLEOTIDASE (E. COLI) WITH AN ENGINEERED DISULFIDE BRIDGE (S228C, P513C)	3.1.3.5 3.6.1.45
1OIF	FAMILY 1 B-GLUCOSIDASE FROM THERMOTOGA MARITIMA	3.2.1.21
1OIL	STRUCTURE OF LIPASE	3.1.1.3
1OIM	FAMILY 1 B-GLUCOSIDASE FROM THERMOTOGA MARITIMA	3.2.1.21
1OIN	FAMILY 1 B-GLUCOSIDASE FROM THERMOTOGA MARITIMA	3.2.1.21
1OJI	ANATOMY OF GLYCOSYNTHESIS: STRUCTURE AND KINETICS OF THE HUMICOLA INSOLENS CEL7B E197A AND E197S GLYCOSYNTHASE MUTANTS	3.2.1.4
1OJJ	ANATOMY OF GLYCOSYNTHESIS: STRUCTURE AND KINETICS OF THE HUMICOLA INSOLENS CEL7BE197A AND E197S GLYCOSYNTHASE MUTANTS	3.2.1.4
1OJK	ANATOMY OF GLYCOSYNTHESIS: STRUCTURE AND KINETICS OF THE HUMICOLA INSOLENS CEL7BE197A AND E197S GLYCOSYNTHASE MUTANTS	3.2.1.4
1OK8	CRYSTAL STRUCTURE OF THE DENGUE 2 VIRUS ENVELOPE GLYCOPROTEIN IN THE POSTFUSION CONFORMATION	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
1OKB	CRYSTAL STRUCTURE OF URACIL-DNA GLYCOSYLASE FROM ATLANTIC COD (GADUS MORHUA)	3.2.2.3 3.2.2.27
1OKE	CRYSTAL STRUCTURE OF THE DENGUE 2 VIRUS ENVELOPE PROTEIN IN COMPLEX WITH N-OCTYL-BETA-D-GLUCOSIDE	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
1OKJ	CRYSTAL STRUCTURE OF THE ESSENTIAL E. COLI YEAZ PROTEIN BY MAD METHOD USING THE GADOLINIUM COMPLEX DOTMA""	3.4
1OKX	BINDING STRUCTURE OF ELASTASE INHIBITOR SCYPTOLIN A	3.4.21.36
1OLP	ALPHA TOXIN FROM CLOSTRIDIUM ABSONUM	3.1.4.3
1OLQ	THE TRICHODERMA REESEI CEL12A P201C MUTANT, STRUCTURE AT 1.7 A RESOLUTION	3.2.1.4
1OLR	THE HUMICOLA GRISEA CEL12A ENZYME STRUCTURE AT 1.2 A RESOLUTION	3.2.1.4
1OM6	CRYSTAL STRUCTURE OF A COLD ADAPTED ALKALINE PROTEASE FROM PSEUDOMONAS TAC II 18, CO-CRYSTALLIZED WITH 5MM EDTA (2 MONTHS)	3.4.24.40
1OM7	CRYSTAL STRUCTURE OF A COLD ADAPTED ALKALINE PROTEASE FROM PSEUDOMONAS TAC II 18, SOAKED IN 85 MM EDTA	3.4.24.40
1OM8	CRYSTAL STRUCTURE OF A COLD ADAPTED ALKALINE PROTEASE FROM PSEUDOMONAS TAC II 18, CO-CRYSTALLYZED WITH 10 MM EDTA	3.4.24.40
1OME	CRYSTAL STRUCTURE OF THE OMEGA LOOP DELETION MUTANT (RESIDUES 163-178 DELETED) OF BETA-LACTAMASE FROM STAPHYLOCOCCUS AUREUS PC1	3.5.2.6
1OMJ	CRYSTAL STRUCTURE OF A PSYCHROPHILIC ALKALINE PROTEASE FROM PSEUDOMONAS TAC II 18	3.4.24.40
1ONB	SOLUTION STRUCTURE OF AN ENGINEERED ARGININE-RICH SUBDOMAIN 2 OF THE HEPATITIS C VIRUS NS3 RNA HELICASE	3.4.21.98 3.4.22 3.6.1.15 3.6.4.13 2.7.7.48
1ONC	THE REFINED 1.7 ANGSTROMS X-RAY CRYSTALLOGRAPHIC STRUCTURE OF P-30, AN AMPHIBIAN RIBONUCLEASE WITH ANTI-TUMOR ACTIVITY	3.1.27
1ONG	SHV-1 BETA-LACTAMASE WITH A PENEM INHIBITOR	3.5.2.6
1ONH	GC1 BETA-LACTAMASE WITH A PENEM INHIBITOR	3.5.2.6
1ONI	CRYSTAL STRUCTURE OF A HUMAN P14.5, A TRANSLATIONAL INHIBITOR REVEALS DIFFERENT MODE OF LIGAND BINDING NEAR THE INVARIANT RESIDUES OF THE YJGF/UK114 PROTEIN FAMILY	3.5.99.10
1ONK	MISTLETOE LECTIN I FROM VISCUM ALBUM	3.2.2.22
1ONS	CRYSTAL STRUCTURE OF ESCHERICHIA COLI HEAT SHOCK PROTEIN YEDU	3.1.2 3.5.1 3.5.1.124 4.2.1.130
1ONW	CRYSTAL STRUCTURE OF ISOASPARTYL DIPEPTIDASE FROM E. COLI	3.4.19
1ONX	CRYSTAL STRUCTURE OF ISOASPARTYL DIPEPTIDASE FROM ESCHERICHIA COLI COMPLEXED WITH ASPARTATE	3.4.19
1ONY	OXALYL-ARYL-AMINO BENZOIC ACID INHIBITORS OF PTP1B, COMPOUND 17	3.1.3.48
1ONZ	OXALYL-ARYL-AMINO BENZOIC ACID INHIBITORS OF PTP1B, COMPOUND 8B	3.1.3.48
1OO9	ORIENTATION IN SOLUTION OF MMP-3 CATALYTIC DOMAIN AND N-TIMP-1 FROM RESIDUAL DIPOLAR COUPLINGS	3.4.24.17
1OOK	CRYSTAL STRUCTURE OF THE COMPLEX OF PLATELET RECEPTOR GPIB-ALPHA AND HUMAN ALPHA-THROMBIN	3.4.21.5
1OOP	THE CRYSTAL STRUCTURE OF SWINE VESICULAR DISEASE VIRUS	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1OP0	CRYSTAL STRUCTURE OF AAV-SP-I, A GLYCOSYLATED SNAKE VENOM SERINE PROTEINASE FROM AGKISTRODON ACUTUS	3.4.21
1OP2	CRYSTAL STRUCTURE OF AAV-SP-II, A GLYCOSYLATED SNAKE VENOM SERINE PROTEINASE FROM AGKISTRODON ACUTUS	3.4.21
1OP8	CRYSTAL STRUCTURE OF HUMAN GRANZYME A	3.4.21.78
1OPZ	A CORE MUTATION AFFECTING THE FOLDING PROPERTIES OF A SOLUBLE DOMAIN OF THE ATPASE PROTEIN COPA FROM BACILLUS SUBTILIS	3.6.3.4 7.2.2.8
1OQ3	A CORE MUTATION AFFECTING THE FOLDING PROPERTIES OF A SOLUBLE DOMAIN OF THE ATPASE PROTEIN COPA FROM BACILLUS SUBTILIS	3.6.3.4 7.2.2.8
1OQ6	SOLUTION STRUCTURE OF COPPER-S46V COPA FROM BACILLUS SUBTILIS	3.6.3.4 7.2.2.8
1OQK	STRUCTURE OF MTH11: A HOMOLOGUE OF HUMAN RNASE P PROTEIN RPP29	3.1.26.5
1OQL	MISTLETOE LECTIN I FROM VISCUM ALBUM COMPLEXED WITH GALACTOSE	3.2.2.22
1OQS	CRYSTAL STRUCTURE OF RV4/RV7 COMPLEX	3.1.1.4
1OR0	CRYSTAL STRUCTURES OF GLUTARYL 7-AMINOCEPHALOSPORANIC ACID ACYLASE: INSIGHT INTO AUTOPROTEOLYTIC ACTIVATION	3.5.1 3.5.1.93
1ORF	THE OLIGOMERIC STRUCTURE OF HUMAN GRANZYME A REVEALS THE MOLECULAR DETERMINANTS OF SUBSTRATE SPECIFICITY	3.4.21.78
1OS0	THERMOLYSIN WITH AN ALPHA-AMINO PHOSPHINIC INHIBITOR	3.4.24.27
1OS2	TERNARY ENZYME-PRODUCT-INHIBITOR COMPLEXES OF HUMAN MMP12	3.4.24.65
1OS5	CRYSTAL STRUCTURE OF HCV NS5B RNA POLYMERASE COMPLEXED WITH A NOVEL NON-COMPETITIVE INHIBITOR.	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
1OS8	RECOMBINANT STREPTOMYCES GRISEUS TRYPSIN	3.4.21.4
1OS9	BINARY ENZYME-PRODUCT COMPLEXES OF HUMAN MMP12	3.4.24.65
1OSE	PORCINE PANCREATIC ALPHA-AMYLASE COMPLEXED WITH ACARBOSE	3.2.1.1
1OSS	T190P STREPTOMYCES GRISEUS TRYPSIN IN COMPLEX WITH BENZAMIDINE	3.4.21.4
1OT5	THE 2.4 ANGSTROM CRYSTAL STRUCTURE OF KEX2 IN COMPLEX WITH A PEPTIDYL-BORONIC ACID INHIBITOR	3.4.21.61
1OUA	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: X-RAY STRUCTURE OF THE I56T MUTANT	3.2.1.17
1OUB	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: X-RAY STRUCTURE OF THE V100A MUTANT	3.2.1.17
1OUC	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: X-RAY STRUCTURE OF THE V110A MUTANT	3.2.1.17
1OUD	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: X-RAY STRUCTURE OF THE V121A MUTANT	3.2.1.17
1OUE	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: X-RAY STRUCTURE OF THE V125A MUTANT	3.2.1.17
1OUF	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: X-RAY STRUCTURE OF THE V130A MUTANT	3.2.1.17
1OUG	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: X-RAY STRUCTURE OF THE V2A MUTANT	3.2.1.17
1OUH	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: X-RAY STRUCTURE OF THE V74A MUTANT	3.2.1.17
1OUI	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: X-RAY STRUCTURE OF THE V93A MUTANT	3.2.1.17
1OUJ	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: X-RAY STRUCTURE OF THE V99A MUTANT	3.2.1.17
1OUO	CRYSTAL STRUCTURE OF THE PERIPLASMIC ENDONUCLEASE VVN	3.1
1OUP	CRYSTAL STRUCTURE OF THE PERIPLASMIC ENDONUCLEASE VVN COMPLEXED WITH OCTAMER DOUBLE STRANDED DNA	3.1
1OUV	HELICOBACTER CYSTEINE RICH PROTEIN C (HCPC)	3.5.2.6
1OV5	T4 LYSOZYME CAVITY MUTANT L99A/M102Q BOUND WITH 2-ALLYLPHENOL	3.2.1.17
1OV7	T4 LYSOZYME CAVITY MUTANT L99A/M102Q BOUND WITH 2-ALLYL-6-METHYL-PHENOL	3.2.1.17
1OVH	T4 LYSOZYME CAVITY MUTANT L99A/M102Q BOUND WITH 2-CHLORO-6-METHYL-ANILINE	3.2.1.17
1OVJ	T4 LYSOZYME CAVITY MUTANT L99A/M102Q BOUND WITH 3-FLUORO-2-METHYL_ANILINE	3.2.1.17
1OVK	T4 LYSOZYME CAVITY MUTANT L99A/M102Q BOUND WITH N-ALLYL-ANILINE	3.2.1.17
1OVQ	SOLUTION STRUCTURE OF THE HYPOTHETICAL PROTEIN YQGF FROM ESCHERICHIA COLI	3.1
1OVW	ENDOGLUCANASE I COMPLEXED WITH NON-HYDROLYSABLE SUBSTRATE ANALOGUE	3.2.1.4
1OWD	SUBSTITUTED 2-NAPHTHAMIDINE INHIBITORS OF UROKINASE	3.4.21.73
1OWE	SUBSTITUTED 2-NAPHTHAMIDINE INHIBITORS OF UROKINASE	3.4.21.73
1OWH	SUBSTITUTED 2-NAPHTHAMIDINE INHIBITORS OF UROKINASE	3.4.21.73
1OWI	SUBSTITUTED 2-NAPHTHAMIDINE INHIBITORS OF UROKINASE	3.4.21.73
1OWJ	SUBSTITUTED 2-NAPHTHAMIDINE INHIBITORS OF UROKINASE	3.4.21.73
1OWK	SUBSTITUTED 2-NAPHTHAMIDINE INHIBITORS OF UROKINASE	3.4.21.73
1OWS	CRYSTAL STRUCTURE OF A C49 PHOSPHOLIPASE A2 FROM INDIAN COBRA REVEALS CARBOHYDRATE BINDING IN THE HYDROPHOBIC CHANNEL	3.1.1.4
1OWY	T4 LYSOZYME CAVITY MUTANT L99A/M102Q BOUND WITH 2-PROPYL-ANILINE	3.2.1.17
1OWZ	T4 LYSOZYME CAVITY MUTANT L99A/M102Q BOUND WITH 4-FLUOROPHENETHYL ALCOHOL	3.2.1.17
1OX1	CRYSTAL STRUCTURE OF THE BOVINE TRYPSIN COMPLEX WITH A SYNTHETIC 11 PEPTIDE INHIBITOR	3.4.21.4
1OX4	TOWARDS UNDERSTANDING THE MECHANISM OF THE COMPLEX CYCLIZATION REACTION CATALYZED BY IMIDAZOLE GLYCEROPHOSPHATE SYNTHASE	2.4.2 4.1.3 4.3.2.10 3.5.1.2
1OX5	TOWARDS UNDERSTANDING THE MECHANISM OF THE COMPLEX CYCLIZATION REACTION CATALYZED BY IMIDAZOLE GLYCEROPHOSPHATE SYNTHASE	2.4.2 4.1.3 4.3.2.10 3.5.1.2
1OX6	TOWARDS UNDERSTANDING THE MECHANISM OF THE COMPLEX CYCLIZATION REACTION CATALYZED BY IMIDAZOLE GLYCEROPHOSPHATE SYNTHASE	2.4.2 4.1.3 4.3.2.10 3.5.1.2
1OX7	CRYSTAL STRUCTURE OF YEAST CYTOSINE DEAMINASE APO-ENZYME: INORGANIC ZINC BOUND	3.5.4.1
1OXG	CRYSTAL STRUCTURE OF A COMPLEX FORMED BETWEEN ORGANIC SOLVENT TREATED BOVINE ALPHA-CHYMOTRYPSIN AND ITS AUTOCATALYTICALLY PRODUCED HIGHLY POTENT 14-RESIDUE PEPTIDE AT 2.2 RESOLUTION	3.4.21.1
1OXL	INHIBITION OF PHOSPHOLIPASE A2 (PLA2) BY (2-CARBAMOYLMETHYL-5-PROPYL-OCTAHYDRO-INDOL-7-YL)-ACETIC ACID (INDOLE): CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PLA2 FROM RUSSELL'S VIPER AND INDOLE AT 1.8 RESOLUTION	3.1.1.4
1OXM	STRUCTURE OF CUTINASE	3.1.1 3.1.1.74
1OXR	ASPIRIN INDUCES ITS ANTI-INFLAMMATORY EFFECTS THROUGH ITS SPECIFIC BINDING TO PHOSPHOLIPASE A2: CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 AND ASPIRIN AT 1.9A RESOLUTION	3.1.1.4
1OXW	THE CRYSTAL STRUCTURE OF SEMET PATATIN	3.1.1
1OYF	CRYSTAL STRUCTURE OF RUSSELLES VIPER (DABOIA RUSSELLII PULCHELLA) PHOSPHOLIPASE A2 IN A COMPLEX WITH VENOM 6-METHYL HEPTANOL	3.1.1.4
1OYN	CRYSTAL STRUCTURE OF PDE4D2 IN COMPLEX WITH (R,S)-ROLIPRAM	3.1.4.17 3.1.4.53
1OYO	REGULATION OF PROTEASE ACTIVITY BY MELANIN: CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PROTEINASE K AND MELANIN MONOMERS AT 2.0 RESOLUTION	3.4.21.64
1OYQ	TRYPSIN INHIBITOR COMPLEX	3.4.21.4
1OYT	COMPLEX OF RECOMBINANT HUMAN THROMBIN WITH A DESIGNED FLUORINATED INHIBITOR	3.4.21.5
1OYU	LONG-DISTANCE CONFORMATIONAL CHANGES IN A PROTEIN ENGINEERED BY MODULATED SEQUENCE DUPLICATION	3.2.1.17
1OYV	CRYSTAL STRUCTURE OF TOMATO INHIBITOR-II IN A TERNARY COMPLEX WITH SUBTILISIN CARLSBERG	3.4.21.62
1OYW	STRUCTURE OF THE RECQ CATALYTIC CORE	3.6.1 3.6.4.12
1OYY	STRUCTURE OF THE RECQ CATALYTIC CORE BOUND TO ATP-GAMMA-S	3.6.1 3.6.4.12
1OZ0	CRYSTAL STRUCTURE OF THE HOMODIMERIC BIFUNCTIONAL TRANSFORMYLASE AND CYCLOHYDROLASE ENZYME AVIAN ATIC IN COMPLEX WITH A MULTISUBSTRATE ADDUCT INHIBITOR BETA-DADF.	2.1.2.3 3.5.4.10
1OZ6	X-RAY STRUCTURE OF ACIDIC PHOSPHOLIPASE A2 FROM INDIAN SAW-SCALED VIPER (ECHIS CARINATUS) WITH A POTENT PLATELET AGGREGATION INHIBITORY ACTIVITY	3.1.1.4
1OZ9	CRYSTAL STRUCTURE OF AQ_1354, A HYPOTHETICAL PROTEIN FROM AQUIFEX AEOLICUS	3.1
1OZI	THE ALTERNATIVELY SPLICED PDZ2 DOMAIN OF PTP-BL	3.1.3.48
1OZY	CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 (MIPLA3) FROM MICROPECHIS IKAHEKA	3.1.1.4
1P01	SERINE PROTEASE MECHANISM. STRUCTURE OF AN INHIBITORY COMPLEX OF ALPHA-LYTIC PROTEASE AND A TIGHTLY BOUND PEPTIDE BORONIC ACID	3.4.21.12
1P02	STRUCTURE ANALYSIS OF SPECIFICITY. ALPHA-LYTIC PROTEASE COMPLEXES WITH ANALOGUES OF REACTION INTERMEDIATES	3.4.21.12
1P03	STRUCTURE ANALYSIS OF SPECIFICITY. ALPHA-LYTIC PROTEASE COMPLEXES WITH ANALOGUES OF REACTION INTERMEDIATES	3.4.21.12
1P04	STRUCTURE ANALYSIS OF SPECIFICITY. ALPHA-LYTIC PROTEASE COMPLEXES WITH ANALOGUES OF REACTION INTERMEDIATES	3.4.21.12
1P05	STRUCTURE ANALYSIS OF SPECIFICITY. ALPHA-LYTIC PROTEASE COMPLEXES WITH ANALOGUES OF REACTION INTERMEDIATES	3.4.21.12
1P06	STRUCTURE ANALYSIS OF SPECIFICITY. ALPHA-LYTIC PROTEASE COMPLEXES WITH ANALOGUES OF REACTION INTERMEDIATES	3.4.21.12
1P09	STRUCTURAL PLASTICITY AS A DETERMINANT OF ENZYME SPECIFICITY. CREATING BROADLY SPECIFIC PROTEASES	3.4.21.12
1P0I	CRYSTAL STRUCTURE OF HUMAN BUTYRYL CHOLINESTERASE	3.1.1.8
1P0M	CRYSTAL STRUCTURE OF HUMAN BUTYRYL CHOLINESTERASE IN COMPLEX WITH A CHOLINE MOLECULE	3.1.1.8
1P0P	CRYSTAL STRUCTURE OF SOMAN-AGED HUMAN BUTYRYL CHOLINESTERASE IN COMPLEX WITH THE SUBSTRATE ANALOG BUTYRYLTHIOCHOLINE	3.1.1.8
1P0Q	CRYSTAL STRUCTURE OF SOMAN-AGED HUMAN BUTYRYL CHOLINESTERASE	3.1.1.8
1P10	STRUCTURAL PLASTICITY AS A DETERMINANT OF ENZYME SPECIFICITY. CREATING BROADLY SPECIFIC PROTEASES	3.4.21.12
1P11	CRYSTAL STRUCTURES OF ALPHA-LYTIC PROTEASE COMPLEXES WITH IRREVERSIBLY BOUND PHOSPHONATE ESTERS	3.4.21.12
1P12	CRYSTAL STRUCTURES OF ALPHA-LYTIC PROTEASE COMPLEXES WITH IRREVERSIBLY BOUND PHOSPHONATE ESTERS	3.4.21.12
1P15	CRYSTAL STRUCTURE OF THE D2 DOMAIN OF RPTPA	3.1.3.48
1P1M	STRUCTURE OF THERMOTOGA MARITIMA AMIDOHYDROLASE TM0936 BOUND TO NI AND METHIONINE	3.5.4.28 3.5.4.31
1P2I	STRUCTURAL CONSEQUENCES OF ACCOMMODATION OF FOUR NON-COGNATE AMINO-ACID RESIDUES IN THE S1 POCKET OF BOVINE TRYPSIN AND CHYMOTRYPSIN	3.4.21.4
1P2J	STRUCTURAL CONSEQUENCES OF ACCOMMODATION OF FOUR NON-COGNATE AMINO-ACID RESIDUES IN THE S1 POCKET OF BOVINE TRYPSIN AND CHYMOTRYPSIN	3.4.21.4
1P2K	STRUCTURAL CONSEQUENCES OF ACCOMMODATION OF FOUR NON-COGNATE AMINO-ACID RESIDUES IN THE S1 POCKET OF BOVINE TRYPSIN AND CHYMOTRYPSIN	3.4.21.4
1P2L	T4 LYSOZYME CORE REPACKING MUTANT V87I/TA	3.2.1.17
1P2M	STRUCTURAL CONSEQUENCES OF ACCOMMODATION OF FOUR NON-COGNATE AMINO-ACID RESIDUES IN THE S1 POCKET OF BOVINE TRYPSIN AND CHYMOTRYPSIN	3.4.21.1
1P2N	STRUCTURAL CONSEQUENCES OF ACCOMMODATION OF FOUR NON-COGNATE AMINO-ACID RESIDUES IN THE S1 POCKET OF BOVINE TRYPSIN AND CHYMOTRYPSIN	3.4.21.1
1P2O	STRUCTURAL CONSEQUENCES OF ACCOMMODATION OF FOUR NON-COGNATE AMINO-ACID RESIDUES IN THE S1 POCKET OF BOVINE TRYPSIN AND CHYMOTRYPSIN	3.4.21.1
1P2P	STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2 AT 2.6 ANGSTROMS RESOLUTION AND COMPARISON WITH BOVINE PHOSPHOLIPASE A2	3.1.1.4
1P2Q	STRUCTURAL CONSEQUENCES OF ACCOMMODATION OF FOUR NON-COGNATE AMINO-ACID RESIDUES IN THE S1 POCKET OF BOVINE TRYPSIN AND CHYMOTRYPSIN	3.4.21.1
1P2R	T4 LYSOZYME CORE REPACKING MUTANT I78V/TA	3.2.1.17
1P2S	H-RAS 166 IN 50% 2,2,2 TRIFLOUROETHANOL	3.6.5.2
1P2T	H-RAS 166 IN AQUEOUS MOTHER LIQOUR, RT	3.6.5.2
1P2U	H-RAS IN 50% ISOPROPANOL	3.6.5.2
1P36	T4 LYOSZYME CORE REPACKING MUTANT I100V/TA	3.2.1.17
1P37	T4 LYSOZYME CORE REPACKING BACK-REVERTANT L102M/CORE10	3.2.1.17
1P3C	GLUTAMYL ENDOPEPTIDASE FROM BACILLUS INTERMEDIUS	3.4.21
1P3E	STRUCTURE OF GLU ENDOPEPTIDASE IN COMPLEX WITH MPD	3.4.21
1P3N	CORE REDESIGN BACK-REVERTANT I103V/CORE10	3.2.1.17
1P42	CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS LPXC DEACETYLASE (ZINC-INHIBITED FORM)	3.5.1 3.5.1.108
1P46	T4 LYSOZYME CORE REPACKING MUTANT M106I/TA	3.2.1.17
1P49	STRUCTURE OF HUMAN PLACENTAL ESTRONE/DHEA SULFATASE	3.1.6.2
1P4D	F FACTOR TRAI RELAXASE DOMAIN	3.6.1 5.6.2.1 3.6.4.12
1P4K	CRYSTAL STRUCTURE OF THE GLYCOSYLASPARAGINASE PRECURSOR D151N MUTANT	3.5.1.26
1P4R	CRYSTAL STRUCTURE OF HUMAN ATIC IN COMPLEX WITH FOLATE-BASED INHIBITOR BW1540U88UD	2.1.2.3 3.5.4.10
1P4V	CRYSTAL STRUCTURE OF THE GLYCOSYLASPARAGINASE PRECURSOR D151N MUTANT WITH GLYCINE	3.5.1.26
1P56	DUPLICATION-EXTENSION OF HELIX A OF T4 LYSOZYME	3.2.1.17
1P57	EXTRACELLULAR DOMAIN OF HUMAN HEPSIN	3.4.21 3.4.21.106
1P58	COMPLEX ORGANIZATION OF DENGUE VIRUS MEMBRANE PROTEINS AS REVEALED BY 9.5 ANGSTROM CRYO-EM RECONSTRUCTION	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
1P5C	CIRCULAR PERMUTATION OF HELIX A IN T4 LYSOZYME	3.2.1.17
1P5F	CRYSTAL STRUCTURE OF HUMAN DJ-1	3.1.2 3.5.1 3.5.1.124
1P5X	STRUCTURE OF THE D55N MUTANT OF PHOSPHOLIPASE C FROM BACILLUS CEREUS	3.1.4.3
1P64	T4 LYSOZYME CORE REPACKING MUTANT L133F/TA	3.2.1.17
1P6B	X-RAY STRUCTURE OF PHOSPHOTRIESTERASE, TRIPLE MUTANT H254G/H257W/L303T	3.1.8.1
1P6C	CRYSTAL STRUCTURE OF PHOSPHOTRIESTERASE TRIPLE MUTANT H254G/H257W/L303T COMPLEXED WITH DIISOPROPYLMETHYLPHOSPHONATE	3.1.8.1
1P6D	STRUCTURE OF THE D55N MUTANT OF PHOSPHOLIPASE C FROM BACILLUS CEREUS IN COMPLEX WITH (3S)-3,4,DI-N-HEXANOYLOXYBUTYL-1-PHOSPHOCHOLINE	3.1.4.3
1P6E	STRUCTURE OF THE D55N MUTANT OF PHOSPHOLIPASE C FROM BACILLUS CEREUS IN COMPLEX WITH 1,2-DI-N-PENTANOYL-SN-GLYCERO-3-DITHIOPHOSPHOCHOLINE	3.1.4.3
1P6O	THE CRYSTAL STRUCTURE OF YEAST CYTOSINE DEAMINASE BOUND TO 4(R)-HYDROXYL-3,4-DIHYDROPYRIMIDINE AT 1.14 ANGSTROMS.	3.5.4.1
1P6T	STRUCTURE CHARACTERIZATION OF THE WATER SOLUBLE REGION OF P-TYPE ATPASE COPA FROM BACILLUS SUBTILIS	3.6.3.4 7.2.2.8
1P6W	CRYSTAL STRUCTURE OF BARLEY ALPHA-AMYLASE ISOZYME 1 (AMY1) IN COMPLEX WITH THE SUBSTRATE ANALOGUE, METHYL 4I,4II,4III-TRI-THIOMALTOTETRAOSIDE (THIO-DP4)	3.2.1.1
1P6Y	T4 LYSOZYME CORE REPACKING MUTANT M120Y/TA	3.2.1.17
1P7D	CRYSTAL STRUCTURE OF THE LAMBDA INTEGRASE (RESIDUES 75-356) BOUND TO DNA	2.7.7 3.1
1P7M	SOLUTION STRUCTURE AND BASE PERTURBATION STUDIES REVEAL A NOVEL MODE OF ALKYLATED BASE RECOGNITION BY 3-METHYLADENINE DNA GLYCOSYLASE I	3.2.2.20
1P7N	DIMERIC ROUS SARCOMA VIRUS CAPSID PROTEIN STRUCTURE WITH AN UPSTREAM 25-AMINO ACID RESIDUE EXTENSION OF C-TERMINAL OF GAG P10 PROTEIN	3.4.23
1P7O	CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 (MIPLA4) FROM MICROPECHIS IKAHEKA	3.1.1.4
1P7S	T4 LYSOZYME CORE REPACKING MUTANT V103I/TA	3.2.1.17
1P7V	STRUCTURE OF A COMPLEX FORMED BETWEEN PROTEINASE K AND A DESIGNED HEPTAPEPTIDE INHIBITOR PRO-ALA-PRO-PHE-ALA-ALA-ALA AT ATOMIC RESOLUTION	3.4.21.64
1P7W	CRYSTAL STRUCTURE OF THE COMPLEX OF PROTEINASE K WITH A DESIGNED HEPTAPEPTIDE INHIBITOR PRO-ALA-PRO-PHE-ALA-SER-ALA AT ATOMIC RESOLUTION	3.4.21.64
1P8A	SOLUTION STRUCTURE OF THE LOW MOLECULAR WEIGHT PROTEIN TYROSINE PHOSPHATASE FROM TRITRICHOMONAS FOETUS	3.1.3.48 3.1.3.2
1P8M	STRUCTURAL AND FUNCTIONAL IMPORTANCE OF FIRST-SHELL METAL LIGANDS IN THE BINUCLEAR MANGANESE CLUSTER OF ARGINASE I.	3.5.3.1
1P8N	STRUCTURAL AND FUNCTIONAL IMPORTANCE OF FIRST-SHELL METAL LIGANDS IN THE BINUCLEAR MANGANESE CLUSTER OF ARGINASE I.	3.5.3.1
1P8O	STRUCTURAL AND FUNCTIONAL IMPORTANCE OF FIRST-SHELL METAL LIGANDS IN THE BINUCLEAR MANGANESE CLUSTER OF ARGINASE I.	3.5.3.1
1P8P	STRUCTURAL AND FUNCTIONAL IMPORTANCE OF FIRST-SHELL METAL LIGANDS IN THE BINUCLEAR MANGANESE CLUSTER OF ARGINASE I.	3.5.3.1
1P8Q	STRUCTURAL AND FUNCTIONAL IMPORTANCE OF FIRST-SHELL METAL LIGANDS IN THE BINUCLEAR CLUSTER OF ARGINASE I.	3.5.3.1
1P8R	STRUCTURAL AND FUNCTIONAL IMPORTANCE OF FIRST-SHELL METAL LIGANDS IN THE BINUCLEAR MANGANESE CLUSTER OF ARGINASE I.	3.5.3.1
1P8S	STRUCTURAL AND FUNCTIONAL IMPORTANCE OF FIRST-SHELL METAL LIGANDS IN THE BINUCLEAR MANGANESE CLUSTER OF ARGINASE I.	3.5.3.1
1P9E	CRYSTAL STRUCTURE ANALYSIS OF METHYL PARATHION HYDROLASE FROM PSEUDOMONAS SP WBC-3	3.1.8.1
1P9S	CORONAVIRUS MAIN PROTEINASE (3CLPRO) STRUCTURE: BASIS FOR DESIGN OF ANTI-SARS DRUGS	3.4.24 3.4.19.12 3.4.22
1P9U	CORONAVIRUS MAIN PROTEINASE (3CLPRO) STRUCTURE: BASIS FOR DESIGN OF ANTI-SARS DRUGS	3.4.19.12 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 3.1.13 3.1 2.1.1
1PA0	CRYSTAL STRUCTURE OF BNSP-7, A LYS49-PHOSPHOLIPASE A2	3.1.1.4
1PA1	CRYSTAL STRUCTURE OF THE C215D MUTANT OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
1PA9	YERSINIA PROTEIN-TYROSINE PHOSPHATASE COMPLEXED WITH PNCS (YOP51,PASTEURELLA X,PTPASE,YOP51DELTA162) (CATALYTIC DOMAIN, RESIDUES 163-468) MUTANT WITH CYS 235 REPLACED BY ARG (C235R)	3.1.3.48
1PAD	BINDING OF CHLOROMETHYL KETONE SUBSTRATE ANALOGUES TO CRYSTALLINE PAPAIN	3.4.22.2
1PAF	THE 2.5 ANGSTROMS STRUCTURE OF POKEWEED ANTIVIRAL PROTEIN	3.2.2.22
1PAG	THE 2.5 ANGSTROMS STRUCTURE OF POKEWEED ANTIVIRAL PROTEIN	3.2.2.22
1PAU	CRYSTAL STRUCTURE OF THE COMPLEX OF APOPAIN WITH THE TETRAPEPTIDE ALDEHYDE INHIBITOR AC-DEVD-CHO	3.4.22 3.4.22.56
1PB0	YCDX PROTEIN IN AUTOINHIBITED STATE	3.1.3
1PBA	THE NMR STRUCTURE OF THE ACTIVATION DOMAIN ISOLATED FROM PORCINE PROCARBOXYPEPTIDASE B	3.4.17.2
1PBG	THE THREE-DIMENSIONAL STRUCTURE OF 6-PHOSPHO-BETA GALACTOSIDASE FROM LACTOCOCCUS LACTIS	3.2.1.85
1PBH	CRYSTAL STRUCTURE OF HUMAN RECOMBINANT PROCATHEPSIN B AT 3.2 ANGSTROM RESOLUTION	3.4.22.1
1PBT	THE CRYSTAL STRUCTURE OF TM1154, OXIDOREDUCTASE, SOL/DEVB FAMILY FROM THERMOTOGA MARITIMA	3.1.1.31
1PC0	NMR STRUCTURE OF THE ARCHAEAL HOMOLOGUE OF RNASE P PROTEIN RPP29	3.1.26.5
1PC8	CRYSTAL STRUCTURE OF A NOVEL FORM OF MISTLETOE LECTIN FROM HIMALAYAN VISCUM ALBUM L. AT 3.8A RESOLUTION	3.2.2.22
1PC9	CRYSTAL STRUCTURE OF BNSP-6, A LYS49-PHOSPHOLIPASE A2	3.1.1.4
1PCA	THREE DIMENSIONAL STRUCTURE OF PORCINE PANCREATIC PROCARBOXYPEPTIDASE A. A COMPARISON OF THE A AND B ZYMOGENS AND THEIR DETERMINANTS FOR INHIBITION AND ACTIVATION	3.4.17.1
1PCI	PROCARICAIN	3.4.22.6 3.4.22.30
1PDV	CRYSTAL STRUCTURE OF HUMAN DJ-1, P 31 2 1 SPACE GROUP	3.1.2 3.5.1 3.5.1.124
1PDW	CRYSTAL STRUCTURE OF HUMAN DJ-1, P 1 21 1 SPACE GROUP	3.1.2 3.5.1 3.5.1.124
1PE0	CRYSTAL STRUCTURE OF THE K130R MUTANT OF HUMAN DJ-1	3.1.2 3.5.1 3.5.1.124
1PE5	THERMOLYSIN WITH TRICYCLIC INHIBITOR	3.4.24.27
1PE6	REFINED X-RAY STRUCTURE OF PAPAIN(DOT)E-64-C COMPLEX AT 2.1-ANGSTROMS RESOLUTION	3.4.22.2
1PE7	THERMOLYSIN WITH BICYCLIC INHIBITOR	3.4.24.27
1PE8	THERMOLYSIN WITH MONOCYCLIC INHIBITOR	3.4.24.27
1PEX	COLLAGENASE-3 (MMP-13) C-TERMINAL HEMOPEXIN-LIKE DOMAIN	3.4.24
1PFG	STRATEGY TO DESIGN INHIBITORS: STRUCTURE OF A COMPLEX OF PROTEINASE K WITH A DESIGNED OCTAPEPTIDE INHIBITOR N-AC-PRO-ALA-PRO-PHE-DALA-ALA-ALA-ALA-NH2 AT 2.5A RESOLUTION	3.4.21.64
1PFQ	CRYSTAL STRUCTURE OF HUMAN APO DIPEPTIDYL PEPTIDASE IV / CD26	3.4.14.5
1PFX	PORCINE FACTOR IXA	3.4.21.22
1PFZ	PROPLASMEPSIN II FROM PLASMODIUM FALCIPARUM	3.4.23.39
1PGS	THE THREE-DIMENSIONAL STRUCTURE OF PNGASE F, A GLYCOSYLASPARAGINASE FROM FLAVOBACTERIUM MENINGOSEPTICUM	3.5.1.52
1PH0	NON-CARBOXYLIC ACID-CONTAINING INHIBITOR OF PTP1B TARGETING THE SECOND PHOSPHOTYROSINE SITE	3.1.3.48
1PHR	THE CRYSTAL STRUCTURE OF A LOW MOLECULAR PHOSPHOTYROSINE PROTEIN PHOSPHATASE	3.1.3.48 3.1.3.2
1PI4	STRUCTURE OF N289A MUTANT OF AMPC IN COMPLEX WITH SM3, A PHENYLGLYCLBORONIC ACID BEARING THE CEPHALOTHIN R1 SIDE CHAIN	3.5.2.6
1PI5	STRUCTURE OF N289A MUTANT OF AMPC IN COMPLEX WITH SM2, CARBOXYPHENYLGLYCYLBORONIC ACID BEARING THE CEPHALOTHIN R1 SIDE CHAIN	3.5.2.6
1PIF	PIG ALPHA-AMYLASE	3.2.1.1
1PIG	PIG PANCREATIC ALPHA-AMYLASE COMPLEXED WITH THE OLIGOSACCHARIDE V-1532	3.2.1.1
1PIO	AN ENGINEERED STAPHYLOCOCCUS AUREUS PC1 BETA-LACTAMASE THAT HYDROLYSES THIRD GENERATION CEPHALOSPORINS	3.5.2.6
1PIP	CRYSTAL STRUCTURE OF PAPAIN-SUCCINYL-GLN-VAL-VAL-ALA-ALA-P-NITROANILIDE COMPLEX AT 1.7 ANGSTROMS RESOLUTION: NONCOVALENT BINDING MODE OF A COMMON SEQUENCE OF ENDOGENOUS THIOL PROTEASE INHIBITORS	3.4.22.2
1PIR	SOLUTION STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2	3.1.1.4
1PIS	SOLUTION STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2	3.1.1.4
1PJ8	STRUCTURE OF A TERNARY COMPLEX OF PROTEINASE K, MERCURY AND A SUBSTRATE-ANALOGUE HEXAPEPTIDE AT 2.2 A RESOLUTION	3.4.21.64
1PJA	THE CRYSTAL STRUCTURE OF PALMITOYL PROTEIN THIOESTERASE-2 REVEALS THE BASIS FOR DIVERGENT SUBSTRATE SPECIFICITIES OF THE TWO LYSOSOMAL THIOESTERASES (PPT1 AND PPT2)	3.1.2.22 3.1.2
1PJI	CRYSTAL STRUCTURE OF WILD TYPE LACTOCOCCUS LACTIS FPG COMPLEXED TO A 1,3 PROPANEDIOL CONTAINING DNA	3.2.2.23 4.2.99.18
1PJJ	COMPLEX BETWEEN THE LACTOCOCCUS LACTIS FPG AND AN ABASIC SITE CONTAINING DNA.	3.2.2.23 4.2.99.18
1PJP	THE 2.2 A CRYSTAL STRUCTURE OF HUMAN CHYMASE IN COMPLEX WITH SUCCINYL-ALA-ALA-PRO-PHE-CHLOROMETHYLKETONE	3.4.21.39
1PJR	STRUCTURE OF DNA HELICASE	3.6.4.12
1PJW	SOLUTION STRUCTURE OF THE DOMAIN III OF THE JAPAN ENCEPHALITIS VIRUS ENVELOPE PROTEIN	3.4.21.91 3.6.1.15 3.6.4.13
1PJX	0.85 ANGSTROM STRUCTURE OF SQUID GANGLION DFPASE	3.1.8.2
1PK2	SOLUTION STRUCTURE OF THE TISSUE-TYPE PLASMINOGEN ACTIVATOR KRINGLE 2 DOMAIN COMPLEXED TO 6-AMINOHEXANOIC ACID AN ANTIFIBRINOLYTIC DRUG	3.4.21.68
1PK4	CRYSTAL AND MOLECULAR STRUCTURE OF HUMAN PLASMINOGEN KRINGLE 4 REFINED AT 1.9-ANGSTROMS RESOLUTION	3.4.21.7
1PKH	STRUCTURAL BASIS FOR RECOGNITION AND CATALYSIS BY THE BIFUNCTIONAL DCTP DEAMINASE AND DUTPASE FROM METHANOCOCCUS JANNASCHII	3.5.4.13 3.6.1.23 3.5.4.30
1PKJ	STRUCTURAL BASIS FOR RECOGNITION AND CATALYSIS BY THE BIFUNCTIONAL DCTP DEAMINASE AND DUTPASE FROM METHANOCOCCUS JANNASCHII	3.5.4.13 3.6.1.23 3.5.4.30
1PKK	STRUCTURAL BASIS FOR RECOGNITION AND CATALYSIS BY THE BIFUNCTIONAL DCTP DEAMINASE AND DUTPASE FROM METHANOCOCCUS JANNASCHII	3.5.4.13 3.6.1.23 3.5.4.30
1PKR	THE STRUCTURE OF RECOMBINANT PLASMINOGEN KRINGLE 1 AND THE FIBRIN BINDING SITE	3.4.21.7
1PKX	CRYSTAL STRUCTURE OF HUMAN ATIC IN COMPLEX WITH XMP	2.1.2.3 3.5.4.10
1PL0	CRYSTAL STRUCTURE OF HUMAN ATIC IN COMPLEX WITH FOLATE-BASED INHIBITOR, BW2315U89UC	2.1.2.3 3.5.4.10
1PLJ	CRYSTALLOGRAPHIC STUDIES ON P21H-RAS USING SYNCHROTRON LAUE METHOD: IMPROVEMENT OF CRYSTAL QUALITY AND MONITORING OF THE GTPASE REACTION AT DIFFERENT TIME POINTS	3.6.5.2
1PLK	CRYSTALLOGRAPHIC STUDIES ON P21H-RAS USING SYNCHROTRON LAUE METHOD: IMPROVEMENT OF CRYSTAL QUALITY AND MONITORING OF THE GTPASE REACTION AT DIFFERENT TIME POINTS	3.6.5.2
1PLL	CRYSTALLOGRAPHIC STUDIES ON P21H-RAS USING SYNCHROTRON LAUE METHOD: IMPROVEMENT OF CRYSTAL QUALITY AND MONITORING OF THE GTPASE REACTION AT DIFFERENT TIME POINTS	3.6.5.2
1PM5	CRYSTAL STRUCTURE OF WILD TYPE LACTOCOCCUS LACTIS FPG COMPLEXED TO A TETRAHYDROFURAN CONTAINING DNA	3.2.2.23 4.2.99.18
1PMH	CRYSTAL STRUCTURE OF CALDICELLULOSIRUPTOR SACCHAROLYTICUS CBM27-1 IN COMPLEX WITH MANNOHEXAOSE	3.2.1.78
1PMJ	CRYSTAL STRUCTURE OF CALDICELLULOSIRUPTOR SACCHAROLYTICUS CBM27-1	3.2.1.78
1PMK	KRINGLE-KRINGLE INTERACTIONS IN MULTIMER KRINGLE STRUCTURES	3.4.21.7
1PML	KRINGLE-KRINGLE INTERACTIONS IN MULTIMER KRINGLE STRUCTURES	3.4.21.68
1PNF	PNGASE F COMPLEX WITH DI-N-ACETYLCHITOBIOSE	3.5.1.52
1PNG	CRYSTAL STRUCTURE OF PEPTIDE-N(4)-(N-ACETYL-BETA-D-GLUCOSAMINYL) ASPARAGINE AMIDASE AT 2.2 ANGSTROMS RESOLUTION	3.5.1.52
1PNK	PENICILLIN ACYLASE HAS A SINGLE-AMINO-ACID CATALYTIC CENTRE	3.5.1.11
1PNL	PENICILLIN ACYLASE HAS A SINGLE-AMINO-ACID CATALYTIC CENTRE	3.5.1.11
1PNM	PENICILLIN ACYLASE HAS A SINGLE-AMINO-ACID CATALYTIC CENTRE	3.5.1.11
1PNT	CRYSTAL STRUCTURE OF BOVINE HEART PHOSPHOTYROSYL PHOSPHATASE AT 2.2 ANGSTROMS RESOLUTION	3.1.3.2 3.1.3.48
1PO8	CRYSTAL STRUCTURE OF A COMPLEX FORMED BETWEEN KRAIT VENOM PHOSPHOLIPASE A2 AND HEPTANOIC ACID AT 2.7 A RESOLUTION.	3.1.1.4
1PO9	CRYTSAL STRUCTURE OF ISOASPARTYL DIPEPTIDASE	3.4.19
1POA	INTERFACIAL CATALYSIS: THE MECHANISM OF PHOSPHOLIPASE A2	3.1.1.4
1POB	CRYSTAL STRUCTURE OF COBRA-VENOM PHOSPHOLIPASE A2 IN A COMPLEX WITH A TRANSITION-STATE ANALOGUE	3.1.1.4
1POC	CRYSTAL STRUCTURE OF BEE-VENOM PHOSPHOLIPASE A2 IN A COMPLEX WITH A TRANSITION-STATE ANALOGUE	3.1.1.4
1POD	STRUCTURES OF FREE AND INHIBITED HUMAN SECRETORY PHOSPHOLIPASE A2 FROM INFLAMMATORY EXUDATE	3.1.1.4
1POE	STRUCTURES OF FREE AND INHIBITED HUMAN SECRETORY PHOSPHOLIPASE A2 FROM INFLAMMATORY EXUDATE	3.1.1.4
1POJ	ISOASPARTYL DIPEPTIDASE WITH BOUND INHIBITOR	3.4.19
1POK	CRYSTAL STRUCTURE OF ISOASPARTYL DIPEPTIDASE	3.4.19
1POO	THERMOSTABLE PHYTASE FROM BACILLUS SP	3.1.3.8
1POP	X-RAY CRYSTALLOGRAPHIC STRUCTURE OF A PAPAIN-LEUPEPTIN COMPLEX	3.4.22.2
1POV	ROLE AND MECHANISM OF THE MATURATION CLEAVAGE OF VP0 IN POLIOVIRUS ASSEMBLY: STRUCTURE OF THE EMPTY CAPSID ASSEMBLY INTERMEDIATE AT 2.9 ANGSTROMS RESOLUTION	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1PP2	THE REFINED CRYSTAL STRUCTURE OF DIMERIC PHOSPHOLIPASE A2 AT 2.5 ANGSTROMS. ACCESS TO A SHIELDED CATALYTIC CENTER	3.1.1.4
1PP4	THE CRYSTAL STRUCTURE OF RHAMNOGALACTURONAN ACETYLESTERASE IN SPACE GROUP P3121	3.1.1 3.1.1.86
1PPA	THE CRYSTAL STRUCTURE OF A LYSINE 49 PHOSPHOLIPASE A2 FROM THE VENOM OF THE COTTONMOUTH SNAKE AT 2.0 ANGSTROMS RESOLUTION	3.1.1.4
1PPB	THE REFINED 1.9 ANGSTROMS CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN: INTERACTION WITH D-PHE-PRO-ARG CHLOROMETHYLKETONE AND SIGNIFICANCE OF THE TYR-PRO-PRO-TRP INSERTION SEGMENT	3.4.21.5
1PPC	GEOMETRY OF BINDING OF THE BENZAMIDINE-AND ARGININE-BASED INHIBITORS N-ALPHA-(2-NAPHTHYL-SULPHONYL-GLYCYL)-DL-P-AMIDINOPHENYLALANYL-PIPERIDINE (NAPAP) AND (2R,4R)-4-METHYL-1-[N-ALPHA-(3-METHYL-1,2,3,4-TETRAHYDRO-8-QUINOLINESULPHONYL)-L-ARGINYL]-2-PIPERIDINE CARBOXYLIC ACID (MQPA) TO HUMAN ALPHA-THROMBIN: X-RAY CRYSTALLOGRAPHIC DETERMINATION OF THE NAPAP-TRYPSIN COMPLEX AND MODELING OF NAPAP-THROMBIN AND MQPA-THROMBIN	3.4.21.4
1PPD	RESTRAINED LEAST-SQUARES REFINEMENT OF THE SULFHYDRYL PROTEASE PAPAIN TO 2.0 ANGSTROMS	3.4.22.2
1PPE	THE REFINED 2.0 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN BOVINE BETA-TRYPSIN AND CMTI-I, A TRYPSIN INHIBITOR FROM SQUASH SEEDS (CUCURBITA MAXIMA): TOPOLOGICAL SIMILARITY OF THE SQUASH SEED INHIBITORS WITH THE CARBOXYPEPTIDASE A INHIBITOR FROM POTATOES	3.4.21.4
1PPF	X-RAY CRYSTAL STRUCTURE OF THE COMPLEX OF HUMAN LEUKOCYTE ELASTASE (PMN ELASTASE) AND THE THIRD DOMAIN OF THE TURKEY OVOMUCOID INHIBITOR	3.4.21.37
1PPG	THE REFINED 2.3 ANGSTROMS CRYSTAL STRUCTURE OF HUMAN LEUKOCYTE ELASTASE IN A COMPLEX WITH A VALINE CHLOROMETHYL KETONE INHIBITOR	3.4.21.37
1PPH	GEOMETRY OF BINDING OF THE NALPHA-TOSYLATED PIPERIDIDES OF M-AMIDINO-, P-AMIDINO-AND P-GUANIDINO PHENYLALANINE TO THROMBIN AND TRYPSIN: X-RAY CRYSTAL STRUCTURES OF THEIR TRYPSIN COMPLEXES AND MODELING OF THEIR THROMBIN COMPLEXES	3.4.21.4
1PPI	THE ACTIVE CENTER OF A MAMMALIAN ALPHA-AMYLASE. THE STRUCTURE OF THE COMPLEX OF A PANCREATIC ALPHA-AMYLASE WITH A CARBOHYDRATE INHIBITOR REFINED TO 2.2 ANGSTROMS RESOLUTION	3.2.1.1
1PPK	CRYSTALLOGRAPHIC ANALYSIS OF TRANSITION STATE MIMICS BOUND TO PENICILLOPEPSIN: PHOSPHOROUS-CONTAINING PEPTIDE ANALOGUES	3.4.23.20
1PPL	CRYSTALLOGRAPHIC ANALYSIS OF TRANSITION-STATE MIMICS BOUND TO PENICILLOPEPSIN: PHOSPHORUS-CONTAINING PEPTIDE ANALOGUES	3.4.23.20
1PPM	CRYSTALLOGRAPHIC ANALYSIS OF TRANSITION-STATE MIMICS BOUND TO PENICILLOPEPSIN: PHOSPHORUS-CONTAINING PEPTIDE ANALOGUES	3.4.23.20
1PPN	STRUCTURE OF MONOCLINIC PAPAIN AT 1.60 ANGSTROMS RESOLUTION	3.4.22.2
1PPO	DETERMINATION OF THE STRUCTURE OF PAPAYA PROTEASE OMEGA	3.4.22.30
1PPP	CRYSTAL STRUCTURE OF PAPAIN-E64-C COMPLEX. BINDING DIVERSITY OF E64-C TO PAPAIN S2 AND S3 SUBSITES	3.4.22.2
1PPX	SOLUTION STRUCTURE OF THE MUTT PYROPHOSPHOHYDROLASE COMPLEXED WITH MG(2+) AND 8-OXO-DGMP, A TIGHTLY-BOUND PRODUCT	3.6.1 3.6.1.55
1PPZ	TRYPSIN COMPLEXES AT ATOMIC AND ULTRA-HIGH RESOLUTION	3.4.21.4
1PQ3	HUMAN ARGINASE II: CRYSTAL STRUCTURE AND PHYSIOLOGICAL ROLE IN MALE AND FEMALE SEXUAL AROUSAL	3.5.3.1
1PQ5	TRYPSIN AT PH 5, 0.85 A	3.4.21.4
1PQ7	TRYPSIN AT 0.8 A, PH5 / BORAX	3.4.21.4
1PQ8	TRYPSIN AT PH 4 AT ATOMIC RESOLUTION	3.4.21.4
1PQA	TRYPSIN WITH PMSF AT ATOMIC RESOLUTION	3.4.21.4
1PQD	T4 LYSOZYME CORE REPACKING MUTANT CORE10/TA	3.2.1.17
1PQI	T4 LYSOZYME CORE REPACKING MUTANT I118L/CORE7/TA	3.2.1.17
1PQJ	T4 LYSOZYME CORE REPACKING MUTANT A111V/CORE10/TA	3.2.1.17
1PQK	REPACKING OF THE CORE OF T4 LYSOZYME BY AUTOMATED DESIGN	3.2.1.17
1PQM	T4 LYSOZYME CORE REPACKING MUTANT V149I/T152V/TA	3.2.1.17
1PQO	T4 LYSOZYME CORE REPACKING MUTANT L118I/TA	3.2.1.17
1PRO	HIV-1 PROTEASE DIMER COMPLEXED WITH A-98881	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1PRX	HORF6 A NOVEL HUMAN PEROXIDASE ENZYME	1.11.1.27 3.1.1.4 2.3.1.23
1PS3	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH KIFUNENSINE	3.2.1.114
1PS5	STRUCTURE OF THE MONOCLINIC C2 FORM OF HEN EGG-WHITE LYSOZYME AT 2.0 ANGSTROMS RESOLUTION	3.2.1.17
1PSA	STRUCTURE OF A PEPSIN(SLASH)RENIN INHIBITOR COMPLEX REVEALS A NOVEL CRYSTAL PACKING INDUCED BY MINOR CHEMICAL ALTERATIONS IN THE INHIBITOR	3.4.23.1
1PSC	PHOSPHOTRIESTERASE FROM PSEUDOMONAS DIMINUTA	3.1.8.1
1PSH	CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 FROM INDIAN COBRA REVEALS A TRIMERIC ASSOCIATION	3.1.1.4
1PSJ	ACIDIC PHOSPHOLIPASE A2 FROM AGKISTRODON HALYS PALLAS	3.1.1.4
1PSN	THE CRYSTAL STRUCTURE OF HUMAN PEPSIN AND ITS COMPLEX WITH PEPSTATIN	3.4.23.1
1PSO	THE CRYSTAL STRUCTURE OF HUMAN PEPSIN AND ITS COMPLEX WITH PEPSTATIN	3.4.23.1
1PSU	STRUCTURE OF THE E. COLI PAAI PROTEIN FROM THE PHYENYLACETIC ACID DEGRADATION OPERON	3.1.2
1PT3	CRYSTAL STRUCTURES OF NUCLEASE-COLE7 COMPLEXED WITH OCTAMER DNA	3.1
1PTA	THREE-DIMENSIONAL STRUCTURE OF PHOSPHOTRIESTERASE: AN ENZYME CAPABLE OF DETOXIFYING ORGANOPHOSPHATE NERVE AGENTS	3.5 3.1.8.1
1PTD	PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C	3.1.4.10 4.6.1.13
1PTG	PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C IN COMPLEX WITH MYO-INOSITOL	3.1.4.10 4.6.1.13
1PTK	STUDIES ON THE INHIBITORY ACTION OF MERCURY UPON PROTEINASE K	3.4.21.64
1PTT	CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH PHOSPHOTYROSINE-CONTAINING TETRA-PEPTIDE (AC-DEPYL-NH2)	3.1.3.48
1PTU	CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH PHOSPHOTYROSINE-CONTAINING HEXA-PEPTIDE (DADEPYL-NH2)	3.1.3.48
1PTV	CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH PHOSPHOTYROSINE	3.1.3.48
1PTW	THE CRYSTAL STRUCTURE OF AMP-BOUND PDE4 SUGGESTS A MECHANISM FOR PHOSPHODIESTERASE CATALYSIS	3.1.4.17 3.1.4.53
1PTY	CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH TWO PHOSPHOTYROSINE MOLECULES	3.1.3.48
1PU3	THE SOLUTION NMR STRUCTURE AND DYNAMICS OF A RECOMBINANT ONCONASE WITH ALTERED N-TERMINAL AND MET23 RESIDUES	3.1.27
1PUM	MISTLETOE LECTIN I IN COMPLEX WITH GALACTOSE	3.2.2.22
1PUN	SOLUTION STRUCTURE OF THE MUTT PYROPHOSPHOHYDROLASE COMPLEXED WITH MG(2+) AND 8-OXO-DGMP, A TIGHTLY-BOUND PRODUCT	3.6.1 3.6.1.55
1PUQ	SOLUTION STRUCTURE OF THE MUTT PYROPHOSPHOHYDROLASE COMPLEXED WITH MG(2+) AND 8-OXO-DGMP, A TIGHTLY-BOUND PRODUCT	3.6.1 3.6.1.55
1PUS	SOLUTION STRUCTURE OF THE MUTT PYROPHOSPHOHYDROLASE COMPLEXED WITH MG(2+) AND 8-OXO-DGMP, A TIGHTLY-BOUND PRODUCT	3.6.1 3.6.1.55
1PUU	MISTLETOE LECTIN I IN COMPLEX WITH LACTOSE	3.2.2.22
1PV1	CRYSTAL STRUCTURE ANALYSIS OF YEAST HYPOTHETICAL PROTEIN: YJG8_YEAST	3.1.1 3.1.2.12
1PV2	NATIVE FORM 2 E.COLI CHAPERONE HSP31	3.1.2 3.5.1 3.5.1.124 4.2.1.130
1PV9	PROLIDASE FROM PYROCOCCUS FURIOSUS	3.4.13.9
1PVI	STRUCTURE OF PVUII ENDONUCLEASE WITH COGNATE DNA	3.1.21.4
1PVJ	CRYSTAL STRUCTURE OF THE STREPTOCOCCAL PYROGENIC EXOTOXIN B (SPEB)- INHIBITOR COMPLEX	3.4.22.10
1PVS	3-METHYLADENINE GLCOSYLASE II(ALKA) HYPOXANTHINE COMPLEX	3.2.2.21
1PVU	THE CRYSTAL STRUCTURE OF PVUII ENDONUCLEASE REVEALS EXTENSIVE STRUCTURAL HOMOLOGIES TO ECORV	3.1.21.4
1PVX	DO-1,4-BETA-XYLANASE, ROOM TEMPERATURE, PH 4.5	3.2.1.8
1PW1	NON-COVALENT COMPLEX OF STREPTOMYCES R61 DD-PEPTIDASE WITH A HIGHLY SPECIFIC PENICILLIN	3.4.16.4
1PW8	COVALENT ACYL ENZYME COMPLEX OF THE R61 DD-PEPTIDASE WITH A HIGHLY SPECIFIC CEPHALOSPORIN	3.4.16.4
1PWC	PENICILLOYL ACYL ENZYME COMPLEX OF THE STREPTOMYCES R61 DD-PEPTIDASE WITH PENICILLIN G	3.4.16.4
1PWD	COVALENT ACYL ENZYME COMPLEX OF THE STREPTOMYCES R61 DD-PEPTIDASE WITH CEPHALOSPORIN C	3.4.16.4
1PWG	COVALENT PENICILLOYL ACYL ENZYME COMPLEX OF THE STREPTOMYCES R61 DD-PEPTIDASE WITH A HIGHLY SPECIFIC PENICILLIN	3.4.16.4
1PWO	CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 (MIPLA2) FROM MICROPECHIS IKAHEKA	3.1.1.4
1PWP	CRYSTAL STRUCTURE OF THE ANTHRAX LETHAL FACTOR COMPLEXED WITH SMALL MOLECULE INHIBITOR NSC 12155	3.4.24.83
1PWQ	CRYSTAL STRUCTURE OF ANTHRAX LETHAL FACTOR COMPLEXED WITH THIOACETYL-TYR-PRO-MET-AMIDE, A METAL-CHELATING PEPTIDYL SMALL MOLECULE INHIBITOR	3.4.24.83
1PWU	CRYSTAL STRUCTURE OF ANTHRAX LETHAL FACTOR COMPLEXED WITH (3-(N-HYDROXYCARBOXAMIDO)-2-ISOBUTYLPROPANOYL-TRP-METHYLAMIDE), A KNOWN SMALL MOLECULE INHIBITOR OF MATRIX METALLOPROTEASES.	3.4.24 3.4.24.83
1PWV	CRYSTAL STRUCTURE OF ANTHRAX LETHAL FACTOR WILD-TYPE PROTEIN COMPLEXED WITH AN OPTIMISED PEPTIDE SUBSTRATE.	3.4.24 3.4.24.83
1PWW	CRYSTAL STRUCTURE OF ANTHRAX LETHAL FACTOR ACTIVE SITE MUTANT PROTEIN COMPLEXED WITH AN OPTIMISED PEPTIDE SUBSTRATE IN THE PRESENCE OF ZINC.	3.4.24 3.4.24.83
1PX8	CRYSTAL STRUCTURE OF BETA-D-XYLOSIDASE FROM THERMOANAEROBACTERIUM SACCHAROLYTICUM, A FAMILY 39 GLYCOSIDE HYDROLASE	3.2.1.37
1PXH	CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B WITH POTENT AND SELECTIVE BIDENTATE INHIBITOR COMPOUND 2	3.1.3.48
1PXV	THE STAPHOSTATIN-STAPHOPAIN COMPLEX: A FORWARD BINDING INHIBITOR IN COMPLEX WITH ITS TARGET CYSTEINE PROTEASE	3.4.22
1PYN	DUAL-SITE POTENT, SELECTIVE PROTEIN TYROSINE PHOSPHATASE 1B INHIBITOR USING A LINKED FRAGMENT STRATEGY AND A MALONATE HEAD ON THE FIRST SITE	3.1.3.48
1PYO	CRYSTAL STRUCTURE OF HUMAN CASPASE-2 IN COMPLEX WITH ACETYL-LEU-ASP-GLU-SER-ASP-CHO	3.4.22 3.4.22.55
1PYP	X-RAY DIFFRACTION STUDY OF INORGANIC PYROPHOSPHATASE FROM BAKER,S YEAST AT THE 3 ANGSTROMS RESOLUTION (RUSSIAN)	3.6.1.1
1PYT	TERNARY COMPLEX OF PROCARBOXYPEPTIDASE A, PROPROTEINASE E, AND CHYMOTRYPSINOGEN C	3.4.17.1
1PYV	NMR SOLUTION STRUCTURE OF THE MITOCHONDRIAL F1B PRESEQUENCE PEPTIDE FROM NICOTIANA PLUMBAGINIFOLIA	3.6.3.14 7.1.2.2
1PZ2	CRYSTAL STRUCTURE OF A TRANSIENT COVALENT REACTION INTERMEDIATE OF A FAMILY 51 ALPHA-L-ARABINOFURANOSIDASE	3.2.1.55
1PZ3	CRYSTAL STRUCTURE OF A FAMILY 51 (GH51) ALPHA-L-ARABINOFURANOSIDASE FROM GEOBACILLUS STEAROTHERMOPHILUS T6	3.2.1.55
1PZO	TEM-1 BETA-LACTAMASE IN COMPLEX WITH A NOVEL, CORE-DISRUPTING, ALLOSTERIC INHIBITOR	3.5.2.6
1PZP	TEM-1 BETA-LACTAMASE IN COMPLEX WITH A NOVEL, CORE-DISRUPTING, ALLOSTERIC INHIBITOR	3.5.2.6
1Q0P	A DOMAIN OF FACTOR B	3.4.21.47
1Q0R	CRYSTAL STRUCTURE OF ACLACINOMYCIN METHYLESTERASE (RDMC) WITH BOUND PRODUCT ANALOGUE, 10-DECARBOXYMETHYLACLACINOMYCIN T (DCMAT)	3.1.1.95
1Q0Z	CRYSTAL STRUCTURE OF ACLACINOMYCIN METHYLESTERASE (RDMC) WITH BOUND PRODUCT ANALOGUE, 10-DECARBOXYMETHYLACLACINOMYCIN A (DCMA)	3.1.1.95
1Q1M	A HIGHLY EFFICIENT APPROACH TO A SELECTIVE AND CELL ACTIVE PTP1B INHIBITORS	3.1.3.48
1Q1Y	CRYSTAL STRUCTURES OF PEPTIDE DEFORMYLASE FROM STAPHYLOCOCCUS AUREUS COMPLEXED WITH ACTINONIN	3.5.1.88
1Q21	CRYSTAL STRUCTURES AT 2.2 ANGSTROMS RESOLUTION OF THE CATALYTIC DOMAINS OF NORMAL RAS PROTEIN AND AN ONCOGENIC MUTANT COMPLEXED WITH GSP	3.6.5.2
1Q27	NMR SOLUTION STRUCTURE OF DR0079: AN HYPOTHETICAL NUDIX PROTEIN FROM D. RADIODURANS	3.6.1
1Q2B	CELLOBIOHYDROLASE CEL7A WITH DISULPHIDE BRIDGE ADDED ACROSS EXO-LOOP BY MUTATIONS D241C AND D249C	3.2.1.91
1Q2E	CELLOBIOHYDROLASE CEL7A WITH LOOP DELETION 245-252 AND BOUND NON-HYDROLYSABLE CELLOTETRAOSE	3.2.1.91
1Q2L	CRYSTAL STRUCTURE OF PITRILYSIN	3.4.24.55
1Q2P	SHV-1 CLASS A BETA-LACTAMASE COMPLEXED WITH PENEM WAY185229	3.5.2.6
1Q2Q	ENTEROBACTER CLOACAE GC1 CLASS C BETA-LACTAMASE COMPLEXED WITH PENEM WAY185229	3.5.2.6
1Q2U	CRYSTAL STRUCTURE OF DJ-1/RS AND IMPLICATION ON FAMILIAL PARKINSON'S DISEASE	3.1.2 3.5.1 3.5.1.124
1Q2V	CRYSTAL STRUCTURE OF THE CHAPERONIN FROM THERMOCOCCUS STRAIN KS-1 (NUCLEOTIDE-FREE FORM)	3.6.4.9
1Q2W	X-RAY CRYSTAL STRUCTURE OF THE SARS CORONAVIRUS MAIN PROTEASE	3.4.22 3.4.19.12 3.4.22.69
1Q2Z	THE 3D SOLUTION STRUCTURE OF THE C-TERMINAL REGION OF KU86	3.6.4
1Q31	CRYSTAL STRUCTURE OF THE TOBACCO ETCH VIRUS PROTEASE C151A MUTANT	3.4.22.44 3.4 3.4.22.45 3.6.4 2.7.7.48
1Q33	CRYSTAL STRUCTURE OF HUMAN ADP-RIBOSE PYROPHOSPHATASE NUDT9	3.6.1.13
1Q39	CRYSTAL STRUCTURE OF THE DNA REPAIR ENZYME ENDONUCLEASE-VIII (NEI) FROM E. COLI: THE WT ENZYME AT 2.8 RESOLUTION.	3.2.2 4.2.99.18
1Q3A	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MATRIX METALLOPROTEINASE 10	3.4.24.22
1Q3B	CRYSTAL STRUCTURE OF THE DNA REPAIR ENZYME ENDONUCLEASE-VIII (NEI) FROM E. COLI: THE R252A MUTANT AT 2.05 RESOLUTION.	3.2.2 4.2.99.18
1Q3C	CRYSTAL STRUCTURE OF THE DNA REPAIR ENZYME ENDONUCLEASE-VIII (NEI) FROM E. COLI: THE E2A MUTANT AT 2.3 RESOLUTION.	3.2.2 4.2.99.18
1Q3F	URACIL DNA GLYCOSYLASE BOUND TO A CATIONIC 1-AZA-2'-DEOXYRIBOSE-CONTAINING DNA	3.2.2 3.2.2.27
1Q3I	CRYSTAL STRUCTURE OF NA,K-ATPASE N-DOMAIN	3.6.3.9 7.2.2.13
1Q3K	CRYSTAL STRUCTURE OF CREATININE AMIDOHYDROLASE (CREATININASE)	3.5.2.10
1Q3Q	CRYSTAL STRUCTURE OF THE CHAPERONIN FROM THERMOCOCCUS STRAIN KS-1 (TWO-POINT MUTANT COMPLEXED WITH AMP-PNP)	3.6.4.9
1Q3R	CRYSTAL STRUCTURE OF THE CHAPERONIN FROM THERMOCOCCUS STRAIN KS-1 (NUCLEOTIDE-FREE FORM OF SINGLE MUTANT)	3.6.4.9
1Q3X	CRYSTAL STRUCTURE OF THE CATALYTIC REGION OF HUMAN MASP-2	3.4.21 3.4.21.104
1Q4N	STRUCTURAL STUDIES OF PHE256TRP OF HUMAN SALIVARY ALPHA-AMYLASE: IMPLICATIONS FOR THE ROLE OF A CONSERVED WATER MOLECULE AND ITS ASSOCIATED CHAIN IN ENZYME ACTIVITY	3.2.1.1
1Q4S	CRYSTAL STRUCTURE OF ARTHROBACTER SP. STRAIN SU 4-HYDROXYBENZOYL COA THIOESTERASE COMPLEXED WITH COA AND 4-HYDROXYBENZOIC ACID	3.1.2.23
1Q4T	CRYSTAL STRUCTURE OF 4-HYDROXYBENZOYL COA THIOESTERASE FROM ARTHROBACTER SP. STRAIN SU COMPLEXED WITH 4-HYDROXYPHENYL COA	3.1.2.23
1Q4U	CRYSTAL STRUCTURE OF 4-HYDROXYBENZOYL COA THIOESTERASE FROM ARTHROBACTER SP. STRAIN SU COMPLEXED WITH 4-HYDROXYBENZYL COA	3.1.2.23
1Q57	THE CRYSTAL STRUCTURE OF THE BIFUNCTIONAL PRIMASE-HELICASE OF BACTERIOPHAGE T7	2.7.7 3.6.4.12
1Q5H	HUMAN DUTP PYROPHOSPHATASE COMPLEX WITH DUDP	3.6.1.23
1Q5P	S156E/S166D VARIANT OF BACILLUS LENTUS SUBTILISIN	3.4.21.62
1Q5Q	THE RHODOCOCCUS 20S PROTEASOME	3.4.25.1
1Q5U	HUMAN DUTP PYROPHOSPHATASE	3.6.1.23
1Q6C	CRYSTAL STRUCTURE OF SOYBEAN BETA-AMYLASE COMPLEXED WITH MALTOSE	3.2.1.2
1Q6D	CRYSTAL STRUCTURE OF SOYBEAN BETA-AMYLASE MUTANT (M51T) WITH INCREASED PH OPTIMUM	3.2.1.2
1Q6E	CRYSTAL STRUCTURE OF SOYBEAN BETA-AMYLASE MUTANT (E178Y) WITH INCREASED PH OPTIMUM AT PH 5.4	3.2.1.2
1Q6F	CRYSTAL STRUCTURE OF SOYBEAN BETA-AMYLASE MUTANT (E178Y) WITH INCREASED PH OPTIMUM AT PH 7.1	3.2.1.2
1Q6G	CRYSTAL STRUCTURE OF SOYBEAN BETA-AMYLASE MUTANT (N340T) WITH INCREASED PH OPTIMUM	3.2.1.2
1Q6J	THE STRUCTURE OF PHOSPHOTYROSINE PHOSPHATASE 1B IN COMPLEX WITH COMPOUND 2	3.1.3.48
1Q6K	CATHEPSIN K COMPLEXED WITH T-BUTYL(1S)-1-CYCLOHEXYL-2-OXOETHYLCARBAMATE	3.4.22.38
1Q6M	THE STRUCTURE OF PHOSPHOTYROSINE PHOSPHATASE 1B IN COMPLEX WITH COMPOUND 3	3.1.3.48
1Q6N	THE STRUCTURE OF PHOSPHOTYROSINE PHOSPHATASE 1B IN COMPLEX WITH COMPOUND 4	3.1.3.48
1Q6P	THE STRUCTURE OF PHOSPHOTYROSINE PHOSPHATASE 1B IN COMPLEX WITH COMPOUND 6	3.1.3.48
1Q6S	THE STRUCTURE OF PHOSPHOTYROSINE PHOSPHATASE 1B IN COMPLEX WITH COMPOUND 9	3.1.3.48
1Q6T	THE STRUCTURE OF PHOSPHOTYROSINE PHOSPHATASE 1B IN COMPLEX WITH COMPOUND 11	3.1.3.48
1Q6V	FIRST CRYSTAL STRUCTURE OF A C49 MONOMER PLA2 FROM THE VENOM OF DABOIA RUSSELLI PULCHELLA AT 1.8 A RESOLUTION	3.1.1.4
1Q74	THE CRYSTAL STRUCTURE OF 1D-MYO-INOSITOL 2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSIDE DEACETYLASE (MSHB)	3.5.1.103
1Q7A	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN RUSSELL'S VIPER PHOSPHOLIPASE A2 AND AN ANTIINFLAMMATORY AGENT OXYPHENBUTAZONE AT 1.6A RESOLUTION	3.1.1.4
1Q7I	STRUCTURAL ANALYSIS OF INTEGRIN ALPHA IIB BETA 3- DISINTEGRIN WITH THE AKGDWN MOTIF	3.4.24
1Q7J	STRUCTURAL ANALYSIS OF INTEGRIN ALPHA IIB BETA 3- DISINTEGRIN WITH THE AKGDWN MOTIF	3.4.24
1Q7L	ZN-BINDING DOMAIN OF THE T347G MUTANT OF HUMAN AMINOACYLASE-I	3.5.1.14
1Q7R	X-RAY CRYSTALLOGRAPHIC ANALYSIS OF A PREDICTED AMIDOTRANSFERASE FROM B. STEAROTHERMOPHILUS AT 1.9 A RESOLUTION	4.3.3.6 3.5.1.2
1Q7S	CRYSTAL STRUCTURE OF BIT1	3.1.1.29
1Q7T	RV1170 (MSHB) FROM MYCOBACTERIUM TUBERCULOSIS	3.5.1.103
1Q7X	SOLUTION STRUCTURE OF THE ALTERNATIVELY SPLICED PDZ2 DOMAIN (PDZ2B) OF PTP-BAS (HPTP1E)	3.1.3.48
1Q83	CRYSTAL STRUCTURE OF THE MOUSE ACETYLCHOLINESTERASE-TZ2PA6 SYN COMPLEX	3.1.1.7
1Q84	CRYSTAL STRUCTURE OF THE MOUSE ACETYLCHOLINESTERASE-TZ2PA6 ANTI COMPLEX	3.1.1.7
1Q8F	CRYSTAL STRUCTURE OF THE E.COLI PYRIMIDINE NUCLEOSIDE HYDROLASE YEIK	3.2.2.8
1Q8R	STRUCTURE OF E.COLI RUSA HOLLIDAY JUNCTION RESOLVASE	3.1.22 3.1.22.4
1Q91	CRYSTAL STRUCTURE OF HUMAN MITOCHONDRIAL DEOXYRIBONUCLEOTIDASE IN COMPLEX WITH THE INHIBITOR DPB-T	3.1.3.5 3.1.3
1Q92	CRYSTAL STRUCTURE OF HUMAN MITOCHONDRIAL DEOXYRIBONUCLEOTIDASE IN COMPLEX WITH THE INHIBITOR PMCP-U	3.1.3.5 3.1.3
1Q9D	FRUCTOSE-1,6-BISPHOSPHATASE COMPLEXED WITH A NEW ALLOSTERIC SITE INHIBITOR (I-STATE)	3.1.3.11
1Q9E	RNASE T1 VARIANT WITH ADENINE SPECIFICITY	3.1.27.3 4.6.1.24
1Q9H	3-DIMENSIONAL STRUCTURE OF NATIVE CEL7A FROM TALAROMYCES EMERSONII	3.2.1.91 3.2.1
1Q9M	THREE DIMENSIONAL STRUCTURES OF PDE4D IN COMPLEX WITH ROLIPRAMS AND IMPLICATION ON INHIBITOR SELECTIVITY	3.1.4.17 3.1.4.53
1Q9P	SOLUTION STRUCTURE OF THE MATURE HIV-1 PROTEASE MONOMER	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1Q9X	CRYSTAL STRUCTURE OF ENTEROBACTERIA PHAGE RB69 GP43 DNA POLYMERASE COMPLEXED WITH TETRAHYDROFURAN CONTAINING DNA	2.7.7.7 3.1.11
1Q9Y	CRYSTAL STRUCTURE OF ENTEROBACTERIA PHAGE RB69 GP43 DNA POLYMERASE COMPLEXED WITH 8-OXOGUANOSINE CONTAINING DNA	2.7.7.7 3.1.11
1QA0	BOVINE TRYPSIN 2-AMINOBENZIMIDAZOLE COMPLEX	3.4.21.4
1QA1	TAILSPIKE PROTEIN, MUTANT V331G	3.2.1
1QA2	TAILSPIKE PROTEIN, MUTANT A334V	3.2.1
1QA3	TAILSPIKE PROTEIN, MUTANT A334I	3.2.1
1QA7	CRYSTAL COMPLEX OF THE 3C PROTEINASE FROM HEPATITIS A VIRUS WITH ITS INHIBITOR AND IMPLICATIONS FOR THE POLYPROTEIN PROCESSING IN HAV	3.6.1.15 3.4.22.28 2.7.7.48
1QAE	THE ACTIVE SITE OF SERRATIA ENDONUCLEASE CONTAINS A CONSERVED MAGNESIUM-WATER CLUSTER	3.1.30.2
1QAH	CRYSTAL STRUCTURE OF PERCHLORIC ACID SOLUBLE PROTEIN-A TRANSLATIONAL INHIBITOR	3.5.99.10
1QAI	CRYSTAL STRUCTURES OF THE N-TERMINAL FRAGMENT FROM MOLONEY MURINE LEUKEMIA VIRUS REVERSE TRANSCRIPTASE COMPLEXED WITH NUCLEIC ACID: FUNCTIONAL IMPLICATIONS FOR TEMPLATE-PRIMER BINDING TO THE FINGERS DOMAIN	2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1
1QAJ	CRYSTAL STRUCTURES OF THE N-TERMINAL FRAGMENT FROM MOLONEY MURINE LEUKEMIA VIRUS REVERSE TRANSCRIPTASE COMPLEXED WITH NUCLEIC ACID: FUNCTIONAL IMPLICATIONS FOR TEMPLATE-PRIMER BINDING TO THE FINGERS DOMAIN	2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1
1QAS	1-PHOSPHATIDYLINOSITOL-4,5-BISPHOSPHATE PHOSPHODIESTERASE DELTA 1	3.1.4.11
1QAT	1-PHOSPHATIDYLINOSITOL-4,5-BISPHOSPHATE PHOSPHODIESTERASE DELTA COMPLEX WITH SAMARIUM (III) CHLORIDE	3.1.4.11
1QAZ	CRYSTAL STRUCTURE OF ALGINATE LYASE A1-III FROM SPHINGOMONAS SPECIES A1 AT 1.78A RESOLUTION	3.5.1.45
1QB0	HUMAN CDC25B CATALYTIC DOMAIN	3.1.3.48
1QB1	BOVINE TRYPSIN WITH 1-[2-[5-[AMINO(IMINO)METHYL]-2-HYDROXYPHENOXY]-6-[3-(4,5-DIHYDRO-1-METHYL-1H-IMIDAZOL-2-YL)PHENOXY]PYRIDIN-4-YL]PIPERIDINE-3-CARBOXYLIC ACID (ZK-806974)	3.4.21.4
1QB2	CRYSTAL STRUCTURE OF THE CONSERVED SUBDOMAIN OF HUMAN PROTEIN SRP54M AT 2.1A RESOLUTION: EVIDENCE FOR THE MECHANISM OF SIGNAL PEPTIDE BINDING	3.6.5
1QB6	BOVINE TRYPSIN 3,3'-[3,5-DIFLUORO-4-METHYL-2, 6-PYRIDINEDIYLBIS(OXY)]BIS(BENZENECARBOXIMIDAMIDE) (ZK-805623) COMPLEX	3.4.21.4
1QB9	BOVINE TRYPSIN 7-[[2-[[1-(1-IMINOETHYL)PIPERIDIN-4-YL]OXY]-9H-CARBOZOL-9-YL] METHYL]NAPHTHALENE-2-CARBOXIMIDAMIDE (ZK-806450) COMPLEX	3.4.21.4
1QBA	BACTERIAL CHITOBIASE, GLYCOSYL HYDROLASE FAMILY 20	3.2.1.52
1QBB	BACTERIAL CHITOBIASE COMPLEXED WITH CHITOBIOSE (DINAG)	3.2.1.52
1QBJ	CRYSTAL STRUCTURE OF THE ZALPHA Z-DNA COMPLEX	3.5.4.37
1QBN	BOVINE TRYPSIN 2-[AMINO(IMINO)METHYL]-2-HYDROXYPHENOXY]-6-[3-(4,5-DIHYDRO-1H-IMIDAZOL-2-YL)PHENOXY]PYRIDINE-4-CARBOXYLIC ACID (ZK-806688) COMPLEX	3.4.21.4
1QBO	BOVINE TRYPSIN 7-[[6-[[1-(1-IMINOETHYL)PIPERIDIN-4-YL]OXY]-2-METHYL-BENZIMIDAZOL-1-YL]METHYL]NAPHTHALENE-2-CARBOXIMIDAMID ZK-806711 INHIBITOR COMPLEX	3.4.21.4
1QBR	HIV-1 PROTEASE INHIBITORS WIIH LOW NANOMOLAR POTENCY	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1QBS	HIV-1 PROTEASE INHIBITORS WIIH LOW NANOMOLAR POTENCY	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1QBT	HIV-1 PROTEASE INHIBITORS WIIH LOW NANOMOLAR POTENCY	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1QBU	HIV-1 PROTEASE INHIBITORS WIIH LOW NANOMOLAR POTENCY	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1QC9	THE CRYSTALLOGRAPHIC STRUCTURE OF RESTRICTION ENDONUCLEASE ECO RI AT 3.3 A IN THE ABSENSE OF DNA	3.1.21.4
1QCG	LOW TEMPERATURE STRUCTURE OF POKEWEED ANTIVIRAL PROTEIN	3.2.2.22
1QCI	LOW TEMPERATURE STRUCTURE OF POKEWEED ANTIVIRAL PROTEIN COMPLEXED WITH ADENINE	3.2.2.22
1QCJ	LOW TEMPERATURE COMPLEX OF POKEWEED ANTIVIRAL PROTEIN WITH PTEORIC ACID	3.2.2.22
1QCN	CRYSTAL STRUCTURE OF FUMARYLACETOACETATE HYDROLASE	3.7.1.2
1QCO	CRYSTAL STRUCTURE OF FUMARYLACETOACETATE HYDROLASE COMPLEXED WITH FUMARATE AND ACETOACETATE	3.7.1.2
1QCP	CRYSTAL STRUCTURE OF THE RWJ-51084 BOVINE PANCREATIC BETA-TRYPSIN AT 1.8 A	3.4.21.4
1QCS	N-TERMINAL DOMAIN OF N-ETHYLMALEIMIDE SENSITIVE FACTOR (NSF)	3.6.4.6
1QD2	CRYSTAL STRUCTURE OF THE COMPLEX OF TRICHOSANTHIN WITH ADENINE, OBTAINED FROM TRICHOSANTHIN COMPLEXED WITH THE DINUCLEOTIDE APG	3.2.2.22
1QD5	OUTER MEMBRANE PHOSPHOLIPASE A FROM ESCHERICHIA COLI	3.1.1.32 3.1.1.4
1QD9	BACILLUS SUBTILIS YABJ	3.5.99.10
1QDE	CRYSTAL STRUCTURE OF THE ATPASE DOMAIN OF TRANSLATION INITIATION FACTOR 4A FROM SACCHAROMYCES CEREVISIAE-THE PROTOTYPE OF THE DEAD BOX PROTEIN FAMILY	3.6.4.13
1QDM	CRYSTAL STRUCTURE OF PROPHYTEPSIN, A ZYMOGEN OF A BARLEY VACUOLAR ASPARTIC PROTEINASE.	3.4.23.40
1QDN	AMINO TERMINAL DOMAIN OF THE N-ETHYLMALEIMIDE SENSITIVE FUSION PROTEIN (NSF)	3.6.4.6
1QDQ	X-RAY CRYSTAL STRUCTURE OF BOVINE CATHEPSIN B-CA074 COMPLEX	3.4.22.1
1QDR	2.1 A RESOLUTION STRUCTURE OF ESCHERICHIA COLI LYTIC TRANSGLYCOSYLASE SLT35	3.2.1 4.2.2
1QDU	CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-8 WITH THE TRIPEPTIDE KETONE INHIBITOR ZEVD-DCBMK	3.4.22 3.4.22.61
1QE1	CRYSTAL STRUCTURE OF 3TC-RESISTANT M184I MUTANT OF HIV-1 REVERSE TRANSCRIPTASE	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1QE3	PNB ESTERASE	3.1.1
1QEZ	SULFOLOBUS ACIDOCALDARIUS INORGANIC PYROPHOSPHATASE: AN ARCHAEL PYROPHOSPHATASE.	3.6.1.1
1QF0	THERMOLYSIN (E.C.3.4.24.27) COMPLEXED WITH (2-SULPHANYL-3-PHENYLPROPANOYL)-PHE-TYR. PARAMETERS FOR ZN-BIDENTATION OF MERCAPTOACYLDIPEPTIDES IN METALLOENDOPEPTIDASE	3.4.24.27
1QF1	THERMOLYSIN (E.C.3.4.24.27) COMPLEXED WITH (2-SULPHANYLHEPTANOYL)-PHE-ALA. PARAMETERS FOR ZN-BIDENTATION OF MERCAPTOACYLDIPEPTIDES IN METALLOENDOPEPTIDASE	3.4.24.27
1QF2	THERMOLYSIN (E.C.3.4.24.27) COMPLEXED WITH (2-SULPHANYL-3-PHENYLPROPANOYL)-GLY-(5-PHENYLPROLINE). PARAMETERS FOR ZN-MONODENTATION OF MERCAPTOACYLDIPEPTIDES IN METALLOENDOPEPTIDASE	3.4.24.27
1QFC	STRUCTURE OF RAT PURPLE ACID PHOSPHATASE	3.1.3.2
1QFK	STRUCTURE OF HUMAN FACTOR VIIA AND ITS IMPLICATIONS FOR THE TRIGGERING OF BLOOD COAGULATION	3.4.21.21
1QFM	PROLYL OLIGOPEPTIDASE FROM PORCINE MUSCLE	3.4.21.26
1QFS	PROLYL OLIGOPEPTIDASE FROM PORCINE MUSCLE WITH COVALENTLY BOUND INHIBITOR Z-PRO-PROLINAL	3.4.21.26
1QFX	PH 2.5 ACID PHOSPHATASE FROM ASPERGILLUS NIGER	3.1.3.8
1QGC	STRUCTURE OF THE COMPLEX OF A FAB FRAGMENT OF A NEUTRALIZING ANTIBODY WITH FOOT AND MOUTH DISEASE VIRUS	3.4.22.46 3.6.1.15 3.4.22.28 2.7.7.48
1QGE	NEW CRYSTAL FORM OF PSEUDOMONAS GLUMAE (FORMERLY CHROMOBACTERIUM VISCOSUM ATCC 6918) LIPASE	3.1.1.3
1QGF	PORCINE PANCREATIC ELASTASE COMPLEXED WITH (3R, 4S)N-PARA-TOLUENESULPHONYL-3-ETHYL-4-(CARBOXYLIC ACID)PYRROLIDIN-2-ONE	3.4.21.36
1QGI	CHITOSANASE FROM BACILLUS CIRCULANS	3.2.1.132
1QGP	NMR STRUCTURE OF THE Z-ALPHA DOMAIN OF ADAR1, 15 STRUCTURES	3.5.4.37
1QGX	X-RAY STRUCTURE OF YEAST HAL2P	3.1.3.7
1QH3	HUMAN GLYOXALASE II WITH CACODYLATE AND ACETATE IONS PRESENT IN THE ACTIVE SITE	3.1.2.6
1QH5	HUMAN GLYOXALASE II WITH S-(N-HYDROXY-N-BROMOPHENYLCARBAMOYL)GLUTATHIONE	3.1.2.6
1QH6	CATALYSIS AND SPECIFICITY IN ENZYMATIC GLYCOSIDE HYDROLASES: A 2,5B CONFORMATION FOR THE GLYCOSYL-ENZYME INTERMIDIATE REVEALED BY THE STRUCTURE OF THE BACILLUS AGARADHAERENS FAMILY 11 XYLANASE	3.2.1.8
1QH7	CATALYSIS AND SPECIFICITY IN ENZYMATIC GLYCOSIDE HYDROLASES: A 2,5B CONFORMATION FOR THE GLYCOSYL-ENZYME INTERMIDIATE REVEALED BY THE STRUCTURE OF THE BACILLUS AGARADHAERENS FAMILY 11 XYLANASE	3.2.1.8
1QH9	ENZYME-PRODUCT COMPLEX OF L-2-HALOACID DEHALOGENASE	3.8.1.2
1QHC	CRYSTAL STRUCTURE OF RIBONUCLEASE A IN COMPLEX WITH 5'-PHOSPHO-2'-DEOXYURIDINE-3'-PYROPHOSPHATE ADENOSINE-3'-PHOSPHATE	3.1.27.5 4.6.1.18
1QHG	STRUCTURE OF DNA HELICASE MUTANT WITH ADPNP	3.6.4.12
1QHH	STRUCTURE OF DNA HELICASE WITH ADPNP	3.6.4.12
1QHK	N-TERMINAL DOMAIN OF SACCHAROMYCES CEREVISIAE RNASE HI REVEALS A FOLD WITH A RESEMBLANCE TO THE N-TERMINAL DOMAIN OF RIBOSOMAL PROTEIN L9	3.1.26.4
1QHO	FIVE-DOMAIN ALPHA-AMYLASE FROM BACILLUS STEAROTHERMOPHILUS, MALTOSE/ACARBOSE COMPLEX	3.2.1.133
1QHP	FIVE-DOMAIN ALPHA-AMYLASE FROM BACILLUS STEAROTHERMOPHILUS, MALTOSE COMPLEX	3.2.1.133
1QHR	NOVEL COVALENT ACTIVE SITE THROMBIN INHIBITORS	3.4.21.5
1QHW	PURPLE ACID PHOSPHATASE FROM RAT BONE	3.1.3.2
1QHZ	NATIVE TETRAGONAL STRUCTURE OF THE ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHAERENS	3.2.1.4
1QI0	ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHAERENS IN THE TETRAGONAL CRYSTAL FORM IN COMPLEX WITH CELLOBIOSE	3.2.1.4
1QI2	ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHAERENS IN THE TETRAGONAL CRYSTAL FORM IN COMPLEX WITH 2',4'-DINITROPHENYL 2-DEOXY-2-FLUORO-B-D-CELLOTRIOSIDE	3.2.1.4
1QI3	MUTANT (D193N) MALTOTETRAOSE-FORMING EXO-AMYLASE IN COMPLEX WITH MALTOTETRAOSE	3.2.1.60
1QI4	MUTANT (E219G) MALTOTETRAOSE-FORMING EXO-AMYLASE IN COMPLEX WITH MALTOTETRAOSE	3.2.1.60
1QI5	MUTANT (D294N) MALTOTETRAOSE-FORMING EXO-AMYLASE IN COMPLEX WITH MALTOTETRAOSE	3.2.1.60
1QI7	THE CRYSTAL STRUCTURE AT 2.0 A OF SAPORIN SO6, A RIBOSOME INACTIVATING PROTEIN FROM SAPONARIA OFFICINALIS	3.2.2.22
1QIA	CRYSTAL STRUCTURE OF STROMELYSIN CATALYTIC DOMAIN	3.4.24.17
1QIB	CRYSTAL STRUCTURE OF GELATINASE A CATALYTIC DOMAIN	3.4.24.24
1QIC	CRYSTAL STRUCTURE OF STROMELYSIN CATALYTIC DOMAIN	3.4.24.17
1QID	SPECIFIC CHEMICAL AND STRUCTURAL DAMAGE AT NINE TIME POINTS (POINT A) CAUSED BY INTENSE SYNCHROTRON RADIATION TO TORPEDO CALIFORNICA ACETYLCHOLINESTERASE	3.1.1.7
1QIE	SPECIFIC CHEMICAL AND STRUCTURAL DAMAGE AT NINE TIME POINTS (POINT B) CAUSED BY INTENSE SYNCHROTRON RADIATION TO TORPEDO CALIFORNICA ACETYLCHOLINESTERASE	3.1.1.7
1QIF	SPECIFIC CHEMICAL AND STRUCTURAL DAMAGE AT NINE TIME POINTS (POINT C) CAUSED BY INTENSE SYNCHROTRON RADIATION TO TORPEDO CALIFORNICA ACETYLCHOLINESTERASE	3.1.1.7
1QIG	SPECIFIC CHEMICAL AND STRUCTURAL DAMAGE AT NINE TIME POINTS (POINT D) CAUSED BY INTENSE SYNCHROTRON RADIATION TO TORPEDO CALIFORNICA ACETYLCHOLINESTERASE	3.1.1.7
1QIH	SPECIFIC CHEMICAL AND STRUCTURAL DAMAGE AT NINE TIME POINTS (POINT E) CAUSED BY INTENSE SYNCHROTRON RADIATION TO TORPEDO CALIFORNICA ACETYLCHOLINESTERASE	3.1.1.7
1QII	SPECIFIC CHEMICAL AND STRUCTURAL DAMAGE AT NINE TIME POINTS (POINT F) CAUSED BY INTENSE SYNCHROTRON RADIATION TO TORPEDO CALIFORNICA ACETYLCHOLINESTERASE	3.1.1.7
1QIJ	SPECIFIC CHEMICAL AND STRUCTURAL DAMAGE AT NINE TIME POINTS (POINT G) CAUSED BY INTENSE SYNCHROTRON RADIATION TO TORPEDO CALIFORNICA ACETYLCHOLINESTERASE	3.1.1.7
1QIK	SPECIFIC CHEMICAL AND STRUCTURAL DAMAGE AT NINE TIME POINTS (POINT H) CAUSED BY INTENSE SYNCHROTRON RADIATION TO TORPEDO CALIFORNICA ACETYLCHOLINESTERASE	3.1.1.7
1QIM	SPECIFIC CHEMICAL AND STRUCTURAL DAMAGE AT NINE TIME POINTS (POINT I) CAUSED BY INTENSE SYNCHROTRON RADIATION TO TORPEDO CALIFORNICA ACETYLCHOLINESTERASE	3.1.1.7
1QIO	SPECIFIC CHEMICAL AND STRUCTURAL DAMAGE CAUSED BY INTENSE SYNCHROTRON RADIATION TO HEN EGG WHITE LYSOZYME	3.2.1.17
1QJ1	NOVEL COVALENT ACTIVE SITE THROMBIN INHIBITORS	3.4.21.5
1QJ6	NOVEL COVALENT ACTIVE SITE THROMBIN INHIBITORS	3.4.21.5
1QJ7	NOVEL COVALENT ACTIVE SITE THROMBIN INHIBITORS	3.4.21.5
1QJI	STRUCTURE OF ASTACIN WITH A TRANSITION-STATE ANALOGUE INHIBITOR	3.4.24.21
1QJJ	STRUCTURE OF ASTACIN WITH A HYDROXAMIC ACID INHIBITOR	3.4.24.21
1QJM	CRYSTAL STRUCTURE OF A COMPLEX OF LACTOFERRIN WITH A LANTHANIDE ION (SM3+) AT 3.4 ANGSTROM RESOLUTION	3.4.21
1QJV	PECTIN METHYLESTERASE PEMA FROM ERWINIA CHRYSANTHEMI	3.1.1.11
1QJW	CEL6A (Y169F) WITH A NON-HYDROLYSABLE CELLOTETRAOSE	3.2.1.91
1QK0	CEL6A WITH A NON-HYDROLYSABLE CELLOTETRAOSE	3.2.1.91
1QK2	WILD TYPE CEL6A WITH A NON-HYDROLYSABLE CELLOTETRAOSE	3.2.1.91
1QKQ	CHARCOT-LEYDEN CRYSTAL PROTEIN - MANNOSE COMPLEX	3.1.1.5
1QL0	SM ENDONUCLEASE FROM SERATIA MARCENSCENS AT ATOMIC RESOLUTION	3.1.30.2
1QL7	FACTOR XA SPECIFIC INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN	3.4.21.4
1QL8	FACTOR XA SPECIFIC INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN	3.4.21.4
1QL9	FACTOR XA SPECIFIC INHIBITOR IN COMPLEX WITH RAT TRYPSIN MUTANT X99RT	3.4.21.4
1QLD	SOLUTION STRUCTURE OF TYPE X CBM	3.2.1.8
1QLG	CRYSTAL STRUCTURE OF PHYTASE WITH MAGNESIUM FROM BACILLUS AMYLOLIQUEFACIENS	3.1.3.8
1QLL	PIRATOXIN-II (PRTX-II) - A K49 PLA2 FROM BOTHROPS PIRAJAI	3.1.1.4
1QLM	THE CRYSTAL STRUCTURE OF METHENYLTETRAHYDROMETHANOPTERIN CYCLOHYDROLASE FROM THE HYPERTHERMOPHILIC ARCHAEON METHANOPYRUS KANDLERI	3.5.4.27
1QM6	CLOSED FORM OF CLOSTRIDIUM PERFRINGENS ALPHA-TOXIN STRAIN NCTC8237	3.1.4.3
1QMC	C-TERMINAL DNA-BINDING DOMAIN OF HIV-1 INTEGRASE, NMR, 42 STRUCTURES	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1QMD	CALCIUM BOUND CLOSED FORM ALPHA-TOXIN FROM CLOSTRIDIUM PERFRINGENS	3.1.4.3
1QMT	RECOMBINANT HUMAN EOSINOPHIL CATIONIC PROTEIN	3.1.27
1QMU	DUCK CARBOXYPEPTIDASE D DOMAIN II	3.4.17.22
1QMY	FMDV LEADER PROTEASE (LBSHORT-C51A-C133S)	3.4.22.46 3.6.1.15 3.4.22.28 2.7.7.48
1QNJ	THE STRUCTURE OF NATIVE PORCINE PANCREATIC ELASTASE AT ATOMIC RESOLUTION (1.1 A)	3.4.21.36
1QNO	THE 3-D STRUCTURE OF A TRICHODERMA REESEI B-MANNANASE FROM GLYCOSIDE HYDROLASE FAMILY 5	3.2.1.78
1QNP	THE 3-D STRUCTURE OF A TRICHODERMA REESEI B-MANNANASE FROM GLYCOSIDE HYDROLASE FAMILY 5	3.2.1.78
1QNQ	THE 3-D STRUCTURE OF A TRICHODERMA REESEI B-MANNANASE FROM GLYCOSIDE HYDROLASE FAMILY 5	3.2.1.78
1QNR	THE 3-D STRUCTURE OF A TRICHODERMA REESEI B-MANNANASE FROM GLYCOSIDE HYDROLASE FAMILY 5	3.2.1.78
1QNS	THE 3-D STRUCTURE OF A TRICHODERMA REESEI B-MANNANASE FROM GLYCOSIDE HYDROLASE FAMILY 5	3.2.1.78
1QO7	STRUCTURE OF ASPERGILLUS NIGER EPOXIDE HYDROLASE	3.3.2.3
1QO9	NATIVE ACETYLCHOLINESTERASE FROM DROSOPHILA MELANOGASTER	3.1.1.7
1QOL	STRUCTURE OF THE FMDV LEADER PROTEASE	3.4.22.46 3.6.1.15 3.4.22.28 2.7.7.48
1QON	ACHE FROM DROSOPHILA MELANOGASTER COMPLEX WITH TACRINE DERIVATIVE 9-(3-IODOBENZYLAMINO)-1,2,3,4-TETRAHYDROACRIDINE	3.1.1.7
1QOZ	CATALYTIC CORE DOMAIN OF ACETYL XYLAN ESTERASE FROM TRICHODERMA REESEI	3.1.1.72
1QPK	MUTANT (D193G) MALTOTETRAOSE-FORMING EXO-AMYLASE IN COMPLEX WITH MALTOTETRAOSE	3.2.1.60
1QPS	THE CRYSTAL STRUCTURE OF A POST-REACTIVE COGNATE DNA-ECO RI COMPLEX AT 2.50 A IN THE PRESENCE OF MN2+ ION	3.1.21.4
1QQ1	TAILSPIKE PROTEIN, MUTANT E359G	3.2.1
1QQ4	CRYSTAL STRUCTURE OF AN ALPHA-LYTIC PROTEASE MUTANT WITH ACCELERATED FOLDING KINETICS, R102H/G134S	3.4.21.12
1QQ5	STRUCTURE OF L-2-HALOACID DEHALOGENASE FROM XANTHOBACTER AUTOTROPHICUS	3.8.1.2
1QQ6	STRUCTURE OF L-2-HALOACID DEHALOGENASE FROM XANTHOBACTER AUTOTROPHICUS WITH CHLOROACETIC ACID COVALENTLY BOUND	3.8.1.2
1QQ7	STRUCTURE OF L-2-HALOACID DEHALOGENASE FROM XANTHOBACTER AUTOTROPHICUS WITH CHLOROPROPIONIC ACID COVALENTLY BOUND	3.8.1.2
1QQ9	STREPTOMYCES GRISEUS AMINOPEPTIDASE COMPLEXED WITH METHIONINE	3.4.11 3.4.11.24
1QQJ	CRYSTAL STRUCTURE OF MOUSE FUMARYLACETOACETATE HYDROLASE REFINED AT 1.55 ANGSTROM RESOLUTION	3.7.1.2
1QQP	FOOT-AND-MOUTH DISEASE VIRUS/ OLIGOSACCHARIDE RECEPTOR COMPLEX.	3.4.22.46 3.6.1.15 3.4.22.28 2.7.7.48
1QQU	CRYSTAL STRUCTURE OF PORCINE BETA TRYPSIN WITH BOUND ACETATE ION	3.4.21.4
1QQY	X-RAY CRYSTAL STRUCTURE ANALYSIS OF CANINE MILK LYSOZYME (APO-TYPE)	3.2.1.17
1QR3	STRUCTURE OF PORCINE PANCREATIC ELASTASE IN COMPLEX WITH FR901277, A NOVEL MACROCYCLIC INHIBITOR OF ELASTASES AT 1.6 ANGSTROM RESOLUTION	3.4.21.36
1QRA	STRUCTURE OF P21RAS IN COMPLEX WITH GTP AT 100 K	3.6.5.2
1QRB	PLASTICITY AND STERIC STRAIN IN A PARALLEL BETA-HELIX: RATIONAL MUTATIONS IN P22 TAILSPIKE PROTEIN	3.2.1
1QRC	TAILSPIKE PROTEIN, MUTANT W391A	3.2.1
1QRH	X-RAY STRUCTURE OF THE DNA-ECO RI ENDONUCLEASE COMPLEXES WITH AN R145K MUTATION AT 2.7 A	3.1.21.4
1QRI	X-RAY STRUCTURE OF THE DNA-ECO RI ENDONUCLEASE COMPLEXES WITH AN E144D MUTATION AT 2.7 A	3.1.21.4
1QRP	HUMAN PEPSIN 3A IN COMPLEX WITH A PHOSPHONATE INHIBITOR IVA-VAL-VAL-LEU(P)-(O)PHE-ALA-ALA-OME	3.4.23.1
1QRR	CRYSTAL STRUCTURE OF SQD1 PROTEIN COMPLEX WITH NAD AND UDP-GLUCOSE	3.13.1.1
1QRW	CRYSTAL STRUCTURE OF AN ALPHA-LYTIC PROTEASE MUTANT WITH ACCELERATED FOLDING KINETICS, R102H/G134S, PH 8	3.4.21.12
1QRX	CRYSTAL STRUCTURE OF WILD-TYPE ALPHA-LYTIC PROTEASE AT 1.6 A, PH 5.14	3.4.21.12
1QRZ	CATALYTIC DOMAIN OF PLASMINOGEN	3.4.21.7
1QS4	CORE DOMAIN OF HIV-1 INTEGRASE COMPLEXED WITH MG++ AND 1-(5-CHLOROINDOL-3-YL)-3-HYDROXY-3-(2H-TETRAZOL-5-YL)-PROPENONE	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1QS5	THE INTRODUCTION OF STRAIN AND ITS EFFECTS ON THE STRUCTURE AND STABILITY OF T4 LYSOZYME	3.2.1.17
1QS9	THE INTRODUCTION OF STRAIN AND ITS EFFECTS ON THE STRUCTURE AND STABILITY OF T4 LYSOZYME	3.2.1.17
1QSA	CRYSTAL STRUCTURE OF THE 70 KDA SOLUBLE LYTIC TRANSGLYCOSYLASE SLT70 FROM ESCHERICHIA COLI AT 1.65 ANGSTROMS RESOLUTION	3.2.1 4.2.2
1QSB	THE INTRODUCTION OF STRAIN AND ITS EFFECTS ON THE STRUCTURE AND STABILITY OF T4 LYSOZYME	3.2.1.17
1QSQ	CAVITY CREATING MUTATION	3.2.1.17
1QSW	CRYSTAL STRUCTURE ANALYSIS OF A HUMAN LYSOZYME MUTANT W64C C65A	3.2.1.17
1QT3	T26D MUTANT OF T4 LYSOZYME	3.2.1.17
1QT4	T26Q MUTANT OF T4 LYSOZYME	3.2.1.17
1QT5	D20E MUTANT STRUCTURE OF T4 LYSOZYME	3.2.1.17
1QT6	E11H MUTANT OF T4 LYSOZYME	3.2.1.17
1QT7	E11N MUTANT OF T4 LYSOZYME	3.2.1.17
1QT8	T26H MUTANT OF T4 LYSOZYME	3.2.1.17
1QTB	THE INTRODUCTION OF STRAIN AND ITS EFFECTS ON THE STRUCTURE AND STABILITY OF T4 LYSOZYME	3.2.1.17
1QTC	THE INTRODUCTION OF STRAIN AND ITS EFFECTS ON THE STRUCTURE AND STABILITY OF T4 LYSOZYME	3.2.1.17
1QTD	THE INTRODUCTION OF STRAIN AND ITS EFFECTS ON THE STRUCTURE AND STABILITY OF T4 LYSOZYME	3.2.1.17
1QTE	CRYSTAL STRUCTURE OF THE 70 KDA SOLUBLE LYTIC TRANSGLYCOSYLASE SLT70 FROM ESCHERICHIA COLI AT 1.90 A RESOLUTION IN COMPLEX WITH A 1,6-ANHYDROMUROTRIPEPTIDE	3.2.1 4.2.2
1QTF	CRYSTAL STRUCTURE OF EXFOLIATIVE TOXIN B	3.4.21
1QTH	THE INTRODUCTION OF STRAIN AND ITS EFFECTS ON THE STRUCTURE AND STABILITY OF T4 LYSOZYME	3.2.1.17
1QTI	ACETYLCHOLINESTERASE (E.C.3.1.1.7)	3.1.1.7
1QTK	CRYSTAL STRUCTURE OF HEW LYSOZYME UNDER PRESSURE OF KRYPTON (55 BAR)	3.2.1.17
1QTN	CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-8 WITH THE TETRAPEPTIDE INHIBITOR ACE-IETD-ALDEHYDE	3.4.22 3.4.22.61
1QTR	CRYSTAL STRUCTURE ANALYSIS OF THE PROLYL AMINOPEPTIDASE FROM SERRATIA MARCESCENS	3.4.11.5
1QTV	T26E APO STRUCTURE OF T4 LYSOZYME	3.2.1.17
1QTW	HIGH-RESOLUTION CRYSTAL STRUCTURE OF THE ESCHERICHIA COLI DNA REPAIR ENZYME ENDONUCLEASE IV	3.1.21.2
1QTZ	D20C MUTANT OF T4 LYSOZYME	3.2.1.17
1QU9	1.2 A CRYSTAL STRUCTURE OF YJGF GENE PRODUCT FROM E. COLI	3.5.99.10
1QUA	CRYSTAL STRUCTURE OF ACUTOLYSIN-C, A HEMORRHAGIC TOXIN FROM THE SNAKE VENOM OF AGKISTRODON ACUTUS, AT 2.2 A RESOLUTION	3.4.24
1QUD	L99G MUTANT OF T4 LYSOZYME	3.2.1.17
1QUG	E108V MUTANT OF T4 LYSOZYME	3.2.1.17
1QUH	L99G/E108V MUTANT OF T4 LYSOZYME	3.2.1.17
1QUM	CRYSTAL STRUCTURE OF ESCHERICHIA COLI ENDONUCLEASE IV IN COMPLEX WITH DAMAGED DNA	3.1.21.2
1QUO	L99A/E108V MUTANT OF T4 LYSOZYME	3.2.1.17
1QUR	HUMAN ALPHA-THROMBIN IN COMPLEX WITH BIVALENT, BENZAMIDINE-BASED SYNTHETIC INHIBITOR	3.4.21.5
1QUS	1.7 A RESOLUTION STRUCTURE OF THE SOLUBLE LYTIC TRANSGLYCOSYLASE SLT35 FROM ESCHERICHIA COLI	3.2.1 4.2.2
1QUT	THE SOLUBLE LYTIC TRANSGLYCOSYLASE SLT35 FROM ESCHERICHIA COLI IN COMPLEX WITH N-ACETYLGLUCOSAMINE	3.2.1 4.2.2
1QUV	CRYSTAL STRUCTURE OF THE RNA DIRECTED RNA POLYMERASE OF HEPATITIS C VIRUS	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
1QVA	YEAST INITIATION FACTOR 4A N-TERMINAL DOMAIN	3.6.4.13
1QVJ	STRUCTURE OF NUDT9 COMPLEXED WITH RIBOSE-5-PHOSPHATE	3.6.1.13
1QW7	STRUCTURE OF AN ENGINEERED ORGANOPHOSPHOROUS HYDROLASE WITH INCREASED ACTIVITY TOWARD HYDROLYSIS OF PHOSPHOTHIOLATE BONDS	3.1.8.1
1QW8	CRYSTAL STRUCTURE OF A FAMILY 51 ALPHA-L-ARABINOFURANOSIDASE IN COMPLEX WITH ARA-ALPHA(1,3)-XYL	3.2.1.55
1QW9	CRYSTAL STRUCTURE OF A FAMILY 51 ALPHA-L-ARABINOFURANOSIDASE IN COMPLEX WITH 4-NITROPHENYL-ARA	3.2.1.55
1QWN	GOLGI ALPHA-MANNOSIDASE II COVALENT INTERMEDIATE COMPLEX WITH 5-FLUORO-GULOSYL-FLUORIDE	3.2.1.114
1QWO	CRYSTAL STRUCTURE OF A PHOSPHORYLATED PHYTASE FROM ASPERGILLUS FUMIGATUS, REVEALING THE STRUCTURAL BASIS FOR ITS HEAT RESILIENCE AND CATALYTIC PATHWAY	3.1.3.8
1QWQ	SOLUTION STRUCTURE OF THE MONOMERIC N67D MUTANT OF BOVINE SEMINAL RIBONUCLEASE	3.1.27.5 4.6.1.18
1QWU	GOLGI ALPHA-MANNOSIDASE II D341N MUTANT COMPLEX WITH 5-F-GULOSIDE	3.2.1.114
1QWY	LATENT LYTM AT 1.3 A RESOLUTION	3.4.24.75
1QWZ	CRYSTAL STRUCTURE OF SORTASE B FROM S. AUREUS COMPLEXED WITH MTSET	3.4.22.71
1QX1	GOLGI ALPHA-MANNOSIDASE II D341N MUTANT COMPLEX WITH 2-F-MANNOSYL-F	3.2.1.114
1QX3	CONFORMATIONAL RESTRICTIONS IN THE ACTIVE SITE OF UNLIGANDED HUMAN CASPASE-3	3.4.22 3.4.22.56
1QX6	CRYSTAL STRUCTURE OF SORTASE B COMPLEXED WITH E-64	3.4.22.71
1QXA	CRYSTAL STRUCTURE OF SORTASE B COMPLEXED WITH GLY3	3.4.22.71
1QXK	MONOACID-BASED, CELL PERMEABLE, SELECTIVE INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
1QXL	CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE COMPLEXED WITH FR235380	3.5.4.4
1QXP	CRYSTAL STRUCTURE OF A MU-LIKE CALPAIN	3.4.22.52 3.4.22.53
1QXW	CRYSTAL STRUCTURE OF STAPHYLOCCOCUS AUREUS IN COMPLEX WITH AN AMINOKETONE INHIBITOR 54135.	3.4.11.18
1QXY	CRYSTAL STRUCTURE OF S. AUREUS METHIONINE AMINOPEPTIDASE IN COMPLEX WITH A KETOHETEROCYCLE 618	3.4.11.18
1QXZ	CRYSTAL STRUCTURE OF S. AUREUS METHIONINE AMINOPEPTIDASE IN COMPLEX WITH A KETOHETEROCYCLE INHIBITOR 119	3.4.11.18
1QY6	STRUCTUE OF V8 PROTEASE FROM STAPHYLOCOCCUS AUREUS	3.4.21.19
1QZ0	CRYSTAL STRUCTURE OF THE YERSINIA PESTIS PHOSPHATASE YOPH IN COMPLEX WITH A PHOSPHOTYROSYL MIMETIC-CONTAINING HEXAPEPTIDE	3.1.3.48
1QZ8	CRYSTAL STRUCTURE OF SARS CORONAVIRUS NSP9	3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
1QZ9	THE THREE DIMENSIONAL STRUCTURE OF KYNURENINASE FROM PSEUDOMONAS FLUORESCENS	3.7.1.3
1QZM	ALPHA-DOMAIN OF ATPASE	3.4.21.53
1QZQ	HUMAN TYROSYL DNA PHOSPHODIESTERASE	3.1.4
1QZY	HUMAN METHIONINE AMINOPEPTIDASE IN COMPLEX WITH BENGAMIDE INHIBITOR LAF153 AND COBALT	3.4.11.18
1R08	STRUCTURAL ANALYSIS OF ANTIVIRAL AGENTS THAT INTERACT WITH THE CAPSID OF HUMAN RHINOVIRUSES	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1R09	HUMAN RHINOVIRUS 14 COMPLEXED WITH ANTIVIRAL COMPOUND R 61837	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1R0A	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE COVALENTLY TETHERED TO DNA TEMPLATE-PRIMER SOLVED TO 2.8 ANGSTROMS	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1R0R	1.1 ANGSTROM RESOLUTION STRUCTURE OF THE COMPLEX BETWEEN THE PROTEIN INHIBITOR, OMTKY3, AND THE SERINE PROTEASE, SUBTILISIN CARLSBERG	3.4.21.62
1R0S	CRYSTAL STRUCTURE OF ADP-RIBOSYL CYCLASE GLU179ALA MUTANT	3.2.2.5 3.2.2.6 2.4.99.20
1R0V	STRUCTURE DETERMINATION OF THE DIMERIC ENDONUCLEASE IN A PSEUDO-FACE-CENTERD P21212 SPACE GROUP	3.1.27.9 4.6.1.16
1R11	STRUCTURE DETERMINATION OF THE DIMERIC ENDONUCLEASE IN A PSEUDO-FACE-CENTERD P21 SPACE GROUP	3.1.27.9 4.6.1.16
1R12	NATIVE APLYSIA ADP RIBOSYL CYCLASE	3.2.2.5 3.2.2.6 2.4.99.20
1R15	APLYSIA ADP RIBOSYL CYCLASE WITH BOUND NICOTINAMIDE AND R5P	3.2.2.5 3.2.2.6 2.4.99.20
1R16	APLYSIA ADP RIBOSYL CYCLASE WITH BOUND PYRIDYLCARBINOL AND R5P	3.2.2.5 3.2.2.6 2.4.99.20
1R1A	CRYSTAL STRUCTURE OF HUMAN RHINOVIRUS SEROTYPE 1A (HRV1A)	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1R1D	STRUCTURE OF A CARBOXYLESTERASE FROM BACILLUS STEAROTHERMOPHILUS	3.1.1.1
1R1H	STRUCTURAL ANALYSIS OF NEPRILYSIN WITH VARIOUS SPECIFIC AND POTENT INHIBITORS	3.4.24.11
1R1I	STRUCTURAL ANALYSIS OF NEPRILYSIN WITH VARIOUS SPECIFIC AND POTENT INHIBITORS	3.4.24.11
1R1J	STRUCTURAL ANALYSIS OF NEPRILYSIN WITH VARIOUS SPECIFIC AND POTENT INHIBITORS	3.4.24.11
1R1O	AMINO ACID SULFONAMIDES AS TRANSITION-STATE ANALOGUE INHIBITORS OF ARGINASE	3.5.3.1
1R2Q	CRYSTAL STRUCTURE OF HUMAN RAB5A GTPASE DOMAIN AT 1.05 A RESOLUTION	3.6.5.2
1R2Y	MUTM (FPG) BOUND TO 8-OXOGUANINE (OXOG) CONTAINING DNA	3.2.2.23 4.2.99.18
1R2Z	MUTM (FPG) BOUND TO 5,6-DIHYDROURACIL (DHU) CONTAINING DNA	3.2.2.23 4.2.99.18
1R33	GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH 5-THIO-D-MANNOPYRANOSYLAMINE	3.2.1.114
1R34	GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH 5-THIO-D-MANNOPYRANOSYLAMIDINIUM SALT	3.2.1.114
1R3M	CRYSTAL STRUCTURE OF THE DIMERIC UNSWAPPED FORM OF BOVINE SEMINAL RIBONUCLEASE	3.1.27.5 4.6.1.18
1R3N	CRYSTAL STRUCTURE OF BETA-ALANINE SYNTHASE FROM SACCHAROMYCES KLUYVERI	3.5.1.6
1R42	NATIVE HUMAN ANGIOTENSIN CONVERTING ENZYME-RELATED CARBOXYPEPTIDASE (ACE2)	3.4.17.23 3.4.17
1R43	CRYSTAL STRUCTURE OF BETA-ALANINE SYNTHASE FROM SACCHAROMYCES KLUYVERI (SELENOMETHIONINE SUBSTITUTED PROTEIN)	3.5.1.6
1R44	CRYSTAL STRUCTURE OF VANX	3.4.13 3.4.13.22
1R46	STRUCTURE OF HUMAN ALPHA-GALACTOSIDASE	3.2.1.22 3.2.1.47
1R47	STRUCTURE OF HUMAN ALPHA-GALACTOSIDASE	3.2.1.22 3.2.1.47
1R4F	INOSINE-ADENOSINE-GUANOSINE PREFERRING NUCLEOSIDE HYDROLASE FROM TRYPANOSOMA VIVAX: TRP260ALA MUTANT IN COMPLEX WITH 3-DEAZA-ADENOSINE	3.2.2.1
1R4L	INHIBITOR BOUND HUMAN ANGIOTENSIN CONVERTING ENZYME-RELATED CARBOXYPEPTIDASE (ACE2)	3.4.17.23 3.4.17
1R4P	SHIGA TOXIN TYPE 2	3.2.2.22
1R4Q	SHIGA TOXIN	3.2.2.22
1R4Y	SOLUTION STRUCTURE OF THE DELETION MUTANT DELTA(7-22) OF THE CYTOTOXIC RIBONUCLEASE ALPHA-SARCIN	3.1.27.10 4.6.1.23
1R4Z	BACILLUS SUBTILIS LIPASE A WITH COVALENTLY BOUND RC-IPG-PHOSPHONATE-INHIBITOR	3.1.1.3
1R50	BACILLUS SUBTILIS LIPASE A WITH COVALENTLY BOUND SC-IPG-PHOSPHONATE-INHIBITOR	3.1.1.3
1R54	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN ADAM33	3.4.24
1R55	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN ADAM 33	3.4.24
1R58	CRYSTAL STRUCTURE OF METAP2 COMPLEXED WITH A357300	3.4.11.18
1R5C	X-RAY STRUCTURE OF THE COMPLEX OF BOVINE SEMINAL RIBONUCLEASE SWAPPING DIMER WITH D(CPA)	3.1.27.5 4.6.1.18
1R5D	X-RAY STRUCTURE OF BOVINE SEMINAL RIBONUCLEASE SWAPPING DIMER FROM A NEW CRYSTAL FORM	3.1.27.5 4.6.1.18
1R5G	CRYSTAL STRUCTURE OF METAP2 COMPLEXED WITH A311263	3.4.11.18
1R5H	CRYSTAL STRUCTURE OF METAP2 COMPLEXED WITH A320282	3.4.11.18
1R5T	THE CRYSTAL STRUCTURE OF CYTIDINE DEAMINASE CDD1, AN ORPHAN C TO U EDITASE FROM YEAST	3.5.4.5
1R5Z	CRYSTAL STRUCTURE OF SUBUNIT C OF V-ATPASE	3.6.3.14
1R62	CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF THE TWO-COMPONENT SYSTEM TRANSMITTER PROTEIN NRII (NTRB)	2.7.3 2.7.13.3 3.1.3
1R64	THE 2.2 A CRYSTAL STRUCTURE OF KEX2 PROTEASE IN COMPLEX WITH AC-ARG-GLU-LYS-BOROARG PEPTIDYL BORONIC ACID INHIBITOR	3.4.21.61
1R6A	STRUCTURE OF THE DENGUE VIRUS 2'O METHYLTRANSFERASE IN COMPLEX WITH S-ADENOSYL HOMOCYSTEINE AND RIBAVIRIN 5' TRIPHOSPHATE	2.7.7.48 3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57
1R6H	SOLUTION STRUCTURE OF HUMAN PRL-3	3.1.3.48
1R6R	SOLUTION STRUCTURE OF DENGUE VIRUS CAPSID PROTEIN REVEALS A NEW FOLD	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
1R6V	CRYSTAL STRUCTURE OF FERVIDOLYSIN FROM FERVIDOBACTERIUM PENNIVORANS, A KERATINOLYTIC ENZYME RELATED TO SUBTILISIN	3.4.21
1R77	CRYSTAL STRUCTURE OF THE CELL WALL TARGETING DOMAIN OF PEPTIDYLGLYCAN HYDROLASE ALE-1	3.4.24.7 3.4.24.75
1R7M	THE HOMING ENDONUCLEASE I-SCEI BOUND TO ITS DNA RECOGNITION REGION	3.1
1R7O	CRYSTAL STRUCTURE OF APO-MANNANASE 26A FROM PSUDOMONAS CELLULOSA	3.2.1.78
1R7R	THE CRYSTAL STRUCTURE OF MURINE P97/VCP AT 3.6A	3.6.4.6
1R8L	THE STRUCTURE OF ENDO-BETA-1,4-GALACTANASE FROM BACILLUS LICHENIFORMIS	3.2.1.89
1R9G	THREE-DIMENSIONAL STRUCTURE OF YAAE FROM BACILLUS SUBTILIS	4.3.3.6 3.5.1.2
1R9M	CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE IV AT 2.1 ANG. RESOLUTION.	3.4.14.5
1R9W	CRYSTAL STRUCTURE OF THE DNA-BINDING DOMAIN OF THE HUMAN PAPILLOMAVIRUS TYPE 18 (HPV-18) REPLICATION INITIATION PROTEIN E1	3.6.4.12
1R9X	BACTERIAL CYTOSINE DEAMINASE D314G MUTANT.	3.5.4.1 3.5.4
1R9Y	BACTERIAL CYTOSINE DEAMINASE D314A MUTANT.	3.5.4.1 3.5.4
1R9Z	BACTERIAL CYTOSINE DEAMINASE D314S MUTANT.	3.5.4.1 3.5.4
1RA0	BACTERIAL CYTOSINE DEAMINASE D314G MUTANT BOUND TO 5-FLUORO-4-(S)-HYDROXY-3,4-DIHYDROPYRIMIDINE.	3.5.4.1 3.5.4
1RA5	BACTERIAL CYTOSINE DEAMINASE D314A MUTANT BOUND TO 5-FLUORO-4-(S)-HYDROXYL-3,4-DIHYDROPYRIMIDINE.	3.5.4.1 3.5.4
1RA6	POLIOVIRUS POLYMERASE FULL LENGTH APO STRUCTURE	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
1RA7	POLIOVIRUS POLYMERASE WITH GTP	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
1RAK	BACTERIAL CYTOSINE DEAMINASE D314S MUTANT BOUND TO 5-FLUORO-4-(S)-HYDROXYL-3,4-DIHYDROPYRIMIDINE.	3.5.4.1 3.5.4
1RAR	CRYSTAL STRUCTURE OF A FLUORESCENT DERIVATIVE OF RNASE A	3.1.27.5 4.6.1.18
1RAS	CRYSTAL STRUCTURE OF A FLUORESCENT DERIVATIVE OF RNASE A	3.1.27.5 4.6.1.18
1RAT	EFFECTS OF TEMPERATURE ON PROTEIN STRUCTURE AND DYNAMICS: X-RAY CRYSTALLOGRAPHIC STUDIES OF THE PROTEIN RIBONUCLEASE-A AT NINE DIFFERENT TEMPERATURES FROM 98 TO 320 K	3.1.27.5 4.6.1.18
1RB7	YEAST CYTOSINE DEAMINASE CRYSTAL FORM P212121 WITH SODIUM ACETATE.	3.5.4.1
1RBB	THE CRYSTAL STRUCTURE OF RIBONUCLEASE B AT 2.5-ANGSTROMS RESOLUTION	3.1.27.5 4.6.1.18
1RBC	CRYSTALLOGRAPHIC STRUCTURES OF RIBONUCLEASE S VARIANTS WITH NONPOLAR SUBSTITUTION AT POSITION 13: PACKING AND CAVITIES	3.1.27.5 4.6.1.18
1RBD	CRYSTALLOGRAPHIC STRUCTURES OF RIBONUCLEASE S VARIANTS WITH NONPOLAR SUBSTITUTION AT POSITION 13: PACKING AND CAVITIES	3.1.27.5 4.6.1.18
1RBE	CRYSTALLOGRAPHIC STRUCTURES OF RIBONUCLEASE S VARIANTS WITH NONPOLAR SUBSTITUTION AT POSITION 13: PACKING AND CAVITIES	3.1.27.5 4.6.1.18
1RBF	CRYSTALLOGRAPHIC STRUCTURES OF RIBONUCLEASE S VARIANTS WITH NONPOLAR SUBSTITUTION AT POSITION 13: PACKING AND CAVITIES	3.1.27.5 4.6.1.18
1RBG	CRYSTALLOGRAPHIC STRUCTURES OF RIBONUCLEASE S VARIANTS WITH NONPOLAR SUBSTITUTION AT POSITION 13: PACKING AND CAVITIES	3.1.27.5 4.6.1.18
1RBH	CRYSTALLOGRAPHIC STRUCTURES OF RIBONUCLEASE S VARIANTS WITH NONPOLAR SUBSTITUTION AT POSITION 13: PACKING AND CAVITIES	3.1.27.5 4.6.1.18
1RBI	CRYSTALLOGRAPHIC STRUCTURES OF RIBONUCLEASE S VARIANTS WITH NONPOLAR SUBSTITUTION AT POSITION 13: PACKING AND CAVITIES	3.1.27.5 4.6.1.18
1RBJ	RIBONUCLEASE B COMPLEX WITH D(TETRA-(DEOXY-ADENYLATE))	3.1.27.5 4.6.1.18
1RBN	THE STRUCTURE OF RIBONUCLEASE A DERIVATIVE II AT 2.1 ANGSTROMS RESOLUTION	3.1.27.5 4.6.1.18
1RBR	STRUCTURAL STUDY OF MUTANTS OF ESCHERICHIA COLI RIBONUCLEASE HI WITH ENHANCED THERMOSTABILITY	3.1.26.4
1RBS	STRUCTURAL STUDY OF MUTANTS OF ESCHERICHIA COLI RIBONUCLEASE HI WITH ENHANCED THERMOSTABILITY	3.1.26.4
1RBT	STRUCTURAL STUDY OF MUTANTS OF ESCHERICHIA COLI RIBONUCLEASE HI WITH ENHANCED THERMOSTABILITY	3.1.26.4
1RBU	STRUCTURAL STUDY OF MUTANTS OF ESCHERICHIA COLI RIBONUCLEASE HI WITH ENHANCED THERMOSTABILITY	3.1.26.4
1RBV	STRUCTURAL STUDY OF MUTANTS OF ESCHERICHIA COLI RIBONUCLEASE HI WITH ENHANCED THERMOSTABILITY	3.1.26.4
1RBW	RIBONUCLEASE A (E.C.3.1.27.5) WITH GUANIDINIUM	3.1.27.5 4.6.1.18
1RBX	RIBONUCLEASE A (E.C.3.1.27.5) CONTROL	3.1.27.5 4.6.1.18
1RC5	CRYSTAL STRUCTURE OF MG(II)-COMPLEX OF RNASE III ENDONUCLEASE DOMAIN FROM AQUIFEX AEOLICUS AT 2.30 ANGSTROM RESOLUTION	3.1.26.3
1RC6	CRYSTAL STRUCTURE OF PROTEIN YLBA FROM E. COLI, PFAM DUF861	3.5.3.26
1RC7	CRYSTAL STRUCTURE OF RNASE III MUTANT E110K FROM AQUIFEX AEOLICUS COMPLEXED WITH DS-RNA AT 2.15 ANGSTROM RESOLUTION	3.1.26.3
1RC8	T4 POLYNUCLEOTIDE KINASE BOUND TO 5'-GTCAC-3' SSDNA	2.7.1.78 3.1.3.34
1RCA	STRUCTURE OF THE CRYSTALLINE COMPLEX OF DEOXYCYTIDYLYL-3',5'-GUANOSINE (3',5'-DCPDG) CO-CRYSTALISED WITH RIBONUCLEASE AT 1.9 ANGSTROMS RESOLUTION. RETROBINDING IN PANCREATIC RNASEA IS INDEPENDENT OF MODE OF INHIBITOR INTROMISSION	3.1.27.5 4.6.1.18
1RCH	SOLUTION NMR STRUCTURE OF RIBONUCLEASE HI FROM ESCHERICHIA COLI, 8 STRUCTURES	3.1.26.4
1RCJ	CRYSTAL STRUCTURE OF E166A MUTANT OF SHV-1 BETA-LACTAMASE WITH THE TRANS-ENAMINE INTERMEDIATE OF TAZOBACTAM	3.5.2.6
1RCK	THE THREE DIMENSIONAL STRUCTURE OF GUANINE-SPECIFIC RIBONUCLEASE F1 IN SOLUTION DETERMINED BY NMR SPECTROSCOPY AND DISTANCE GEOMETRY	3.1.27.3 4.6.1.24
1RCL	THE THREE DIMENSIONAL STRUCTURE OF GUANINE-SPECIFIC RIBONUCLEASE F1 IN SOLUTION DETERMINED BY NMR SPECTROSCOPY AND DISTANCE GEOMETRY	3.1.27.3 4.6.1.24
1RCM	CRYSTAL STRUCTURE OF A UBIQUITIN-DEPENDENT DEGRADATION SUBSTRATE: A THREE-DISULFIDE FORM OF LYSOZYME	3.2.1.17
1RD3	2.5A STRUCTURE OF ANTICOAGULANT THROMBIN VARIANT E217K	3.4.21.5
1RD6	CRYSTAL STRUCTURE OF S. MARCESCENS CHITINASE A MUTANT W167A	3.2.1.14
1RDA	CRYSTAL STRUCTURES OF RIBONUCLEASE HI ACTIVE SITE MUTANTS FROM ESCHERICHIA COLI	3.1.26.4
1RDB	CRYSTAL STRUCTURES OF RIBONUCLEASE HI ACTIVE SITE MUTANTS FROM ESCHERICHIA COLI	3.1.26.4
1RDC	CRYSTAL STRUCTURES OF RIBONUCLEASE HI ACTIVE SITE MUTANTS FROM ESCHERICHIA COLI	3.1.26.4
1RDD	CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNASE HI IN COMPLEX WITH MG2+ AT 2.8 ANGSTROMS RESOLUTION: PROOF FOR A SINGLE MG2+ SITE	3.1.26.4
1RDF	G50P MUTANT OF PHOSPHONOACETALDEHYDE HYDROLASE IN COMPLEX WITH SUBSTRATE ANALOGUE VINYL SULFONATE	3.11.1.1
1RDR	POLIOVIRUS 3D POLYMERASE	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
1RDS	CRYSTAL STRUCTURE OF RIBONUCLEASE MS (AS RIBONUCLEASE T1 HOMOLOGUE) COMPLEXED WITH A GUANYLYL-3',5'-CYTIDINE ANALOGUE	3.1.27.3 4.6.1.24
1RDX	R-STATE STRUCTURE OF THE ARG 243 TO ALA MUTANT OF PIG KIDNEY FRUCTOSE 1,6-BISPHOSPHATASE EXPRESSED IN E. COLI	3.1.3.11
1RDY	T-STATE STRUCTURE OF THE ARG 243 TO ALA MUTANT OF PIG KIDNEY FRUCTOSE 1,6-BISPHOSPHATASE EXPRESSED IN E. COLI	3.1.3.11
1RDZ	T-STATE STRUCTURE OF THE ARG 243 TO ALA MUTANT OF PIG KIDNEY FRUCTOSE 1,6-BISPHOSPHATASE EXPRESSED IN E. COLI	3.1.3.11
1RE1	CRYSTAL STRUCTURE OF CASPASE-3 WITH A NICOTINIC ACID ALDEHYDE INHIBITOR	3.4.22 3.4.22.56
1RE2	HUMAN LYSOZYME LABELLED WITH TWO 2',3'-EPOXYPROPYL BETA-GLYCOSIDE OF N-ACETYLLACTOSAMINE	3.2.1.17
1RED	ENDO-1,4-BETA-XYLANASE II COMPLEX WITH 4,5-EPOXYPENTYL-BETA-D-XYLOSIDE	3.2.1.8
1REE	ENDO-1,4-BETA-XYLANASE II COMPLEX WITH 3,4-EPOXYBUTYL-BETA-D-XYLOSIDE	3.2.1.8
1REF	ENDO-1,4-BETA-XYLANASE II COMPLEX WITH 2,3-EPOXYPROPYL-BETA-D-XYLOSIDE	3.2.1.8
1REM	HUMAN LYSOZYME WITH MAN-B1,4-GLCNAC COVALENTLY ATTACHED TO ASP53	3.2.1.17
1RER	CRYSTAL STRUCTURE OF THE HOMOTRIMER OF FUSION GLYCOPROTEIN E1 FROM SEMLIKI FOREST VIRUS.	3.4.21.90
1REV	HIV-1 REVERSE TRANSCRIPTASE	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1REX	NATIVE HUMAN LYSOZYME	3.2.1.17
1REY	HUMAN LYSOZYME-N,N'-DIACETYLCHITOBIOSE COMPLEX	3.2.1.17
1REZ	HUMAN LYSOZYME-N-ACETYLLACTOSAMINE COMPLEX	3.2.1.17
1RFF	CRYSTAL STRUCTURE OF HUMAN TYROSYL-DNA PHOSPHODIESTERASE COMPLEXED WITH VANADATE, OCTAPEPTIDE KLNYYDPR, AND TETRANUCLEOTIDE AGTT.	3.1.4
1RFI	CRYSTAL STRUCTURE OF HUMAN TYROSYL-DNA PHOSPHODIESTERASE COMPLEXED WITH VANADATE, PENTAPEPTIDE KLNYK, AND TETRANUCLEOTIDE AGTC	3.1.4
1RFL	NMR DATA DRIVEN STRUCTURAL MODEL OF G-DOMAIN OF MNME PROTEIN	3.6
1RFN	HUMAN COAGULATION FACTOR IXA IN COMPLEX WITH P-AMINO BENZAMIDINE	3.4.21.22
1RFP	ANALYSIS OF THE STABILIZATION OF HEN LYSOZYME WITH THE HELIX DIPOLE AND CHARGED SIDE CHAINS	3.2.1.17
1RG1	CRYSTAL STRUCTURE OF HUMAN TYROSYL-DNA PHOSPHODIESTERASE COMPLEXED WITH VANADATE, OCTOPAMINE, AND TETRANUCLEOTIDE AGTT	3.1.4
1RG2	CRYSTAL STRUCTURE OF HUMAN TYROSYL-DNA PHOSPHODIESTERASE COMPLEXED WITH VANADATE, OCTOPAMINE, AND TETRANUCLEOTIDE AGTA	3.1.4
1RGA	CRYSTAL STRUCTURE OF RNASE T1 WITH 3'-GMP AND GUANOSINE: A PRODUCT COMPLEX	3.1.27.3 4.6.1.24
1RGB	PHOSPHOLIPASE A2 FROM VIPERA AMMODYTES MERIDIONALIS	3.1.1.4
1RGC	THE COMPLEX BETWEEN RIBONUCLEASE T1 AND 3'-GUANYLIC ACID SUGGESTS GEOMETRY OF ENZYMATIC REACTION PATH. AN X-RAY STUDY	3.1.27.3 4.6.1.24
1RGE	HYDROLASE, GUANYLORIBONUCLEASE	3.1.27.3 4.6.1.24
1RGF	HYDROLASE, GUANYLORIBONUCLEASE	3.1.27.3 4.6.1.24
1RGG	HYDROLASE, GUANYLORIBONUCLEASE	3.1.27.3 4.6.1.24
1RGH	HYDROLASE, GUANYLORIBONUCLEASE	3.1.27.3 4.6.1.24
1RGK	RNASE T1 MUTANT GLU46GLN BINDS THE INHIBITORS 2'GMP AND 2'AMP AT THE 3' SUBSITE	3.1.27.3 4.6.1.24
1RGL	RNASE T1 MUTANT GLU46GLN BINDS THE INHIBITORS 2'GMP AND 2'AMP AT THE 3' SUBSITE	3.1.27.3 4.6.1.24
1RGQ	M9A HCV PROTEASE COMPLEX WITH PENTAPEPTIDE KETO-AMIDE INHIBITOR	3.4.21.98 3.4.22 3.6.1.15 3.6.4.13 2.7.7.48
1RGT	CRYSTAL STRUCTURE OF HUMAN TYROSYL-DNA PHOSPHODIESTERASE COMPLEXED WITH VANADATE, OCTOPAMINE, AND TETRANUCLEOTIDE AGTC	3.1.4
1RGU	THE CRYSTAL STRUCTURE OF HUMAN TYROSYL-DNA PHOSPHODIESTERASE COMPLEXED WITH VANADATE, OCTOPAMINE, AND TETRANUCLEOTIDE AGTG	3.1.4
1RGY	CITROBACTER FREUNDII GN346 CLASS C BETA-LACTAMASE COMPLEXED WITH TRANSITION-STATE ANALOG OF CEFOTAXIME	3.5.2.6
1RGZ	ENTEROBACTER CLOACAE GC1 CLASS C BETA-LACTAMASE COMPLEXED WITH TRANSITION-STATE ANALOG OF CEFOTAXIME	3.5.2.6
1RH0	CRYSTAL STRUCTURE OF HUMAN TYROSYL-DNA PHOSPHODIESTERASE COMPLEXED WITH VANADATE, OCTOPAMINE AND TRINUCLEOTIDE GTT	3.1.4
1RH9	FAMILY GH5 ENDO-BETA-MANNANASE FROM LYCOPERSICON ESCULENTUM (TOMATO)	3.2.1.78
1RHA	WATER DEPENDENT DOMAIN MOTION AND FLEXIBILITY IN RIBONUCLEASE A AND THE INVARIANT FEATURES IN ITS HYDRATION SHELL. AN X-RAY STUDY OF TWO LOW HUMIDITY CRYSTAL FORMS OF THE ENZYME	3.1.27.5 4.6.1.18
1RHB	WATER DEPENDENT DOMAIN MOTION AND FLEXIBILITY IN RIBONUCLEASE A AND THE INVARIANT FEATURES IN ITS HYDRATION SHELL. AN X-RAY STUDY OF TWO LOW HUMIDITY CRYSTAL FORMS OF THE ENZYME	3.1.27.5 4.6.1.18
1RHI	HUMAN RHINOVIRUS 3 COAT PROTEIN	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1RHJ	CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-3 WITH A PRYAZINONE INHIBITOR	3.4.22 3.4.22.56
1RHK	CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-3 WITH A PHENYL-PROPYL-KETONE INHIBITOR	3.4.22 3.4.22.56
1RHL	RIBONUCLEASE T1 COMPLEXED WITH 2'GMP/G23A MUTANT	3.1.27.3 4.6.1.24
1RHM	CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-3 WITH A NICOTINIC ACID ALDEHYDE INHIBITOR	3.4.22 3.4.22.56
1RHQ	CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-3 WITH A BROMOMETHOXYPHENYL INHIBITOR	3.4.22 3.4.22.56
1RHR	CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-3 WITH A CINNAMIC ACID METHYL ESTER INHIBITOR	3.4.22 3.4.22.56
1RHU	CRYSTAL STRUCTURE OF THE COMPLEX OF CASPASE-3 WITH A 5,6,7 TRICYCLIC PEPTIDOMIMETIC INHIBITOR	3.4.22 3.4.22.56
1RI6	STRUCTURE OF A PUTATIVE ISOMERASE FROM E. COLI	3.1.1.31
1RIF	CRYSTAL STRUCTURE OF THE UVSW HELICASE FROM BACTERIOPHAGE T4	3.6.4.12
1RIL	CRYSTAL STRUCTURE OF RIBONUCLEASE H FROM THERMUS THERMOPHILUS HB8 REFINED AT 2.8 ANGSTROMS RESOLUTION	3.1.26.4
1RIW	THROMBIN IN COMPLEX WITH NATURAL PRODUCT INHIBITOR OSCILLARIN	3.4.21.5
1RJP	CRYSTAL STRUCTURE OF D-AMINOACYLASE IN COMPLEX WITH 100MM CUCL2	3.5.1.81
1RJQ	THE CRYSTAL STRUCTURE OF THE D-AMINOACYLASE MUTANT D366A	3.5.1.81
1RJR	THE CRYSTAL STRUCTURE OF THE D-AMINOACYLASE D366A MUTANT IN COMPLEX WITH 100MM ZNCL2	3.5.1.81
1RJX	HUMAN PLASMINOGEN CATALYTIC DOMAIN, K698M MUTANT	3.4.21.7
1RK5	THE D-AMINOACYLASE MUTANT D366A IN COMPLEX WITH 100MM CUCL2	3.5.1.81
1RK6	THE ENZYME IN COMPLEX WITH 50MM CDCL2	3.5.1.81
1RKN	SOLUTION STRUCTURE OF 1-110 FRAGMENT OF STAPHYLOCOCCAL NUCLEASE WITH G88W MUTATION	3.1.31.1
1RKP	CRYSTAL STRUCTURE OF PDE5A1-IBMX	3.1.4.17 3.1.4.35
1RKQ	CRYSTAL STRUCTURE OF HAD-LIKE PHOSPHATASE YIDA FROM E. COLI	3.1.3.23
1RKU	CRYSTAL STRUCTURE OF THRH GENE PRODUCT OF PSEUDOMONAS AERUGINOSA	3.1.3.3
1RKV	STRUCTURE OF PHOSPHATE COMPLEX OF THRH FROM PSEUDOMONAS AERUGINOSA	3.1.3.3
1RL0	CRYSTAL STRUCTURE OF A NEW RIBOSOME-INACTIVATING PROTEIN (RIP): DIANTHIN 30	3.2.2.22
1RL4	PLASMODIUM FALCIPARUM PEPTIDE DEFORMYLASE COMPLEX WITH INHIBITOR	3.5.1.31 3.5.1.88
1RL8	CRYSTAL STRUCTURE OF THE COMPLEX OF RESISTANT STRAIN OF HIV-1 PROTEASE(V82A MUTANT) WITH RITONAVIR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RLA	THREE-DIMENSIONAL STRUCTURE OF RAT LIVER ARGINASE, THE BINUCLEAR MANGANESE METALLOENZYME OF THE UREA CYCLE	3.5.3.1
1RLK	STRUCTURE OF CONSERVED PROTEIN OF UNKNOWN FUNCTION TA0108 FROM THERMOPLASMA ACIDOPHILUM	3.1.1.29
1RLM	CRYSTAL STRUCTURE OF YBIV FROM ESCHERICHIA COLI K12	3.1.3 3.1.3.23
1RLO	PHOSPHO-ASPARTYL INTERMEDIATE ANALOGUE OF YBIV FROM E. COLI K12	3.1.3 3.1.3.23
1RLS	CRYSTAL STRUCTURE OF RNASE T1 COMPLEXED WITH THE PRODUCT NUCLEOTIDE 3'-GMP. STRUCTURAL EVIDENCE FOR DIRECT INTERACTION OF HISTIDINE 40 AND GLUTAMIC ACID 58 WITH THE 2'-HYDROXYL GROUP OF RIBOSE	3.1.27.3 4.6.1.24
1RLT	TRANSITION STATE ANALOGUE OF YBIV FROM E. COLI K12	3.1.3 3.1.3.23
1RLV	CRYSTAL STRUCTURE OF A DIMERIC ARCHAEAL SPLICING ENDONUCLEASE	3.1.27.9 4.6.1.16
1RLW	CALCIUM-PHOSPHOLIPID BINDING DOMAIN FROM CYTOSOLIC PHOSPHOLIPASE A2	3.1.1.4 3.1.1.5
1RM8	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF MMP-16/MT3-MMP: CHARACTERIZATION OF MT-MMP SPECIFIC FEATURES	3.4.24
1RMD	RAG1 DIMERIZATION DOMAIN	3.1 2.3.2.27
1RMG	RHAMNOGALACTURONASE A FROM ASPERGILLUS ACULEATUS	3.2.1 3.2.1.171
1RMQ	CRYSTAL STRUCTURE OF APHA CLASS B ACID PHOSPHATASE/PHOSPHOTRANSFERASE WITH OSMIATE MIMICKING THE CATALYTIC INTERMEDIATE	3.1.3.2
1RMS	CRYSTAL STRUCTURES OF RIBONUCLEASE MS COMPLEXED WITH 3'-GUANYLIC ACID A GP*C ANALOGUE, 2'-DEOXY-2'-FLUOROGUANYLYL-3',5'-CYTIDINE	3.1.4.23 4.6.1.24
1RMT	CRYSTAL STRUCTURE OF APHA CLASS B ACID PHOSPHATASE/PHOSPHOTRANSFERASE COMPLEXED WITH ADENOSINE.	3.1.3.2
1RMU	THREE-DIMENSIONAL STRUCTURES OF DRUG-RESISTANT MUTANTS OF HUMAN RHINOVIRUS 14	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1RMY	CRYSTAL STRUCTURE OF APHA CLASS B ACID PHOSPHATASE/PHOSPHOTRANSFERASE TERNARY COMPLEX WITH DEOXYCYTOSINE AND PHOSPHATE BOUND TO THE CATALYTIC METAL	3.1.3.2
1RMZ	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH THE INHIBITOR NNGH AT 1.3 A RESOLUTION	3.4.24.65
1RN1	THREE-DIMENSIONAL STRUCTURE OF GLN 25-RIBONUCLEASE T1 AT 1.84 ANGSTROMS RESOLUTION: STRUCTURAL VARIATIONS AT THE BASE RECOGNITION AND CATALYTIC SITES	3.1.27.3 4.6.1.24
1RN4	HIS92ALA MUTATION IN RIBONUCLEASE T1 INDUCES SEGMENTAL FLEXIBILITY. AN X-RAY STUDY	3.1.27.3 4.6.1.24
1RN8	CRYSTAL STRUCTURE OF DUTPASE COMPLEXED WITH SUBSTRATE ANALOGUE IMIDO-DUTP	3.6.1.23
1RNB	CRYSTAL STRUCTURE OF A BARNASE-D(*GP*C) COMPLEX AT 1.9 ANGSTROMS RESOLUTION	3.1.27
1RNC	NEWLY OBSERVED BINDING MODE IN PANCREATIC RIBONUCLEASE	3.1.27.5 4.6.1.18
1RND	NEWLY OBSERVED BINDING MODE IN PANCREATIC RIBONUCLEASE	3.1.27.5 4.6.1.18
1RNE	THE CRYSTAL STRUCTURE OF RECOMBINANT GLYCOSYLATED HUMAN RENIN ALONE AND IN COMPLEX WITH A TRANSITION STATE ANALOG INHIBITOR	3.4.23.15
1RNF	X-RAY CRYSTAL STRUCTURE OF UNLIGANDED HUMAN RIBONUCLEASE 4	3.1.27
1RNH	STRUCTURE OF RIBONUCLEASE H PHASED AT 2 ANGSTROMS RESOLUTION BY MAD ANALYSIS OF THE SELENOMETHIONYL PROTEIN	3.1.26.4
1RNJ	CRYSTAL STRUCTURE OF INACTIVE MUTANT DUTPASE COMPLEXED WITH SUBSTRATE ANALOGUE IMIDO-DUTP	3.6.1.23
1RNM	RIBONUCLEASE A COMPLEX WITH CYTIDYLIC ACID (5'CMP) CRYSTALLIZED FROM 80% AMMONIUM SULPHATE	3.1.27.5 4.6.1.18
1RNN	RIBONUCLEASE A COMPLEX WITH CYTIDYLIC ACID (5'CMP) CRYSTALLIZED FROM 8M SODIUM FORMATE	3.1.27.5 4.6.1.18
1RNO	RIBONUCLEASE A CRYSTALLIZED FROM 80% AMMONIUM SULPHATE	3.1.27.5 4.6.1.18
1RNQ	RIBONUCLEASE A CRYSTALLIZED FROM 8M SODIUM FORMATE	3.1.27.5 4.6.1.18
1RNT	RESTRAINED LEAST-SQUARES REFINEMENT OF THE CRYSTAL STRUCTURE OF THE RIBONUCLEASE T1(ASTERISK)2(PRIME)-GUANYLIC ACID COMPLEX AT 1.9 ANGSTROMS RESOLUTION	3.1.27.3 4.6.1.24
1RNU	REFINEMENT OF THE CRYSTAL STRUCTURE OF RIBONUCLEASE S. COMPARISON WITH AND BETWEEN THE VARIOUS RIBONUCLEASE A STRUCTURES	3.1.27.5 4.6.1.18
1RNV	REFINEMENT OF THE CRYSTAL STRUCTURE OF RIBONUCLEASE S. COMPARISON WITH AND BETWEEN THE VARIOUS RIBONUCLEASE A STRUCTURES	3.1.27.5 4.6.1.18
1RNW	RECOMBINANT RIBONUCLEASE A CRYSTALLIZED FROM 80% AMMONIUM SULPHATE	3.1.27.5 4.6.1.18
1RNX	RIBONUCLEASE A CRYSTALLIZED FROM 3M SODIUM CHLORIDE, 30% AMMONIUM SULFATE	3.1.27.5 4.6.1.18
1RNY	RIBONUCLEASE A CRYSTALLIZED FROM 3M CESIUM CHLORIDE, 30% AMMONIUM SULFATE	3.1.27.5 4.6.1.18
1RNZ	RIBONUCLEASE A CRYSTALLIZED FROM 2.5M SODIUM CHLORIDE, 3.3M SODIUM FORMATE	3.1.27.5 4.6.1.18
1RO6	CRYSTAL STRUCTURE OF PDE4B2B COMPLEXED WITH ROLIPRAM (R & S)	3.1.4.17 3.1.4.53
1RO9	CRYSTAL STRUCTURES OF THE CATALYTIC DOMAIN OF PHOSPHODIESTERASE 4B2B COMPLEXED WITH 8-BR-AMP	3.1.4.17 3.1.4.53
1ROB	STRUCTURE OF THE CRYSTALLINE COMPLEX OF CYTIDYLIC ACID (2'-CMP) WITH RIBONUCLEASE AT 1.6 ANGSTROMS RESOLUTION	3.1.27.5 4.6.1.18
1ROR	CRYSTAL STRUCTURES OF THE CATALYTIC DOMAIN OF PHOSPHODIESTERASE 4B2B COMPLEXED WITH AMP	3.1.4.17 3.1.4.53
1ROS	CRYSTAL STRUCTURE OF MMP-12 COMPLEXED TO 2-(1,3-DIOXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)ETHYL-4-(4-ETHOXY[1,1-BIPHENYL]-4-YL)-4-OXOBUTANOIC ACID	3.4.24.65
1RP1	DOG PANCREATIC LIPASE RELATED PROTEIN 1	3.1.1.3
1RP5	PBP2X FROM STREPTOCOCCUS PNEUMONIAE STRAIN 5259 WITH REDUCED SUSCEPTIBILITY TO BETA-LACTAM ANTIBIOTICS	3.4
1RP8	CRYSTAL STRUCTURE OF BARLEY ALPHA-AMYLASE ISOZYME 1 (AMY1) INACTIVE MUTANT D180A IN COMPLEX WITH MALTOHEPTAOSE	3.2.1.1
1RP9	CRYSTAL STRUCTURE OF BARLEY ALPHA-AMYLASE ISOZYME 1 (AMY1) INACTIVE MUTANT D180A IN COMPLEX WITH ACARBOSE	3.2.1.1
1RPA	THREE-DIMENSIONAL STRUCTURE OF RAT ACID PHOSPHATASE IN COMPLEX WITH L(+) TARTRATE	3.1.3.2 3.1.3.5
1RPF	THE STRUCTURES OF RNASE COMPLEXED WITH 3'-CMP AND D(CPA): ACTIVE SITE CONFORMATION AND CONSERVED WATER MOLECULES	3.1.27.5 4.6.1.18
1RPG	STRUCTURES OF RNASE A COMPLEXED WITH 3'-CMP AND D(CPA): ACTIVE SITE CONFORMATION AND CONSERVED WATER MOLECULES	3.1.27.5 4.6.1.18
1RPH	STRUCTURES OF RNASE A COMPLEXED WITH 3'-CMP AND D(CPA): ACTIVE SITE CONFORMATION AND CONSERVED WATER MOLECULES	3.1.27.5 4.6.1.18
1RPI	CRYSTAL STRUCTURES OF A MULTIDRUG-RESISTANT HIV-1 PROTEASE REVEAL AN EXPANDED ACTIVE SITE CAVITY	3.4.23.16
1RPK	CRYSTAL STRUCTURE OF BARLEY ALPHA-AMYLASE ISOZYME 1 (AMY1) IN COMPLEX WITH ACARBOSE	3.2.1.1
1RPM	HUMAN RECEPTOR PROTEIN TYROSINE PHOSPHATASE MU, DOMAIN 1	3.1.3.48
1RPT	CRYSTAL STRUCTURES OF RAT ACID PHOSPHATASE COMPLEXED WITH THE TRANSITIONS STATE ANALOGS VANADATE AND MOLYBDATE: IMPLICATIONS FOR THE REACTION MECHANISM	3.1.3.2 3.1.3.5
1RPZ	T4 POLYNUCLEOTIDE KINASE BOUND TO 5'-TGCAC-3' SSDNA	2.7.1.78 3.1.3.34
1RQ5	STRUCTURAL BASIS FOR THE EXOCELLULASE ACTIVITY OF THE CELLOBIOHYDROLASE CBHA FROM C. THERMOCELLUM	3.2.1.91 3.2.1
1RQ9	CRYSTAL STRUCTURES OF A MULTIDRUG-RESISTANT HIV-1 PROTEASE REVEAL AN EXPANDED ACTIVE SITE CAVITY	3.4.23.16
1RQC	CRYSTALS OF PEPTIDE DEFORMYLASE FROM PLASMODIUM FALCIPARUM WITH TEN SUBUNITS PER ASYMMETRIC UNIT REVEAL CRITICAL CHARACTERISTICS OF THE ACTIVE SITE FOR DRUG DESIGN	3.5.1.88
1RQL	CRYSTAL STRUCTURE OF PHOSPONOACETALDEHYDE HYDROLASE COMPLEXED WITH MAGNESIUM AND THE INHIBITOR VINYL SULFONATE	3.11.1.1
1RQN	PHOSPHONOACETALDEHYDE HYDROLASE COMPLEXED WITH MAGNESIUM	3.11.1.1
1RQX	CRYSTAL STRUCTURE OF ACC DEAMINASE COMPLEXED WITH INHIBITOR	3.5.99.7
1RR9	CATALYTIC DOMAIN OF E.COLI LON PROTEASE	3.4.21.53
1RRA	RIBONUCLEASE A FROM RATTUS NORVEGICUS (COMMON RAT)	3.1.27.5 4.6.1.18
1RRC	T4 POLYNUCLEOTIDE KINASE BOUND TO 5'-GTC-3' SSDNA	2.7.1.78 3.1.3.34
1RRE	CRYSTAL STRUCTURE OF E.COLI LON PROTEOLYTIC DOMAIN	3.4.21.53
1RRK	CRYSTAL STRUCTURE ANALYSIS OF THE BB SEGMENT OF FACTOR B	3.4.21.47
1RRQ	MUTY ADENINE GLYCOSYLASE IN COMPLEX WITH DNA CONTAINING AN A:OXOG PAIR	3.2.2 3.2.2.31
1RRS	MUTY ADENINE GLYCOSYLASE IN COMPLEX WITH DNA CONTAINING AN ABASIC SITE	3.2.2 3.2.2.31
1RS0	CRYSTAL STRUCTURE ANALYSIS OF THE BB SEGMENT OF FACTOR B COMPLEXED WITH DI-ISOPROPYL-PHOSPHATE (DIP)	3.4.21.47
1RSM	THE 2-ANGSTROMS RESOLUTION STRUCTURE OF A THERMOSTABLE RIBONUCLEASE A CHEMICALLY CROSS-LINKED BETWEEN LYSINE RESIDUES 7 AND 41	3.1.27.5 4.6.1.18
1RSN	RIBONUCLEASE (RNASE SA) (E.C.3.1.4.8) COMPLEXED WITH EXO-2',3'-CYCLOPHOSPHOROTHIOATE	3.1.27.3 4.6.1.24
1RT1	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE COMPLEXED WITH MKC-442	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RT2	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE COMPLEXED WITH TNK-651	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RT3	AZT DRUG RESISTANT HIV-1 REVERSE TRANSCRIPTASE COMPLEXED WITH 1051U91	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RT4	HIV-1 REVERSE TRANSCRIPTASE COMPLEXED WITH UC781	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RT5	HIV-1 REVERSE TRANSCRIPTASE COMPLEXED WITH UC10	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RT6	HIV-1 REVERSE TRANSCRIPTASE COMPLEXED WITH UC38	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RT7	HIV-1 REVERSE TRANSCRIPTASE COMPLEXED WITH UC84	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RTB	CRYSTAL STRUCTURE DISPOSITION OF THYMIDYLIC ACID TETRAMER IN COMPLEX WITH RIBONUCLEASE A	3.1.27.5 4.6.1.18
1RTC	THE STRUCTURE OF RECOMBINANT RICIN A CHAIN AT 2.3 ANGSTROMS	3.2.2.22
1RTD	STRUCTURE OF A CATALYTIC COMPLEX OF HIV-1 REVERSE TRANSCRIPTASE: IMPLICATIONS FOR NUCLEOSIDE ANALOG DRUG RESISTANCE	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RTF	COMPLEX OF BENZAMIDINE WITH THE CATALYTIC DOMAIN OF HUMAN TWO CHAIN TISSUE PLASMINOGEN ACTIVATOR [(TC)-T-PA]	3.4.21.68
1RTG	C-TERMINAL DOMAIN (HAEMOPEXIN-LIKE DOMAIN) OF HUMAN MATRIX METALLOPROTEINASE-2	3.4.24.24
1RTH	HIGH RESOLUTION STRUCTURES OF HIV-1 RT FROM FOUR RT-INHIBITOR COMPLEXES	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RTI	HIGH RESOLUTION STRUCTURES OF HIV-1 RT FROM FOUR RT-INHIBITOR COMPLEXES	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RTJ	MECHANISM OF INHIBITION OF HIV-1 REVERSE TRANSCRIPTASE BY NON-NUCLEOSIDE INHIBITORS	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1RTK	CRYSTAL STRUCTURE ANALYSIS OF THE BB SEGMENT OF FACTOR B COMPLEXED WITH 4-GUANIDINOBENZOIC ACID	3.4.21.47
1RTL	CRYSTAL STRUCTURE OF HCV NS3 PROTEASE DOMAIN: NS4A PEPTIDE COMPLEX WITH COVALENTLY BOUND PYRROLIDINE-5,5-TRANSLACTAM INHIBITOR	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
1RTQ	THE 0.95 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF THE AMINOPEPTIDASE FROM AEROMONAS PROTEOLYTICA	3.4.11.10
1RUC	RHINOVIRUS 14 MUTANT N1105S COMPLEXED WITH ANTIVIRAL COMPOUND WIN 52035	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1RUD	RHINOVIRUS 14 MUTANT N1105S COMPLEXED WITH ANTIVIRAL COMPOUND WIN 52084	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1RUE	RHINOVIRUS 14 SITE DIRECTED MUTANT N1219A COMPLEXED WITH ANTIVIRAL COMPOUND WIN 52035	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1RUF	RHINOVIRUS 14 (HRV14) (MUTANT WITH ASN 1 219 REPLACED BY ALA (N219A IN CHAIN 1)	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1RUG	RHINOVIRUS 14 MUTANT N1219S COMPLEXED WITH ANTIVIRAL COMPOUND WIN 52035	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1RUH	RHINOVIRUS 14 MUTANT N1219S COMPLEXED WITH ANTIVIRAL COMPOUND WIN 52084	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1RUI	RHINOVIRUS 14 MUTANT S1223G COMPLEXED WITH ANTIVIRAL COMPOUND WIN 52084	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1RUJ	RHINOVIRUS 14 MUTANT WITH SER 1 223 REPLACED BY GLY (S1223G)	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1RUV	RIBONUCLEASE A-URIDINE VANADATE COMPLEX: HIGH RESOLUTION RESOLUTION X-RAY STRUCTURE (1.3 A)	3.1.27.5 4.6.1.18
1RV5	COMPLEX OF ECORV ENDONUCLEASE WITH D(AAAGAT)/D(ATCTT)	3.1.21.4
1RV7	CRYSTAL STRUCTURES OF A MULTIDRUG-RESISTANT HIV-1 PROTEASE REVEAL AN EXPANDED ACTIVE SITE CAVITY	3.4.23.16
1RVA	MG2+ BINDING TO THE ACTIVE SITE OF ECO RV ENDONUCLEASE: A CRYSTALLOGRAPHIC STUDY OF COMPLEXES WITH SUBSTRATE AND PRODUCT DNA AT 2 ANGSTROMS RESOLUTION	3.1.21.4
1RVB	MG2+ BINDING TO THE ACTIVE SITE OF ECO RV ENDONUCLEASE: A CRYSTALLOGRAPHIC STUDY OF COMPLEXES WITH SUBSTRATE AND PRODUCT DNA AT 2 ANGSTROMS RESOLUTION	3.1.21.4
1RVC	MG2+ BINDING TO THE ACTIVE SITE OF ECO RV ENDONUCLEASE: A CRYSTALLOGRAPHIC STUDY OF COMPLEXES WITH SUBSTRATE AND PRODUCT DNA AT 2 ANGSTROMS RESOLUTION	3.1.21.4
1RVD	H-RAS COMPLEXED WITH DIAMINOBENZOPHENONE-BETA,GAMMA-IMIDO-GTP	3.6.5.2
1RVE	THE CRYSTAL STRUCTURE OF ECORV ENDONUCLEASE AND OF ITS COMPLEXES WITH COGNATE AND NON-COGNATE DNA FRAGMENTS	3.1.21.4
1RVF	FAB COMPLEXED WITH INTACT HUMAN RHINOVIRUS	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1RW2	THREE-DIMENSIONAL STRUCTURE OF KU80 CTD	3.6.4
1RWK	CRYSTAL STRUCTURE OF HUMAN CASPASE-1 IN COMPLEX WITH 3-(2-MERCAPTO-ACETYLAMINO)-4-OXO-PENTANOIC ACID	3.4.22.36
1RWM	CRYSTAL STRUCTURE OF HUMAN CASPASE-1 IN COMPLEX WITH 4-OXO-3-[2-(5-{[4-(QUINOXALIN-2-YLAMINO)-BENZOYLAMINO]-METHYL}-THIOPHEN-2-YL)-ACETYLAMINO]-PENTANOIC ACID	3.4.22.36
1RWN	CRYSTAL STRUCTURE OF HUMAN CASPASE-1 IN COMPLEX WITH 3-{2-ETHYL-6-[4-(QUINOXALIN-2-YLAMINO)-BENZOYLAMINO]-HEXANOYLAMINO}-4-OXO-BUTYRIC ACID	3.4.22.36
1RWO	CRYSTAL STRUCTURE OF HUMAN CASPASE-1 IN COMPLEX WITH 4-OXO-3-{6-[4-(QUINOXALIN-2-YLAMINO)-BENZOYLAMINO]-2-THIOPHEN-2-YL-HEXANOYLAMINO}-PENTANOIC ACID	3.4.22.36
1RWP	CRYSTAL STRUCTURE OF HUMAN CASPASE-1 IN COMPLEX WITH 3-{6-[(8-HYDROXY-QUINOLINE-2-CARBONYL)-AMINO]-2-THIOPHEN-2-YL-HEXANOYLAMINO}-4-OXO-BUTYRIC ACID	3.4.22.36
1RWQ	HUMAN DIPEPTIDYL PEPTIDASE IV IN COMPLEX WITH 5-AMINOMETHYL-6-(2,4-DICHLORO-PHENYL)-2-(3,5-DIMETHOXY-PHENYL)-PYRIMIDIN-4-YLAMINE	3.4.14.5
1RWV	CRYSTAL STRUCTURE OF HUMAN CASPASE-1 IN COMPLEX WITH 5-[5-(1-CARBOXYMETHYL-2-OXO-PROPYLCARBAMOYL)-5-PHENYL-PENTYLSULFAMOYL]-2-HYDROXY-BENZOIC ACID	3.4.22.36
1RWW	CRYSTAL STRUCTURE OF HUMAN CASPASE-1 IN COMPLEX WITH 4-OXO-3-[(6-{[4-(QUINOXALIN-2-YLAMINO)-BENZOYLAMINO]-METHYL}-PYRIDINE-3-CARBONYL)-AMINO]-BUTYRIC ACID	3.4.22.36
1RWX	CRYSTAL STRUCTURE OF HUMAN CASPASE-1 IN COMPLEX WITH 4-OXO-3-{6-[4-(QUINOXALIN-2-YLOXY)-BENZOYLAMINO]-2-THIOPHEN-2-YL-HEXANOYLAMINO}-BUTYRIC ACID	3.4.22.36
1RXD	CRYSTAL STRUCTURE OF HUMAN PROTEIN TYROSINE PHOSPHATASE 4A1	3.1.3.48
1RXP	STRUCTURE OF TRYPSIN (ORTHORHOMBIC) WITH 1-(4-TERT-BUTYLCARBAMOYL- PIPERAZINE-1-CARBONYL)-3-(3-GUANIDINO-PROPYL)-4-OXO-AZETIDINE-2-CARBOXYLIC ACID	3.4.21.4
1RXQ	YFIT FROM BACILLUS SUBTILIS IS A PROBABLE METAL-DEPENDENT HYDROLASE WITH AN UNUSUAL FOUR-HELIX BUNDLE TOPOLOGY	3
1RXV	CRYSTAL STRUCTURE OF A. FULGIDUS FEN-1 BOUND TO DNA	3.1
1RXW	CRYSTAL STRUCTURE OF A. FULGIDUS FEN-1 BOUND TO DNA	3.1
1RXX	STRUCTURE OF ARGININE DEIMINASE	3.5.3.6
1RYA	CRYSTAL STRUCTURE OF THE E. COLI GDP-MANNOSE MANNOSYL HYDROLASE IN COMPLEX WITH GDP AND MG	3.6.1
1RYB	CRYSTAL STRUCTURE OF THE CHLOROPLAST GROUP II INTRON SPLICING FACTOR CRS2	3.1.1.29
1RYF	ALTERNATIVE SPLICING OF RAC1 GENERATES RAC1B, A SELF-ACTIVATING GTPASE	3.6.5.2
1RYH	ALTERNATIVE SPLICING OF RAC1 GENERATES RAC1B, A SELF-ACTIVATING GTPASE	3.6.5.2
1RZ2	1.6A CRYSTAL STRUCTURE OF THE PROTEIN BA4783/Q81L49 (SIMILAR TO SORTASE B) FROM BACILLUS ANTHRACIS.	3.4.22.71
1RZN	CRYSTAL STRUCTURE OF PENICILLIN-BINDING PROTEIN-RELATED FACTOR A FROM BACILLUS SUBTILIS.	3.1.22.4
1RZO	AGGLUTININ FROM RICINUS COMMUNIS WITH GALACTOAZA	3.2.2.22
1RZW	THE SOLUTION STRUCTURE OF THE ARCHAEGLOBUS FULGIDIS PROTEIN AF2095. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET GR4	3.1.1.29
1RZY	CRYSTAL STRUCTURE OF RABBIT HINT COMPLEXED WITH N-ETHYLSULFAMOYLADENOSINE	3
1S01	LARGE INCREASES IN GENERAL STABILITY FOR SUBTILISIN BPN(PRIME) THROUGH INCREMENTAL CHANGES IN THE FREE ENERGY OF UNFOLDING	3.4.21.62
1S02	EFFECTS OF ENGINEERED SALT BRIDGES ON THE STABILITY OF SUBTILISIN BPN'	3.4.21.14 3.4.21.62
1S0B	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN TYPE B AT PH 4.0	3.4.24.69
1S0C	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN TYPE B AT PH 5.0	3.4.24.69
1S0D	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN TYPE B AT PH 5.5	3.4.24.69
1S0E	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN TYPE B AT PH 6.0	3.4.24.69
1S0F	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN TYPE B AT PH 7.0	3.4.24.69
1S0G	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN TYPE B APO FORM	3.4.24.69
1S0I	TRYPANOSOMA CRUZI TRANS-SIALIDASE IN COMPLEX WITH SIALYL-LACTOSE (MICHAELIS COMPLEX)	3.2.1.18
1S0J	TRYPANOSOMA CRUZI TRANS-SIALIDASE IN COMPLEX WITH MUNANA (MICHAELIS COMPLEX)	3.2.1.18
1S0Q	NATIVE BOVINE PANCREATIC TRYPSIN	3.4.21.4
1S0R	BOVINE PANCREATIC TRYPSIN INHIBITED WITH BENZAMIDINE AT ATOMIC RESOLUTION	3.4.21.4
1S0U	EIF2GAMMA APO	3.6.5.3
1S0W	1B LACTAMSE/ B LACTAMASE INHIBITOR	3.5.2.6
1S17	IDENTIFICATION OF NOVEL POTENT BICYCLIC PEPTIDE DEFORMYLASE INHIBITORS	3.5.1.88
1S18	STRUCTURE AND PROTEIN DESIGN OF HUMAN APYRASE	3.6.1.5 3.6.1.6
1S1C	CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THE HUMAN RHOA AND RHO-BINDING DOMAIN OF HUMAN ROCKI	3.6.5.2
1S1D	STRUCTURE AND PROTEIN DESIGN OF HUMAN APYRASE	3.6.1.5 3.6.1.6
1S1T	CRYSTAL STRUCTURE OF L100I MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH UC-781	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1S1U	CRYSTAL STRUCTURE OF L100I MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH NEVIRAPINE	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1S1V	CRYSTAL STRUCTURE OF L100I MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH TNK-651	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1S1W	CRYSTAL STRUCTURE OF V106A MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH UC-781	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1S1X	CRYSTAL STRUCTURE OF V108I MUTANT HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH NEVIRAPINE	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1S2B	STRUCTURE OF SCP-B THE FIRST MEMBER OF THE EQOLISIN FAMILY OF PEPTIDASES TO HAVE ITS STRUCTURE DETERMINED	3.4.23.32
1S2J	CRYSTAL STRUCTURE OF THE DROSOPHILA PATTERN-RECOGNITION RECEPTOR PGRP-SA	3.4.17.13
1S2K	STRUCTURE OF SCP-B A MEMBER OF THE EQOLISIN FAMILY OF PEPTIDASES IN A COMPLEX WITH A TRIPEPTIDE ALA-ILE-HIS	3.4.23.32
1S2M	CRYSTAL STRUCTURE OF THE DEAD BOX PROTEIN DHH1P	3.6.4.13
1S2N	CRYSTAL STRUCTURE OF A COLD ADAPTED SUBTILISIN-LIKE SERINE PROTEINASE	3.4.21
1S2O	X-RAY STRUCTURE OF THE SUCROSE-PHOSPHATASE (SPP) FROM SYNECHOCYSTIS SP. PCC6803 AT 1.40 A RESOLUTION	3.1.3.24
1S3L	STRUCTURAL AND FUNCTIONAL CHARACTERIZATION OF A NOVEL ARCHAEAL PHOSPHODIESTERASE	3.1.4
1S3M	STRUCTURAL AND FUNCTIONAL CHARACTERIZATION OF A NOVEL ARCHAEAL PHOSPHODIESTERASE	3.1.4
1S3N	STRUCTURAL AND FUNCTIONAL CHARACTERIZATION OF A NOVEL ARCHAEAL PHOSPHODIESTERASE	3.1.4
1S3T	BORATE INHIBITED BACILLUS PASTEURII UREASE CRYSTAL STRUCTURE	3.5.1.5
1S48	CRYSTAL STRUCTURE OF RNA-DEPENDENT RNA POLYMERASE CONSTRUCT 1 (RESIDUES 71-679) FROM BVDV	3.4.22 3.4.21.113 3.6.1.15 3.6.4.13 2.7.7.48
1S49	CRYSTAL STRUCTURE OF RNA-DEPENDENT RNA POLYMERASE CONSTRUCT 1 (RESIDUES 71-679) FROM BOVINE VIRAL DIARRHEA VIRUS COMPLEXED WITH GTP	3.4.22 3.4.21.113 3.6.1.15 3.6.4.13 2.7.7.48
1S4B	CRYSTAL STRUCTURE OF HUMAN THIMET OLIGOPEPTIDASE.	3.4.24.15
1S4V	THE 2.0 A CRYSTAL STRUCTURE OF THE KDEL-TAILED CYSTEINE ENDOPEPTIDASE FUNCTIONING IN PROGRAMMED CELL DEATH OF RICINUS COMMUNIS ENDOSPERM	3.4.22
1S58	THE STRUCTURE OF B19 PARVOVIRUS CAPSID	3.1.1.4
1S5P	STRUCTURE AND SUBSTRATE BINDING PROPERTIES OF COBB, A SIR2 HOMOLOG PROTEIN DEACETYLASE FROM ESCHERICIA COLI.	3.5.1 2.3.1.286
1S5S	PORCINE TRYPSIN COMPLEXED WITH GUANIDINE-3-PROPANOL INHIBITOR	3.4.21.4
1S5U	CRYSTAL STRUCTURE OF HYPOTHETICAL PROTEIN EC709 FROM ESCHERICHIA COLI	3.1.2
1S66	CRYSTAL STRUCTURE OF HEME DOMAIN OF DIRECT OXYGEN SENSOR FROM E. COLI	3.1.4.52
1S67	CRYSTAL STRUCTURE OF HEME DOMAIN OF DIRECT OXYGEN SENSOR FROM E. COLI	3.1.4.52
1S6B	X-RAY CRYSTAL STRUCTURE OF A COMPLEX FORMED BETWEEN TWO HOMOLOGOUS ISOFORMS OF PHOSPHOLIPASE A2 FROM NAJA NAJA SAGITTIFERA: PRINCIPLE OF MOLECULAR ASSOCIATION AND INACTIVATION	3.1.1.4
1S6F	PORCINE TRYPSIN COVALENT COMPLEX WITH BORATE AND GUANIDINE-3 INHIBITOR	3.4.21.4
1S6H	PORCINE TRYPSIN COMPLEXED WITH GUANIDINE-3-PROPANOL INHIBITOR	3.4.21.4
1S6O	SOLUTION STRUCTURE AND BACKBONE DYNAMICS OF THE APO-FORM OF THE SECOND METAL-BINDING DOMAIN OF THE MENKES PROTEIN ATP7A	3.6.3.4 7.2.2.8
1S6P	CRYSTAL STRUCTURE OF HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH JANSSEN-R100943	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1S6Q	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH JANSSEN-R147681	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1S6R	908R CLASS C BETA-LACTAMASE BOUND TO IODO-ACETAMIDO-PHENYL BORONIC ACID	3.5.2.6
1S6U	SOLUTION STRUCTURE AND BACKBONE DYNAMICS OF THE CU(I) FORM OF THE SECOND METAL-BINDING DOMAIN OF THE MENKES PROTEIN ATP7A	3.6.3.4 7.2.2.8
1S6Y	2.3A CRYSTAL STRUCTURE OF PHOSPHO-BETA-GLUCOSIDASE	3.2.1.86
1S70	COMPLEX BETWEEN PROTEIN SER/THR PHOSPHATASE-1 (DELTA) AND THE MYOSIN PHOSPHATASE TARGETING SUBUNIT 1 (MYPT1)	3.1.3.16 3.1.3.53
1S7G	STRUCTURAL BASIS FOR THE MECHANISM AND REGULATION OF SIR2 ENZYMES	3.5.1 2.3.1.286
1S81	PORCINE TRYPSIN WITH NO INHIBITOR BOUND	3.4.21.4
1S82	PORCINE TRYPSIN COMPLEXED WITH BORATE AND ETHYLENE GLYCOL	3.4.21.4
1S83	PORCINE TRYPSIN COMPLEXED WITH 4-AMINO PROPANOL	3.4.21.4
1S84	PORCINE TRYPSIN COVALENT COMPLEX WITH 4-AMINO BUTANOL, BORATE AND ETHYLENE GLYCOL	3.4.21.4
1S85	PORCINE TRYPSIN COMPLEXED WITH P-HYDROXYMETHYL BENZAMIDINE AND BORATE	3.4.21.4
1S8E	CRYSTAL STRUCTURE OF MRE11-3	3.1
1S8G	CRYSTAL STRUCTURE OF LYS49-PHOSPHOLIPASE A2 FROM AGKISTRODON CONTORTRIX LATICINCTUS, FATTY ACID BOUND FORM	3.1.1.4
1S8H	CRYSTAL STRUCTURE OF LYS49-PHOSPHOLIPASE A2 FROM AGKISTRODON CONTORTRIX LATICINCTUS, FIRST FATTY ACID FREE FORM	3.1.1.4
1S8I	CRYSTAL STRUCTURE OF LYS49-PHOSPHOLIPASE A2 FROM AGKISTRODON CONTORTRIX LATICINCTUS, SECOND FATTY ACID FREE FORM	3.1.1.4
1S8O	HUMAN SOLUBLE EPOXIDE HYDROLASE	3.3.2.3 3.3.2.10 3.1.3.76
1S95	STRUCTURE OF SERINE/THREONINE PROTEIN PHOSPHATASE 5	3.1.3.16
1S9E	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH JANSSEN-R129385	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1S9G	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH JANSSEN-R120394.	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1S9H	CRYSTAL STRUCTURE OF ADENO-ASSOCIATED VIRUS TYPE 2 REP40	3.6.4.12
1S9R	CRYSTAL STRUCTURE OF ARGININE DEIMINASE COVALENTLY LINKED WITH A REACTION INTERMEDIATE	3.5.3.6
1SA3	AN ASYMMETRIC COMPLEX OF RESTRICTION ENDONUCLEASE MSPI ON ITS PALINDROMIC DNA RECOGNITION SITE	3.1.21.4
1SAT	CRYSTAL STRUCTURE OF THE 50 KDA METALLO PROTEASE FROM S. MARCESCENS	3.4.24.40
1SAW	X-RAY STRUCTURE OF HOMO SAPIENS PROTEIN FLJ36880	3.7.1.5 4.1.1.112
1SB1	NOVEL NON-COVALENT THROMBIN INHIBITORS INCORPORATING P1 4,5,6,7-TETRAHYDROBENZOTHIAZOLE ARGININE SIDE CHAIN MIMETICS	3.4.21.5
1SBC	THE REFINED CRYSTAL STRUCTURE OF SUBTILISIN CARLSBERG AT 2.5 ANGSTROMS RESOLUTION	3.4.21.62
1SBG	AN ORALLY-BIOAVAILABLE HIV-1 PROTEASE INHIBITOR CONTAINING AN IMIDAZOLE-DERIVED PEPTIDE BOND REPLACEMENT. CRYSTALLOGRAPHIC AND PHARMACOKINETIC ANALYSIS	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1SBH	SUBTILISIN BPN' 8397+1 (E.C. 3.4.21.14) MUTANT (M50F, N76D, G169A, Q206C, N218S, K256Y)	3.4.21.62
1SBI	SUBTILISIN BPN' 8397 (E.C. 3.4.21.14) MUTANT (M50F, N76D, G169A, Q206C, N218S)	3.4.21.62
1SBK	X-RAY STRUCTURE OF YDII_ECOLI NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET ER29.	3.1.2.28
1SBN	REFINED CRYSTAL STRUCTURES OF SUBTILISIN NOVO IN COMPLEX WITH WILD-TYPE AND TWO MUTANT EGLINS. COMPARISON WITH OTHER SERINE PROTEINASE INHIBITOR COMPLEXES	3.4.21.62
1SBT	ATOMIC COORDINATES FOR SUBTILISIN BPN (OR NOVO)	3.4.21.14 3.4.21.62
1SBW	CRYSTAL STRUCTURE OF MUNG BEAN INHIBITOR LYSINE ACTIVE FRAGMENT COMPLEX WITH BOVINE BETA-TRYPSIN AT 1.8A RESOLUTION	3.4.21.4
1SC0	X-RAY STRUCTURE OF YB61_HAEIN NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET IR63	3.1.2
1SC1	CRYSTAL STRUCTURE OF AN ACTIVE-SITE LIGAND-FREE FORM OF THE HUMAN CASPASE-1 C285A MUTANT	3.4.22.36
1SC3	CRYSTAL STRUCTURE OF THE HUMAN CASPASE-1 C285A MUTANT IN COMPLEX WITH MALONATE	3.4.22.36
1SC4	CRYSTAL STRUCTURE OF THE HUMAN CASPASE-1 C285A MUTANT AFTER REMOVAL OF MALONATE	3.4.22.36
1SC8	UROKINASE PLASMINOGEN ACTIVATOR B-CHAIN-J435 COMPLEX	3.4.21.73
1SCA	ENZYME CRYSTAL STRUCTURE IN A NEAT ORGANIC SOLVENT	3.4.21.62
1SCB	ENZYME CRYSTAL STRUCTURE IN A NEAT ORGANIC SOLVENT	3.4.21.62
1SCD	X-RAY CRYSTAL STRUCTURE OF CROSS-LINKED SUBTILISM CARLSBERG IN WATER VS. ACETONITRILE	3.4.21.62
1SCJ	CRYSTAL STRUCTURE OF SUBTILISIN-PROPEPTIDE COMPLEX	3.4.21.62
1SCN	INACTIVATION OF SUBTILISIN CARLSBERG BY N-(TERT-BUTOXYCARBONYL-ALANYL-PROLYL-PHENYLALANYL)-O-BENZOL HYDROXYLAMINE: FORMATION OF COVALENT ENZYME-INHIBITOR LINKAGE IN THE FORM OF A CARBAMATE DERIVATIVE	3.4.21.62
1SCW	TOWARD BETTER ANTIBIOTICS: CRYSTAL STRUCTURE OF R61 DD-PEPTIDASE INHIBITED BY A NOVEL MONOCYCLIC PHOSPHATE INHIBITOR	3.4.16.4
1SDE	TOWARD BETTER ANTIBIOTICS: CRYSTAL STRUCTURE OF D-ALA-D-ALA PEPTIDASE INHIBITED BY A NOVEL BICYCLIC PHOSPHATE INHIBITOR	3.4.16.4
1SDN	CRYSTAL STRUCTURE OF A DEACYLATION-DEFECTIVE MUTANT OF PENICILLIN-BINDING PROTEIN 5 MODIFIED BY MERCURY	3.4.16.4 3.5.2.6
1SDO	CRYSTAL STRUCTURE OF RESTRICTION ENDONUCLEASE BSTYI	3.1.21.4
1SDT	CRYSTAL STRUCTURES OF HIV PROTEASE V82A AND L90M MUTANTS REVEAL CHANGES IN INDINAVIR BINDING SITE.	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1SDU	CRYSTAL STRUCTURES OF HIV PROTEASE V82A AND L90M MUTANTS REVEAL CHANGES IN INDINAVIR BINDING SITE.	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1SDV	CRYSTAL STRUCTURES OF HIV PROTEASE V82A AND L90M MUTANTS REVEAL CHANGES IN INDINAVIR BINDING SITE.	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1SDX	CRYSTAL STRUCTURE OF THE ZINC SATURATED C-TERMINAL HALF OF BOVINE LACTOFERRIN AT 2.0 A RESOLUTION REVEALS TWO ADDITIONAL ZINC BINDING SITES	3.4.21
1SEH	CRYSTAL STRUCTURE OF E. COLI DUTPASE COMPLEXED WITH THE PRODUCT DUMP	3.6.1.23
1SEL	CRYSTAL STRUCTURE OF SELENOSUBTILISIN AT 2.0-ANGSTROMS RESOLUTION	3.4.21.62
1SF4	BINDING OF N,N'-DIACETYLCHITOBIOSE TO HEW LYSOZYME: A POWDER DIFFRACTION STUDY	3.2.1.17
1SF6	BINDING OF N,N',N-TRIACETYLCHITOTRIOSE TO HEW LYSOZYME: A POWDER DIFFRACTION STUDY"	3.2.1.17
1SF7	BINDING OF TETRA-N-ACETYLCHITOTETRAOSE TO HEW LYSOZYME: A POWDER DIFFRACTION STUDY	3.2.1.17
1SFB	BINDING OF PENTA-N-ACETYLCHITOPENTAOSE TO HEW LYSOZYME: A POWDER DIFFRACTION STUDY	3.2.1.17
1SFG	BINDING OF HEXA-N-ACETYLCHITOHEXAOSE: A POWDER DIFFRACTION STUDY	3.2.1.17
1SFI	HIGH RESOLUTION STRUCTURE OF A POTENT, CYCLIC PROTEASE INHIBITOR FROM SUNFLOWER SEEDS	3.4.21.4
1SFK	CORE (C) PROTEIN FROM WEST NILE VIRUS, SUBTYPE KUNJIN	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
1SFQ	FAST FORM OF THROMBIN MUTANT R(77A)A BOUND TO PPACK	3.4.21.5
1SFV	PORCINE PANCREAS PHOSPHOLIPASE A2, NMR, MINIMIZED AVERAGE STRUCTURE	3.1.1.4
1SFW	PORCINE PANCREAS PHOSPHOLIPASE A2, NMR, 18 STRUCTURES	3.1.1.4
1SG3	STRUCTURE OF ALLANTOICASE	3.5.3.4
1SG8	CRYSTAL STRUCTURE OF THE PROCOAGULANT FAST FORM OF THROMBIN	3.4.21.5
1SGC	THE 1.8 ANGSTROMS STRUCTURE OF THE COMPLEX BETWEEN CHYMOSTATIN AND STREPTOMYCES GRISEUS PROTEASE A. A MODEL FOR SERINE PROTEASE CATALYTIC TETRAHEDRAL INTERMEDIATES	3.4.21.80
1SGD	ASP 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B AT PH 6.5	3.4.21.81
1SGE	GLU 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B AT PH 6.5	3.4.21.81
1SGF	CRYSTAL STRUCTURE OF 7S NGF: A COMPLEX OF NERVE GROWTH FACTOR WITH FOUR BINDING PROTEINS (SERINE PROTEINASES)	3.4.21.35
1SGI	CRYSTAL STRUCTURE OF THE ANTICOAGULANT SLOW FORM OF THROMBIN	3.4.21.5
1SGL	THE THREE-DIMENSIONAL STRUCTURE AND X-RAY SEQUENCE REVEAL THAT TRICHOMAGLIN IS A NOVEL S-LIKE RIBONUCLEASE	3.1
1SGN	ASN 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B	3.4.21.81
1SGP	ALA 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B	3.4.21.81
1SGQ	GLY 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B	3.4.21.81
1SGR	LEU 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B	3.4.21.81
1SGT	REFINED CRYSTAL STRUCTURE OF STREPTOMYCES GRISEUS TRYPSIN AT 1.7 ANGSTROMS RESOLUTION	3.4.21.4
1SGU	COMPARING THE ACCUMULATION OF ACTIVE SITE AND NON-ACTIVE SITE MUTATIONS IN THE HIV-1 PROTEASE	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1SGY	TYR 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH STREPTOMYCES GRISEUS PROTEINASE B AT PH 6.5	3.4.21.81
1SGZ	CRYSTAL STRUCTURE OF UNBOUND BETA-SECRETASE CATALYTIC DOMAIN.	3.4.23.46
1SH0	CRYSTAL STRUCTURE OF NORWALK VIRUS POLYMERASE (TRICLINIC)	2.7.7.48 3.4.22.66 3.6.1.15
1SH2	CRYSTAL STRUCTURE OF NORWALK VIRUS POLYMERASE (METAL-FREE, CENTERED ORTHORHOMBIC)	2.7.7.48 3.4.22.66 3.6.1.15
1SH3	CRYSTAL STRUCTURE OF NORWALK VIRUS POLYMERASE (MGSO4 CRYSTAL FORM)	2.7.7.48 3.4.22.66 3.6.1.15
1SH7	CRYSTAL STRUCTURE OF A COLD ADAPTED SUBTILISIN-LIKE SERINE PROTEINASE	3.4.21
1SH9	COMPARING THE ACCUMULATION OF ACTIVE SITE AND NON-ACTIVE SITE MUTATIONS IN THE HIV-1 PROTEASE	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1SHH	SLOW FORM OF THROMBIN BOUND WITH PPACK	3.4.21.5
1SHJ	CASPASE-7 IN COMPLEX WITH DICA ALLOSTERIC INHIBITOR	3.4.22 3.4.22.60
1SHL	CASPASE-7 IN COMPLEX WITH FICA ALLOSTERIC INHIBITOR	3.4.22 3.4.22.60
1SHN	CRYSTAL STRUCTURE OF SHRIMP ALKALINE PHOSPHATASE WITH PHOSPHATE BOUND	3.1.3.1
1SHQ	CRYSTAL STRUCTURE OF SHRIMP ALKALINE PHOSPHATASE WITH MAGNESIUM IN M3	3.1.3.1
1SHV	STRUCTURE OF SHV-1 BETA-LACTAMASE	3.5.2.6
1SIB	REFINED CRYSTAL STRUCTURES OF SUBTILISIN NOVO IN COMPLEX WITH WILD-TYPE AND TWO MUTANT EGLINS. COMPARISON WITH OTHER SERINE PROTEINASE INHIBITOR COMPLEXES	3.4.21.62
1SIP	ALTERNATIVE NATIVE FLAP CONFORMATION REVEALED BY 2.3 ANGSTROMS RESOLUTION STRUCTURE OF SIV PROTEINASE	3.4.23 2.7.7.49 3.1.13.2 3.1.26.13
1SIV	THREE-DIMENSIONAL STRUCTURE OF A SIV PROTEASE(SLASH)INHIBITOR COMPLEX. IMPLICATIONS FOR THE DESIGN OF HIV-1 AND HIV-2 PROTEASE INHIBITORS	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1SIX	MYCOBACTERIUM TUBERCULOSIS DUTPASE COMPLEXED WITH MAGNESIUM AND ALPHA,BETA-IMIDO-DUTP	3.6.1.23
1SJN	MYCOBACTERIUM TUBERCULOSIS DUTPASE COMPLEXED WITH MAGNESIUM AND ALPHA,BETA-IMIDO-DUTP	3.6.1.23
1SJY	CRYSTAL STRUCTURE OF NUDIX HYDROLASE DR1025 FROM DEINOCOCCUS RADIODURANS	3.6.1
1SK8	CRYSTALLOGRAPHIC SNAPSHOTS OF ASPERGILLUS FUMIGATUS PHYTASE REVEALING ITS ENZYMATIC DYNAMICS	3.1.3.8
1SK9	CRYSTALLOGRAPHIC SNAPSHOTS OF ASPERGILLUS FUMIGATUS PHYTASE REVEALING ITS ENZYMATIC DYNAMICS	3.1.3.8
1SKA	CRYSTALLOGRAPHIC SNAPSHOTS OF ASPERGILLUS FUMIGATUS PHYTASE REVEALING ITS ENZYMATIC DYNAMICS	3.1.3.8
1SKB	CRYSTALLOGRAPHIC SNAPSHOTS OF ASPERGILLUS FUMIGATUS PHYTASE REVEALING ITS ENZYMATIC DYNAMICS	3.1.3.8
1SKF	CRYSTAL STRUCTURE OF THE STREPTOMYCES K15 DD-TRANSPEPTIDASE	3.4.16.4
1SKG	STRUCTURE-BASED RATIONAL DRUG DESIGN: CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 AND A PENTAPEPTIDE VAL-ALA-PHE-ARG-SER	3.1.1.4
1SKR	T7 DNA POLYMERASE COMPLEXED TO DNA PRIMER/TEMPLATE AND DDATP	2.7.7.7 3.1.11
1SKS	BINARY 3' COMPLEX OF T7 DNA POLYMERASE WITH A DNA PRIMER/TEMPLATE CONTAINING A CIS-SYN THYMINE DIMER ON THE TEMPLATE	2.7.7.7 3.1.11
1SKW	BINARY 3' COMPLEX OF T7 DNA POLYMERASE WITH A DNA PRIMER/TEMPLATE CONTAINING A DISORDERED CIS-SYN THYMINE DIMER ON THE TEMPLATE	2.7.7.7 3.1.11
1SL0	TERNARY 3' COMPLEX OF T7 DNA POLYMERASE WITH A DNA PRIMER/TEMPLATE CONTAINING A DISORDERED CIS-SYN THYMINE DIMER ON THE TEMPLATE AND AN INCOMING NUCLEOTIDE	2.7.7.7 3.1.11
1SL1	BINARY 5' COMPLEX OF T7 DNA POLYMERASE WITH A DNA PRIMER/TEMPLATE CONTAINING A CIS-SYN THYMINE DIMER ON THE TEMPLATE	2.7.7.7 3.1.11
1SL2	TERNARY 5' COMPLEX OF T7 DNA POLYMERASE WITH A DNA PRIMER/TEMPLATE CONTAINING A CIS-SYN THYMINE DIMER ON THE TEMPLATE AND AN INCOMING NUCLEOTIDE	2.7.7.7 3.1.11
1SL3	CRYSTAL STRUCTUE OF THROMBIN IN COMPLEX WITH A POTENT P1 HETEROCYCLE-ARYL BASED INHIBITOR	3.4.21.5
1SLH	MYCOBACTERIUM TUBERCULOSIS DUTPASE COMPLEXED WITH MAGNESIUM AND DUDP	3.6.1.23
1SLI	LEECH INTRAMOLECULAR TRANS-SIALIDASE COMPLEXED WITH DANA	3.2.1.18 4.2.2.15
1SLJ	SOLUTION STRUCTURE OF THE S1 DOMAIN OF RNASE E FROM E. COLI	3.1.4 3.1.26.12
1SLL	SIALIDASE L FROM LEECH MACROBDELLA DECORA	3.2.1.18 4.2.2.15
1SLM	CRYSTAL STRUCTURE OF FIBROBLAST STROMELYSIN-1: THE C-TRUNCATED HUMAN PROENZYME	3.4.24.17
1SLN	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN FIBROBLAST STROMELYSIN-1 INHIBITED WITH THE N-CARBOXY-ALKYL INHIBITOR L-702,842	3.4.24.17
1SLY	COMPLEX OF THE 70-KDA SOLUBLE LYTIC TRANSGLYCOSYLASE WITH BULGECIN A	3.2.1 4.2.2
1SM8	M. TUBERCULOSIS DUTPASE COMPLEXED WITH CHROMIUM AND DUTP	3.6.1.23
1SMC	MYCOBACTERIUM TUBERCULOSIS DUTPASE COMPLEXED WITH DUTP IN THE ABSENCE OF METAL ION.	3.6.1.23
1SMD	HUMAN SALIVARY AMYLASE	3.2.1.1
1SME	PLASMEPSIN II, A HEMOGLOBIN-DEGRADING ENZYME FROM PLASMODIUM FALCIPARUM, IN COMPLEX WITH PEPSTATIN A	3.4.23.39
1SMF	STUDIES ON AN ARTIFICIAL TRYPSIN INHIBITOR PEPTIDE DERIVED FROM THE MUNG BEAN INHIBITOR	3.4.21.4
1SML	METALLO BETA LACTAMASE L1 FROM STENOTROPHOMONAS MALTOPHILIA	3.5.2.6
1SMN	IDENTIFICATION OF THE SERRATIA ENDONUCLEASE DIMER: STRUCTURAL BASIS AND IMPLICATIONS FOR CATALYSIS	3.1.30.2
1SMP	CRYSTAL STRUCTURE OF A COMPLEX BETWEEN SERRATIA MARCESCENS METALLO-PROTEASE AND AN INHIBITOR FROM ERWINIA CHRYSANTHEMI	3.4.24.40
1SMR	THE 3-D STRUCTURE OF MOUSE SUBMAXILLARY RENIN COMPLEXED WITH A DECAPEPTIDE INHIBITOR CH-66 BASED ON THE 4-16 FRAGMENT OF RAT ANGIOTENSINOGEN	3.4.23.15
1SMX	CRYSTAL STRUCTURE OF THE S1 DOMAIN OF RNASE E FROM E. COLI (NATIVE)	3.1.4 3.1.26.12
1SN8	CRYSTAL STRUCTURE OF THE S1 DOMAIN OF RNASE E FROM E. COLI (PB DERIVATIVE)	3.1.4 3.1.26.12
1SNC	THE CRYSTAL STRUCTURE OF THE TERNARY COMPLEX OF STAPHYLOCOCCAL NUCLEASE, CA2+, AND THE INHIBITOR PD*TP, REFINED AT 1.65 ANGSTROMS	3.1.31.1
1SND	STAPHYLOCOCCAL NUCLEASE DIMER CONTAINING A DELETION OF RESIDUES 114-119 COMPLEXED WITH CALCIUM CHLORIDE AND THE COMPETITIVE INHIBITOR DEOXYTHYMIDINE-3',5'-DIPHOSPHATE	3.1.31.1
1SNF	MYCOBACTERIUM TUBERCULOSIS DUTPASE COMPLEXED WITH MAGNESIUM AND DEOXYURIDINE 5'-MONOPHOSPHATE	3.6.1.23
1SNK	CATHEPSIN K COMPLEXED WITH CARBAMATE DERIVATIZED NORLEUCINE ALDEHYDE	3.4.22.38
1SNM	ACTIVE SITE MUTANT GLU-43 (RIGHT ARROW) ASP IN STAPHYLOCOCCAL NUCLEASE DISPLAYS NONLOCAL STRUCTURAL CHANGES	3.1.31.1
1SNO	PROTEIN STABILITY IN STAPHYLOCOCCAL NUCLEASE	3.1.31.1
1SNP	PROTEIN STABILITY IN STAPHYLOCOCCAL NUCLEASE	3.1.31.1
1SNQ	PROTEIN STABILITY IN STAPHYLOCOCCAL NUCLEASE	3.1.31.1
1SNT	STRUCTURE OF THE HUMAN CYTOSOLIC SIALIDASE NEU2	3.2.1.18
1SO2	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 3B IN COMPLEX WITH A DIHYDROPYRIDAZINE INHIBITOR	3.1.4.17
1SO7	MALTOSE-INDUCED STRUCTURE OF THE HUMAN CYTOLSOLIC SIALIDASE NEU2	3.2.1.18
1SOA	HUMAN DJ-1 WITH SULFINIC ACID	3.1.2 3.5.1 3.5.1.124
1SOJ	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 3B IN COMPLEX WITH IBMX	3.1.4.17
1SOM	TORPEDO CALIFORNICA ACETYLCHOLINESTERASE INHIBITED BY NERVE AGENT GD (SOMAN).	3.1.1.7
1SOT	CRYSTAL STRUCTURE OF THE DEGS STRESS SENSOR	3.4.21 3.4.21.107
1SOZ	CRYSTAL STRUCTURE OF DEGS PROTEASE IN COMPLEX WITH AN ACTIVATING PEPTIDE	3.4.21 3.4.21.107
1SP4	CRYSTAL STRUCTURE OF NS-134 IN COMPLEX WITH BOVINE CATHEPSIN B: A TWO HEADED EPOXYSUCCINYL INHIBITOR EXTENDS ALONG THE WHOLE ACTIVE SITE CLEFT	3.4.22.1
1SP5	CRYSTAL STRUCTURE OF HIV-1 PROTEASE COMPLEXED WITH A PRODUCT OF AUTOPROTEOLYSIS	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1SPB	SUBTILISIN BPN' PROSEGMENT (77 RESIDUES) COMPLEXED WITH A MUTANT SUBTILISIN BPN' (266 RESIDUES). CRYSTAL PH 4.6. CRYSTALLIZATION TEMPERATURE 20 C DIFFRACTION TEMPERATURE-160 C	3.4.21.62
1SPI	CRYSTAL STRUCTURE OF SPINACH CHLOROPLAST FRUCTOSE-1,6-BISPHOSPHATASE AT 2.8 ANGSTROMS RESOLUTION	3.1.3.11
1SPJ	STRUCTURE OF MATURE HUMAN TISSUE KALLIKREIN (HUMAN KALLIKREIN 1 OR KLK1) AT 1.70 ANGSTROM RESOLUTION WITH VACANT ACTIVE SITE	3.4.21.35
1SPV	CRYSTAL STRUCTURE OF THE PUTATIVE PHOSPHATASE OF ESCHERICHIA COLI, NORTHEAST STRUCTURAL GENOMOICS TARGET ER58	3.1.1.106
1SQ2	CRYSTAL STRUCTURE ANALYSIS OF THE NURSE SHARK NEW ANTIGEN RECEPTOR (NAR) VARIABLE DOMAIN IN COMPLEX WITH LYSOZYME	3.2.1.17
1SQA	SUBSTITUTED 2-NAPHTHAMIDINE INHIBITORS OF UROKINASE	3.4.21.73
1SQJ	CRYSTAL STRUCTURE ANALYSIS OF OLIGOXYLOGLUCAN REDUCING-END-SPECIFIC CELLOBIOHYDROLASE (OXG-RCBH)	3.2.1.150
1SQM	STRUCTURE OF [R563A] LEUKOTRIENE A4 HYDROLASE	3.3.2.6 3.4.11.4
1SQO	SUBSTITUTED 2-NAPHTHAMIDINE INHIBITORS OF UROKINASE	3.4.21.73
1SQT	SUBSTITUTED 2-NAPHTHAMIDINE INHIBITORS OF UROKINASE	3.4.21.73
1SQU	STRUCTURAL GENOMICS, CRYSTAL STRUCTURE OF THE CHEX PROTEIN FROM THERMOTOGA MARITIMA	3
1SQY	STRUCTURE OF HUMAN DIFERRIC LACTOFERRIN AT 2.5A RESOLUTION USING CRYSTALS GROWN AT PH 6.5	3.4.21
1SQZ	DESIGN OF SPECIFIC INHIBITORS OF PHOPHOLIPASE A2: CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN GROUP II PHOPHOLIPASE A2 AND A DESIGNED PEPTIDE DEHYDRO-ILE-ALA-ARG-SER AT 1.2A RESOLUTION	3.1.1.4
1SRN	THE REFINED CRYSTAL STRUCTURE OF A FULLY ACTIVE SEMISYNTHETIC RIBONUCLEASE AT 1.8 ANGSTROMS RESOLUTION	3.1.27.5 4.6.1.18
1SRP	STRUCTURAL ANALYSIS OF SERRATIA PROTEASE	3.4.24.40
1SSO	SOLUTION STRUCTURE AND DNA-BINDING PROPERTIES OF A THERMOSTABLE PROTEIN FROM THE ARCHAEON SULFOLOBUS SOLFATARICUS	3.1.27
1SSW	CRYSTAL STRUCTURE OF PHAGE T4 LYSOZYME MUTANT Y24A/Y25A/T26A/I27A/C54T/C97A	3.2.1.17
1SSX	0.83A RESOLUTION CRYSTAL STRUCTURE OF ALPHA-LYTIC PROTEASE AT PH 8	3.4.21.12
1SSY	CRYSTAL STRUCTURE OF PHAGE T4 LYSOZYME MUTANT G28A/I29A/G30A/C54T/C97A	3.2.1.17
1ST0	STRUCTURE OF DCPS BOUND TO M7GPPPG	3.6.1.59
1ST2	THE THREE-DIMENSIONAL STRUCTURE OF BACILLUS AMYLOLIQUEFACIENS SUBTILISIN AT 1.8 ANGSTROMS AND AN ANALYSIS OF THE STRUCTURAL CONSEQUENCES OF PEROXIDE INACTIVATION	3.4.21.14 3.4.21.62
1ST3	THE CRYSTAL STRUCTURE OF THE BACILLUS LENTUS ALKALINE PROTEASE, SUBTILISIN BL, AT 1.4 ANGSTROMS RESOLUTION	3.4.21.62
1ST4	STRUCTURE OF DCPS BOUND TO M7GPPPA	3.6.1.59
1ST8	CRYSTAL STRUCTURE OF FRUCTAN 1-EXOHYDROLASE IIA FROM CICHORIUM INTYBUS	3.2.1.80
1STA	ACCOMMODATION OF INSERTION MUTATIONS ON THE SURFACE AND IN THE INTERIOR OF STAPHYLOCOCCAL NUCLEASE	3.1.31.1
1STB	ACCOMMODATION OF INSERTION MUTATIONS ON THE SURFACE AND IN THE INTERIOR OF STAPHYLOCOCCAL NUCLEASE	3.1.31.1
1STF	THE REFINED 2.4 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF RECOMBINANT HUMAN STEFIN B IN COMPLEX WITH THE CYSTEINE PROTEINASE PAPAIN: A NOVEL TYPE OF PROTEINASE INHIBITOR INTERACTION	3.4.22.2
1STG	TWO DISTINCTLY DIFFERENT METAL BINDING MODES ARE SEEN IN X-RAY CRYSTAL STRUCTURES OF STAPHYLOCOCCAL NUCLEASE-COBALT(II)-NUCLEOTIDE COMPLEXES	3.1.31.1
1STH	TWO DISTINCTLY DIFFERENT METAL BINDING MODES ARE SEEN IN X-RAY CRYSTAL STRUCTURES OF STAPHYLOCOCCAL NUCLEASE-COBALT(II)-NUCLEOTIDE COMPLEXES	3.1.31.1
1STN	THE CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE REFINED AT 1.7 ANGSTROMS RESOLUTION	3.1.31.1
1STX	STRUCTURE OF THE K38A MUTANT OF ECORV BOUND TO COGNATE DNA AND MN2+	3.1.21.4
1STY	THE ALPHA ANEURISM: A STRUCTURAL MOTIF REVEALED IN AN INSERTION MUTANT OF STAPHYLOCOCCAL NUCLEASE	3.1.31.1
1SU1	STRUCTURAL AND BIOCHEMICAL CHARACTERIZATION OF YFCE, A PHOSPHOESTERASE FROM E. COLI	3.1.4
1SU4	CRYSTAL STRUCTURE OF CALCIUM ATPASE WITH TWO BOUND CALCIUM IONS	3.6.3.8 7.2.2.10
1SUA	SUBTILISIN BPN'	3.4.21.62
1SUB	CALCIUM-INDEPENDENT SUBTILISIN BY DESIGN	3.4.21.62
1SUC	CALCIUM-INDEPENDENT SUBTILISIN BY DESIGN	3.4.21.62
1SUD	CALCIUM-INDEPENDENT SUBTILISIN BY DESIGN	3.4.21.62
1SUE	SUBTILISIN BPN' FROM BACILLUS AMYLOLIQUEFACIENS, MUTANT	3.4.21.62
1SUG	1.95 A STRUCTURE OF APO PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
1SUP	SUBTILISIN BPN' AT 1.6 ANGSTROMS RESOLUTION: ANALYSIS OF DISCRETE DISORDER AND COMPARISON OF CRYSTAL FORMS	3.4.21.62
1SUQ	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH JANSSEN-R185545	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1SUZ	THE STRUCTURE OF K92A ECORV BOUND TO COGNATE DNA AND MG2+	3.1.21.4
1SV2	CRYSTAL STRUCTURE OF PEPTIDE DEFORMYLASE FROM LEPTOSPIRA INTERROGANS (LIPDF) AT PH7.5	3.5.1.88
1SV3	STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 AND 4-METHOXYBENZOIC ACID AT 1.3A RESOLUTION.	3.1.1.4
1SV5	CRYSTAL STRUCTURE OF K103N MUTANT HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH JANSSEN-R165335	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1SV9	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN GROUPII PHOSPHOLIPASE A2 AND ANTI-INFLAMMATORY AGENT 2-[(2,6-DICHLOROPHENYL)AMINO] BENZENEACETIC ACID AT 2.7A RESOLUTION	3.1.1.4
1SVB	ENVELOPE GLYCOPROTEIN FROM TICK-BORNE ENCEPHALITIS VIRUS	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
1SVJ	THE SOLUTION STRUCTURE OF THE NUCLEOTIDE BINDING DOMAIN OF KDPB	3.6.3.12 7.2.2.6
1SVK	STRUCTURE OF THE K180P MUTANT OF GI ALPHA SUBUNIT BOUND TO ALF4 AND GDP	3.6.1.46
1SVL	CO-CRYSTAL STRUCTURE OF SV40 LARGE T ANTIGEN HELICASE DOMAIN AND ADP	3.6.4
1SVM	CO-CRYSTAL STRUCTURE OF SV40 LARGE T ANTIGEN HELICASE DOMAIN AND ATP	3.6.4
1SVN	SAVINASE	3.4.21.62
1SVO	STRUCTURE OF SV40 LARGE T ANTIGEN HELICASE DOMAIN	3.6.4
1SVP	SINDBIS VIRUS CAPSID PROTEIN	3.4.21 3.4.21.90
1SVS	STRUCTURE OF THE K180P MUTANT OF GI ALPHA SUBUNIT BOUND TO GPPNHP.	3.6.1.46
1SWV	CRYSTAL STRUCTURE OF THE D12A MUTANT OF PHOSPHONOACETALDEHYDE HYDROLASE COMPLEXED WITH MAGNESIUM	3.11.1.1
1SWW	CRYSTAL STRUCTURE OF THE PHOSPHONOACETALDEHYDE HYDROLASE D12A MUTANT COMPLEXED WITH MAGNESIUM AND SUBSTRATE PHOSPHONOACETALDEHYDE	3.11.1.1
1SWY	USE OF A HALIDE BINDING SITE TO BYPASS THE 1000-ATOM LIMIT TO AB INITIO STRUCTURE DETERMINATION	3.2.1.17
1SWZ	USE OF AN ION-BINDING SITE TO BYPASS THE 1000-ATOM LIMIT TO AB INITIO STRUCTURE DETERMINATION BY DIRECT METHODS	3.2.1.17
1SX2	USE OF A HALIDE BINDING SITE TO BYPASS THE 1000-ATOM LIMIT TO STRUCTURE DETERMINATION BY DIRECT METHODS	3.2.1.17
1SX5	K38A ECORV BOUND TO CLEAVED DNA AND MN2+: P1 CRYSTAL FORM	3.1.21.4
1SX7	USE OF AN ION-BINDING SITE TO BYPASS THE 1000-ATOM LIMIT TO AB INITIO STRUCTURE DETERMINATION BY DIRECT METHODS	3.2.1.17
1SX8	ECORV BOUND TO COGNATE DNA AND MN2+	3.1.21.4
1SXK	CRYSTAL STRUCTURE OF A COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 AND A NON-SPECIFIC ANTI-INFLAMMATORY AMINO SALICYLIC ACID AT 1.2 A RESOLUTION	3.1.1.4
1SXR	DROSOPHILA PEPTIDOGLYCAN RECOGNITION PROTEIN (PGRP)-SA	3.4.17.13
1SXV	1.3A CRYSTAL STRUCTURE OF RV3628, MYCOBACTERIUM TUBERCULOSIS INORGANIC PYROPHOSPHATASE (PPASE) AT PH5.0	3.6.1.1
1SYB	TRANSFER OF A BETA-TURN STRUCTURE TO A NEW PROTEIN CONTEXT	3.1.31.1
1SYC	ENGINEERING ALTERNATIVE BETA-TURN TYPES IN STAPHYLOCOCCAL NUCLEASE	3.1.31.1
1SYD	ENGINEERING ALTERNATIVE BETA-TURN TYPES IN STAPHYLOCOCCAL NUCLEASE	3.1.31.1
1SYE	ENGINEERING ALTERNATIVE BETA-TURN TYPES IN STAPHYLOCOCCAL NUCLEASE	3.1.31.1
1SYF	ENGINEERING ALTERNATIVE BETA-TURN TYPES IN STAPHYLOCOCCAL NUCLEASE	3.1.31.1
1SYG	ENGINEERING ALTERNATIVE BETA-TURN TYPES IN STAPHYLOCOCCAL NUCLEASE	3.1.31.1
1SYL	CRYSTAL STRUCTURE OF INACTIVE MUTANT DUTPASE COMPLEXED WITH SUBSTRATE DUTP	3.6.1.23
1SZ3	CRYSTAL STRUCTURE OF NUDIX HYDROLASE DR1025 IN COMPLEXED WITH GNP AND MG+2	3.6.1
1SZ6	MISTLETOE LECTIN I FROM VISCUM ALBUM. CRYSTAL STRUCTURE AT 2.05 A RESOLUTION	3.2.2.22
1SZ8	CRYSTAL STRUCTURE OF AN ACIDIC PHOSPHOLIPASE A2 FROM NAJA NAJA SAGITTIFERA AT 1.5 A RESOLUTION	3.1.1.4
1SZB	CRYSTAL STRUCTURE OF THE HUMAN MBL-ASSOCIATED PROTEIN 19 (MAP19)	3.4.21.104
1SZC	STRUCTURAL BASIS FOR NICOTINAMIDE CLEAVAGE AND ADP-RIBOSE TRANSFER BY NAD+-DEPENDENT SIR2 HISTONE/PROTEIN DEACETYLASES	3.5.1 2.3.1.286
1SZD	STRUCTURAL BASIS FOR NICOTINAMIDE CLEAVAGE AND ADP-RIBOSE TRANSFER BY NAD+-DEPENDENT SIR2 HISTONE/PROTEIN DEACETYLASES	3.5.1 2.3.1.286
1SZN	THE STRUCTURE OF ALPHA-GALACTOSIDASE	3.2.1.22
1SZO	CRYSTAL STRUCTURE ANALYSIS OF THE 6-OXO CAMPHOR HYDROLASE HIS122ALA MUTANT BOUND TO ITS NATURAL PRODUCT (2S,4S)-ALPHA-CAMPHOLINIC ACID	3.7.1.18
1SZZ	CRYSTAL STRUCTURE OF PEPTIDE DEFORMYLASE FROM LEPTOSPIRA INTERROGANS COMPLEXED WITH INHIBITOR ACTINONIN	3.5.1.88
1T03	HIV-1 REVERSE TRANSCRIPTASE CROSSLINKED TO TENOFOVIR TERMINATED TEMPLATE-PRIMER (COMPLEX P)	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1T05	HIV-1 REVERSE TRANSCRIPTASE CROSSLINKED TO TEMPLATE-PRIMER WITH TENOFOVIR-DIPHOSPHATE BOUND AS THE INCOMING NUCLEOTIDE SUBSTRATE	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1T0O	THE STRUCTURE OF ALPHA-GALACTOSIDASE FROM TRICHODERMA REESEI COMPLEXED WITH BETA-D-GALACTOSE	3.2.1.22
1T2H	Y81W MUTANT OF RNASE SA FROM STREPTOMYCES AUREOFACIENS	3.1.27.3 4.6.1.24
1T2I	T76W MUTANT OF RNASE SA FROM STREPTOMYCES AUREOFACIENS	3.1.27.3 4.6.1.24
1T2N	STRUCTURE OF A THERMOSTABLE TRIPLE MUTANT OF BACILLUS SUBTILIS LIPASE OBTAINED THROUGH DIRECTED EVOLUTION	3.1.1.3
1T2T	CRYSTAL STRUCTURE OF THE DNA-BINDING DOMAIN OF INTRON ENDONUCLEASE I-TEVI WITH OPERATOR SITE	3.1
1T31	A DUAL INHIBITOR OF THE LEUKOCYTE PROTEASES CATHEPSIN G AND CHYMASE WITH THERAPEUTIC EFFICACY IN ANIMALS MODELS OF INFLAMMATION	3.4.21.39
1T32	A DUAL INHIBITOR OF THE LEUKOCYTE PROTEASES CATHEPSIN G AND CHYMASE WITH THERAPEUTIC EFFICACY IN ANIMALS MODELS OF INFLAMMATION	3.4.21.20
1T37	DESIGN OF SPECIFIC INHIBITORS OF PHOSPHOLIPASE A2: CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN GROUP I PHOSPHOLIPASE A2 AND A DESIGNED PENTAPEPTIDE LEU-ALA-ILE-TYR-SER AT 2.6A RESOLUTION	3.1.1.4
1T3A	CRYSTAL STRUCTURE OF CLOSTRIDIUM BOTULINUM NEUROTOXIN TYPE E CATALYTIC DOMAIN	3.4.24.69
1T3C	CLOSTRIDIUM BOTULINUM TYPE E CATALYTIC DOMAIN E212Q MUTANT	3.4.24.69
1T3G	CRYSTAL STRUCTURE OF THE TOLL/INTERLEUKIN-1 RECEPTOR (TIR) DOMAIN OF HUMAN IL-1RAPL	3.2.2.6
1T3J	MITOFUSIN DOMAIN HR2 V686M/I708M MUTANT	3.6.5
1T3K	NMR STRUCTURE OF A CDC25-LIKE DUAL-SPECIFICITY TYROSINE PHOSPHATASE OF ARABIDOPSIS THALIANA	3.1.3.48 1.20.4.1
1T3M	STRUCTURE OF THE ISOASPARTYL PEPTIDASE WITH L-ASPARAGINASE ACTIVITY FROM E. COLI	3.5.1.1 3.4.19.5
1T3P	HALF-SANDWICH ARENE RUTHENIUM(II)-ENZYME COMPLEX	3.2.1.17
1T3R	HIV PROTEASE WILD-TYPE IN COMPLEX WITH TMC114 INHIBITOR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1T48	ALLOSTERIC INHIBITION OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
1T49	ALLOSTERIC INHIBITION OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
1T4J	ALLOSTERIC INHIBITION OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
1T4M	STRUCTURE OF A THERMOSTABLE DOUBLE MUTANT OF BACILLUS SUBTILIS LIPASE OBTAINED THROUGH DIRECTED EVOLUTION	3.1.1.3
1T4N	SOLUTION STRUCTURE OF RNT1P DSRBD	3.1.26.3
1T4O	CRYSTAL STRUCTURE OF RNT1P DSRBD	3.1.26.3
1T4P	ARGINASE-DEHYDRO-ABH COMPLEX	3.5.3.1
1T4R	ARGINASE-DESCARBOXY-NOR-NOHA COMPLEX	3.5.3.1
1T4S	ARGINASE-L-VALINE COMPLEX	3.5.3.1
1T4T	ARGINASE-DINOR-NOHA COMPLEX	3.5.3.1
1T4U	CRYSTAL STRUCTURE ANALYSIS OF A NOVEL OXYGUANIDINE BOUND TO THROMBIN	3.4.21.5
1T4V	CRYSTAL STRUCTURE ANALYSIS OF A NOVEL OXYGUANIDINE BOUND TO THROMBIN	3.4.21.5
1T5B	STRUCTURAL GENOMICS, A PROTEIN FROM SALMONELLA TYPHIMURIUM SIMILAR TO E. COLI ACYL CARRIER PROTEIN PHOSPHODIESTERASE	3.1.4.14 1.7.1.17
1T5F	ARGINASE I-AOH COMPLEX	3.5.3.1
1T5G	ARGINASE-F2-L-ARGININE COMPLEX	3.5.3.1
1T5I	CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF UAP56	3.6.4.13
1T5J	CRYSTAL STRUCTURE OF RIBOSYLGLYCOHYDROLASE MJ1187 FROM METHANOCOCCUS JANNASCHII	3.2.2
1T5S	STRUCTURE OF THE (SR)CA2+-ATPASE CA2-E1-AMPPCP FORM	3.6.3.8 7.2.2.10
1T5T	STRUCTURE OF THE (SR)CA2+-ATPASE CA2-E1-ADP:ALF4- FORM	3.6.3.8 7.2.2.10
1T64	CRYSTAL STRUCTURE OF HUMAN HDAC8 COMPLEXED WITH TRICHOSTATIN A	3.5.1.98
1T67	CRYSTAL STRUCTURE OF HUMAN HDAC8 COMPLEXED WITH MS-344	3.5.1.98
1T69	CRYSTAL STRUCTURE OF HUMAN HDAC8 COMPLEXED WITH SAHA	3.5.1.98
1T6C	STRUCTURAL CHARACTERIZATION OF THE PPX/GPPA PROTEIN FAMILY: CRYSTAL STRUCTURE OF THE AQUIFEX AEOLICUS FAMILY MEMBER	3.6.1.11 3.6.1.40
1T6D	MIRAS PHASING OF THE AQUIFEX AEOLICUS PPX/GPPA PHOSPHATASE: CRYSTAL STRUCTURE OF THE TYPE II VARIANT	3.6.1.11 3.6.1.40
1T6E	CRYSTAL STRUCTURE OF THE TRITICUM AESTIVUM XYLANASE INHIBITOR I	3.2.1.8
1T6G	CRYSTAL STRUCTURE OF THE TRITICUM AESTIVUM XYLANASE INHIBITOR-I IN COMPLEX WITH ASPERGILLUS NIGER XYLANASE-I	3.2.1.8
1T6H	CRYSTAL STRUCTURE T4 LYSOZYME INCORPORATING AN UNNATURAL AMINO ACID P-IODO-L-PHENYLALANINE AT POSITION 153	3.2.1.17
1T6N	CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF HUMAN UAP56	3.6.4.13
1T6V	CRYSTAL STRUCTURE ANALYSIS OF THE NURSE SHARK NEW ANTIGEN RECEPTOR (NAR) VARIABLE DOMAIN IN COMPLEX WITH LYSOZYME	3.2.1.17
1T70	CRYSTAL STRUCTURE OF A NOVEL PHOSPHATASE FROM DEINOCOCCUS RADIODURANS	3.1.4.16 3.1.3.60
1T71	CRYSTAL STRUCTURE OF A NOVEL PHOSPHATASE MYCOPLASMA PNEUMONIAEFROM	3.1
1T7C	CRYSTAL STRUCTURE OF THE P1 GLU BPTI MUTANT- BOVINE CHYMOTRYPSIN COMPLEX	3.4.21.1
1T7D	CRYSTAL STRUCTURE OF ESCHERICHIA COLI TYPE I SIGNAL PEPTIDASE IN COMPLEX WITH A LIPOPEPTIDE INHIBITOR	3.4.21.89
1T7I	THE STRUCTURAL AND THERMODYNAMIC BASIS FOR THE BINDING OF TMC114, A NEXT-GENERATION HIV-1 PROTEASE INHIBITOR.	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1T7J	CRYSTAL STRUCTURE OF INHIBITOR AMPRENAVIR IN COMPLEX WITH A MULTI-DRUG RESISTANT VARIANT OF HIV-1 PROTEASE (L63P/V82T/I84V)	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1T7K	CRYSTAL STRUCTURE OF HIV PROTEASE COMPLEXED WITH ARYLSULFONAMIDE AZACYCLIC UREA	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1T7P	T7 DNA POLYMERASE COMPLEXED TO DNA PRIMER/TEMPLATE,A NUCLEOSIDE TRIPHOSPHATE, AND ITS PROCESSIVITY FACTOR THIOREDOXIN	2.7.7.7 3.1.11
1T8A	USE OF SEQUENCE DUPLICATION TO ENGINEER A LIGAND-TRIGGERED LONG-DISTANCE MOLECULAR SWITCH IN T4 LYSOZYME	3.2.1.17
1T8E	T7 DNA POLYMERASE TERNARY COMPLEX WITH DCTP AT THE INSERTION SITE.	2.7.7.7 3.1.11
1T8F	CRYSTAL STRUCTURE OF PHAGE T4 LYSOZYME MUTANT R14A/K16A/I17A/K19A/T21A/E22A/C54T/C97A	3.2.1.17
1T8G	CRYSTAL STRUCTURE OF PHAGE T4 LYSOZYME MUTANT L32A/L33A/T34A/C54T/C97A/E108V	3.2.1.17
1T8H	1.8 A CRYSTAL STRUCTURE OF AN UNCHARACTERIZED B. STEAROTHERMOPHILUS PROTEIN	2.4.2.1 3.5.4.4 2.4.2.28
1T8L	CRYSTAL STRUCTURE OF THE P1 MET BPTI MUTANT- BOVINE CHYMOTRYPSIN COMPLEX	3.4.21.1
1T8M	CRYSTAL STRUCTURE OF THE P1 HIS BPTI MUTANT- BOVINE CHYMOTRYPSIN COMPLEX	3.4.21.1
1T8N	CRYSTAL STRUCTURE OF THE P1 THR BPTI MUTANT- BOVINE CHYMOTRYPSIN COMPLEX	3.4.21.1
1T8O	CRYSTAL STRUCTURE OF THE P1 TRP BPTI MUTANT- BOVINE CHYMOTRYPSIN COMPLEX	3.4.21.1
1T8Q	STRUCTURAL GENOMICS, CRYSTAL STRUCTURE OF GLYCEROPHOSPHORYL DIESTER PHOSPHODIESTERASE FROM E. COLI	3.1.4.46
1T8W	CRYSTAL STRUCTURE OF E. COLI AMP NUCLEOSIDASE	3.2.2.4
1T97	USE OF SEQUENCE DUPLICATION TO ENGINEER A LIGAND-TRIGGERED LONG-DISTANCE MOLECULAR SWITCH IN T4 LYSOZYME	3.2.1.17
1T9H	THE CRYSTAL STRUCTURE OF YLOQ, A CIRCULARLY PERMUTED GTPASE.	3.6.1
1T9I	I-CREI(D20N)/DNA COMPLEX	3.1
1T9J	I-CREI(Q47E)/DNA COMPLEX	3.1
1T9R	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 5A	3.1.4.17 3.1.4.35
1T9S	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 5A IN COMPLEX WITH GMP	3.1.4.17 3.1.4.35
1T9Z	THREE-DIMENSIONAL STRUCTURE OF A RNA-POLYMERASE II BINDING PROTEIN.	3.1.3.16
1TA0	THREE-DIMENSIONAL STRUCTURE OF A RNA-POLYMERASE II BINDING PROTEIN WITH ASSOCIATED LIGAND.	3.1.3.16
1TA1	H141C MUTANT OF RAT LIVER ARGINASE I	3.5.3.1
1TA2	CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH COMPOUND 1	3.4.21.5
1TA6	CRYSTAL STRUCTURE OF THROMBIN IN COMPLEX WITH COMPOUND 14B	3.4.21.5
1TAB	STRUCTURE OF THE TRYPSIN-BINDING DOMAIN OF BOWMAN-BIRK TYPE PROTEASE INHIBITOR AND ITS INTERACTION WITH TRYPSIN	3.4.21.4
1TAL	ALPHA-LYTIC PROTEASE AT 120 K (SINGLE STRUCTURE MODEL)	3.4.21.12
1TAM	HUMAN IMMUNODEFICIENCY VIRUS, NMR, MINIMIZED AVERAGE STRUCTURE	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1TAW	BOVINE TRYPSIN COMPLEXED TO APPI	3.4.21.4
1TAY	DISSECTION OF THE FUNCTIONAL ROLE OF STRUCTURAL ELEMENTS OF TYROSINE-63 IN THE CATALYTIC ACTION OF HUMAN LYSOZYME	3.2.1.17
1TAZ	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 1B	3.1.4.17
1TB5	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH AMP	3.1.4.17 3.1.4.53
1TB6	2.5A CRYSTAL STRUCTURE OF THE ANTITHROMBIN-THROMBIN-HEPARIN TERNARY COMPLEX	3.4.21.5
1TB7	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4D IN COMPLEX WITH AMP	3.1.4.17 3.1.4.53
1TBB	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4D IN COMPLEX WITH ROLIPRAM	3.1.4.17 3.1.4.53
1TBD	SOLUTION STRUCTURE OF THE ORIGIN DNA BINDING DOMAIN OF SV40 T-ANTIGEN, NMR, MINIMIZED AVERAGE STRUCTURE	3.6.4
1TBF	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 5A IN COMPLEX WITH SILDENAFIL	3.1.4.17 3.1.4.35
1TBH	H141D MUTANT OF RAT LIVER ARGINASE I	3.5.3.1
1TBJ	H141A MUTANT OF RAT LIVER ARGINASE I	3.5.3.1
1TBL	H141N MUTANT OF RAT LIVER ARGINASE I	3.5.3.1
1TBQ	CRYSTAL STRUCTURE OF INSECT DERIVED DOUBLE DOMAIN KAZAL INHIBITOR RHODNIIN IN COMPLEX WITH THROMBIN	3.4.21.5
1TBR	CRYSTAL STRUCTURE OF INSECT DERIVED DOUBLE DOMAIN KAZAL INHIBITOR RHODNIIN IN COMPLEX WITH THROMBIN	3.4.21.5
1TBU	CRYSTAL STRUCTURE OF N-TERMINAL DOMAIN OF YEAST PEROXISOMAL THIOESTERASE-1	3.1.2.2
1TBY	DISSECTION OF THE FUNCTIONAL ROLE OF STRUCTURAL ELEMENTS OF TYROSINE-63 IN THE CATALYTIC ACTION OF HUMAN LYSOZYME	3.2.1.17
1TBZ	HUMAN THROMBIN WITH ACTIVE SITE N-METHYL-D PHENYLALANYL-N-[5-(AMINOIMINOMETHYL)AMINO]-1-{{BENZOTHIAZOLYL)CARBONYL] BUTYL]-L-PROLINAMIDE TRIFLUROACETATE AND EXOSITE-HIRUGEN	3.4.21.5
1TC5	STRUCTURAL ANALYSIS OF A PROBABLE EUKARYOTIC D-AMINO ACID TRNA DEACYLASE	3.1
1TC8	CRYSTAL STRUCTURE OF KRAIT-VENOM PHOSPHOLIPASE A2 IN A COMPLEX WITH A NATURAL FATTY ACID TRIDECANOIC ACID	3.1.1.4
1TCA	THE SEQUENCE, CRYSTAL STRUCTURE DETERMINATION AND REFINEMENT OF TWO CRYSTAL FORMS OF LIPASE B FROM CANDIDA ANTARCTICA	3.1.1.3
1TCB	THE SEQUENCE, CRYSTAL STRUCTURE DETERMINATION AND REFINEMENT OF TWO CRYSTAL FORMS OF LIPASE B FROM CANDIDA ANTARCTICA	3.1.1.3
1TCC	THE SEQUENCE, CRYSTAL STRUCTURE DETERMINATION AND REFINEMENT OF TWO CRYSTAL FORMS OF LIPASE B FROM CANDIDA ANTARCTICA	3.1.1.3
1TCO	TERNARY COMPLEX OF A CALCINEURIN A FRAGMENT, CALCINEURIN B, FKBP12 AND THE IMMUNOSUPPRESSANT DRUG FK506 (TACROLIMUS)	3.1.3.16
1TCS	CRYSTAL STRUCTURE OF TRICHOSANTHIN-NADPH COMPLEX AT 1.7 ANGSTROMS RESOLUTION REVEALS ACTIVE-SITE ARCHITECTURE	3.2.2.22
1TCW	SIV PROTEASE COMPLEXED WITH INHIBITOR SB203386	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1TCX	HIV TRIPLE MUTANT PROTEASE COMPLEXED WITH INHIBITOR SB203386	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1TCY	DISSECTION OF THE FUNCTIONAL ROLE OF STRUCTURAL ELEMENTS OF TYROSINE-63 IN THE CATALYTIC ACTION OF HUMAN LYSOZYME	3.2.1.17
1TD7	INTERACTIONS OF A SPECIFIC NON-STEROIDAL ANTI-INFLAMMATORY DRUG (NSAID) WITH GROUP I PHOSPHOLIPASE A2 (PLA2): CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PLA2 AND NIFLUMIC ACID AT 2.5 A RESOLUTION	3.1.1.4
1TDG	COMPLEX OF S130G SHV-1 BETA-LACTAMASE WITH TAZOBACTAM	3.5.2.6
1TDH	CRYSTAL STRUCTURE OF HUMAN ENDONUCLEASE VIII-LIKE 1 (NEIL1)	3.2.2 4.2.99.18
1TDL	STRUCTURE OF SER130GLY SHV-1 BETA-LACTAMASE	3.5.2.6
1TDV	NON-SPECIFIC BINDING TO PHOSPHOLIPASE A2:CRYSTAL STRUCTURE OF THE COMPLEX OF PLA2 WITH A DESIGNED PEPTIDE TYR-TRP-ALA-ALA-ALA-ALA AT 1.7A RESOLUTION	3.1.1.4
1TDY	DISSECTION OF THE FUNCTIONAL ROLE OF STRUCTURAL ELEMENTS OF TYROSINE-63 IN THE CATALYTIC ACTION OF HUMAN LYSOZYME	3.2.1.17
1TDZ	CRYSTAL STRUCTURE COMPLEX BETWEEN THE LACTOCOCCUS LACTIS FPG (MUTM) AND A FAPY-DG CONTAINING DNA	3.2.2.23 4.2.99.18
1TE0	STRUCTURAL ANALYSIS OF DEGS, A STRESS SENSOR OF THE BACTERIAL PERIPLASM	3.4.21 3.4.21.107
1TE2	PUTATIVE PHOSPHATASE YNIC FROM ESCHERICHIA COLI K12	3.1.3.18 3.1.3.68 3.1.3.22 3.1.3.50 3.1.3.23
1TE7	SOLUTION NMR STRUCTURE OF PROTEIN YQFB FROM ESCHERICHIA COLI. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET ET99	3.5.1.135
1TEC	CRYSTALLOGRAPHIC REFINEMENT BY INCORPORATION OF MOLECULAR DYNAMICS. THE THERMOSTABLE SERINE PROTEASE THERMITASE COMPLEXED WITH EGLIN-C	3.4.21.66
1TEM	6 ALPHA HYDROXYMETHYL PENICILLOIC ACID ACYLATED ON THE TEM-1 BETA-LACTAMASE FROM ESCHERICHIA COLI	3.5.2.6
1TEW	STRUCTURE OF HEXAGONAL TURKEY EGG WHITE LYSOZYME AT 1.65 ANGSTROMS RESOLUTION	3.2.1.17
1TF4	ENDO/EXOCELLULASE FROM THERMOMONOSPORA	3.2.1.4
1TF8	STREPTOMYCES GRISEUS AMINOPEPTIDASE COMPLEXED WITH L-TRYPTOPHAN	3.4.11 3.4.11.24
1TF9	STREPTOMYCES GRISEUS AMINOPEPTIDASE COMPLEXED WITH P-IODO-L-PHENYLALANINE	3.4.11 3.4.11.24
1TFF	STRUCTURE OF OTUBAIN-2	3.4 3.4.19.12
1TFM	CRYSTAL STRUCTURE OF A RIBOSOME INACTIVATING PROTEIN IN ITS NATURALLY INHIBITED FORM	3.2.2.22
1TFR	RNASE H FROM BACTERIOPHAGE T4	3.1.26.4
1TFX	COMPLEX OF THE SECOND KUNITZ DOMAIN OF TISSUE FACTOR PATHWAY INHIBITOR WITH PORCINE TRYPSIN	3.4.21.4
1TG1	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN RUSSELLS VIPER PHOSPHOLIPASE A2 AND A DESIGNED PEPTIDE INHIBITOR PHQ-LEU-VAL-ARG-TYR AT 1.2A RESOLUTION	3.1.1.4
1TG4	DESIGN OF SPECIFIC INHIBITORS OF GROUPII PHOSPHOLIPASE A2(PLA2): CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN RUSSELLS VIPER PLA2 AND DESIGNED PEPTIDE PHE-LEU-ALA-TYR-LYS AT 1.7A RESOLUTION	3.1.1.4
1TG6	CRYSTALLOGRAPHY AND MUTAGENESIS POINT TO AN ESSENTIAL ROLE FOR THE N-TERMINUS OF HUMAN MITOCHONDRIAL CLPP	3.4.21.92
1TG7	NATIVE STRUCTURE OF BETA-GALACTOSIDASE FROM PENICILLIUM SP.	3.2.1.23
1TG8	THE STRUCTURE OF DENGUE VIRUS E GLYCOPROTEIN	3.4.21.91 3.6.1.15 3.6.4.13
1TGB	CRYSTAL STRUCTURE OF BOVINE TRYPSINOGEN AT 1.8 ANGSTROMS RESOLUTION. II. CRYSTALLOGRAPHIC REFINEMENT, REFINED CRYSTAL STRUCTURE AND COMPARISON WITH BOVINE TRYPSIN	3.4.21.4
1TGC	ON THE DISORDERED ACTIVATION DOMAIN IN TRYPSINOGEN. CHEMICAL LABELLING AND LOW-TEMPERATURE CRYSTALLOGRAPHY	3.4.21.4
1TGM	CRYSTAL STRUCTURE OF A COMPLEX FORMED BETWEEN GROUP II PHOSPHOLIPASE A2 AND ASPIRIN AT 1.86 A RESOLUTION	3.1.1.4
1TGN	STRUCTURE OF BOVINE TRYPSINOGEN AT 1.9 ANGSTROMS RESOLUTION	3.4.21.4
1TGT	ON THE DISORDERED ACTIVATION DOMAIN IN TRYPSINOGEN. CHEMICAL LABELLING AND LOW-TEMPERATURE CRYSTALLOGRAPHY	3.4.21.4
1TGZ	STRUCTURE OF HUMAN SENP2 IN COMPLEX WITH SUMO-1	3.4.22
1TH0	STRUCTURE OF HUMAN SENP2	3.4.22
1TH6	CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 IN COMPLEX WITH ATROPINE AT 1.23A RESOLUTION	3.1.1.4
1THD	COMPLEX ORGANIZATION OF DENGUE VIRUS E PROTEIN AS REVEALED BY 9.5 ANGSTROM CRYO-EM RECONSTRUCTION	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
1THE	CRYSTAL STRUCTURES OF RECOMBINANT RAT CATHEPSIN B AND A CATHEPSIN B-INHIBITOR COMPLEX: IMPLICATIONS FOR STRUCTURE-BASED INHIBITOR DESIGN	3.4.22.1
1THG	1.8 ANGSTROMS REFINED STRUCTURE OF THE LIPASE FROM GEOTRICHUM CANDIDUM	3.1.1.3
1THL	THERMOLYSIN COMPLEXED WITH A NOVEL GLUTARAMIDE DERIVATIVE, N-(1-(2(R,S)-CARBOXY-4-PHENYLBUTYL) CYCLOPENTYLCARBONYL)-(S)-TRYPTOPHAN	3.4.24.27
1THM	CRYSTAL STRUCTURE OF THERMITASE AT 1.4 ANGSTROMS RESOLUTION	3.4.21.66
1THP	STRUCTURE OF HUMAN ALPHA-THROMBIN Y225P MUTANT BOUND TO D-PHE-PRO-ARG-CHLOROMETHYLKETONE	3.4.21.5
1THR	STRUCTURES OF THROMBIN COMPLEXES WITH A DESIGNED AND A NATURAL EXOSITE INHIBITOR	3.4.21.5
1THS	STRUCTURES OF THROMBIN COMPLEXES WITH A DESIGNED AND A NATURAL EXOSITE INHIBITOR	3.4.21.5
1THZ	CRYSTAL STRUCTURE OF AVIAN AICAR TRANSFORMYLASE IN COMPLEX WITH A NOVEL INHIBITOR IDENTIFIED BY VIRTUAL LIGAND SCREENING	2.1.2.3 3.5.4.10
1TIB	CONFORMATIONAL LABILITY OF LIPASES OBSERVED IN THE ABSENCE OF AN OIL-WATER INTERFACE: CRYSTALLOGRAPHIC STUDIES OF ENZYMES FROM THE FUNGI HUMICOLA LANUGINOSA AND RHIZOPUS DELEMAR	3.1.1.3
1TIC	CONFORMATIONAL LABILITY OF LIPASES OBSERVED IN THE ABSENCE OF AN OIL-WATER INTERFACE: CRYSTALLOGRAPHIC STUDIES OF ENZYMES FROM THE FUNGI HUMICOLA LANUGINOSA AND RHIZOPUS DELEMAR	3.1.1.3
1TIK	CRYSTAL STRUCTURE OF ACYL CARRIER PROTEIN PHOSPHODIESTERASE	3.1.4.14 1.7.1.17
1TIO	HIGH PACKING DENSITY FORM OF BOVINE BETA-TRYPSIN IN CYCLOHEXANE	3.4.21.4
1TIP	THE BISPHOSPHATASE DOMAIN OF THE BIFUNCTIONAL RAT LIVER 6-PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE	3.1.3.46 2.7.1.105
1TIY	X-RAY STRUCTURE OF GUANINE DEAMINASE FROM BACILLUS SUBTILIS NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET SR160	3.5.4.3
1TJ3	X-RAY STRUCTURE OF THE SUCROSE-PHOSPHATASE (SPP) FROM SYNECHOCYSTIS SP. PCC6803 IN A CLOSED CONFORMATION	3.1.3.24
1TJ4	X-RAY STRUCTURE OF THE SUCROSE-PHOSPHATASE (SPP) FROM SYNECHOCYSTIS SP. PCC6803 IN COMPLEX WITH SUCROSE	3.1.3.24
1TJ5	X-RAY STRUCTURE OF THE SUCROSE-PHOSPHATASE (SPP) FROM SYNECHOCYSTIS SP. PCC6803 IN COMPLEX WITH SUCROSE AND PHOSPHATE	3.1.3.24
1TJ9	STRUCTURE OF THE COMPLEXED FORMED BETWEEN GROUP II PHOSPHOLIPASE A2 AND A RATIONALLY DESIGNED TETRA PEPTIDE,VAL-ALA-ARG-SER AT 1.1A RESOLUTION	3.1.1.4
1TJK	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN GROUP II PHOSPHOLIPASE A2 WITH A DESIGNED PENTAPEPTIDE, PHE- LEU- SER- THR- LYS AT 1.2 A RESOLUTION	3.1.1.4
1TK0	T7 DNA POLYMERASE TERNARY COMPLEX WITH 8 OXO GUANOSINE AND DDCTP AT THE INSERTION SITE	2.7.7.7 3.1.11
1TK2	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN ALKALINE PROTEINASE SAVINASE AND GRAMICIDIN S AT 1.5A RESOLUTION	3.4.21.62
1TK3	CRYSTAL STRUCTURE OF HUMAN APO DIPEPTIDYL PEPTIDASE IV/CD26	3.4.14.5
1TK4	CRYSTAL STRUCTURE OF RUSSELLS VIPER PHOSPHOLIPASE A2 IN COMPLEX WITH A SPECIFICALLY DESIGNED TETRAPEPTIDE ALA-ILE-ARG-SER AT 1.1 A RESOLUTION	3.1.1.4
1TK5	T7 DNA POLYMERASE BINARY COMPLEX WITH 8 OXO GUANOSINE IN THE TEMPLATING STRAND	2.7.7.7 3.1.11
1TK8	T7 DNA POLYMERASE TERNARY COMPLEX WITH 8 OXO GUANOSINE AND DAMP AT THE ELONGATION SITE	2.7.7.7 3.1.11
1TKD	T7 DNA POLYMERASE TERNARY COMPLEX WITH 8 OXO GUANOSINE AND DCMP AT THE ELONGATION SITE	2.7.7.7 3.1.11
1TKF	STREPTOMYCES GRISEUS AMINOPEPTIDASE COMPLEXED WITH D-TRYPTOPHAN	3.4.11 3.4.11.24
1TKH	STREPTOMYCES GRISEUS AMINOPEPTIDASE COMPLEXED WITH D-PHENYLALANINE	3.4.11 3.4.11.24
1TKJ	STREPTOMYCES GRISEUS AMINOPEPTIDASE COMPLEXED WITH D-METHIONINE	3.4.11 3.4.11.24
1TKR	HUMAN DIPEPTIDYL PEPTIDASE IV/CD26 INHIBITED WITH DIISOPROPYL FLUOROPHOSPHATE	3.4.14.5
1TKT	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW426318	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1TKX	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW490745	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1TKZ	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW429576	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1TL1	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW451211	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1TL3	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH GW450557	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1TL9	HIGH RESOLUTION CRYSTAL STRUCTURE OF CALPAIN I PROTEASE CORE IN COMPLEX WITH LEUPEPTIN	3.4.22.52
1TLA	HYDROPHOBIC CORE REPACKING AND AROMATIC-AROMATIC INTERACTION IN THE THERMOSTABLE MUTANT OF T4 LYSOZYME SER 117 (RIGHT ARROW) PHE	3.2.1.17
1TLD	CRYSTAL STRUCTURE OF BOVINE BETA-TRYPSIN AT 1.5 ANGSTROMS RESOLUTION IN A CRYSTAL FORM WITH LOW MOLECULAR PACKING DENSITY. ACTIVE SITE GEOMETRY, ION PAIRS AND SOLVENT STRUCTURE	3.4.21.4
1TLI	THERMOLYSIN (2% ISOPROPANOL SOAKED CRYSTALS)	3.4.24.27
1TLO	HIGH RESOLUTION CRYSTAL STRUCTURE OF CALPAIN I PROTEASE CORE IN COMPLEX WITH E64	3.4.22.52
1TLP	CRYSTALLOGRAPHIC STRUCTURAL ANALYSIS OF PHOSPHORAMIDATES AS INHIBITORS AND TRANSITION-STATE ANALOGS OF THERMOLYSIN	3.4.24.27
1TLX	THERMOLYSIN (NATIVE)	3.4.24.27
1TM1	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2	3.4.21.62
1TM3	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 M59K MUTANT	3.4.21.62
1TM4	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILSIN BPN'WITH CHYMOTRYPSIN INHIBITOR 2 M59G MUTANT	3.4.21.62
1TM5	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 M59A MUTANT	3.4.21.62
1TM7	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 M59Y MUTANT	3.4.21.62
1TMB	MOLECULAR BASIS FOR THE INHIBITION OF HUMAN ALPHA-THROMBIN BY THE MACROCYCLIC PEPTIDE CYCLOTHEONAMIDE A	3.4.21.5
1TME	THREE-DIMENSIONAL STRUCTURE OF THEILER VIRUS	3.6.4.13 3.4.22.28 2.7.7.48
1TMF	THREE-DIMENSIONAL STRUCTURE OF THEILER MURINE ENCEPHALOMYELITIS VIRUS (BEAN STRAIN)	3.6.4.13 3.4.22.28 2.7.7.48
1TMG	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 M59F MUTANT	3.4.21.62
1TML	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF A THERMOPHILIC ENDOCELLULASE	3.2.1.4
1TMN	BINDING OF N-CARBOXYMETHYL DIPEPTIDE INHIBITORS TO THERMOLYSIN DETERMINED BY X-RAY CRYSTALLOGRAPHY. A NOVEL CLASS OF TRANSITION-STATE ANALOGUES FOR ZINC PEPTIDASES	3.4.24.27
1TMQ	STRUCTURE OF TENEBRIO MOLITOR LARVAL ALPHA-AMYLASE IN COMPLEX WITH RAGI BIFUNCTIONAL INHIBITOR	3.2.1.1
1TMT	CHANGES IN INTERACTIONS IN COMPLEXES OF HIRUDIN DERIVATIVES AND HUMAN ALPHA-THROMBIN DUE TO DIFFERENT CRYSTAL FORMS	3.4.21.5
1TMU	CHANGES IN INTERACTIONS IN COMPLEXES OF HIRUDIN DERIVATIVES AND HUMAN ALPHA-THROMBIN DUE TO DIFFERENT CRYSTAL FORMS	3.4.21.5
1TNG	PREDICTION OF NOVEL SERINE PROTEASE INHIBITORS	3.4.21.4
1TNH	PREDICTION OF NOVEL SERINE PROTEASE INHIBITORS	3.4.21.4
1TNI	PREDICTION OF NOVEL SERINE PROTEASE INHIBITORS	3.4.21.4
1TNJ	PREDICTION OF NOVEL SERINE PROTEASE INHIBITORS	3.4.21.4
1TNK	PREDICTION OF NOVEL SERINE PROTEASE INHIBITORS	3.4.21.4
1TNL	PREDICTION OF NOVEL SERINE PROTEASE INHIBITORS	3.4.21.4
1TNS	A NOVEL CLASS OF WINGED HELIX-TURN-HELIX PROTEIN: THE DNA-BINDING DOMAIN OF MU TRANSPOSASE	3.1.22 6.5.1
1TNT	A NOVEL CLASS OF WINGED HELIX-TURN-HELIX PROTEIN: THE DNA-BINDING DOMAIN OF MU TRANSPOSASE	3.1.22 6.5.1
1TO1	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 Y61A MUTANT	3.4.21.62
1TO2	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 M59K, IN PH 9 CRYOSOAK	3.4.21.62
1TO9	CRYSTAL STRUCTURE OF THI-4 PROTEIN FROM BACILLUS SUBTILIS	3.5.99.2
1TOC	STRUCTURE OF SERINE PROTEINASE	3.4.21.5
1TOM	ALPHA-THROMBIN COMPLEXED WITH HIRUGEN	3.4.21.5
1TON	RAT SUBMAXILLARY GLAND SERINE PROTEASE, TONIN. STRUCTURE SOLUTION AND REFINEMENT AT 1.8 ANGSTROMS RESOLUTION	3.4.21.35
1TP2	CRYSTAL STRUCTURE OF THE COMPLEX OF GROUP II PHOSPHOLIPASEA2 DIMER WITH A FATTY ACID TRIDECANOIC ACID AT 2.4 A RESOLUTION	3.1.1.4
1TPA	THE GEOMETRY OF THE REACTIVE SITE AND OF THE PEPTIDE GROUPS IN TRYPSIN, TRYPSINOGEN AND ITS COMPLEXES WITH INHIBITORS	3.4.21.4
1TPG	F1-G MODULE PAIR RESIDUES 1-91 (C83S) OF TISSUE-TYPE PLASMINOGEN ACTIVATOR (T-PA) (NMR, 298K, PH2.95, REPRESENTATIVE STRUCTURE)	3.4.21.68
1TPK	CRYSTAL STRUCTURE OF THE KRINGLE-2 DOMAIN OF TISSUE PLASMINOGEN ACTIVATOR AT 2.4-ANGSTROMS RESOLUTION	3.4.21.31 3.4.21.68
1TPM	SOLUTION STRUCTURE OF THE FIBRIN BINDING FINGER DOMAIN OF TISSUE-TYPE PLASMINOGEN ACTIVATOR DETERMINED BY 1H NUCLEAR MAGNETIC RESONANCE	3.4.21.68
1TPN	SOLUTION STRUCTURE OF THE FIBRIN BINDING FINGER DOMAIN OF TISSUE-TYPE PLASMINOGEN ACTIVATOR DETERMINED BY 1H NUCLEAR MAGNETIC RESONANCE	3.4.21.68
1TPO	THE GEOMETRY OF THE REACTIVE SITE AND OF THE PEPTIDE GROUPS IN TRYPSIN, TRYPSINOGEN AND ITS COMPLEXES WITH INHIBITORS	3.4.21.4
1TPP	THE GEOMETRY OF THE REACTIVE SITE AND OF THE PEPTIDE GROUPS IN TRYPSIN, TRYPSINOGEN AND ITS COMPLEXES WITH INHIBITORS	3.4.21.4
1TPS	ATOMIC STRUCTURE OF THE TRYPSIN-A90720A COMPLEX: A UNIFIED APPROACH TO STRUCTURE AND FUNCTION	3.4.21.4
1TPZ	CRYSTAL STRUCTURE OF IIGP1: A PARADIGM FOR INTERFERON INDUCIBLE P47 RESISTANCE GTPASES	3.6.5
1TQ2	CRYSTAL STRUCTURE OF IIGP1: A PARADIGM FOR INTERFERON INDUCIBLE P47 RESISTANCE GTPASES	3.6.5
1TQ4	CRYSTAL STRUCTURE OF IIGP1: A PARADIGM FOR INTERFERON INDUCIBLE P47 RESISTANCE GTPASES	3.6.5
1TQ6	CRYSTAL STRUCTURE OF IIGP1: A PARADIGM FOR INTERFERON INDUCIBLE P47 RESISTANCE GTPASES	3.6.5
1TQ7	CRYSTAL STRUCTURE OF THE ANTICOAGULANT THROMBIN MUTANT W215A/E217A BOUND TO PPACK	3.4.21.5
1TQ9	NON-COVALENT SWAPPED DIMER OF BOVINE SEMINAL RIBONUCLEASE IN COMPLEX WITH 2'-DEOXYCYTIDINE-2'-DEOXYADENOSINE-3',5'-MONOPHOSPHATE	3.1.27.5 4.6.1.18
1TQD	CRYSTAL STRUCTURE OF IIGP1: A PARADIGM FOR INTERFERON INDUCIBLE P47 RESISTANCE GTPASES	3.6.5
1TQF	CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE COMPLEXED WITH INHIBITOR	3.4.23.46
1TQH	COVALENT REACTION INTERMEDIATE REVEALED IN CRYSTAL STRUCTURE OF THE GEOBACILLUS STEAROTHERMOPHILUS CARBOXYLESTERASE EST30	3.1.1.1
1TQO	CRYOGENIC CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT TRUNCATED DELTA+PHS I92E	3.1.31.1
1TQS	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH SALACINOL	3.2.1.114
1TQT	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH A DIASTEREOMER OF SALACINOL	3.2.1.114
1TQU	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH THE SALACINOL ANALOG GHAVAMIOL	3.2.1.114
1TQV	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH SELENO-SALACINOL (BLINTOL)	3.2.1.114
1TQW	GOLGI ALPHA-MANNOSIDASE II IN COMPLEX WITH A DIASTEREOMER OF SELENO-SALACINOL	3.2.1.114
1TR1	CRYSTAL STRUCTURE OF E96K MUTATED BETA-GLUCOSIDASE A FROM BACILLUS POLYMYXA, AN ENZYME WITH INCREASED THERMORESISTANCE	3.2.1.21
1TR5	ROOM TEMPERATURE STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT TRUNCATED DELTA+PHS I92E	3.1.31.1
1TR9	STRUCTURE OF BETA-HEXOSAMINIDASE FROM VIBRIO CHOLERAE	3.2.1.52
1TRH	TWO CONFORMATIONAL STATES OF CANDIDA RUGOSA LIPASE	3.1.1.3
1TRL	NMR SOLUTION STRUCTURE OF THE C-TERMINAL FRAGMENT 255-316 OF THERMOLYSIN: A DIMER FORMED BY SUBUNITS HAVING THE NATIVE STRUCTURE	3.4.24.27
1TRM	THE THREE-DIMENSIONAL STRUCTURE OF ASN102 MUTANT OF TRYPSIN. ROLE OF ASP102 IN SERINE PROTEASE CATALYSIS	3.4.21.4
1TRN	CRYSTAL STRUCTURE OF HUMAN TRYPSIN 1: UNEXPECTED PHOSPHORYLATION OF TYROSINE 151	3.4.21.4
1TRP	X-RAY CRYSTALLOGRAPHIC AND CALORIMERIC STUDIES OF THE EFFECTS OF THE MUTATION TRP 59 TYR IN RIBONUCLEASE T1	3.1.27.3 4.6.1.24
1TRQ	X-RAY CRYSTALLOGRAPHIC AND CALORIMERIC STUDIES OF THE EFFECTS OF THE MUTATION TRP 59 TYR IN RIBONUCLEASE T1	3.1.27.3 4.6.1.24
1TRY	STRUCTURE OF INHIBITED TRYPSIN FROM FUSARIUM OXYSPORUM AT 1.55 ANGSTROMS	3.4.21.4
1TS9	CRYSTAL STRUCTURE OF THE ARCHAEAL HOMOLOG OF HUMAN RNASE P PROTEIN RPP29 FROM ARCHAEOGLOBUS FULGIDUS	3.1.26.5
1TSF	CRYSTAL STRUCTURE OF THE ARCHAEAL HOMOLOG OF HUMAN RNASE P PROTEIN RPP29 FROM ARCHAEOGLOBUS FULGIDUS	3.1.26.5
1TSP	CRYSTAL STRUCTURE OF P22 TAILSPIKE PROTEIN: INTERDIGITATED SUBUNITS IN A THERMOSTABLE TRIMER	3.2.1
1TSQ	CRYSTAL STRUCTURE OF AP2V SUBSTRATE VARIANT OF NC-P1 DECAMER PEPTIDE IN COMPLEX WITH V82A/D25N HIV-1 PROTEASE MUTANT	3.4.23.16
1TSU	CRYSTAL STRUCTURE OF DECAMER NCP1 SUBSTRATE PEPTIDE IN COMPLEX WITH WILD-TYPE D25N HIV-1 PROTEASE VARIANT	3.4.23.16
1TT2	CRYOGENIC CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE VARIANT TRUNCATED DELTA+PHS I92K	3.1.31.1
1TTO	CRYSTAL STRUCTURE OF THE RNASE T1 VARIANT R2	3.1.27.3 4.6.1.24
1TU3	CRYSTAL STRUCTURE OF RAB5 COMPLEX WITH RABAPTIN5 C-TERMINAL DOMAIN	3.6.5.2
1TU4	CRYSTAL STRUCTURE OF RAB5-GDP COMPLEX	3.6.5.2
1TUM	MUTT PYROPHOSPHOHYDROLASE-METAL-NUCLEOTIDE-METAL COMPLEX, NMR, 16 STRUCTURES	3.6.1 3.6.1.55
1TUX	HIGH RESOLUTION CRYSTAL STRUCTURE OF A THERMOSTABLE XYLANASE FROM THERMOASCUS AURANTIACUS	3.2.1.8
1TV6	HIV-1 REVERSE TRANSCRIPTASE COMPLEXED WITH CP-94,707	2.7.7.4 3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1TVI	SOLUTION STRUCTURE OF TM1509 FROM THERMOTOGA MARITIMA: VT1, A NESGC TARGET PROTEIN	3.1
1TVN	CELLULASE CEL5G FROM PSEUDOALTEROMONAS HALOPLANKTIS, A FAMILY GH 5-2 ENZYME	3.2.1.4
1TVP	ENDOGLUCANASE CEL5G FROM PSEUDOALTEROMONAS HALOPLANKTIS IN COMPLEX WITH CELLOBIOSE	3.2.1.4
1TVR	HIV-1 RT/9-CL TIBO	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1TW7	WIDE OPEN 1.3A STRUCTURE OF A MULTI-DRUG RESISTANT HIV-1 PROTEASE REPRESENTS A NOVEL DRUG TARGET	3.4.23.16
1TW8	HINCII BOUND TO CA2+ AND COGNATE DNA GTCGAC	3.1.21.4
1TWL	INORGANIC PYROPHOSPHATASE FROM PYROCOCCUS FURIOSUS PFU-264096-001	3.6.1.1
1TWX	CRYSTAL STRUCTURE OF THE THROMBIN MUTANT D221A/D222K	3.4.21.5
1TX3	HINCII BOUND TO COGNATE DNA	3.1.21.4
1TX6	TRYPSIN:BBI COMPLEX	3.4.21.4
1TX7	BOVINE TRYPSIN COMPLEXED WITH P-AMIDINOPHENYLMETHYLPHOSPHINIC ACID (AMPA)	3.4.21.4
1TX8	BOVINE TRYPSIN COMPLEXED WITH AMSO	3.4.21.4
1TXO	CRYSTAL STRUCTURE OF THE MYCOBACTERIUM TUBERCULOSIS SERINE/THREONINE PHOSPHATASE PSTP/PPP AT 1.95 A.	3.1.3.16
1TXR	X-RAY CRYSTAL STRUCTURE OF BESTATIN BOUND TO AAP	3.4.11.10
1TXZ	CRYSTAL STRUCTURE OF YEAST YMX7, AN ADP-RIBOSE-1''-MONOPHOSPHATASE, COMPLEXED WITH ADP-RIBOSE	3.1.3.84
1TY8	CRYSTAL STRUCTURE OF YEAST YMX7, AN ADP-RIBOSE-1''-MONOPHOSPHATASE, COMPLEXED WITH ADP	3.1.3.84
1TYF	THE STRUCTURE OF CLPP AT 2.3 ANGSTROM RESOLUTION SUGGESTS A MODEL FOR ATP-DEPENDENT PROTEOLYSIS	3.4.21.92
1TYH	CRYSTAL STRUCTURE OF TRANSCRIPTIONAL ACTIVATOR TENA FROM BACILLUS SUBTILIS	3.5.99.2
1TYN	ATOMIC STRUCTURE OF THE TRYPSIN-CYCLOTHEONAMIDE A COMPLEX: LESSONS FOR THE DESIGN OF SERINE PROTEASE INHIBITORS	3.4.21.4
1TYU	STRUCTURE OF TAILSPIKE-PROTEIN	3.2.1
1TYV	STRUCTURE OF TAILSPIKE-PROTEIN	3.2.1
1TYW	STRUCTURE OF TAILSPIKE-PROTEIN	3.2.1
1TYX	TITLE OF TAILSPIKE-PROTEIN	3.2.1
1TYY	CRYSTAL STRUCTURE OF AMINOIMIDAZOLE RIBOSIDE KINASE FROM SALMONELLA ENTERICA	2.7.1.4 3.6.1.26
1TYZ	CRYSTAL STRUCTURE OF 1-AMINOCYCLOPROPANE-1-CARBOYXLATE DEAMINASE FROM PSEUDOMONAS	3.5.99.7
1TZ2	CRYSTAL STRUCTURE OF 1-AMINOCYCLOPROPANE-1-CARBOYXLATE DEAMINASE COMPLEXED WITH ACC	3.5.99.7
1TZ3	CRYSTAL STRUCTURE OF AMINOIMIDAZOLE RIBOSIDE KINASE COMPLEXED WITH AMINOIMIDAZOLE RIBOSIDE	2.7.1.4 3.6.1.26
1TZ6	CRYSTAL STRUCTURE OF AMINOIMIDAZOLE RIBOSIDE KINASE FROM SALMONELLA ENTERICA COMPLEXED WITH AMINOIMIDAZOLE RIBOSIDE AND ATP ANALOG	2.7.1.4 3.6.1.26
1TZJ	CRYSTAL STRUCTURE OF 1-AMINOCYCLOPROPANE-1-CARBOXYLATE DEAMINASE COMPLEXED WITH D-VINYL GLYCINE	3.5.99.7
1TZK	CRYSTAL STRUCTURE OF 1-AMINOCYCLOPROPANE-1-CARBOXYLATE-DEAMINASE COMPLEXED WITH ALPHA-KETO-BUTYRATE	3.5.99.7
1TZM	CRYSTAL STRUCTURE OF ACC DEAMINASE COMPLEXED WITH SUBSTRATE ANALOG B-CHLORO-D-ALANINE	3.5.99.7
1TZP	MEPA, INACTIVE FORM WITHOUT ZN IN P21	3.4.99 3.4.24
1TZS	CRYSTAL STRUCTURE OF AN ACTIVATION INTERMEDIATE OF CATHEPSIN E	3.4.23.34
1U02	CRYSTAL STRUCTURE OF TREHALOSE-6-PHOSPHATE PHOSPHATASE RELATED PROTEIN	3.1.3.12
1U05	CRYSTAL STRUCTURE OF PROTEIN YFIH FROM SHIGELLA FLEXNERI, PFAM DUF152	2.4.2.1 3.5.4.4 2.4.2.28
1U09	FOOTAND MOUTH DISEASE VIRUS RNA-DEPENDENT RNA POLYMERASE	2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15
1U0A	CRYSTAL STRUCTURE OF THE ENGINEERED BETA-1,3-1,4-ENDOGLUCANASE H(A16-M) IN COMPLEX WITH BETA-GLUCAN TETRASACCHARIDE	3.2.1.73
1U0C	Y33C MUTANT OF HOMING ENDONUCLEASE I-CREI	3.1
1U0D	Y33H MUTANT OF HOMING ENDONUCLEASE I-CREI	3.1
1U0J	CRYSTAL STRUCTURE OF AAV2 REP40-ADP COMPLEX	3.6.4.12
1U0L	CRYSTAL STRUCTURE OF YJEQ FROM THERMOTOGA MARITIMA	3.6.1
1U10	MEPA, ACTIVE FORM WITH ZN IN P1	3.4.99 3.4.24
1U14	THE CRYSTAL STRUCTURE OF HYPOTHETICAL UPF0244 PROTEIN YJJX AT RESOLUTION 1.68 ANGSTROM	3.6.1.73
1U1B	STRUCTURE OF BOVINE PANCREATIC RIBONUCLEASE A IN COMPLEX WITH 3'-PHOSPHOTHYMIDINE (3'-5')-PYROPHOSPHATE ADENOSINE 3'-PHOSPHATE	3.1.27.5 4.6.1.18
1U20	CRYSTAL STRUCTURE OF XENOPUS LAEVIS NUDIX HYDROLASE NUCLEAR SNORNA DECAPPING PROTEIN X29	3.6.1.62 3.6.1.64
1U24	CRYSTAL STRUCTURE OF SELENOMONAS RUMINANTIUM PHYTASE	3.1.3.72
1U25	CRYSTAL STRUCTURE OF SELENOMONAS RUMINANTIUM PHYTASE COMPLEXED WITH PERSULFATED PHYTATE IN THE C2221 CRYSTAL FORM	3.1.3.72
1U26	CRYSTAL STRUCTURE OF SELENOMONAS RUMINANTIUM PHYTASE COMPLEXED WITH PERSULFATED PHYTATE	3.1.3.72
1U2E	CRYSTAL STRUCTURE OF THE C-C BOND HYDROLASE MHPC	3.7.1 3.7.1.14
1U2P	CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS LOW MOLECULAR PROTEIN TYROSINE PHOSPHATASE (MPTPA) AT 1.9A RESOLUTION	3.1.3.48
1U2Q	CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS LOW MOLECULAR WEIGHT PROTEIN TYROSINE PHOSPHATASE (MPTPA) AT 2.5A RESOLUTION WITH GLYCEROL IN THE ACTIVE SITE	3.1.3.48
1U2S	X-RAY STRUCTURE OF THE SUCROSE-PHOSPHATASE (SPP) FROM SYNECHOCYSTIS SP. PCC6803 IN COMPLEX WITH GLUCOSE	3.1.3.24
1U2T	X-RAY STRUCTURE OF THE SUCROSE-PHOSPHATASE (SPP) FROM SYNECHOCYSTIS SP. PCC6803 IN COMPLEX WITH SUCROSE6P	3.1.3.24
1U2Y	IN SITU EXTENSION AS AN APPROACH FOR IDENTIFYING NOVEL ALPHA-AMYLASE INHIBITORS, STRUCTURE CONTAINING D-GLUCONHYDROXIMO-1,5-LACTAM	3.2.1.1
1U30	IN SITU EXTENSION AS AN APPROACH FOR IDENTIFYING NOVEL ALPHA-AMYLASE INHIBITORS, STRUCTURE CONTAINING MALTOSYL-ALPHA (1,4)-D-GLUCONHYDROXIMO-1,5-LACTAM	3.2.1.1
1U32	CRYSTAL STRUCTURE OF A PROTEIN PHOSPHATASE-1: CALCINEURIN HYBRID BOUND TO OKADAIC ACID	3.1.3.16
1U33	IN SITU EXTENSION AS AN APPROACH FOR IDENTIFYING NOVEL ALPHA-AMYLASE INHIBITORS	3.2.1.1
1U4G	ELASTASE OF PSEUDOMONAS AERUGINOSA WITH AN INHIBITOR	3.4.24.26
1U4J	CRYSTAL STRUCTURE OF A CARBOHYDRATE INDUCED DIMER OF GROUP I PHOSPHOLIPASE A2 FROM BUNGARUS CAERULEUS AT 2.1 A RESOLUTION	3.1.1.4
1U5I	CRYSTAL STRUCTURE ANALYSIS OF RAT M-CALPAIN MUTANT LYS10 THR	3.4.22.53
1U5W	CRYSTAL STRUCTURE OF HYPOTHETICAL PROTEIN YJJX FROM ESCHERICHIA COLI	3.6.1.73
1U60	MCSG APC5046 PROBABLE GLUTAMINASE YBAS	3.5.1.2
1U61	CRYSTAL STRUCTURE OF PUTATIVE RIBONUCLEASE III FROM BACILLUS CEREUS	3.1.26
1U62	NMR STRUCTURE ANALYSIS OF THE LACTOFERRIN-BASED PEPTIDE FQWQRNIRKVR IN COMPLEX WITH LIPOPOLYSACCHARIDE	3.4.21
1U65	ACHE W. CPT-11	3.1.1.7
1U6Q	SUBSTITUTED 2-NAPHTHAMADINE INHIBITORS OF UROKINASE	3.4.21.73
1U6Z	STRUCTURE OF AN E. COLI EXOPOLYPHOSPHATASE: INSIGHT INTO THE PROCESSIVE HYDROLYSIS OF POLYPHOSPHATE AND ITS REGULATION	3.6.1.11
1U73	CRYSTAL STRUCTURE OF A DIMERIC ACIDIC PLATELET AGGREGATION INHIBITOR AND HYPOTENSIVE PHOSPHOLIPASE A2 FROM BOTHROPS JARARACUSSU	3.1.1.4
1U7L	CRYSTAL STRUCTURE OF SUBUNIT C (VMA5P) OF THE YEAST V-ATPASE	3.6.3.14
1U7O	MAGNESIUM DEPENDENT PHOSPHATASE 1 (MDP-1)	3.1.3 3.1.3.48
1U7P	X-RAY CRYSTAL STRUCTURE OF THE HYPOTHETICAL PHOSPHOTYROSINE PHOSPHATASE MDP-1 OF THE HALOACID DEHALOGENASE SUPERFAMILY	3.1.3 3.1.3.48
1U7Q	THE SOLUTION STRUCTURE OF THE NUCLEOTIDE BINDING DOMAIN OF KDPB	3.6.3.12 7.2.2.6
1U8E	HUMAN DIPEPTIDYL PEPTIDASE IV/CD26 MUTANT Y547F	3.4.14.5
1U8G	CRYSTAL STRUCTURE OF A HIV-1 PROTEASE IN COMPLEX WITH PEPTIDOMIMETIC INHIBITOR KI2-PHE-GLU-GLU-NH2	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1U8U	E. COLI THIOESTERASE I/PROTEASE I/LYSOPHOSPHOLIASE L1 IN COMPLEXED WITH OCTANOIC ACID	3.1.1.5 3.1.2 3.1.2.2 3.1.1.2 3.1.2.14 3.4.21
1U8X	CRYSTAL STRUCTURE OF GLVA FROM BACILLUS SUBTILIS, A METAL-REQUIRING, NAD-DEPENDENT 6-PHOSPHO-ALPHA-GLUCOSIDASE	3.2.1.122
1U8Y	CRYSTAL STRUCTURES OF RAL-GPPNHP AND RAL-GDP REVEAL TWO NOVEL BINDING SITES THAT ARE ALSO PRESENT IN RAS AND RAP	3.6.5.2
1U8Z	CRYSTAL STRUCTURES OF RAL-GPPNHP AND RAL-GDP REVEAL TWO NOVEL BINDING SITES THAT ARE ALSO PRESENT IN RAS AND RAP	3.6.5.2
1U90	CRYSTAL STRUCTURES OF RAL-GPPNHP AND RAL-GDP REVEAL TWO NOVEL BINDING SITES THAT ARE ALSO PRESENT IN RAS AND RAP	3.6.5.2
1U9Q	CRYSTAL STRUCTURE OF CRUZAIN BOUND TO AN ALPHA-KETOESTER	3.4.22.51
1U9R	CRYSTAL STRUCTURE OF STAPHYLOCOCCAL NUCLEASE MUTANT V66E/P117G/H124L/S128A AT ROOM TEMPERATURE	3.1.31.1
1U9V	CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH THE COVALENT INHIBITOR NVP-ABE854	3.4.22.38
1U9W	CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH THE COVALENT INHIBITOR NVP-ABI491	3.4.22.38
1U9X	CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH THE COVALENT INHIBITOR NVP-ABJ688	3.4.22.38
1UA3	CRYSTAL STRUCTURE OF THE PIG PANCREATIC A-AMYLASE COMPLEXED WITH MALTO-OLIGOSACCHARIDES	3.2.1.1
1UA7	CRYSTAL STRUCTURE ANALYSIS OF ALPHA-AMYLASE FROM BACILLUS SUBTILIS COMPLEXED WITH ACARBOSE	3.2.1.1
1UAA	E. COLI REP HELICASE/DNA COMPLEX	3.6.1
1UAD	CRYSTAL STRUCTURE OF THE RALA-GPPNHP-SEC5 RAL-BINDING DOMAIN COMPLEX	3.6.5.2
1UAQ	THE CRYSTAL STRUCTURE OF YEAST CYTOSINE DEAMINASE	3.5.4.1
1UAS	CRYSTAL STRUCTURE OF RICE ALPHA-GALACTOSIDASE	3.2.1.22
1UAX	CRYSTAL STRUCTURE OF THE RIBONUCLEASE H2 FROM PYROCOCCUS HORIKOSHII OT3	3.1.26.4
1UB4	CRYSTAL STRUCTURE OF MAZEF COMPLEX	3.1.27
1UBN	SELENOSUBTILISIN BPN	3.4.21.62
1UBP	CRYSTAL STRUCTURE OF UREASE FROM BACILLUS PASTEURII INHIBITED WITH BETA-MERCAPTOETHANOL AT 1.65 ANGSTROMS RESOLUTION	3.5.1.5
1UBZ	CRYSTAL STRUCTURE OF GLU102-MUTANT HUMAN LYSOZYME DOUBLY LABELED WITH 2',3'-EPOXYPROPYL BETA-GLYCOSIDE OF N-ACETYLLACTOSAMINE	3.2.1.17
1UC0	CRYSTAL STRUCTURE OF WILD-TYPE HEN-EGG WHITE LYSOZYME SINGLY LABELED WITH 2',3'-EPOXYPROPYL BETA-GLYCOSIDE OF N-ACETYLLACTOSAMINE	3.2.1.17
1UC2	HYPOTHETICAL EXTEIN PROTEIN OF PH1602 FROM PYROCOCCUS HORIKOSHII	6.5.1.8 3.1
1UCA	CRYSTAL STRUCTURE OF THE RIBONUCLEASE MC1 FROM BITTER GOURD SEEDS COMPLEXED WITH 2'-UMP	3.1.27.1 4.6.1.19
1UCC	CRYSTAL STRUCTURE OF THE RIBONUCLEASE MC1 FROM BITTER GOURD SEEDS COMPLEXED WITH 3'-UMP.	3.1.27.1 4.6.1.19
1UCD	CRYSTAL STRUCTURE OF RIBONUCLEASE MC1 FROM BITTER GOURD SEEDS COMPLEXED WITH 5'-UMP	3.1.27.1 4.6.1.19
1UCF	THE CRYSTAL STRUCTURE OF DJ-1, A PROTEIN RELATED TO MALE FERTILITY AND PARKINSON'S DISEASE	3.1.2 3.5.1 3.5.1.124
1UCG	CRYSTAL STRUCTURE OF RIBONUCLEASE MC1 N71T MUTANT	3.1.27.1 4.6.1.19
1UCH	DEUBIQUITINATING ENZYME UCH-L3 (HUMAN) AT 1.8 ANGSTROM RESOLUTION	3.1.2.15 3.4.19.12
1UCI	MUTANTS OF RNASE SA	3.1.27.3 4.6.1.24
1UCJ	MUTANTS OF RNASE SA	3.1.27.3 4.6.1.24
1UCK	MUTANTS OF RNASE SA	3.1.27.3 4.6.1.24
1UCL	MUTANTS OF RNASE SA	3.1.27.3 4.6.1.24
1UCO	HEN EGG-WHITE LYSOZYME, LOW HUMIDITY FORM	3.2.1.17
1UCY	THROMBIN COMPLEXED WITH FIBRINOPEPTIDE A ALPHA (RESIDUES 7-19). THREE COMPLEXES, ONE WITH EPSILON-THROMBIN AND TWO WITH ALPHA-THROMBIN	3.4.21.5
1UD2	CRYSTAL STRUCTURE OF CALCIUM-FREE ALPHA-AMYLASE FROM BACILLUS SP. STRAIN KSM-K38 (AMYK38)	3.2.1.1
1UD3	CRYSTAL STRUCTURE OF AMYK38 N289H MUTANT	3.2.1.1
1UD4	CRYSTAL STRUCTURE OF CALCIUM FREE ALPHA AMYLASE FROM BACILLUS SP. STRAIN KSM-K38 (AMYK38, IN CALCIUM CONTAINING SOLUTION)	3.2.1.1
1UD5	CRYSTAL STRUCTURE OF AMYK38 WITH RUBIDIUM ION	3.2.1.1
1UD6	CRYSTAL STRUCTURE OF AMYK38 WITH POTASSIUM ION	3.2.1.1
1UD8	CRYSTAL STRUCTURE OF AMYK38 WITH LITHIUM ION	3.2.1.1
1UDE	CRYSTAL STRUCTURE OF THE INORGANIC PYROPHOSPHATASE FROM THE HYPERTHERMOPHILIC ARCHAEON PYROCOCCUS HORIKOSHII OT3	3.6.1.1
1UDG	THE STRUCTURAL BASIS OF SPECIFIC BASE EXCISION REPAIR BY URACIL-DNA GLYCOSYLASE	3.2.2.3 3.2.2.27
1UDH	THE STRUCTURAL BASIS OF SPECIFIC BASE EXCISION REPAIR BY URACIL-DNA GLYCOSYLASE	3.2.2.3 3.2.2.27
1UDI	NUCLEOTIDE MIMICRY IN THE CRYSTAL STRUCTURE OF THE URACIL-DNA GLYCOSYLASE-URACIL GLYCOSYLASE INHIBITOR PROTEIN COMPLEX	3.2.2.3 3.2.2.27
1UDT	CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 5 COMPLEXED WITH SILDENAFIL(VIAGRA)	3.1.4.17 3.1.4.35
1UDU	CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 5 COMPLEXED WITH TADALAFIL(CIALIS)	3.1.4.17 3.1.4.35
1UDX	CRYSTAL STRUCTURE OF THE CONSERVED PROTEIN TT1381 FROM THERMUS THERMOPHILUS HB8	3.6.5
1UEA	MMP-3/TIMP-1 COMPLEX	3.4.24.17
1UF4	CRYSTAL STRUCTURE OF C171A/V236A MUTANT OF N-CARBAMYL-D-AMINO ACID AMIDOHYDROLASE	3.5.1.77
1UF5	CRYSTAL STRUCTURE OF C171A/V236A MUTANT OF N-CARBAMYL-D-AMINO ACID AMIDOHYDROLASE COMPLEXED WITH N-CARBAMYL-D-METHIONINE	3.5.1.77
1UF7	CRYSTAL STRUCTURE OF C171A/V236A MUTANT OF N-CARBAMYL-D-AMINO ACID AMIDOHYDROLASE COMPLEXED WITH N-CARBAMYL-D-VALINE	3.5.1.77
1UF8	CRYSTAL STRUCTURE OF C171A/V236A MUTANT OF N-CARBAMYL-D-AMINO ACID AMIDOHYDROLASE COMPLEXED WITH N-CARBAMYL-D-PHENYLALANINE	3.5.1.77
1UFW	SOLUTION STRUCTURE OF RNP DOMAIN IN SYNAPTOJANIN 2	3.1.3.36
1UG6	STRUCTURE OF BETA-GLUCOSIDASE AT ATOMIC RESOLUTION FROM THERMUS THERMOPHILUS HB8	3.2.1.21
1UG8	NMR STRUCTURE OF THE R3H DOMAIN FROM POLY(A)-SPECIFIC RIBONUCLEASE	3.1.13.4
1UG9	CRYSTAL STRUCTURE OF GLUCODEXTRANASE FROM ARTHROBACTER GLOBIFORMIS I42	3.2.1.70 3.2.1.3
1UGH	CRYSTAL STRUCTURE OF HUMAN URACIL-DNA GLYCOSYLASE IN COMPLEX WITH A PROTEIN INHIBITOR: PROTEIN MIMICRY OF DNA	3.2.2.3 3.2.2.27
1UH2	THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE/MALTO-HEXAOSE COMPLEX	3.2.1.1 3.2.1.135
1UH3	THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE/ACARBOSE COMPLEX	3.2.1.1 3.2.1.135
1UH4	THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE 1/MALTO-TRIDECAOSE COMPLEX	3.2.1.1 3.2.1.135
1UH7	CRYSTAL STRUCTURE OF RHIZOPUSPEPSIN AT PH 4.6	3.4.23.6 3.4.23.21
1UH8	CRYSTAL STRUCTURE OF RHIZOPUSPEPSIN AT PH 8.0	3.4.23.6 3.4.23.21
1UH9	CRYSTAL STRUCTURE OF RHIZOPUSPEPSIN AT PH 7.0	3.4.23.6 3.4.23.21
1UHB	CRYSTAL STRUCTURE OF PORCINE ALPHA TRYPSIN BOUND WITH AUTO CATALYTICALY PRODUCED NATIVE PEPTIDE AT 2.15 A RESOLUTION	3.4.21.4
1UHO	CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE 5 COMPLEXED WITH VARDENAFIL(LEVITRA)	3.1.4.17 3.1.4.35
1UHV	CRYSTAL STRUCTURE OF BETA-D-XYLOSIDASE FROM THERMOANAEROBACTERIUM SACCHAROLYTICUM, A FAMILY 39 GLYCOSIDE HYDROLASE	3.2.1.37
1UI0	CRYSTAL STRUCTURE OF URACIL-DNA GLYCOSYLASE FROM THERMUS THERMOPHILUS HB8	3.2.2 3.2.2.27
1UI1	CRYSTAL STRUCTURE OF URACIL-DNA GLYCOSYLASE FROM THERMUS THERMOPHILUS HB8	3.2.2 3.2.2.27
1UIA	ANALYSIS OF THE STABILIZATION OF HEN LYSOZYME WITH THE HELIX DIPOLE AND CHARGED SIDE CHAINS	3.2.1.17
1UIB	ANALYSIS OF THE STABILIZATION OF HEN LYSOZYME WITH THE HELIX DIPOLE AND CHARGED SIDE CHAINS	3.2.1.17
1UIC	ANALYSIS OF THE STABILIZATION OF HEN LYSOZYME WITH THE HELIX DIPOLE AND CHARGED SIDE CHAINS	3.2.1.17
1UID	ANALYSIS OF THE STABILIZATION OF HEN LYSOZYME WITH THE HELIX DIPOLE AND CHARGED SIDE CHAINS	3.2.1.17
1UIE	ANALYSIS OF THE STABILIZATION OF HEN LYSOZYME WITH THE HELIX DIPOLE AND CHARGED SIDE CHAINS	3.2.1.17
1UIF	ANALYSIS OF THE STABILIZATION OF HEN LYSOZYME WITH THE HELIX DIPOLE AND CHARGED SIDE CHAINS	3.2.1.17
1UIG	ANALYSIS OF THE STABILIZATION OF HEN LYSOZYME WITH THE HELIX DIPOLE AND CHARGED SIDE CHAINS	3.2.1.17
1UIH	ANALYSIS OF THE STABILIZATION OF HEN LYSOZYME WITH THE HELIX DIPOLE AND CHARGED SIDE CHAINS	3.2.1.17
1UIL	DOUBLE-STRANDED RNA-BINDING MOTIF OF HYPOTHETICAL PROTEIN BAB28848	3.6.4.13
1UIO	ADENOSINE DEAMINASE (HIS 238 ALA MUTANT)	3.5.4.4
1UIP	ADENOSINE DEAMINASE (HIS 238 GLU MUTANT)	3.5.4.4
1UJ1	CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO)	3.4.24 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
1UJB	STRUCTURE OF THE PROTEIN HISTIDINE PHOSPHATASE SIXA	3.1.3
1UJC	STRUCTURE OF THE PROTEIN HISTIDINE PHOSPHATASE SIXA COMPLEXED WITH TUNGSTATE	3.1.3
1UJX	THE FORKHEAD ASSOCIATED (FHA) DOMAIN LIKE STRUCTURE FROM MOUSE POLYNUCLEOTIDE KINASE 3'-PHOSPHATASE	3.1.3.32 2.7.1.78
1UK2	CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) AT PH8.0	3.4.24 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
1UK3	CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) AT PH7.6	3.4.24 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
1UK4	CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (3CLPRO) COMPLEXED WITH AN INHIBITOR	3.4.24 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
1UK6	CRYSTAL STRUCTURE OF A META-CLEAVAGE PRODUCT HYDROLASE (CUMD) COMPLEXED WITH PROPIONATE	3.7.1.9
1UK7	CRYSTAL STRUCTURE OF A META-CLEAVAGE PRODUCT HYDROLASE (CUMD) COMPLEXED WITH N-BUTYRATE	3.7.1.9
1UK8	CRYSTAL STRUCTURE OF A META-CLEAVAGE PRODUCT HYDROLASE (CUMD) COMPLEXED WITH N-VALERATE	3.7.1.9
1UK9	CRYSTAL STRUCTURE OF A META-CLEAVAGE PRODUCT HYDROLASE (CUMD) COMPLEXED WITH ISOVALERATE	3.7.1.9
1UKA	CRYSTAL STRUCTURE OF A META-CLEAVAGE PRODUCT HYDROLASE (CUMD) COMPLEXED WITH (S)-2-METHYLBUTYRATE	3.7.1.9
1UKB	CRYSTAL STRUCTURE OF A META-CLEAVAGE PRODUCT HYDROLASE (CUMD) COMPLEXED WITH BENZOATE	3.7.1.9
1UKC	CRYSTAL STRUCTURE OF ASPERGILLUS NIGER ESTA	3.1.1
1UKF	CRYSTAL STRUCTURE OF PSEUDOMONAS AVIRULENCE PROTEIN AVRPPHB	3.4.22
1UKO	CRYSTAL STRUCTURE OF SOYBEAN BETA-AMYLASE MUTANT SUBSTITUTED AT SURFACE REGION	3.2.1.2
1UKP	CRYSTAL STRUCTURE OF SOYBEAN BETA-AMYLASE MUTANT SUBSTITUTED AT SURFACE REGION	3.2.1.2
1UKR	STRUCTURE OF ENDO-1,4-BETA-XYLANASE C	3.2.1.8
1ULO	N-TERMINAL CELLULOSE-BINDING DOMAIN FROM CELLULOMONAS FIMI BETA-1,4-GLUCANASE C, NMR, MINIMIZED AVERAGE STRUCTURE	3.2.1.4
1ULP	N-TERMINAL CELLULOSE-BINDING DOMAIN FROM CELLULOMONAS FIMI BETA-1,4-GLUCANASE C, NMR, 25 STRUCTURES	3.2.1.4
1ULR	CRYSTAL STRUCTURE OF TT0497 FROM THERMUS THERMOPHILUS HB8	3.6.1.7
1ULV	CRYSTAL STRUCTURE OF GLUCODEXTRANASE COMPLEXED WITH ACARBOSE	3.2.1.70 3.2.1.3
1UM2	CRYSTAL STRUCTURE OF THE VMA1-DERIVED ENDONUCLEASE WITH THE LIGATED EXTEIN SEGMENT	3.6.3.14 7.1.2.2 3.1
1UMA	ALPHA-THROMBIN (HIRUGEN) COMPLEXED WITH NA-(N,N-DIMETHYLCARBAMOYL)-ALPHA-AZALYSINE	3.4.21.5
1UMG	CRYSTAL STRUCTURE OF FRUCTOSE-1,6-BISPHOSPHATASE	3.1.3.11 4.1.2.13
1UML	CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE COMPLEXED WITH A POTENT INHIBITOR FR233624	3.5.4.4
1UMS	STROMELYSIN-1 CATALYTIC DOMAIN WITH HYDROPHOBIC INHIBITOR BOUND, PH 7.0, 32OC, 20 MM CACL2, 15% ACETONITRILE; NMR ENSEMBLE OF 20 STRUCTURES	3.4.24.17
1UMT	STROMELYSIN-1 CATALYTIC DOMAIN WITH HYDROPHOBIC INHIBITOR BOUND, PH 7.0, 32OC, 20 MM CACL2, 15% ACETONITRILE; NMR AVERAGE OF 20 STRUCTURES MINIMIZED WITH RESTRAINTS	3.4.24.17
1UMU	STRUCTURE DETERMINATION OF UMUD' BY MAD PHASING OF THE SELENOMETHIONYL PROTEIN	3.4.21
1UMV	CRYSTAL STRUCTURE OF AN ACIDIC, NON-MYOTOXIC PHOSPHOLIPASE A2 FROM THE VENOM OF BOTHROPS JARARACUSSU	3.1.1.4
1UN3	CRYSTAL STRUCTURE OF HUMAN ANGIOGENIN VARIANT T44D	3.1.27.5 3.1.27
1UN4	CRYSTAL STRUCTURE OF HUMAN ANGIOGENIN VARIANT T80A	3.1.27.5 3.1.27
1UN5	ARH-II, AN ANGIOGENIN/RNASE A CHIMERA	3.1.27.5 3.1.27 4.6.1.18
1UNE	CARBOXYLIC ESTER HYDROLASE, 1.5 ANGSTROM ORTHORHOMBIC FORM OF THE BOVINE RECOMBINANT PLA2	3.1.1.4
1UO6	PORCINE PANCREATIC ELASTASE/XE-COMPLEX	3.4.21.36
1UOC	X-RAY STRUCTURE OF THE RNASE DOMAIN OF THE YEAST POP2 PROTEIN	3.1.13.4
1UOK	CRYSTAL STRUCTURE OF B. CEREUS OLIGO-1,6-GLUCOSIDASE	3.2.1.10
1UOO	PROLYL OLIGOPEPTIDASE FROM PORCINE BRAIN, S554A MUTANT WITH BOUND PEPTIDE LIGAND GLY-PHE-ARG-PRO	3.4.21.26
1UOP	PROLYL OLIGOPEPTIDASE FROM PORCINE BRAIN, S554A MUTANT WITH BOUND PEPTIDE LIGAND GLY-PHE-GLU-PRO	3.4.21.26
1UOQ	PROLYL OLIGOPEPTIDASE FROM PORCINE BRAIN, S554A MUTANT WITH BOUND PEPTIDE LIGAND GLU-PHE-SER-PRO	3.4.21.26
1UOZ	STRUCTURE OF THE ENDOGLUCANASE CEL6 FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH THIOCELLOPENTAOSE AT 1.1 ANGSTROM	3.2.1
1UP0	STRUCTURE OF THE ENDOGLUCANASE CEL6 FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH CELLOBIOSE AT 1.75 ANGSTROM	3.2.1
1UP2	STRUCTURE OF THE ENDOGLUCANASE CEL6 FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH GLUCOSE-ISOFAGOMINE AT 1.9 ANGSTROM	3.2.1
1UP3	STRUCTURE OF THE ENDOGLUCANASE CEL6 FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH METHYL-CELLOBIOSYL-4-DEOXY-4-THIO-BETA-D-CELLOBIOSIDE AT 1.6 ANGSTROM	3.2.1
1UPH	HIV-1 MYRISTOYLATED MATRIX	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1UPJ	HIV-1 PROTEASE COMPLEX WITH U095438 [3-[1-(4-BROMOPHENYL) ISOBUTYL]-4-HYDROXYCOUMARIN	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1UPN	COMPLEX OF ECHOVIRUS TYPE 12 WITH DOMAINS 3 AND 4 OF ITS RECEPTOR DECAY ACCELERATING FACTOR (CD55) BY CRYO ELECTRON MICROSCOPY AT 16 A	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1UQ4	RICIN A-CHAIN (RECOMBINANT) R213D MUTANT	3.2.2.22
1UQ5	RICIN A-CHAIN (RECOMBINANT) N122A MUTANT	3.2.2.22
1UQY	XYLANASE XYN10B MUTANT (E262S) FROM CELLVIBRIO MIXTUS IN COMPLEX WITH XYLOPENTAOSE	3.2.1.8
1UQZ	XYLANASE XYN10B MUTANT (E262S) FROM CELLVIBRIO MIXTUS IN COMPLEX WITH 4-O-METHYL GLUCURONIC ACID	3.2.1.8
1UR0	THE STRUCTURE OF ENDO-BETA-1,4-GALACTANASE FROM BACILLUS LICHENIFORMIS IN COMPLEX WITH TWO OLIGOSACCHARIDE PRODUCTS.	3.2.1.89
1UR1	XYLANASE XYN10B MUTANT (E262S) FROM CELLVIBRIO MIXTUS IN COMPLEX WITH ARABINOFURANOSE ALPHA-1,3 LINKED TO XYLOBIOSE	3.2.1.8
1UR2	XYLANASE XYN10B MUTANT (E262S) FROM CELLVIBRIO MIXTUS IN COMPLEX WITH ARABINOFURANOSE ALPHA 1,3 LINKED TO XYLOTRIOSE	3.2.1.8
1UR4	THE STRUCTURE OF ENDO-BETA-1,4-GALACTANASE FROM BACILLUS LICHENIFORMIS IN COMPLEX WITH TWO OLIGOSACCHARIDE PRODUCTS.	3.2.1.89
1UR8	INTERACTIONS OF A FAMILY 18 CHITINASE WITH THE DESIGNED INHIBITOR HM508, AND ITS DEGRADATION PRODUCT, CHITOBIONO-DELTA-LACTONE	3.2.1.14
1UR9	INTERACTIONS OF A FAMILY 18 CHITINASE WITH THE DESIGNED INHIBITOR HM508, AND ITS DEGRADATION PRODUCT, CHITOBIONO-DELTA-LACTONE	3.2.1.14
1URA	ALKALINE PHOSPHATASE (D51ZN)	3.1.3.1
1URB	ALKALINE PHOSPHATASE (N51MG)	3.1.3.1
1URK	SOLUTION STRUCTURE OF THE AMINO TERMINAL FRAGMENT OF UROKINASE-TYPE PLASMINOGEN ACTIVATOR	3.4.21.73
1URR	A NOVEL DROSOPHILA MELANOGASTER ACYLPHOSPHATASE (ACPDRO2)	3.6.1.7
1URX	CRYSTALLOGRAPHIC STRUCTURE OF BETA-AGARASE A IN COMPLEX WITH OLIGOAGAROSE	3.2.1.81
1US2	XYLANASE10C (MUTANT E385A) FROM CELLVIBRIO JAPONICUS IN COMPLEX WITH XYLOPENTAOSE	3.2.1.8
1US3	NATIVE XYLANASE10C FROM CELLVIBRIO JAPONICUS	3.2.1.8
1USH	5'-NUCLEOTIDASE FROM E. COLI	3.1.3.5 3.6.1.45
1USN	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN FIBROBLAST STROMELYSIN-1 INHIBITED WITH THIADIAZOLE INHIBITOR PNU-142372	3.4.24.17
1USR	NEWCASTLE DISEASE VIRUS HEMAGGLUTININ-NEURAMINIDASE: EVIDENCE FOR A SECOND SIALIC ACID BINDING SITE AND IMPLICATIONS FOR FUSION	3.2.1.18
1USW	CRYSTAL STRUCTURE OF FERULIC ACID ESTERASE FROM ASPERGILLUS NIGER	3.1.1.73
1USX	CRYSTAL STRUCTURE OF THE NEWCASTLE DISEASE VIRUS HEMAGGLUTININ-NEURAMINIDASE COMPLEXED WITH THIOSIALOSIDE	3.2.1.18
1UT5	DIVALENT METAL IONS (MANGANESE) BOUND TO T5 5'-EXONUCLEASE	3.1.11.3 3.1.11
1UT6	STRUCTURE OF ACETYLCHOLINESTERASE (E.C. 3.1.1.7) COMPLEXED WITH N-9-(1',2',3',4'-TETRAHYDROACRIDINYL)-1,8- DIAMINOOCTANE AT 2.4 ANGSTROMS RESOLUTION.	3.1.1.7
1UT8	DIVALENT METAL IONS (ZINC) BOUND TO T5 5'-EXONUCLEASE	3.1.11.3 3.1.11
1UT9	STRUCTURAL BASIS FOR THE EXOCELLULASE ACTIVITY OF THE CELLOBIOHYDROLASE CBHA FROM C. THERMOCELLUM	3.2.1.4
1UTE	PIG PURPLE ACID PHOSPHATASE COMPLEXED WITH PHOSPHATE	3.1.3.2
1UTJ	TRYPSIN SPECIFICITY AS ELUCIDATED BY LIE CALCULATIONS, X-RAY STRUCTURES AND ASSOCIATION CONSTANT MEASUREMENTS	3.4.21.4
1UTK	TRYPSIN SPECIFICITY AS ELUCIDATED BY LIE CALCULATIONS, X-RAY STRUCTURES AND ASSOCIATION CONSTANT MEASUREMENTS	3.4.21.4
1UTL	TRYPSIN SPECIFICITY AS ELUCIDATED BY LIE CALCULATIONS, X-RAY STRUCTURES AND ASSOCIATION CONSTANT MEASUREMENTS	3.4.21.4
1UTM	TRYPSIN SPECIFICITY AS ELUCIDATED BY LIE CALCULATIONS, X-RAY STRUCTURES AND ASSOCIATION CONSTANT MEASUREMENTS	3.4.21.4
1UTN	TRYPSIN SPECIFICITY AS ELUCIDATED BY LIE CALCULATIONS, X-RAY STRUCTURES AND ASSOCIATION CONSTANT MEASUREMENTS	3.4.21.4
1UTO	TRYPSIN SPECIFICITY AS ELUCIDATED BY LIE CALCULATIONS, X-RAY STRUCTURES AND ASSOCIATION CONSTANT MEASUREMENTS	3.4.21.4
1UTP	TRYPSIN SPECIFICITY AS ELUCIDATED BY LIE CALCULATIONS, X-RAY STRUCTURES AND ASSOCIATION CONSTANT MEASUREMENTS	3.4.21.4
1UTQ	TRYPSIN SPECIFICITY AS ELUCIDATED BY LIE CALCULATIONS, X-RAY STRUCTURES AND ASSOCIATION CONSTANT MEASUREMENTS	3.4.21.4
1UTT	CRYSTAL STRUCTURE OF MMP-12 COMPLEXED TO 2-(1,3-DIOXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)ETHYL-4-(4-ETHOXY[1,1-BIPHENYL]-4-YL)-4-OXOBUTANOIC ACID	3.4.24.65
1UTZ	CRYSTAL STRUCTURE OF MMP-12 COMPLEXED TO (2R)-3-({[4-[(PYRIDIN-4-YL)PHENYL]-THIEN-2-YL}CARBOXAMIDO)(PHENYL)PROPANOIC ACID	3.4.24.65
1UU4	X-RAY CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMICOLA GRISEA CEL12A IN COMPLEX WITH CELLOBIOSE	3.2.1.4
1UU5	X-RAY CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMICOLA GRISEA CEL12A SOAKED WITH CELLOTETRAOSE	3.2.1.4
1UU6	X-RAY CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMICOLA GRISEA CEL12A IN COMPLEX WITH A SOAKED CELLOPENTAOSE	3.2.1.4
1UUG	ESCHERICHIA COLI URACIL-DNA GLYCOSYLASE:INHIBITOR COMPLEX WITH WILD-TYPE UDG AND WILD-TYPE UGI	3.2.2.3 3.2.2.27
1UV4	NATIVE BACILLUS SUBTILIS ARABINANASE ARB43A	3.2.1.99
1UVO	STRUCTURE OF THE COMPLEX OF PORCINE PANCREATIC ELASTASE IN COMPLEX WITH CADMIUM REFINED AT 1.85 A RESOLUTION (CRYSTAL A)	3.4.21.36
1UVP	STRUCTURE OF THE COMPLEX OF PORCINE PANCREATIC ELASTASE IN COMPLEX WITH CADMIUM REFINED AT 1.85 A RESOLUTION (CRYSTAL B)	3.4.21.36
1UVS	BOVINE THROMBIN--BM51.1011 COMPLEX	3.4.21.5
1UVT	BOVINE THROMBIN--BM14.1248 COMPLEX	3.4.21.5
1UVU	BOVINE THROMBIN--BM12.1700 COMPLEX	3.4.21.5
1UW7	NSP9 PROTEIN FROM SARS-CORONAVIRUS.	3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
1UWB	TYR 181 CYS HIV-1 RT/8-CL TIBO	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1UWC	FERULOYL ESTERASE FROM ASPERGILLUS NIGER	3.1.1.73
1UWI	CRYSTAL STRUCTURE OF MUTATED BETA-GLYCOSIDASE FROM SULFOLOBUS SOLFATARICUS, WORKING AT MODERATE TEMPERATURE	3.2.1.23
1UWQ	STRUCTURE OF BETA-GLYCOSIDASE FROM SULFOLOBUS SOLFATARICUS	3.2.1.23
1UWR	STRUCTURE OF BETA-GLYCOSIDASE FROM SULFOLOBUS SOLFATARICUS IN COMPLEX WITH 2-DEOXY-2-FLUORO-GALACTOSE	3.2.1.23
1UWS	STRUCTURE OF BETA-GLYCOSIDASE FROM SULFOLOBUS SOLFATARICUS IN COMPLEX WITH 2-DEOXY-2-FLUORO-GLUCOSE	3.2.1.23
1UWT	STRUCTURE OF BETA-GLYCOSIDASE FROM SULFOLOBUS SOLFATARICUS IN COMPLEX WITH D-GALACTOHYDROXIMO-1,5-LACTAM	3.2.1.23
1UWU	STRUCTURE OF BETA-GLYCOSIDASE FROM SULFOLOBUS SOLFATARICUS IN COMPLEX WITH D-GLUCOHYDROXIMO-1,5-LACTAM	3.2.1.23
1UWW	X-RAY CRYSTAL STRUCTURE OF A NON-CRYSTALLINE CELLULOSE SPECIFIC CARBOHYDRATE-BINDING MODULE: CBM28.	3.2.1.4
1UWY	CRYSTAL STRUCTURE OF HUMAN CARBOXYPEPTIDASE M	3.4.17.12
1UWZ	BACILLUS SUBTILIS CYTIDINE DEAMINASE WITH AN ARG56 - ALA SUBSTITUTION	3.5.4.5
1UX0	BACILLUS SUBTILIS CYTIDINE DEAMINASE WITH AN ARG56 - GLN SUBSTITUTION	3.5.4.5
1UX1	BACILLUS SUBTILIS CYTIDINE DEAMINASE WITH A CYS53HIS AND AN ARG56GLN SUBSTITUTION	3.5.4.5
1UX7	CARBOHYDRATE-BINDING MODULE CBM36 IN COMPLEX WITH CALCIUM AND XYLOTRIOSE	3.2.1.55
1UXO	THE CRYSTAL STRUCTURE OF THE YDEN GENE PRODUCT FROM B. SUBTILIS	3
1UXX	CBM6CT FROM CLOSTRIDIUM THERMOCELLUM IN COMPLEX WITH XYLOPENTAOSE	3.2.1.8
1UY1	BINDING SUB-SITE DISSECTION OF A FAMILY 6 CARBOHYDRATE-BINDING MODULE BY X-RAY CRYSTALLOGRAPHY AND ISOTHERMAL TITRATION CALORIMETRY	3.2.1.8
1UY2	BINDING SUB-SITE DISSECTION OF A FAMILY 6 CARBOHYDRATE-BINDING MODULE BY X-RAY CRYSTALLOGRAPHY AND ISOTHERMAL TITRATION CALORIMETRY	3.2.1.8
1UY3	BINDING SUB-SITE DISSECTION OF A FAMILY 6 CARBOHYDRATE-BINDING MODULE BY X-RAY CRYSTALLOGRAPHY AND ISOTHERMAL TITRATION CALORIMETRY	3.2.1.8
1UY4	BINDING SUB-SITE DISSECTION OF A FAMILY 6 CARBOHYDRATE-BINDING MODULE BY X-RAY CRYSTALLOGRAPHY AND ISOTHERMAL TITRATION CALORIMETRY	3.2.1.8
1UYQ	MUTATED B-GLUCOSIDASE A FROM PAENIBACILLUS POLYMYXA SHOWING INCREASED STABILITY	3.2.1.21
1UZ1	FAMILY 1 B-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH ISOFAGOMINE LACTAM	3.2.1.21
1UZA	CRYSTALLOGRAPHIC STRUCTURE OF A FERULOYL ESTERASE FROM ASPERGILLUS NIGER	3.1.1.73
1UZE	COMPLEX OF THE ANTI-HYPERTENSIVE DRUG ENALAPRILAT AND THE HUMAN TESTICULAR ANGIOTENSIN I-CONVERTING ENZYME	3.2.1 3.4.15.1
1UZF	COMPLEX OF THE ANTI-HYPERTENSIVE DRUG CAPTOPRIL AN THE HUMAN TESTICULAR ANGIOTENSIN I-CONVERTING ENZYME	3.2.1 3.4.15.1
1UZG	CRYSTAL STRUCTURE OF THE DENGUE TYPE 3 VIRUS ENVELOPE PROTEIN	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
1V03	CRYSTAL STRUCTURE OF THE SORGHUM BICOLOR DHURRINASE 1	3.2.1.21
1V04	SERUM PARAOXONASE BY DIRECTED EVOLUTION	3.1.1.2 3.1.8.1 3.1.1.81
1V08	CRYSTAL STRUCTURE OF THE ZEA MAZE BETA-GLUCOSIDASE-1 IN COMPLEX WITH GLUCO-TETRAZOLE	3.2.1.21 3.2.1.182
1V0A	FAMILY 11 CARBOHYDRATE-BINDING MODULE OF CELLULOSOMAL CELLULASE LIC26A-CEL5E OF CLOSTRIDIUM THERMOCELLUM	3.2.1.4
1V0D	CRYSTAL STRUCTURE OF CASPASE-ACTIVATED DNASE (CAD)	3
1V0K	XYLANASE XYN10A FROM STREPTOMYCES LIVIDANS IN COMPLEX WITH XYLOBIO-DEOXYNOJIRIMYCIN AT PH 5.8	3.2.1.8
1V0L	XYLANASE XYN10A FROM STREPTOMYCES LIVIDANS IN COMPLEX WITH XYLOBIO-ISOFAGOMINE AT PH 5.8	3.2.1.8
1V0M	XYLANASE XYN10A FROM STREPTOMYCES LIVIDANS IN COMPLEX WITH XYLOBIO-DEOXYNOJIRIMYCIN AT PH 7.5	3.2.1.8
1V0N	XYLANASE XYN10A FROM STREPTOMYCES LIVIDANS IN COMPLEX WITH XYLOBIO-ISOFAGOMINE AT PH 7.5	3.2.1.8
1V0R	TUNGSTATE-INHIBITED PHOSPHOLIPASE D FROM STREPTOMYCES SP. STRAIN PMF	3.1.4.4
1V0S	UNINHIBITED FORM OF PHOSPHOLIPASE D FROM STREPTOMYCES SP. STRAIN PMF	3.1.4.4
1V0T	PHOSPHOLIPASE D FROM STREPTOMYCES SP. STRAIN PMF SOAKED WITH THE PRODUCT GLYCEROPHOSPHATE	3.1.4.4
1V0U	PHOSPHOLIPASE D FROM STREPTOMYCES SP. STRAIN PMF SOAKED WITH THE PRODUCT GLYCEROPHOSPHATE.	3.1.4.4
1V0V	PHOSPHOLIPASE D FROM STREPTOMYCES SP. STRAIN PMF SOAKED WITH THE SUBSTRATE DIBUTYRYLPHOSPHATIDYLCHOLINE.	3.1.4.4
1V0W	PHOSPHOLIPASE D FROM STREPTOMYCES SP. STRAIN PMF SOAKED WITH THE SUBSTRATE DIBUTYRYLPHOSPHATIDYLCHOLINE.	3.1.4.4
1V0Y	PHOSPHOLIPASE D FROM STREPTOMYCES SP. STRAIN PMF SOAKED WITH THE SUBSTRATE DIBUTYRYLPHOSPHATIDYLCHOLINE.	3.1.4.4
1V0Z	STRUCTURE OF NEURAMINIDASE FROM ENGLISH DUCK SUBTYPE N6	3.2.1.18
1V13	CRYSTAL STRUCTURE OF THE MUTANT HIS103ALA OF THE COLICIN E9 DNASE DOMAIN IN COMPLEX WITH ZN+2 (2.0 ANGSTROMS)	3.1
1V14	CRYSTAL STRUCTURE OF THE COLICIN E9, MUTANT HIS103ALA, IN COMPLEX WITH MG+2 AND DSDNA (RESOLUTION 2.9A)	3.1.21.1 3.1
1V15	CRYSTAL STRUCTURE OF THE COLICIN E9, MUTANT HIS103ALA, IN COMPLEX WITH ZN+2 AND DSDNA (RESOLUTION 2.4A)	3.1.21.1 3.1
1V2G	THE L109P MUTANT OF E. COLI THIOESTERASE I/PROTEASE I/LYSOPHOSPHOLIPASE L1 (TAP) IN COMPLEXED WITH OCTANOIC ACID	3.1.1.5 3.1.2 3.1.2.2 3.1.1.2 3.1.2.14 3.4.21
1V2I	STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III	3.2.1.18
1V2J	BENZAMIDINE IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(SSRI)BT.C1	3.4.21.4
1V2K	FACTOR XA SPECIFIC INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(TRIPLE.GLU)BT.D2	3.4.21.4
1V2L	BENZAMIDINE IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(TRIPLE.GLU)BT.D1	3.4.21.4
1V2M	BENZAMIDINE IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(TRIPLE.GLU)BT.A1	3.4.21.4
1V2N	POTENT FACTOR XA INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(99/175/190)BT	3.4.21.4
1V2O	TRYPSIN INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(SSYI)BT.B4	3.4.21.4
1V2P	TRYPSIN INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(SSYI)BT.A4	3.4.21.4
1V2Q	TRYPSIN INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(SSWI)BT.B4	3.4.21.4
1V2R	TRYPSIN INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(SSRI)BT.B4	3.4.21.4
1V2S	BENZAMIDINE IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(SSFI.GLU)BT.D1	3.4.21.4
1V2T	TRYPSIN INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(SSFI.GLU)BT.B4	3.4.21.4
1V2U	BENZAMIDINE IN COMPLEX WITH BOVINE TRYPSIN VARINAT X(SSAI)BT.D1	3.4.21.4
1V2V	BENZAMIDINE IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(SSAI)BT.C1	3.4.21.4
1V2W	TRYPSIN INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN VARIANT X(SSAI)BT.B4	3.4.21.4
1V3A	STRUCTURE OF HUMAN PRL-3, THE PHOSPHATASE ASSOCIATED WITH CANCER METASTASIS	3.1.3.48
1V3B	STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III	3.2.1.18
1V3C	STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III: COMPLEX WITH NEU5AC	3.2.1.18
1V3D	STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III: COMPLEX WITH NEU5AC2EN	3.2.1.18
1V3E	STRUCTURE OF THE HEMAGGLUTININ-NEURAMINIDASE FROM HUMAN PARAINFLUENZA VIRUS TYPE III: COMPLEX WITH ZANAMAVIR	3.2.1.18
1V3H	THE ROLES OF GLU186 AND GLU380 IN THE CATALYTIC REACTION OF SOYBEAN BETA-AMYLASE	3.2.1.2
1V3I	THE ROLES OF GLU186 AND GLU380 IN THE CATALYTIC REACTION OF SOYBEAN BETA-AMYLASE	3.2.1.2
1V3X	FACTOR XA IN COMPLEX WITH THE INHIBITOR 1-[6-METHYL-4,5,6,7-TETRAHYDROTHIAZOLO(5,4-C)PYRIDIN-2-YL] CARBONYL-2-CARBAMOYL-4-(6-CHLORONAPHTH-2-YLSULPHONYL)PIPERAZINE	3.4.21.6
1V3Y	THE CRYSTAL STRUCTURE OF PEPTIDE DEFORMYLASE FROM THERMUS THERMOPHILUS HB8	3.5.1.88
1V3Z	CRYSTAL STRUCTURE OF ACYLPHOSPHATASE FROM PYROCOCCUS HORIKOSHII	3.6.1.7
1V4Y	THE FUNCTIONAL ROLE OF THE BINUCLEAR METAL CENTER IN D-AMINOACYLASE. ONE-METAL ACTIVATION AND SECOND-METAL ATTENUATION	3.5.1.81
1V51	THE FUNCTIONAL ROLE OF THE BINUCLEAR METAL CENTER IN D-AMINOACYLASE. ONE-METAL ACTIVATION AND SECOND-METAL ATTENUATION	3.5.1.81
1V5C	THE CRYSTAL STRUCTURE OF THE INACTIVE FORM CHITOSANASE FROM BACILLUS SP. K17 AT PH3.7	3.2.1.132 3.2.1
1V5D	THE CRYSTAL STRUCTURE OF THE ACTIVE FORM CHITOSANASE FROM BACILLUS SP. K17 AT PH6.4	3.2.1.132 3.2.1
1V5I	CRYSTAL STRUCTURE OF SERINE PROTEASE INHIBITOR POIA1 IN COMPLEX WITH SUBTILISIN BPN'	3.4.21.62
1V5O	SOLUTION STRUCTURE OF THE UBIQUITIN-LIKE DOMAIN FROM MOUSE HYPOTHETICAL 1700011N24RIK PROTEIN	3.4.23
1V5T	SOLUTION STRUCTURE OF THE UBIQUITIN-LIKE DOMAIN FROM MOUSE HYPOTHETICAL 8430435I17RIK PROTEIN	3.1.3.16
1V6C	CRYSTAL STRUCTURE OF PSYCHROPHILIC SUBTILISIN-LIKE PROTEASE APA1 FROM ANTARCTIC PSYCHROTROPH PSEUDOALTEROMONAS SP. AS-11	3.4.21
1V6D	THE CRYSTAL STRUCTURE OF THE TRYPSIN COMPLEX WITH SYNTHETIC HETEROCHIRAL PEPTIDE	3.4.21.4
1V6T	CRYSTAL STRUCTURE OF LACTAM UTILIZATION PROTEIN FROM PYROCOCCUS HORIKOSHII OT3	3.5.2.9
1V6U	CRYSTAL STRUCTURE OF XYLANASE FROM STREPTOMYCES OLIVACEOVIRIDIS E-86 COMPLEXED WITH 2(2)-ALPHA-L-ARABINOFURANOSYL-XYLOBIOSE	3.2.1.8
1V6V	CRYSTAL STRUCTURE OF XYLANASE FROM STREPTOMYCES OLIVACEOVIRIDIS E-86 COMPLEXED WITH 3(2)-ALPHA-L-ARABINOFURANOSYL-XYLOTRIOSE	3.2.1.8
1V6W	CRYSTAL STRUCTURE OF XYLANASE FROM STREPTOMYCES OLIVACEOVIRIDIS E-86 COMPLEXED WITH 2(2)-4-O-METHYL-ALPHA-D-GLUCURONOSYL-XYLOBIOSE	3.2.1.8
1V6X	CRYSTAL STRUCTURE OF XYLANASE FROM STREPTOMYCES OLIVACEOVIRIDIS E-86 COMPLEXED WITH 3(3)-4-O-METHYL-ALPHA-D-GLUCURONOSYL-XYLOTRIOSE	3.2.1.8
1V6Y	CRYSTAL STRUCTURE OF CHIMERIC XYLANASE BETWEEN STREPTOMYCES OLIVACEOVIRIDIS E-86 FXYN AND CELLULOMONAS FIMI CEX	3.2.1.8 3.2.1.91
1V73	CRYSTAL STRUCTURE OF COLD-ACTIVE PROTEIN-TYROSINE PHOSPHATASE OF A PSYCHROPHILE SHEWANELLA SP.	3.1.3.48
1V76	CRYSTAL STRUCTURE OF ARCHAEAL RIBONUCLEASE P PROTEIN PH1771P FROM PYROCOCCUS HORIKOSHII OT3	3.1.26.5
1V77	CRYSTAL STRUCTURE OF THE PH1877 PROTEIN	3.1.26.5
1V79	CRYSTAL STRUCTURES OF ADENOSINE DEAMINASE COMPLEXED WITH POTENT INHIBITORS	3.5.4.4
1V7A	CRYSTAL STRUCTURES OF ADENOSINE DEAMINASE COMPLEXED WITH POTENT INHIBITORS	3.5.4.4
1V7R	STRUCTURE OF NUCLEOTIDE TRIPHOSPHATE PYROPHOSPHATASE FROM PYROCOCCUS HORIKOSHII OT3	3.6.1.19 3.6.1.66
1V7S	TRICLINIC HEN LYSOZYME CRYSTALLIZED AT 313K FROM A D2O SOLUTION	3.2.1.17
1V7T	TRICLINIC LYSOZYME WITH LOW SOLVENT CONTENT OBTAINED BY PHASE TRANSITION	3.2.1.17
1V7Z	CREATININASE-PRODUCT COMPLEX	3.5.2.10
1V8B	CRYSTAL STRUCTURE OF A HYDROLASE	3.3.1.1
1V8E	CRYSTAL STRUCTURE OF GLYCEROPHOSPHORYL DIESTER PHOSPHODIESTERASE FROM THERMUS THERMOPHILUS HB8	3.1.4.46
1V8I	CRYSTAL STRUCTURE ANALYSIS OF THE ADP-RIBOSE PYROPHOSPHATASE	3.6.1.13
1V8L	STRUCTURE ANALYSIS OF THE ADP-RIBOSE PYROPHOSPHATASE COMPLEXED WITH ADP-RIBOSE	3.6.1.13
1V8M	CRYSTAL STRUCTURE ANALYSIS OF ADP-RIBOSE PYROPHOSPHATASE COMPLEXED WITH ADP-RIBOSE AND GD	3.6.1.13
1V8N	CRYSTAL STRUCTURE ANALYSIS OF THE ADP-RIBOSE PYROPHOSPHATASE COMPLEXED WITH ZN	3.6.1.13
1V8O	CRYSTAL STRUCTURE OF PAE2754 FROM PYROBACULUM AEROPHILUM	3.1
1V8P	CRYSTAL STRUCTURE OF PAE2754 FROM PYROBACULUM AEROPHILUM	3.1
1V8R	CRYSTAL STRUCTURE ANALYSIS OF THE ADP-RIBOSE PYROPHOSPHATASE COMPLEXED WITH ADP-RIBOSE AND ZN	3.6.1.13
1V8S	CRYSTAL STRUCTURE ANALUSIS OF THE ADP-RIBOSE PYROPHOSPHATASE COMPLEXED WITH AMP AND MG	3.6.1.13
1V8T	CRYSTAL STRUCTURE ANALYSIS OF THE ADP-RIBOSE PYROPHOSPHATASE COMPLEXED WITH RIBOSE-5'-PHOSPHATE AND ZN	3.6.1.13
1V8U	CRYSTAL STRUCTURE ANALYSIS OF THE ADP-RIBOSE PYROPHOSPHATASE OF E82Q MUTANT WITH SO4 AND MG	3.6.1.13
1V8V	CRYSTAL STRUCTURE ANALYSIS OF THE ADP-RIBOSE PYROPHOSPHATASE OF E86Q MUTANT, COMPLEXED WITH ADP-RIBOSE AND MG	3.6.1.13
1V8W	CRYSTAL STRUCTURE ANALYSIS OF THE ADP-RIBOSE PYROPHOSPHATASE OF E82Q MUTANT, COMPLEXED WITH SO4 AND ZN	3.6.1.13
1V8Y	CRYSTAL STRUCTURE ANALYSIS OF THE ADP-RIBOSE PYROPHOSPHATASE OF E86Q MUTANT, COMPLEXED WITH ADP-RIBOSE AND ZN	3.6.1.13
1V96	CRYSTAL STRUCTURE OF HYPOTHETICAL PROTEIN OF UNKNOWN FUNCTION FROM PYROCOCCUS HORIKOSHII OT3	3.1
1V9H	CRYSTAL STRUCTURE OF THE RNASE MC1 MUTANT Y101A IN COMPLEX WITH 5'-UMP	3.1.27.1 4.6.1.19
1V9M	CRYSTAL STRUCTURE OF THE C SUBUNIT OF V-TYPE ATPASE FROM THERMUS THERMOPHILUS	3.6.3.14
1V9Y	CRYSTAL STRUCTURE OF THE HEME PAS SENSOR DOMAIN OF EC DOS (FERRIC FORM)	3.1.4.52
1V9Z	CRYSTAL STRUCTURE OF THE HEME PAS SENSOR DOMAIN OF EC DOS (FERROUS FORM)	3.1.4.52
1VA4	PSEUDOMONAS FLUORESCENS ARYL ESTERASE	3.1.1.2 1
1VAH	CRYSTAL STRUCTURE OF THE PIG PANCREATIC-AMYLASE COMPLEXED WITH R-NITROPHENYL-A-D-MALTOSIDE	3.2.1.1
1VAP	THE MONOMERIC ASP49 SECRETORY PHOSPHOLIPASE A2 FROM THE VENOM OF AGKISTRIDON PISCIVORUS PISCIVORUS	3.1.1.4
1VAS	ATOMIC MODEL OF A PYRIMIDINE DIMER SPECIFIC EXCISION REPAIR ENZYME COMPLEXED WITH A DNA SUBSTRATE: STRUCTURAL BASIS FOR DAMAGED DNA RECOGNITION	3.2.2.17 4.2.99.18
1VAT	IODINE DERIVATIVE OF HEN EGG-WHITE LYSOZYME	3.2.1.17
1VAU	XENON DERIVATIVE OF HEN EGG-WHITE LYSOZYME	3.2.1.17
1VB6	CRYSTAL STRUCTURE OF THE HEME PAS SENSOR DOMAIN OF EC DOS (OXYGEN-BOUND FORM)	3.1.4.52
1VB9	CRYSTAL STRUCTURE OF THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE II (TVA II) COMPLEXED WITH TRANSGLYCOSYLATED PRODUCT	3.2.1.1 3.2.1.135
1VBR	CRYSTAL STRUCTURE OF COMPLEX XYLANASE 10B FROM THERMOTOGA MARITIMA WITH XYLOBIOSE	3.2.1.8
1VBU	CRYSTAL STRUCTURE OF NATIVE XYLANASE 10B FROM THERMOTOGA MARITIMA	3.2.1.8
1VC8	CRYSTAL STRUCTURE OF A T.THERMOPHILUS HB8 AP6A HYDROLASE NDX1-AP6A COMPLEX	3.6.1.61
1VC9	CRYSTAL STRUCTURE OF A T.THERMOPHILUS HB8 AP6A HYDROLASE E50Q MUTANT-MG2+-ATP COMPLEX	3.6.1.61
1VCD	CRYSTAL STRUCTURE OF A T.THERMOPHILUS HB8 AP6A HYDROLASE NDX1	3.6.1.61
1VCJ	INFLUENZA B VIRUS NEURAMINIDASE COMPLEXED WITH 1-(4-CARBOXY-2-(3-PENTYLAMINO)PHENYL)-5-AMINOMETHYL-5-HYDROXYMETHYL-PYRROLIDIN-2-ONE	3.2.1.18
1VCP	SEMLIKI FOREST VIRUS CAPSID PROTEIN (CRYSTAL FORM I)	3.4.21.90
1VCQ	SEMLIKI FOREST VIRUS CAPSID PROTEIN (CRYSTAL FORM II)	3.4.21.90
1VCU	STRUCTURE OF THE HUMAN CYTOSOLIC SIALIDASE NEU2 IN COMPLEX WITH THE INHIBITOR DANA	3.2.1.18
1VCW	CRYSTAL STRUCTURE OF DEGS AFTER BACKSOAKING THE ACTIVATING PEPTIDE	3.4.21 3.4.21.107
1VCZ	CRYSTAL STRUCTURE OF THE RNASE NT IN COMPLEX WITH 5'-GMP	3.1.27.1
1VD1	CRYSTAL STRUCTURE OF RNASE NT IN COMPLEX WITH 5'-AMP	3.1.27.1
1VD3	RIBONUCLEASE NT IN COMPLEX WITH 2'-UMP	3.1.27.1
1VD5	CRYSTAL STRUCTURE OF UNSATURATED GLUCURONYL HYDROLASE, RESPONSIBLE FOR THE DEGRADATION OF GLYCOSAMINOGLYCAN, FROM BACILLUS SP. GL1 AT 1.8 A RESOLUTION	3.2.1 3.2.1.179
1VD6	CRYSTAL STRUCTURE OF GLYCEROPHOSPHORYL DIESTER PHOSPHODIESTERASE COMPLEXED WITH GLYCEROL	3.1.4.46
1VDE	PI-SCEI, A HOMING ENDONUCLEASE WITH PROTEIN SPLICING ACTIVITY	7.1.2.2 3.1
1VDL	SOLUTION STRUCTURE OF RSGI RUH-013, A UBA DOMAIN IN MOUSE CDNA	3.1.2.15 3.4.19.12
1VDP	THE CRYSTAL STRUCTURE OF THE MONOCLINIC FORM OF HEN EGG WHITE LYSOZYME AT 1.7 ANGSTROMS RESOLUTION IN SPACE	3.2.1.17
1VDQ	THE CRYSTAL STRUCTURE OF THE ORTHORHOMBIC FORM OF HEN EGG WHITE LYSOZYME AT 1.5 ANGSTROMS RESOLUTION	3.2.1.17
1VDS	THE CRYSTAL STRUCTURE OF THE TETRAGONAL FORM OF HEN EGG WHITE LYSOZYME AT 1.6 ANGSTROMS RESOLUTION IN SPACE	3.2.1.17
1VDT	THE CRYSTAL STRUCTURE OF THE TETRAGONAL FORM OF HEN EGG WHITE LYSOZYME AT 1.7 ANGSTROMS RESOLUTION UNDER BASIC CONDITIONS IN SPACE	3.2.1.17
1VDW	A HYPOTHETICAL PROTEIN PH1897 FROM PYROCOCCUS HORIKOSHII WITH SIMILARITIES FOR INOSITOL-1 MONOPHOSPHATASE	3.1.3.11
1VDX	CRYSTAL STRUCTURE OF A PYROCOCCUS HORIKOSHII PROTEIN WITH SIMILARITIES TO 2'5' RNA-LIGASE	6.5.1.3 3.1.4.58
1VDZ	CRYSTAL STRUCTURE OF A-TYPE ATPASE CATALYTIC SUBUNIT A FROM PYROCOCCUS HORIKOSHII OT3	3.6.3.14 7.1.2.2 3.1
1VE6	CRYSTAL STRUCTURE OF AN ACYLPEPTIDE HYDROLASE/ESTERASE FROM AEROPYRUM PERNIX K1	3.4.19.1
1VE7	CRYSTAL STRUCTURE OF AN ACYLPEPTIDE HYDROLASE/ESTERASE FROM AEROPYRUM PERNIX K1 IN COMPLEX WITH P-NITROPHENYL PHOSPHATE	3.4.19.1
1VEC	CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF RCK/P54, A HUMAN DEAD-BOX PROTEIN	3.6.4.13
1VED	THE CRYSTAL STRUCTURE OF THE ORTHORHOMBIC FORM OF HEN EGG WHITE LYSOZYME AT 1.9 ANGSTROMS RESOLUTION IN SPACE	3.2.1.17
1VEK	SOLUTION STRUCTURE OF RSGI RUH-011, A UBA DOMAIN FROM ARABIDOPSIS CDNA	3.4.19.12
1VEM	CRYSTAL STRUCTURE ANALYSIS OF BACILLUS CEREUS BETA-AMYLASE AT THE OPTIMUM PH (6.5)	3.2.1.2
1VEN	CRYSTAL STRUCTURE ANALYSIS OF Y164E/MALTOSE OF BACILUS CEREUS BETA-AMYLASE AT PH 4.6	3.2.1.2
1VEO	CRYSTAL STRUCTURE ANALYSIS OF Y164F/MALTOSE OF BACILLUS CEREUS BETA-AMYLASE AT PH 4.6	3.2.1.2
1VEP	CRYSTAL STRUCTURE ANALYSIS OF TRIPLE (T47M/Y164E/T328N)/MALTOSE OF BACILLUS CEREUS BETA-AMYLASE AT PH 6.5	3.2.1.2
1VEV	CRYSTAL STRUCTURE OF PEPTIDE DEFORMYLASE FROM LEPTOSPIRA INTERROGANS (LIPDF) AT PH6.5	3.5.1.88
1VEY	CRYSTAL STRUCTURE OF PEPTIDE DEFORMYLASE FROM LEPTOSPIRA INTERROGANS (LIPDF) AT PH7.0	3.5.1.88
1VEZ	CRYSTAL STRUCTURE OF PEPTIDE DEFORMYLASE FROM LEPTOSPIRA INTERROGANS(LIPDF) AT PH8.0	3.5.1.88
1VF8	THE CRYSTAL STRUCTURE OF YM1 AT 1.31 A RESOLUTION	3.2.1.52
1VFD	HUMAN LACTOFERRIN, N-TERMINAL LOBE MUTANT WITH ARG 121 REPLACED BY GLU (R121E)	3.4.21
1VFE	HUMAN LACTOFERRIN, N-TERMINAL LOBE MUTANT WITH ARG 121 REPLACED BY SER (R121S)	3.4.21
1VFF	BETA-GLYCOSIDASE FROM PYROCOCCUS HORIKOSHII	3.2.1.21
1VFL	ADENOSINE DEAMINASE	3.5.4.4
1VFM	CRYSTAL STRUCTURE OF THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE 2/ALPHA-CYCLODEXTRIN COMPLEX	3.2.1.135
1VFO	CRYSTAL STRUCTURE OF THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE 2/BETA-CYCLODEXTRIN COMPLEX	3.2.1.135
1VFP	CRYSTAL STRUCTURE OF THE SR CA2+-ATPASE WITH BOUND AMPPCP	3.6.3.8 7.2.2.10
1VFU	CRYSTAL STRUCTURE OF THERMOACTINOMYCES VULGARIS R-47 AMYLASE 2/GAMMA-CYCLODEXTRIN COMPLEX	3.2.1.135
1VG5	SOLUTION STRUCTURE OF RSGI RUH-014, A UBA DOMAIN FROM ARABIDOPSIS CDNA	3.4.21
1VGC	GAMMA-CHYMOTRYPSIN L-PARA-CHLORO-1-ACETAMIDO BORONIC ACID INHIBITOR COMPLEX	3.4.21.1
1VGJ	CRYSTAL STRUCTURE OF 2'-5' RNA LIGASE FROM PYROCOCCUS HORIKOSHII	3.1.4.58
1VGN	STRUCTURE-BASED DESIGN OF THE IRREVERSIBLE INHIBITORS TO METALLO--LACTAMASE (IMP-1)	3.5.2.6
1VGX	CRYSTAL STRUCTURE OF A AUTOINDUCER-2 SYNTHESIS PROTEIN	3.13.1 4.4.1.21
1VGY	CRYSTAL STRUCTURE OF SUCCINYL DIAMINOPIMELATE DESUCCINYLASE	3.5.1.18
1VH2	CRYSTAL STRUCTURE OF A AUTOINDUCER-2 SYNTHESIS PROTEIN	3.13.1 4.4.1.21
1VH5	CRYSTAL STRUCTURE OF A PUTATIVE THIOESTERASE	3.1.2.28
1VH9	CRYSTAL STRUCTURE OF A PUTATIVE THIOESTERASE	3.1.2
1VHE	CRYSTAL STRUCTURE OF A AMINOPEPTIDASE/GLUCANASE HOMOLOG	3.4.11
1VHG	CRYSTAL STRUCTURE OF ADP COMPOUNDS HYDROLASE	3.6.1
1VHR	HUMAN VH1-RELATED DUAL-SPECIFICITY PHOSPHATASE	3.1.3.48 3.1.3.16
1VHU	CRYSTAL STRUCTURE OF A PUTATIVE PHOSPHOESTERASE	3.2.2
1VHX	CRYSTAL STRUCTURE OF PUTATIVE HOLLIDAY JUNCTION RESOLVASE	3.1
1VHZ	CRYSTAL STRUCTURE OF ADP COMPOUNDS HYDROLASE	3.6.1
1VI8	CRYSTAL STRUCTURE OF A PUTATIVE THIOESTERASE	3.1.2.28
1VIJ	HIV-1 PROTEASE COMPLEXED WITH THE INHIBITOR HOE/BAY 793 HEXAGONAL FORM	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1VIK	HIV-1 PROTEASE COMPLEXED WITH THE INHIBITOR HOE/BAY 793 ORTHORHOMBIC FORM	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1VIP	ANTICOAGULANT CLASS II PHOSPHOLIPASE A2 FROM THE VENOM OF VIPERA RUSSELLI RUSSELLI	3.1.1.4
1VIQ	CRYSTAL STRUCTURE OF PUTATIVE ADP RIBOSE PYROPHOSPHATASE	3.6.1.13
1VIT	THROMBIN:HIRUDIN 51-65 COMPLEX	3.4.21.5
1VIU	CRYSTAL STRUCTURE OF PUTATIVE ADP RIBOSE PYROPHOSPHATASE	3.6.1
1VIW	TENEBRIO MOLITOR ALPHA-AMYLASE-INHIBITOR COMPLEX	3.2.1.1
1VIX	CRYSTAL STRUCTURE OF A PUTATIVE PEPTIDASE T	3.4.11.14 3.4.11.4
1VJ5	HUMAN SOLUBLE EPOXIDE HYDROLASE- N-CYCLOHEXYL-N'-(4-IODOPHENYL)UREA COMPLEX	3.3.2.3 3.3.2.10 3.1.3.76
1VJ6	PDZ2 FROM PTP-BL IN COMPLEX WITH THE C-TERMINAL LIGAND FROM THE APC PROTEIN	3.1.3.48
1VJ7	CRYSTAL STRUCTURE OF THE BIFUNCTIONAL CATALYTIC FRAGMENT OF RELSEQ, THE RELA/SPOT HOMOLOG FROM STREPTOCOCCUS EQUISIMILIS.	3.1.7.2 2.7.6.5
1VJ9	UROKINASE PLASMINOGEN ACTIVATOR B-CHAIN-JT464 COMPLEX	3.4.21.73
1VJA	UROKINASE PLASMINOGEN ACTIVATOR B-CHAIN-JT463 COMPLEX	3.4.21.73
1VJE	CRYSTAL STRUCTURE OF A AUTOINDUCER-2 SYNTHESIS PROTEIN WITH BOUND SELENOMETHIONINE	3.13.1 4.4.1.21
1VJR	CRYSTAL STRUCTURE OF 4-NITROPHENYLPHOSPHATASE (TM1742) FROM THERMOTOGA MARITIMA AT 2.40 A RESOLUTION	3.1.3.41
1VJS	STRUCTURE OF ALPHA-AMYLASE PRECURSOR	3.2.1.1
1VJT	CRYSTAL STRUCTURE OF ALPHA-GLUCOSIDASE (TM0752) FROM THERMOTOGA MARITIMA AT 2.50 A RESOLUTION	3.2.1.139
1VJV	CRYSTAL STRUCTURE OF UBIQUITIN CARBOXYL-TERMINAL HYDROLASE 6 (YFR010W) FROM SACCHAROMYCES CEREVISIAE AT 1.74 A RESOLUTION	3.1.2.15 3.4.19.12
1VJZ	CRYSTAL STRUCTURE OF ENDOGLUCANASE (TM1752) FROM THERMOTOGA MARITIMA AT 2.05 A RESOLUTION	3.2.1.4
1VK0	X-RAY STRUCTURE OF GENE PRODUCT FROM ARABIDOPSIS THALIANA AT5G06450	3.1.13.1
1VK2	CRYSTAL STRUCTURE OF URACIL-DNA GLYCOSYLASE (TM0511) FROM THERMOTOGA MARITIMA AT 1.90 A RESOLUTION	3.2.2 3.2.2.27
1VK6	CRYSTAL STRUCTURE OF NADH PYROPHOSPHATASE (1790429) FROM ESCHERICHIA COLI K12 AT 2.20 A RESOLUTION	3.6.1 3.6.1.22
1VKG	CRYSTAL STRUCTURE OF HUMAN HDAC8 COMPLEXED WITH CRA-19156	3.5.1.98
1VKH	CRYSTAL STRUCTURE OF A PUTATIVE SERINE HYDROLASE (YDR428C) FROM SACCHAROMYCES CEREVISIAE AT 1.85 A RESOLUTION	3.5.1.9
1VKP	X-RAY STRUCTURE OF GENE PRODUCT FROM ARABIDOPSIS THALIANA AT5G08170, AGMATINE IMINOHYDROLASE	3.5.3.12
1VKQ	A RE-DETERMINATION OF THE STRUCTURE OF THE TRIPLE MUTANT (K53,56,120M) OF PHOSPHOLIPASE A2 AT 1.6A RESOLUTION USING SULPHUR-SAS AT 1.54A WAVELENGTH	3.1.1.4
1VL1	CRYSTAL STRUCTURE OF 6-PHOSPHOGLUCONOLACTONASE (TM1154) FROM THERMOTOGA MARITIMA AT 1.70A RESOLUTION	3.1.1.31
1VL9	ATOMIC RESOLUTION (0.97A) STRUCTURE OF THE TRIPLE MUTANT (K53,56,121M) OF BOVINE PANCREATIC PHOSPHOLIPASE A2	3.1.1.4
1VLR	CRYSTAL STRUCTURE OF MRNA DECAPPING ENZYME (DCPS) FROM MUS MUSCULUS AT 1.83 A RESOLUTION	3.6.1.59
1VM1	STRUCTURE OF SHV-1 BETA-LACTAMASE INHIBITED BY TAZOBACTAM	3.5.2.6
1VMG	CRYSTAL STRUCTURE OF MAZG NUCLEOTIDE PYROPHOSPHOHYDROLASE (13816655) FROM SULFOLOBUS SOLFATARICUS AT 1.46 A RESOLUTION	3.6.1
1VOT	ACETYLCHOLINESTERASE (E.C. 3.1.1.7) COMPLEXED WITH HUPERZINE A	3.1.1.7
1VP2	CRYSTAL STRUCTURE OF A PUTATIVE XANTHOSINE TRIPHOSPHATE PYROPHOSPHATASE/HAM1 PROTEIN HOMOLOG (TM0159) FROM THERMOTOGA MARITIMA AT 1.78 A RESOLUTION	3.6.1 3.6.1.66
1VP7	CRYSTAL STRUCTURE OF EXODEOXYRIBONUCLEASE VII SMALL SUBUNIT (NP_881400.1) FROM BORDETELLA PERTUSSIS AT 2.40 A RESOLUTION	3.1.11.6
1VPM	CRYSTAL STRUCTURE OF ACYL-COA HYDROLASE (NP_241664.1) FROM BACILLUS HALODURANS AT 1.66 A RESOLUTION	3.1.2
1VQ2	CRYSTAL STRUCTURE OF T4-BACTERIOPHAGE DEOXYCYTIDYLATE DEAMINASE, MUTANT R115E	3.5.4.12
1VR0	CRYSTAL STRUCTURE OF PUTATIVE 2-PHOSPHOSULFOLACTATE PHOSPHATASE (15026306) FROM CLOSTRIDIUM ACETOBUTYLICUM AT 2.6 A RESOLUTION	3.1.3.71
1VR1	SPECIFITY FOR PLASMINOGEN ACTIVATOR INHIBITOR-1	3.4.21.5
1VRH	HRV14/SDZ 880-061 COMPLEX	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1VRL	MUTY ADENINE GLYCOSYLASE IN COMPLEX WITH DNA AND SOAKED ADENINE FREE BASE	3.2.2 3.2.2.31
1VRR	CRYSTAL STRUCTURE OF THE RESTRICTION ENDONUCLEASE BSTYI COMPLEX WITH DNA	3.1.21.4
1VRT	HIGH RESOLUTION STRUCTURES OF HIV-1 RT FROM FOUR RT-INHIBITOR COMPLEXES	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1VRU	HIGH RESOLUTION STRUCTURES OF HIV-1 RT FROM FOUR RT-INHIBITOR COMPLEXES	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1VRX	ENDOCELLULASE E1 FROM ACIDOTHERMUS CELLULOLYTICUS MUTANT Y245G	3.2.1.4
1VSB	SUBTILISIN CARLSBERG L-PARA-CHLOROPHENYL-1-ACETAMIDO BORONIC ACID INHIBITOR COMPLEX	3.4.21.62
1VSD	ASV INTEGRASE CORE DOMAIN WITH MG(II) COFACTOR AND HEPES LIGAND, HIGH MG CONCENTRATION FORM	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
1VSE	ASV INTEGRASE CORE DOMAIN WITH MG(II) COFACTOR AND HEPES LIGAND, LOW MG CONCENTRATION FORM	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
1VSF	ASV INTEGRASE CORE DOMAIN WITH MN(II) COFACTOR AND HEPES LIGAND, HIGH MG CONCENTRATION FORM	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
1VSH	ASV INTEGRASE CORE DOMAIN WITH ZN(II) COFACTORS	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
1VSI	ASV INTEGRASE CORE DOMAIN WITH CA(II) COFACTOR	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
1VSJ	ASV INTEGRASE CORE DOMAIN WITH CD(II) COFACTORS	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
1VSK	ASV INTEGRASE CORE DOMAIN D64N MUTATION IN CITRATE BUFFER PH 6.0	2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1
1VSL	ASV INTEGRASE CORE DOMAIN D64N MUTATION WITH ZINC CATION	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
1VSM	ASV INTEGRASE CORE DOMAIN IN CITRATE BUFFER PH 5.0	2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1
1VSN	CRYSTAL STRUCTURE OF A POTENT SMALL MOLECULE INHIBITOR BOUND TO CATHEPSIN K	3.4.22.38
1VSR	VERY SHORT PATCH REPAIR (VSR) ENDONUCLEASE FROM ESCHERICHIA COLI	3.1
1VXO	METHYLPHOSPHONYLATED ACETYLCHOLINESTERASE (AGED) OBTAINED BY REACTION WITH O-ETHYL-S-[2-[BIS(1-METHYLETHYL)AMINO]ETHYL] METHYLPHOSPHONOTHIOATE (VX)	3.1.1.7
1VXR	O-ETHYLMETHYLPHOSPHONYLATED ACETYLCHOLINESTERASE OBTAINED BY REACTION WITH O-ETHYL-S-[2-[BIS(1-METHYLETHYL)AMINO]ETHYL] METHYLPHOSPHONOTHIOATE (VX)	3.1.1.7
1VYB	ENDONUCLEASE DOMAIN OF HUMAN LINE1 ORF2P	2.7.7.49 3.1.21
1VYQ	NOVEL INHIBITORS OF PLASMODIUM FALCIPARUM DUTPASE PROVIDE A PLATFORM FOR ANTI-MALARIAL DRUG DESIGN	3.6.1.23
1VZ2	PROLYL OLIGOPEPTIDASE FROM PORCINE BRAIN, Y73C/V427C/C255T MUTANT	3.4.21.26
1VZ3	PROLYL OLIGOPEPTIDASE FROM PORCINE BRAIN, T597C MUTANT	3.4.21.26
1VZJ	STRUCTURE OF THE TETRAMERIZATION DOMAIN OF ACETYLCHOLINESTERASE: FOUR-FOLD INTERACTION OF A WWW MOTIF WITH A LEFT-HANDED POLYPROLINE HELIX	3.1.1.7
1VZQ	COMPLEX OF THROMBIN WITH DESIGNED INHIBITOR 7165	3.4.21.5
1VZS	SOLUTION STRUCTURE OF SUBUNIT F6 FROM THE PERIPHERAL STALK REGION OF ATP SYNTHASE FROM BOVINE HEART MITOCHONDRIA	3.6.3.14
1VZV	STRUCTURE OF VARICELLA-ZOSTER VIRUS PROTEASE	3.4.21 3.4.21.97
1W08	STRUCTURE OF T70N HUMAN LYSOZYME	3.2.1.17
1W0H	CRYSTALLOGRAPHIC STRUCTURE OF THE NUCLEASE DOMAIN OF 3'HEXO, A DEDDH FAMILY MEMBER, BOUND TO RAMP	3.1
1W0J	BERYLLIUM FLUORIDE INHIBITED BOVINE F1-ATPASE	3.6.3.14
1W0N	STRUCTURE OF UNCOMPLEXED CARBOHYDRATE BINDING DOMAIN CBM36	3.2.1.8 3.2.1.55
1W0O	VIBRIO CHOLERAE SIALIDASE	3.2.1.18
1W0P	VIBRIO CHOLERAE SIALIDASE WITH ALPHA-2,6-SIALYLLACTOSE	3.2.1.18
1W0Y	TF7A_3771 COMPLEX	3.4.21.21
1W0Z	UROKINASE TYPE PLASMINOGEN ACTIVATOR	3.4.21.73
1W10	UROKINASE TYPE PLASMINOGEN ACTIVATOR	3.4.21.73
1W11	UROKINASE TYPE PLASMINOGEN ACTIVATOR	3.4.21.73
1W12	UROKINASE TYPE PLASMINOGEN ACTIVATOR	3.4.21.73
1W13	UROKINASE TYPE PLASMINOGEN ACTIVATOR	3.4.21.73
1W14	UROKINASE TYPE PLASMINOGEN ACTIVATOR	3.4.21.73
1W17	STRUCTURE OF BACILLUS SUBTILIS PDAA, A FAMILY 4 CARBOHYDRATE ESTERASE.	3 3.5.1
1W1A	STRUCTURE OF BACILLUS SUBTILIS PDAA IN COMPLEX WITH NAG, A FAMILY 4 CARBOHYDRATE ESTERASE.	3.5.1
1W1B	STRUCTURE OF BACILLUS SUBTILIS PDAA WITH CADMIUM, A FAMILY 4 CARBOHYDRATE ESTERASE.	3.5.1
1W1P	CRYSTAL STRUCTURE OF S. MARCESCENS CHITINASE B IN COMPLEX WITH THE CYCLIC DIPEPTIDE INHIBITOR CYCLO-(GLY-L-PRO) AT 2.1 A RESOLUTION	3.2.1.14
1W1T	CRYSTAL STRUCTURE OF S. MARCESCENS CHITINASE B IN COMPLEX WITH THE CYCLIC DIPEPTIDE INHIBITOR CYCLO-(HIS-L-PRO) AT 1.9 A RESOLUTION	3.2.1.14
1W1V	CRYSTAL STRUCTURE OF S. MARCESCENS CHITINASE B IN COMPLEX WITH THE CYCLIC DIPEPTIDE INHIBITOR CYCLO-(L-ARG-L-PRO) AT 1.85 A RESOLUTION	3.2.1.14
1W1X	STRUCTURE OF NEURAMINIDASE FROM ENGLISH DUCK SUBTYPE N6 COMPLEXED WITH 30 MM SIALIC ACID (NANA, NEU5AC), CRYSTAL SOAKED FOR 3 HOURS AT 277 K.	3.2.1.18
1W1Y	CRYSTAL STRUCTURE OF S. MARCESCENS CHITINASE B IN COMPLEX WITH THE CYCLIC DIPEPTIDE INHIBITOR CYCLO-(L-TYR-L-PRO) AT 1.85 A RESOLUTION	3.2.1.14
1W20	STRUCTURE OF NEURAMINIDASE FROM ENGLISH DUCK SUBTYPE N6 COMPLEXED WITH 30 MM SIALIC ACID (NANA, NEU5AC), CRYSTAL SOAKED FOR 3 HOURS AT 291 K	3.2.1.18
1W21	STRUCTURE OF NEURAMINIDASE FROM ENGLISH DUCK SUBTYPE N6 COMPLEXED WITH 30 MM SIALIC ACID (NANA, NEU5AC), CRYSTAL SOAKED FOR 43 HOURS AT 291 K.	3.2.1.18
1W22	CRYSTAL STRUCTURE OF INHIBITED HUMAN HDAC8	3.5.1.98
1W2I	CRYSTAL STRUCTUORE OF ACYLPHOSPHATASE FROM PYROCOCCUS HORIKOSHII COMPLEXED WITH FORMATE	3.6.1.7
1W2K	TF7A_4380 COMPLEX	3.4.21.21
1W2P	THE 3-DIMENSIONAL STRUCTURE OF A XYLANASE (XYN10A) FROM CELLVIBRIO JAPONICUS	3.2.1.8
1W2U	X-RAY CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMICOLA GRISEA CEL12A IN COMPLEX WITH A SOAKED THIO CELLOTETRAOSE	3.2.1.4
1W2V	THE 3-DIMENSIONAL STRUCTURE OF A THERMOSTABLE MUTANT OF A XYLANASE (XYN10A) FROM CELLVIBRIO JAPONICUS	3.2.1.8
1W2Y	THE CRYSTAL STRUCTURE OF A COMPLEX OF CAMPYLOBACTER JEJUNI DUTPASE WITH SUBSTRATE ANALOGUE DUPNHP	3.6.1.23
1W32	THE 3-DIMENSIONAL STRUCTURE OF A THERMOSTABLE MUTANT OF A XYLANASE (XYN10A) FROM CELLVIBRIO JAPONICUS	3.2.1.8
1W3C	CRYSTAL STRUCTURE OF THE HEPATITIS C VIRUS NS3 PROTEASE IN COMPLEX WITH A PEPTIDOMIMETIC INHIBITOR	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
1W3H	THE 3-DIMENSIONAL STRUCTURE OF A THERMOSTABLE MUTANT OF A XYLANASE (XYN10A) FROM CELLVIBRIO JAPONICUS	3.2.1.8
1W3J	FAMILY 1 B-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH TETRAHYDROOXAZINE	3.2.1.21
1W3K	ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHAERENS IN COMPLEX WITH CELLOBIO DERIVED-TETRAHYDROOXAZINE	3.2.1.4
1W3L	ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHAERENS IN COMPLEX WITH CELLOTRI DERIVED-TETRAHYDROOXAZINE	3.2.1.4
1W4L	COMPLEX OF TCACHE WITH BIS-ACTING GALANTHAMINE DERIVATIVE	3.1.1.7
1W4O	BINDING OF NONNATURAL 3'-NUCLEOTIDES TO RIBONUCLEASE A	3.1.27.5 4.6.1.18
1W4P	BINDING OF NONNATURAL 3'-NUCLEOTIDES TO RIBONUCLEASE A	3.1.27.5 4.6.1.18
1W4Q	BINDING OF NONNATURAL 3'-NUCLEOTIDES TO RIBONUCLEASE A	3.1.27.5 4.6.1.18
1W50	APO STRUCTURE OF BACE (BETA SECRETASE)	3.4.23.46
1W51	BACE (BETA SECRETASE) IN COMPLEX WITH A NANOMOLAR NON-PEPTIDIC INHIBITOR	3.4.23.46
1W53	KINASE RECRUITMENT DOMAIN OF THE STRESS PHOSPHATASE RSBU	3.1.3.3
1W5D	CRYSTAL STRUCTURE OF PBP4A FROM BACILLUS SUBTILIS	3.4.16.4
1W5V	HIV-1 PROTEASE IN COMPLEX WITH FLUORO SUBSTITUTED DIOL-BASED C2- SYMMETRIC INHIBITOR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1W5W	HIV-1 PROTEASE IN COMPLEX WITH FLUORO SUBSTITUTED DIOL-BASED C2- SYMMETRIC INHIBITOR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1W5X	HIV-1 PROTEASE IN COMPLEX WITH FLUORO SUBSTITUTED DIOL-BASED C2- SYMMETRIC INHIBITOR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1W5Y	HIV-1 PROTEASE IN COMPLEX WITH FLUORO SUBSTITUTED DIOL-BASED C2- SYMMETRIC INHIBITOR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1W6H	NOVEL PLASMEPSIN II-INHIBITOR COMPLEX	3.4.23.39
1W6I	PLASMEPSIN II-PEPSTATIN A COMPLEX	3.4.23.39
1W6R	COMPLEX OF TCACHE WITH GALANTHAMINE DERIVATIVE	3.1.1.7
1W6V	SOLUTION STRUCTURE OF THE DUSP DOMAIN OF HUSP15	3.1.2.15 3.4.19.12
1W6Z	HIGH ENERGY TETRAGONAL LYSOZYME X-RAY STRUCTURE	3.2.1.17
1W75	NATIVE ORTHORHOMBIC FORM OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE (ACHE)	3.1.1.7
1W76	ORTHORHOMBIC FORM OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE (ACHE) COMPLEXED WITH BIS-ACTING GALANTHAMINE DERIVATIVE	3.1.1.7
1W79	CRYSTAL STRUCTURE OF THE DD-TRANSPEPTIDASE-CARBOXYPEPTIDASE FROM ACTINOMADURA R39	3.4.16.4
1W7F	CRYSTAL STRUCTURE OF THE CLASS A BETA-LACTAMASE BS3 INHIBITED WITH ISOCITRATE	3.5.2.6
1W7G	ALPHA-THROMBIN COMPLEX WITH SULFATED HIRUDIN (RESIDUES 54-65) AND L- ARGININE TEMPLATE INHIBITOR CS107	3.4.21.5
1W7V	ZNMG SUBSTITUTED AMINOPEPTIDASE P FROM E. COLI	3.4.11.9
1W7X	FACTOR7 - 413 COMPLEX	3.4.21.21
1W8B	FACTOR7 - 413 COMPLEX	3.4.21.21
1W8I	THE STRUCTURE OF GENE PRODUCT AF1683 FROM ARCHAEOGLOBUS FULGIDUS.	3.1
1W8N	CONTRIBUTION OF THE ACTIVE SITE ASPARTIC ACID TO CATALYSIS IN THE BACTERIAL NEURAMINIDASE FROM MICROMONOSPORA VIRIDIFACIENS.	3.2.1.18
1W8O	CONTRIBUTION OF THE ACTIVE SITE ASPARTIC ACID TO CATALYSIS IN THE BACTERIAL NEURAMINIDASE FROM MICROMONOSPORA VIRIDIFACIENS	3.2.1.18
1W8Q	CRYSTAL STRUCTURE OF THE DD-TRANSPEPTIDASE-CARBOXYPEPTIDASE FROM ACTINOMADURA R39	3.4.16.4
1W8Y	CRYSTAL STRUCTURE OF THE NITROCEFIN ACYL-DD-PEPTIDASE FROM ACTINOMADURA R39.	3.4.16.4
1W9B	S. ALBA MYROSINASE IN COMPLEX WITH CARBA-GLUCOTROPAEOLIN	3.2.3.1 3.2.1.147
1W9D	S. ALBA MYROSINASE IN COMPLEX WITH S-ETHYL PHENYLACETOTHIOHYDROXIMATE- O-SULFATE	3.2.3.1 3.2.1.147
1W9I	MYOSIN II DICTYOSTELIUM DISCOIDEUM MOTOR DOMAIN S456Y BOUND WITH MGADP-BEFX	3.6.4.1
1W9J	MYOSIN II DICTYOSTELIUM DISCOIDEUM MOTOR DOMAIN S456Y BOUND WITH MGADP-ALF4	3.6.4.1
1W9K	DICTYOSTELIUM DISCOIDEUM MYOSIN II MOTOR DOMAIN S456E WITH BOUND MGADP-BEFX	3.6.4.1
1W9L	MYOSIN II DICTYOSTELIUM DISCOIDEUM MOTOR DOMAIN S456E BOUND WITH MGADP-ALF4	3.6.4.1
1W9P	SPECIFICITY AND AFFINITY OF NATURAL PRODUCT CYCLOPENTAPEPTIDE INHIBITORS AGAINST ASPERGILLUS FUMIGATUS, HUMAN AND BACTERIAL CHITINASEFRA	3.2.1.14
1W9S	STRUCTURE OF A BETA-1,3-GLUCAN BINDING CBM6 FROM BACILLUS HALODURANS	3.2.1.6
1W9T	STRUCTURE OF A BETA-1,3-GLUCAN BINDING CBM6 FROM BACILLUS HALODURANS IN COMPLEX WITH XYLOBIOSE	3.2.1.6
1W9U	SPECIFICITY AND AFFNITY OF NATURAL PRODUCT CYCLOPENTAPEPTIDE INHIBITOR ARGADIN AGAINST ASPERGILLUS FUMIGATUS CHITINASE	3.2.1.14
1W9V	SPECIFICITY AND AFFINITY OF NATURAL PRODUCT CYCLOPENTAPEPTIDE ARGIFIN AGAINST ASPERGILLUS FUMIGATUS	3.2.1.14
1W9W	STRUCTURE OF A BETA-1,3-GLUCAN BINDING CBM6 FROM BACILLUS HALODURANS IN COMPLEX WITH LAMINARIHEXAOSE	3.2.1.6
1W9X	BACILLUS HALMAPALUS ALPHA AMYLASE	3.2.1.1
1WAB	PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE	3.1.1.47
1WAF	DNA POLYMERASE FROM BACTERIOPHAGE RB69	2.7.7.7 3.1.11
1WAJ	DNA POLYMERASE FROM BACTERIOPHAGE RB69	2.7.7.7 3.1.11
1WAO	PP5 STRUCTURE	3.1.3.16
1WAR	RECOMBINANT HUMAN PURPLE ACID PHOSPHATASE EXPRESSED IN PICHIA PASTORIS	3.1.3.2
1WAW	SPECIFICITY AND AFFINITY OF NATURAL PRODUCT CYCLOPENTAPEPTIDE INHIBITOR ARGADIN AGAINST HUMAN CHITINASE	3.2.1.14
1WAX	PROTEIN TYROSINE PHOSPHATASE 1B WITH ACTIVE SITE INHIBITOR	3.1.3.48
1WAY	ACTIVE SITE THROMBIN INHIBITORS	3.4.21.5
1WB0	SPECIFICITY AND AFFINITY OF NATURAL PRODUCT CYCLOPENTAPEPTIDE INHIBITOR ARGIFIN AGAINST HUMAN CHITINASE	3.2.1.14
1WB4	S954A MUTANT OF THE FERULOYL ESTERASE MODULE FROM CLOSTRIDIUM THERMOCELLUM COMPLEXED WITH SINAPINATE	3.2.1.8
1WB5	S954A MUTANT OF THE FERULOYL ESTERASE MODULE FROM CLOSTRIDIUM THERMOCELLUM COMPLEXED WITH SYRINGATE	3.2.1.8
1WB6	S954A MUTANT OF THE FERULOYL ESTERASE MODULE FROM CLOSTRIDIUM THERMOCELLUM COMPLEXED WITH VANILLATE	3.2.1.8
1WBG	ACTIVE SITE THROMBIN INHIBITORS	3.4.21.5
1WBQ	ZNMG SUBSTITUTED AMINOPEPTIDASE P FROM E. COLI	3.4.11.9
1WBU	FRAGMENT BASED LEAD DISCOVERY USING CRYSTALLOGRAPHY	3.1.27.5 4.6.1.18
1WC2	BETA-1,4-D-ENDOGLUCANASE CEL45A FROM BLUE MUSSEL MYTILUS EDULIS AT 1.2A	3.2.1.4
1WCD	CRYSTAL STRUCTURE OF IBDV T1 VIRUS-LIKE PARTICLE REVEALS A MISSING LINK IN ICOSAHEDRAL VIRUSES EVOLUTION	3.4.21
1WCE	CRYSTAL STRUCTURE OF THE T13 IBDV VIRAL PARTICLE REVEALS A MISSING LINK IN ICOSAHEDRAL VIRUSES EVOLUTION	3.4.21
1WCF	1.54 A CRYSTAL STRUCTURE OF RV3628, MYCOBACTERIUM TUBERCULOSIS INORGANIC PYROPHOSPHATASE (PPASE) AT PH7.0	3.6.1.1
1WCG	APHID MYROSINASE	3.2.3.1 3.2.1.147
1WCH	CRYSTAL STRUCTURE OF PTPL1 HUMAN TYROSINE PHOSPHATASE MUTATED IN COLORECTAL CANCER - EVIDENCE FOR A SECOND PHOSPHOTYROSINE SUBSTRATE RECOGNITION POCKET	3.1.3.48
1WCQ	MUTAGENESIS OF THE NUCLEOPHILIC TYROSINE IN A BACTERIAL SIALIDASE TO PHENYLALANINE.	3.2.1.18
1WCS	A MUTANT OF TRYPANOSOMA RANGELI SIALIDASE DISPLAYING TRANS-SIALIDASE ACTIVITY	3.2.1.18
1WCV	STRUCTURE OF THE BACTERIAL CHROMOSOME SEGREGATION PROTEIN SOJ	3.6
1WCY	CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE IV (DPPIV) COMPLEX WITH DIPROTIN A	3.4.14.5
1WCZ	CRYSTAL STRUCTURE OF AN ALKALINE FORM OF V8 PROTEASE FROM STAPHYLOCOCCUS AUREUS	3.4.21.19
1WD3	CRYSTAL STRUCTURE OF ARABINOFURANOSIDASE	3.2.1.55
1WD4	CRYSTAL STRUCTURE OF ARABINOFURANOSIDASE COMPLEXED WITH ARABINOSE	3.2.1.55
1WD8	CALCIUM FREE FORM OF HUMAN PEPTIDYLARGININE DEIMINASE TYPE4 (PAD4)	3.5.3.15
1WD9	CALCIUM BOUND FORM OF HUMAN PEPTIDYLARGININE DEIMINASE TYPE4 (PAD4)	3.5.3.15
1WDA	CRYSTAL STRUCTURE OF HUMAN PEPTIDYLARGININE DEIMINASE TYPE4 (PAD4) IN COMPLEX WITH BENZOYL-L-ARGININE AMIDE	3.5.3.15
1WDP	THE ROLE OF AN INNER LOOP IN THE CATALYTIC MECHANISM OF SOYBEAN BETA-AMYLASE	3.2.1.2
1WDQ	THE ROLE OF AN INNER LOOP IN THE CATALYTIC MECHANISM OF SOYBEAN BETA-AMYLASE	3.2.1.2
1WDR	THE ROLE OF AN INNER LOOP IN THE CATALYTIC MECHANISM OF SOYBEAN BETA-AMYLASE	3.2.1.2
1WDS	THE ROLE OF AN INNER LOOP IN THE CATALYTIC MECHANISM OF SOYBEAN BETA-AMYLASE	3.2.1.2
1WDY	CRYSTAL STRUCTURE OF RIBONUCLEASE	3.1.26
1WE4	CRYSTAL STRUCTURE OF CLASS A BETA-LACTAMASE TOHO-1 G238C MUTANT	3.5.2.6
1WE5	CRYSTAL STRUCTURE OF ALPHA-XYLOSIDASE FROM ESCHERICHIA COLI	3.2.1 3.2.1.177
1WEF	CATALYTIC DOMAIN OF MUTY FROM ESCHERICHIA COLI K20A MUTANT	3.2.2 3.2.2.31
1WEG	CATALYTIC DOMAIN OF MUTY FROM ESCHERICHIA COLI K142A MUTANT	3.2.2 3.2.2.31
1WEI	CATALYTIC DOMAIN OF MUTY FROM ESCHERICHIA COLI K20A MUTANT COMPLEXED TO ADENINE	3.2.2 3.2.2.31
1WEK	CRYSTAL STRUCTURE OF THE CONSERVED HYPOTHETICAL PROTEIN TT1465 FROM THERMUS THERMOPHILUS HB8	3.2.2
1WGG	SOLUTION STRUCTURE OF THE N-TERMINAL UBIQUITIN-LIKE DOMAIN OF MOUSE UBIQUITIN SPECIFIC PROTEASE 14 (USP14)	3.1.2.15 3.4.19.12
1WGI	STRUCTURE OF INORGANIC PYROPHOSPHATASE	3.6.1.1
1WGJ	STRUCTURE OF INORGANIC PYROPHOSPHATASE	3.6.1.1
1WGW	SOLUTION STRUCTURE OF THE N-TERMINAL DOMAIN OF MOUSE PUTATIVE SIGNAL RECOGNITION PARTICLE 54 (SRP54)	3.6.5
1WH0	SOLUTION STRUCTURE OF THE CS DOMAIN OF HUMAN USP19	3.1.2.15 3.4.19.12
1WHB	SOLUTION STRUCTURE OF THE RHODANESE-LIKE DOMAIN IN HUMAN UBIQUITIN SPECIFIC PROTEASE 8 (UBP8)	3.1.2.15 3.4.19.12
1WHE	COAGULATION FACTOR, NMR, 20 STRUCTURES	3.4.21.6
1WHF	COAGULATION FACTOR, NMR, 15 STRUCTURES	3.4.21.6
1WHL	SOLUTION STRUCTURE OF THE 1ST CAP-GLY DOMAIN IN HUMAN CYLINDROMATOSIS TUMOR SUPPRESSOR CYLD	3.4.19.12
1WHM	SOLUTION STRUCTURE OF THE 2ND CAP-GLY DOMAIN IN HUMAN CYLINDROMATOSIS TUMOR SUPPRESSOR CYLD	3.4.19.12
1WHQ	SOLUTION STRUCTURE OF THE N-TERMINAL DSRBD FROM HYPOTHETICAL PROTEIN BAB28848	3.6.4.13
1WHS	STRUCTURE OF THE COMPLEX OF L-BENZYLSUCCINATE WITH WHEAT SERINE CARBOXYPEPTIDASE II AT 2.0 ANGSTROMS RESOLUTION	3.4.16.1 3.4.16.6
1WHT	STRUCTURE OF THE COMPLEX OF L-BENZYLSUCCINATE WITH WHEAT SERINE CARBOXYPEPTIDASE II AT 2.0 ANGSTROMS RESOLUTION	3.4.16.1 3.4.16.6
1WHV	SOLUTION STRUCTURE OF THE RNA BINDING DOMAIN FROM HYPOTHETICAL PROTEIN BAB23382	3.1.13.4
1WIV	SOLUTION STRUCTURE OF RSGI RUH-023, A UBA DOMAIN FROM ARABIDOPSIS CDNA	3.4.19.12
1WJ9	CRYSTAL STRUCTURE OF A CRISPR-ASSOCIATED PROTEIN FROM THERMUS THERMOPHILUS	3.1
1WJA	SOLUTION STRUCTURE OF THE N-TERMINAL ZN BINDING DOMAIN OF HIV-1 INTEGRASE (D FORM), NMR, REGULARIZED MEAN STRUCTURE	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1WJB	SOLUTION STRUCTURE OF THE N-TERMINAL ZN BINDING DOMAIN OF HIV-1 INTEGRASE (D FORM), NMR, 40 STRUCTURES	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1WJC	SOLUTION STRUCTURE OF THE N-TERMINAL ZN BINDING DOMAIN OF HIV-1 INTEGRASE (E FORM), NMR, REGULARIZED MEAN STRUCTURE	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1WJD	SOLUTION STRUCTURE OF THE N-TERMINAL ZN BINDING DOMAIN OF HIV-1 INTEGRASE (E FORM), NMR, 38 STRUCTURES	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1WJE	SOLUTION STRUCTURE OF H12C MUTANT OF THE N-TERMINAL ZN BINDING DOMAIN OF HIV-1 INTEGRASE COMPLEXED TO CADMIUM, NMR, MINIMIZED AVERAGE STRUCTURE	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1WJF	SOLUTION STRUCTURE OF H12C MUTANT OF THE N-TERMINAL ZN BINDING DOMAIN OF HIV-1 INTEGRASE COMPLEXED TO CADMIUM, NMR, 40 STRUCTURES	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1WKM	THE PRODUCT BOUND FORM OF THE MN(II)LOADED METHIONINE AMINOPEPTIDASE FROM HYPERTHERMOPHILE PYROCOCCUS FURIOSUS	3.4.11.18
1WKQ	CRYSTAL STRUCTURE OF BACILLUS SUBTILIS GUANINE DEAMINASE. THE FIRST DOMAIN-SWAPPED STRUCTURE IN THE CYTIDINE DEAMINASE SUPERFAMILY	3.5.4.3
1WKR	CRYSTAL STRUCTURE OF ASPARTIC PROTEINASE FROM IRPEX LACTEUS	3.4.23.29
1WKY	CRYSTAL STRUCTURE OF ALKALINE MANNANASE FROM BACILLUS SP. STRAIN JAMB-602: CATALYTIC DOMAIN AND ITS CARBOHYDRATE BINDING MODULE	3.2.1.78
1WL6	MG-SUBSTITUTED FORM OF E. COLI AMINOPEPTIDASE P	3.4.11.9
1WL7	STRUCTURE OF THE THERMOSTABLE ARABINANASE	3.2.1.99
1WL9	STRUCTURE OF AMINOPEPTIDASE P FROM E. COLI	3.4.11.9
1WLJ	HUMAN ISG20	3.1 3.1.13.1
1WLR	APO AMINOPEPTIDASE P FROM E. COLI	3.4.11.9
1WLS	CRYSTAL STRUCTURE OF L-ASPARAGINASE I HOMOLOGUE PROTEIN FROM PYROCOCCUS HORIKOSHII	3.5.1.1
1WM1	CRYSTAL STRUCTURE OF PROLYL AMINOPEPTIDASE, COMPLEX WITH PRO-TBODA	3.4.11.5
1WM9	STRUCTURE OF GTP CYCLOHYDROLASE I FROM THERMUS THERMOPHILUS HB8	3.5.4.16
1WMD	CRYSTAL STRUCTURE OF ALKALINE SERINE PROTEASE KP-43 FROM BACILLUS SP. KSM-KP43 (1.30 ANGSTROM, 100 K)	3.4.21
1WME	CRYSTAL STRUCTURE OF ALKALINE SERINE PROTEASE KP-43 FROM BACILLUS SP. KSM-KP43 (1.50 ANGSTROM, 293 K)	3.4.21
1WMF	CRYSTAL STRUCTURE OF ALKALINE SERINE PROTEASE KP-43 FROM BACILLUS SP. KSM-KP43 (OXIDIZED FORM, 1.73 ANGSTROM)	3.4.21
1WMR	CRYSTAL STRUCTURE OF ISOPULLULANASE FROM ASPERGILLUS NIGER ATCC 9642	3.2.1.57
1WN1	CRYSTAL STRUCTURE OF DIPEPTIASE FROM PYROCOCCUS HORIKOSHII OT3	3.4
1WN2	CRYSTAL STRUCTURE OF PROJECT ID PH1539 FROM PYROCOCCUS HORIKOSHII OT3	3.1.1.29
1WN5	CRYSTAL STRUCTURE OF BLASTICIDIN S DEAMINASE (BSD) COMPLEXED WITH CACODYLIC ACID	3.5.4.23
1WN6	CRYSTAL STRUCTURE OF BLASTICIDIN S DEAMINASE (BSD) COMPLEXED WITH TETRAHEDRAL INTERMEDIATE OF BLASTICIDIN S	3.5.4.23
1WNE	FOOT AND MOUTH DISEASE VIRUS RNA-DEPENDENT RNA POLYMERASE IN COMPLEX WITH A TEMPLATE-PRIMER RNA	2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15
1WNF	CRYSTAL STRUCTURE OF PH0066 FROM PYROCOCCUS HORIKOSHII	3.5.1.1
1WNI	CRYSTAL STRUCTURE OF H2-PROTEINASE	3.4.24.53
1WNO	CRYSTAL STRUCTURE OF A NATIVE CHITINASE FROM ASPERGILLUS FUMIGATUS YJ-407	3.2.1.14
1WNS	CRYSTAL STRUCTURE OF FAMILY B DNA POLYMERASE FROM HYPERTHERMOPHILIC ARCHAEON PYROCOCCUS KODAKARAENSIS KOD1	2.7.7.7 3.1
1WO2	CRYSTAL STRUCTURE OF THE PIG PANCREATIC ALPHA-AMYLASE COMPLEXED WITH MALTO-OLIGOSAACHARIDES UNDER THE EFFECT OF THE CHLORIDE ION	3.2.1.1
1WOF	CRYSTAL STRUCTURE OF SARS-COV MPRO IN COMPLEX WITH AN INHIBITOR N1	3.4.24 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
1WOG	CRYSTAL STRUCTURE OF AGMATINASE REVEALS STRUCTURAL CONSERVATION AND INHIBITION MECHANISM OF THE UREOHYDROLASE SUPERFAMILY	3.5.3.11
1WOH	CRYSTAL STRUCTURE OF AGMATINASE REVEALS STRUCTURAL CONSERVATION AND INHIBITION MECHANISM OF THE UREOHYDROLASE SUPERFAMILY	3.5.3.11
1WOI	CRYSTAL STRUCTURE OF AGMATINASE REVEALS STRUCTURAL CONSERVATION AND INHIBITION MECHANISM OF THE UREOHYDROLASE SUPERFAMILY	3.5.3.11
1WOJ	CRYSTAL STRUCTURE OF HUMAN PHOSPHODIESTERASE	3.1.4.37
1WP6	CRYSTAL STRUCTURE OF MALTOHEXAOSE-PRODUCING AMYLASE FROM ALKALOPHILIC BACILLUS SP.707.	3.2.1.98
1WPC	CRYSTAL STRUCTURE OF MALTOHEXAOSE-PRODUCING AMYLASE COMPLEXED WITH PSEUDO-MALTONONAOSE	3.2.1.98
1WPG	CRYSTAL STRUCTURE OF THE SR CA2+-ATPASE WITH MGF4	3.6.3.8 7.2.2.10
1WPM	STRUCTURE OF BACILLUS SUBTILIS INORGANIC PYROPHOSPHATASE	3.6.1.1
1WPN	CRYSTAL STRUCTURE OF THE N-TERMINAL CORE OF BACILLUS SUBTILIS INORGANIC PYROPHOSPHATASE	3.6.1.1
1WPO	HYDROLYTIC ENZYME HUMAN CYTOMEGALOVIRUS PROTEASE	3.4.21 3.4.21.97
1WPP	STRUCTURE OF STREPTOCOCCUS GORDONII INORGANIC PYROPHOSPHATASE	3.6.1.1
1WPX	CRYSTAL STRUCTURE OF CARBOXYPEPTIDASE Y INHIBITOR COMPLEXED WITH THE COGNATE PROTEINASE	3.4.16.5
1WQM	CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
1WQN	CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
1WQO	CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
1WQP	CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
1WQQ	CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
1WQR	CONTRIBUTION OF HYDROGEN BONDS TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
1WQS	CRYSTAL STRUCTURE OF NOROVIRUS 3C-LIKE PROTEASE	2.7.7.48 3.4.22.66 3.6.1.15
1WQV	HUMAN FACTOR VIIA-TISSUE FACTOR COMPLEXED WITH PROPYLSULFONAMIDE-D-THR-MET-P-AMINOBENZAMIDINE	3.4.21.21
1WR0	STRUCTURAL CHARACTERIZATION OF THE MIT DOMAIN FROM HUMAN VPS4B	3.6.4.6
1WR8	CRYSTAL STRUCTURE OF HYPOTHETICAL PROTEIN PH1421 FROM PYROCOCCUS HORIKOSHII.	3.1.3.18
1WRA	CRYSTAL STRUCTURE OF PHOSPHORYLCHOLINE ESTERASE DOMAIN OF THE VIRULENCE FACTOR CHOLINE BINDING PROTEIN E FROM STREPTOCOCCUS PNEUMONIAE	3.1.4.38
1WRB	CRYSTAL STRUCTURE OF THE N-TERMINAL RECA-LIKE DOMAIN OF DJVLGB, A PRANARIAN VASA-LIKE RNA HELICASE	3.6.4.13
1WRM	CRYSTAL STRUCTURE OF JSP-1	3.1.3.48 3.1.3.16
1WS0	STRUCTURE ANALYSIS OF PEPTIDE DEFORMYLASE FROM BACILLUS CEREUS	3.5.1.88
1WS1	STRUCTURE ANALYSIS OF PEPTIDE DEFORMYLASE FROM BACILLUS CEREUS	3.5.1.88
1WSA	STRUCTURE OF L-ASPARAGINASE II PRECURSOR	3.5.1.1
1WSD	ALKALINE M-PROTEASE FORM I CRYSTAL STRUCTURE	3.4.21
1WSE	CO-CRYSTAL STRUCTURE OF E.COLI RNASE HI ACTIVE SITE MUTANT (E48A*) WITH MN2+	3.1.26.4
1WSF	CO-CRYSTAL STRUCTURE OF E.COLI RNASE HI ACTIVE SITE MUTANT (D134A*) WITH MN2+	3.1.26.4
1WSG	CO-CRYSTAL STRUCTURE OF E.COLI RNASE HI ACTIVE SITE MUTANT (E48A/D134N*) WITH MN2+	3.1.26.4
1WSH	CRYSTAL STRUCTURE OF E.COLI RNASE HI ACTIVE SITE MUTANT (E48A/K87A)	3.1.26.4
1WSI	CRYSTAL STRUCTURE OF E.COLI RNASE HI ACTIVE SITE MUTANT (E48A/K87A/D134N)	3.1.26.4
1WSJ	CRYSTAL STRUCTURE OF E.COLI RNASE HI ACTIVE SITE MUTANT (K87A/H124A)	3.1.26.4
1WSS	HUMAN FACTOR VIIA-TISSUE FACTOR IN COMPLEX WITH PEPTIDE-MIMETIC INHIBITOR THAT HAS TWO CHARGED GROUPS IN P2 AND P4	3.4.21.21
1WTD	CRYSTAL STRUCTURE OF TYPE II RESTRCITION ENDONUCLEASE, ECOO109I DNA-FREE FORM	3.1.21.4
1WTE	CRYSTAL STRUCTURE OF TYPE II RESTRCITION ENDONUCLEASE, ECOO109I COMPLEXED WITH COGNATE DNA	3.1.21.4
1WTG	HUMAN FACTOR VIIA-TISSUE FACTOR COMPLEXED WITH ETHYLSULFONAMIDE-D-BIPHENYLALANINE-GLN-P-AMINOBENZAMIDINE	3.4.21.21
1WTH	CRYSTAL STRUCTURE OF GP5-S351L MUTANT AND GP27 COMPLEX	3.2.1.17
1WTM	X-RAY STRUCTURE OF HEW LYSOZYME ORTHORHOMBIC CRYSTAL FORMED IN THE EARTH'S MAGNETIC FIELD	3.2.1.17
1WTN	THE STRUCTURE OF HEW LYSOZYME ORTHORHOMBIC CRYSTAL GROWTH UNDER A HIGH MAGNETIC FIELD	3.2.1.17
1WU0	SOLUTION STRUCTURE OF SUBUNIT C OF F1FO-ATP SYNTHASE FROM THE THERMOPHILIC BACILLUS PS3	3.6.3.14
1WU1	FACTOR XA IN COMPLEX WITH THE INHIBITOR 4-[(5-CHLOROINDOL-2-YL)SULFONYL]-2-(2-METHYLPROPYL)-1-[[5-(PYRIDIN-4-YL) PYRIMIDIN-2-YL]CARBONYL]PIPERAZINE	3.4.21.6
1WU4	CRYSTAL STRUCTURE OF REDUCING-END-XYLOSE RELEASING EXO-OLIGOXYLANASE	3.2.1.156
1WU5	CRYSTAL STRUCTURE OF REDUCING-END-XYLOSE RELEASING EXO-OLIGOXYLANASE COMPLEXED WITH XYLOSE	3.2.1.156
1WU6	CRYSTAL STRUCTURE OF REDUCING-END-XYLOSE RELEASING EXO-OLIGOXYLANASE E70A MUTANT COMPLEXED WITH XYLOBIOSE	3.2.1.156
1WUD	E. COLI RECQ HRDC DOMAIN	3.6.1 3.6.4.12
1WUN	HUMAN FACTOR VIIA-TISSUE FACTOR COMPLEXED WITH ETHYLSULFONAMIDE-D-TRP-GLN-P-AMINOBENZAMIDINE	3.4.21.21
1WUO	CRYSTAL STRUCTURE OF METALLO-BETA-LACTAMASE IMP-1 MUTANT (D81A)	3.5.2.6
1WUP	CRYSTAL STRUCTURE OF METALLO-BETA-LACTAMASE IMP-1 MUTANT (D81E)	3.5.2.6
1WUQ	STRUCTURE OF GTP CYCLOHYDROLASE I COMPLEXED WITH 8-OXO-GTP	3.5.4.16
1WUR	STRUCTURE OF GTP CYCLOHYDROLASE I COMPLEXED WITH 8-OXO-DGTP	3.5.4.16
1WV7	HUMAN FACTOR VIIA-TISSUE FACTOR COMPLEXED WITH ETHYLSULFONAMIDE-D-5-PROPOXY-TRP-GLN-P-AMINOBENZAMIDINE	3.4.21.21
1WVA	CRYSTAL STRUCTURE OF HUMAN ARGINASE I FROM TWINNED CRYSTAL	3.5.3.1
1WVB	CRYSTAL STRUCTURE OF HUMAN ARGINASE I: THE MUTANT E256Q	3.5.3.1
1WVM	CRYSTAL STRUCTURE OF PSYCHROPHILIC SUBTILISIN-LIKE SERINE PROTEASE APA1 FROM ANTARCTIC PSYCHROTROPH PSEUDOALEROMONAS SP. AS-11, COMPLEXED WITH INHIBITOR CHYMOSTATIN	3.4.21
1WVU	CRYSTAL STRUCTURE OF CHITINASE C FROM STREPTOMYCES GRISEUS HUT6037	3.2.1.14
1WVV	CRYSTAL STRUCTURE OF CHITINASE C MUTANT E147Q	3.2.1.14
1WW1	CRYSTAL STRUCTURE OF TRNASE Z FROM THERMOTOGA MARITIMA	3.1.26.11
1WW4	AGROCYBE CYLINDRACEA GALECTIN COMPLEXED WITH NEUACA2-3LACTOSE	3.1.21
1WW5	AGROCYBE CYLINDRACEA GALECTIN COMPLEXED WITH 3'-SULFONYL LACTOSE	3.1.21
1WW6	AGROCYBE CYLINDRACEA GALECTIN COMPLEXED WITH LACTOSE	3.1.21
1WW7	AGROCYBE CYLINDRACEA GALECTIN (LIGAND-FREE)	3.1.21
1WWR	CRYSTAL STRUCTURE OF TRNA ADENOSINE DEAMINASE TADA FROM AQUIFEX AEOLICUS	3.5.4 3.5.4.33
1WXR	CRYSTAL STRUCTURE OF HEME BINDING PROTEIN, AN AUTOTRANSPORTER HEMOGLOBINE PROTEASE FROM PATHOGENIC ESCHERICHIA COLI	3.4.21
1WXY	CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE LIGATED WITH A POTENT INHIBITOR	3.5.4.4
1WXZ	CRYSTAL STRUCTURE OF ADENOSINE DEAMINASE LIGATED WITH A POTENT INHIBITOR	3.5.4.4
1WY2	CRYSTAL STRUCTURE OF THE PROLIDASE FROM PYROCOCCUS HORIKOSHII OT3	3.4.13.9
1WYB	STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE	3.5.1.46
1WYC	STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE, DN MUTANT	3.5.1.46
1WYK	SINDBIS VIRUS CAPSID PROTEIN (114-264)	3.4.21 3.4.21.90
1WYW	CRYSTAL STRUCTURE OF SUMO1-CONJUGATED THYMINE DNA GLYCOSYLASE	3.2.2 3.2.2.29
1WZA	CRYSTAL STRUCTURE OF ALPHA-AMYLASE FROM H.ORENII	3.2.1.1
1WZC	CRYSTAL STRUCTURE OF PYROCOCCUS HORIKOSHII MANNOSYL-3-PHOSPHOGLYCERATE PHOSPHATASE COMPLEXED WITH MG2+ AND PHOSPHATE	3.1.3.70
1WZK	THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE II (TVA II) MUTATNT D465N	3.2.1.135
1WZL	THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE II (TVA II) MUTATNT R469L	3.2.1.135
1WZM	THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE II (TVA II) MUTATNT R469K	3.2.1.135
1WZZ	STRUCTURE OF ENDO-BETA-1,4-GLUCANASE CMCAX FROM ACETOBACTER XYLINUM	3.2.1.4
1X0C	IMPROVED CRYSTAL STRUCTURE OF ISOPULLULANASE FROM ASPERGILLUS NIGER ATCC 9642	3.2.1.57
1X0T	CRYSTAL STRUCTURE OF RIBONUCLEASE P PROTEIN PH1601P FROM PYROCOCCUS HORIKOSHII OT3	3.1.26.5
1X10	STRUCTURE OF MUTANT PYRROLIDONE CARBOXYL PEPTIDASE (E192A) FROM A HYPERTHERMOPHILE, PYROCOCCUS FURIOSUS	3.4.19.3
1X12	STRUCTURE OF MUTANT PYRROLIDONE CARBOXYL PEPTIDASE (E192D) FROM A HYPERTHERMOPHILE, PYROCOCCUS FURIOSUS	3.4.19.3
1X1P	CRYSTAL STRUCTURE OF TK-RNASE HII(1-197)-A(28-42)	3.1.26.4
1X1R	CRYSTAL STRUCTURE OF M-RAS IN COMPLEX WITH GDP	3.6.5.2
1X1S	CRYSTAL STRUCTURE OF M-RAS IN COMPLEX WITH GPPNHP	3.6.5.2
1X1U	WATER-MEDIATE INTERACTION AT APROTEIN-PROTEIN INTERFACE	3.1.27
1X1W	WATER-MEDIATE INTERACTION AT APROTEIN-PROTEIN INTERFACE	3.1.27
1X1X	WATER-MEDIATE INTERACTION AT APROTEIN-PROTEIN INTERFACE	3.1.27
1X1Y	WATER-MEDIATE INTERACTION AT APROTEIN-PROTEIN INTERFACE	3.1.27
1X2B	THE CRYSTAL STRUCTURE OF PROLYL AMINOPEPTIDASE COMPLEXED WITH SAR-TBODA	3.4.11.5
1X2E	THE CRYSTAL STRUCTURE OF PROLYL AMINOPEPTIDASE COMPLEXED WITH ALA-TBODA	3.4.11.5
1X37	STRUCTURE OF BACILLUS SUBTILIS LON PROTEASE SSD DOMAIN	3.4.21.53
1X38	CRYSTAL STRUCTURE OF BARLEY BETA-D-GLUCAN GLUCOHYDROLASE ISOENZYME EXO1 IN COMPLEX WITH GLUCO-PHENYLIMIDAZOLE	3.2.1.58
1X39	CRYSTAL STRUCTURE OF BARLEY BETA-D-GLUCAN GLUCOHYDROLASE ISOENZYME EXO1 IN COMPLEX WITH GLUCO-PHENYLIMIDAZOLE	3.2.1.58
1X3W	STRUCTURE OF A PEPTIDE:N-GLYCANASE-RAD23 COMPLEX	3.5.1.52
1X3Z	STRUCTURE OF A PEPTIDE:N-GLYCANASE-RAD23 COMPLEX	3.5.1.52
1X42	CRYSTAL STRUCTURE OF A HALOACID DEHALOGENASE FAMILY PROTEIN (PH0459) FROM PYROCOCCUS HORIKOSHII OT3	3.8.1
1X51	SOLUTION STRUCTURE OF THE NUDIX DOMAIN FROM HUMAN A/G-SPECIFIC ADENINE DNA GLYCOSYLASE ALPHA-3 SPLICE ISOFORM	3.2.2 3.2.2.31
1X52	SOLUTION STRUCTURES OF THE C-TERMINAL DOMAIN OF THE HUMAN PELOTA HOMOLOG (CGI-17)	3.1
1X5Z	SOLUTION STRUCTURE OF THE FIBRONECTIN TYPE-III DOMAIN OF HUMAN PROTEIN TYROSINE PHOSPHATASE, RECEPTOR TYPE, D ISOFORM 4 VARIANT	3.1.3.48
1X60	SOLUTION STRUCTURE OF THE PEPTIDOGLYCAN BINDING DOMAIN OF B. SUBTILIS CELL WALL LYTIC ENZYME CWLC	3.5.1.28
1X6C	SOLUTION STRUCTURES OF THE SH2 DOMAIN OF HUMAN PROTEIN-TYROSINE PHOSPHATASE SHP-1	3.1.3.48
1X6L	CRYSTAL STRUCTURE OF S. MARCESCENS CHITINASE A MUTANT W167A	3.2.1.14
1X6N	CRYSTAL STRUCTURE OF S. MARCESCENS CHITINASE A MUTANT W167A IN COMPLEX WITH ALLOSAMIDIN	3.2.1.14
1X70	HUMAN DIPEPTIDYL PEPTIDASE IV IN COMPLEX WITH A BETA AMINO ACID INHIBITOR	3.4.14.5
1X7A	PORCINE FACTOR IXA COMPLEXED TO 1-{3-[AMINO(IMINO)METHYL]PHENYL}-N-[4-(1H-BENZIMIDAZOL-1-YL)-2-FLUOROPHENYL]-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-5-CARBOXAMIDE	3.4.21.22
1X8G	CRYSTAL STRUCTURE OF THE MONO-ZINC CARBAPENEMASE CPHA FROM AEROMONAS HYDROPHYLA	3.5.2.6
1X8H	THE MONO-ZINC CARBAPENEMASE CPHA (N220G MUTANT) SHOWS A ZN(II)- NH2 ARG COORDINATION	3.5.2.6
1X8I	CRYSTAL STRUCTURE OF THE ZINC CARBAPENEMASE CPHA IN COMPLEX WITH THE ANTIBIOTIC BIAPENEM	3.5.2.6
1X9D	CRYSTAL STRUCTURE OF HUMAN CLASS I ALPHA-1,2-MANNOSIDASE IN COMPLEX WITH THIO-DISACCHARIDE SUBSTRATE ANALOGUE	3.2.1.113
1X9M	T7 DNA POLYMERASE IN COMPLEX WITH AN N-2-ACETYLAMINOFLUORENE-ADDUCTED DNA	2.7.7.7 3.1.11
1X9S	T7 DNA POLYMERASE IN COMPLEX WITH A PRIMER/TEMPLATE DNA CONTAINING A DISORDERED N-2 AMINOFLUORENE ON THE TEMPLATE, CRYSTALLIZED WITH DIDEOXY-CTP AS THE INCOMING NUCLEOTIDE.	2.7.7.7 3.1.11
1X9W	T7 DNA POLYMERASE IN COMPLEX WITH A PRIMER/TEMPLATE DNA CONTAINING A DISORDERED N-2 AMINOFLUORENE ON THE TEMPLATE, CRYSTALLIZED WITH DIDEOXY-ATP AS THE INCOMING NUCLEOTIDE.	2.7.7.7 3.1.11
1X9Y	THE PROSTAPHOPAIN B STRUCTURE	3.4.22
1XAF	CRYSTAL STRUCTURE OF PROTEIN OF UNKNOWN FUNCTION YFIH FROM SHIGELLA FLEXNERI 2A STR. 2457T	2.4.2.1 3.5.4.4 2.4.2.28
1XAX	NMR STRUCTURE OF HI0004, A PUTATIVE ESSENTIAL GENE PRODUCT FROM HAEMOPHILUS INFLUENZAE	3.1
1XBD	INTERNAL XYLAN BINDING DOMAIN FROM CELLULOMONAS FIMI XYLANASE D, NMR, 5 STRUCTURES	3.2.1.8 3.5.1
1XBO	PTP1B COMPLEXED WITH ISOXAZOLE CARBOXYLIC ACID	3.1.3.48
1XBU	STREPTOMYCES GRISEUS AMINOPEPTIDASE COMPLEXED WITH P-IODO-D-PHENYLALANINE	3.4.11 3.4.11.24
1XC6	NATIVE STRUCTURE OF BETA-GALACTOSIDASE FROM PENICILLIUM SP. IN COMPLEX WITH GALACTOSE	3.2.1.23
1XC8	CRYSTAL STRUCTURE COMPLEX BETWEEN THE WILD-TYPE LACTOCOCCUS LACTIS FPG (MUTM) AND A FAPY-DG CONTAINING DNA	3.2.2.23 4.2.99.18
1XCM	CRYSTAL STRUCTURE OF THE GPPNHP-BOUND H-RAS G60A MUTANT	3.6.5.2
1XCR	CRYSTAL STRUCTURE OF LONGER SPLICE VARIANT OF PTD012 FROM HOMO SAPIENS REVEALS A NOVEL ZINC-CONTAINING FOLD	3.1
1XCW	ACARBOSE REARRANGEMENT MECHANISM IMPLIED BY THE KINETIC AND STRUCTURAL ANALYSIS OF HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH ANALOGUES AND THEIR ELONGATED COUNTERPARTS	3.2.1.1
1XCX	ACARBOSE REARRANGEMENT MECHANISM IMPLIED BY THE KINETIC AND STRUCTURAL ANALYSIS OF HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH ANALOGUES AND THEIR ELONGATED COUNTERPARTS	3.2.1.1
1XD0	ACARBOSE REARRANGEMENT MECHANISM IMPLIED BY THE KINETIC AND STRUCTURAL ANALYSIS OF HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH ANALOGUES AND THEIR ELONGATED COUNTERPARTS	3.2.1.1
1XD1	ACARBOSE REARRANGEMENT MECHANISM IMPLIED BY THE KINETIC AND STRUCTURAL ANALYSIS OF HUMAN PANCREATIC ALPHA-AMYLASE IN COMPLEX WITH ANALOGUES AND THEIR ELONGATED COUNTERPARTS	3.2.1.1
1XD2	CRYSTAL STRUCTURE OF A TERNARY RAS:SOS:RAS*GDP COMPLEX	3.6.5.2
1XD3	CRYSTAL STRUCTURE OF UCHL3-UBVME COMPLEX	3.4.19.12
1XDF	CRYSTAL STRUCTURE OF PATHOGENESIS-RELATED PROTEIN LLPR-10.2A FROM YELLOW LUPINE	3.1.27
1XDH	STRUCTURE OF PLASMEPSIN II IN COMPLEX WITH PEPSTATIN A	3.4.23.39
1XE5	STRUCTURE OF PLASMEPSIN II IN COMPLEX OF AN PEPSTATIN ANALOGUE	3.4.23.39
1XE6	STRUCTURE OF PLASMEPSIN II IN COMPLEX OF AN PEPSTATIN ANALOGUE	3.4.23.39
1XEI	THE CRYSTAL STRUCTURES OF LYSOZYME AT VERY LOW LEVELS OF HYDRATION	3.2.1.17
1XEJ	THE CRYSTAL STRUCTURES OF LYSOZYME AT VERY LOW LEVELS OF HYDRATION	3.2.1.17
1XEK	THE CRYSTAL STRUCTURES OF LYSOZYME AT VERY LOW LEVELS OF HYDRATION	3.2.1.17
1XEM	HIGH RESOLUTION CRYSTAL STRUCTURE OF ESCHERICHIA COLI ZINC- PEPTIDE DEFORMYLASE BOUND TO FORMATE	3.5.1.88
1XEN	HIGH RESOLUTION CRYSTAL STRUCTURE OF ESCHERICHIA COLI IRON- PEPTIDE DEFORMYLASE BOUND TO FORMATE	3.5.1.88
1XEO	HIGH RESOLUTION CRYSTALS STRUCTURE OF COBALT- PEPTIDE DEFORMYLASE BOUND TO FORMATE	3.5.1.88
1XEP	CATECHOL IN COMPLEX WITH T4 LYSOZYME L99A/M102Q	3.2.1.17
1XFI	X-RAY STRUCTURE OF GENE PRODUCT FROM ARABIDOPSIS THALIANA AT2G17340	3.1.3
1XFK	1.8A CRYSTAL STRUCTURE OF FORMIMINOGLUTAMASE FROM VIBRIO CHOLERAE O1 BIOVAR ELTOR STR. N16961	3.5.3.8
1XFO	CRYSTAL STRUCTURE OF AN ARCHAEAL AMINOPEPTIDASE	3.4.11
1XFT	SYNCHROTRON X-RAY POWDER DIFFRACTION STUDY OF HEXAGONAL TURKEY EGG-WHITE LYSOZYME	3.2.1.17
1XG2	CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN PECTIN METHYLESTERASE AND ITS INHIBITOR PROTEIN	3.1.1.11
1XG7	CONSERVED HYPOTHETICAL PROTEIN PFU-877259-001 FROM PYROCOCCUS FURIOSUS	3.2.2 4.2.99.18
1XGE	DIHYDROOROTASE FROM ESCHERICHIA COLI: LOOP MOVEMENT AND COOPERATIVITY BETWEEN SUBUNITS	3.5.2.3
1XGI	AMPC BETA-LACTAMASE IN COMPLEX WITH 3-(3-NITRO-PHENYLSULFAMOYL)-THIOPHENE-2-CARBOXYLIC ACID	3.5.2.6
1XGJ	AMPC BETA-LACTAMASE IN COMPLEX WITH 3-(4-CARBOXY-2-HYDROXY-PHENYLSULFAMOYL)-THIOPHENE-2-CARBOXYLIC ACID	3.5.2.6
1XGM	METHIONINE AMINOPEPTIDASE FROM HYPERTHERMOPHILE PYROCOCCUS FURIOSUS	3.4.11.18
1XGN	METHIONINE AMINOPEPTIDASE FROM HYPERTHERMOPHILE PYROCOCCUS FURIOSUS	3.4.11.18
1XGO	METHIONINE AMINOPEPTIDASE FROM HYPERTHERMOPHILE PYROCOCCUS FURIOSUS	3.4.11.18
1XGS	METHIONINE AMINOPEPTIDASE FROM HYPERTHERMOPHILE PYROCOCCUS FURIOSUS	3.4.11.18
1XGZ	STRUCTURE OF THE N298S VARIANT OF HUMAN PANCREATIC ALPHA-AMYLASE	3.2.1.1
1XH0	STRUCTURE OF THE N298S VARIANT OF HUMAN PANCREATIC ALPHA-AMYLASE COMPLEXED WITH ACARBOSE	3.2.1.1
1XH1	STRUCTURE OF THE N298S VARIANT OF HUMAN PANCREATIC ALPHA-AMYLASE COMPLEXED WITH CHLORIDE	3.2.1.1
1XH2	STRUCTURE OF THE N298S VARIANT OF HUMAN PANCREATIC ALPHA-AMYLASE COMPLEXED WITH CHLORIDE AND ACARBOSE	3.2.1.1
1XHK	CRYSTAL STRUCTURE OF M. JANNASCHII LON PROTEOLYTIC DOMAIN	3.4.21
1XHU	HINCII BOUND TO CLEAVED, COGNATE DNA CONTAINING GTCGAC	3.1.21.4
1XHV	HINCII BOUND TO CLEAVED COGNATE DNA GTCGAC AND MN2+	3.1.21.4
1XHX	PHI29 DNA POLYMERASE, ORTHORHOMBIC CRYSTAL FORM	2.7.7.7 3.1.11
1XHZ	PHI29 DNA POLYMERASE, ORTHORHOMBIC CRYSTAL FORM, SSDNA COMPLEX	2.7.7.7 3.1.11
1XI1	PHI29 DNA POLYMERASE SSDNA COMPLEX, MONOCLINIC CRYSTAL FORM	2.7.7.7 3.1.11
1XI6	EXTRAGENIC SUPPRESSOR FROM PYROCOCCUS FURIOSUS PFU-1862794-001	3.1.3.11
1XJ0	CRYSTAL STRUCTURE OF THE GDP-BOUND FORM OF THE RASG60A MUTANT	3.6.5.2
1XJO	STRUCTURE OF AMINOPEPTIDASE	3.4.11 3.4.11.24
1XJT	CRYSTAL STRUCTURE OF ACTIVE FORM OF P1 PHAGE ENDOLYSIN LYZ	3.2.1.17
1XJU	CRYSTAL STRUCTURE OF SECRETED INACTIVE FORM OF P1 PHAGE ENDOLYSIN LYZ	3.2.1.17
1XKA	FACTOR XA COMPLEXED WITH A SYNTHETIC INHIBITOR FX-2212A,(2S)-(3'-AMIDINO-3-BIPHENYLYL)-5-(4-PYRIDYLAMINO)PENTANOIC ACID	3.4.21.6
1XKB	FACTOR XA COMPLEXED WITH A SYNTHETIC INHIBITOR FX-2212A,(2S)-(3'-AMIDINO-3-BIPHENYLYL)-5-(4-PYRIDYLAMINO)PENTANOIC ACID	3.4.21.6
1XKG	CRYSTAL STRUCTURE OF THE MAJOR HOUSE DUST MITE ALLERGEN DER P 1 IN ITS PRO FORM AT 1.61 A RESOLUTION	3.4.22 3.4.22.65
1XKL	CRYSTAL STRUCTURE OF SALICYLIC ACID-BINDING PROTEIN 2 (SABP2) FROM NICOTIANA TABACUM, NESG TARGET AR2241	3.1.1
1XKO	STRUCTURE OF THERMOTOGA MARITIMA CHEX	3
1XKR	X-RAY STRUCTURE OF THERMOTOGA MARITIMA CHEC	3
1XKT	HUMAN FATTY ACID SYNTHASE: STRUCTURE AND SUBSTRATE SELECTIVITY OF THE THIOESTERASE DOMAIN	2.3.1.85 2.3.1.38 2.3.1.39 2.3.1.41 1.1.1.100 4.2.1.59 1.3.1.39 3.1.2.14
1XL2	HIV-1 PROTEASE IN COMPLEX WITH PYRROLIDINMETHANAMINE	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1XL5	HIV-1 PROTEASE IN COMPLEX WITH AMIDHYROXYSULFONE	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1XLU	X-RAY STRUCTURE OF DI-ISOPROPYL-PHOSPHORO-FLUORIDATE (DFP) INHIBITED BUTYRYLCHOLINESTERASE AFTER AGING	3.1.1.8
1XLV	ETHYLPHOSPHORYLATED BUTYRYLCHOLINESTERASE (AGED) OBTAINED BY REACTION WITH ECHOTHIOPHATE	3.1.1.8
1XLW	DIETHYLPHOSPHORYLATED BUTYRYLCHOLINESTERASE (NONAGED) OBTAINED BY REACTION WITH ECHOTHIOPHATE	3.1.1.8
1XLX	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH CILOMILAST	3.1.4.17 3.1.4.53
1XLZ	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH FILAMINAST	3.1.4.17 3.1.4.53
1XM1	NONBASIC THROMBIN INHIBITOR COMPLEX	3.4.21.5
1XM2	CRYSTAL STRUCTURE OF HUMAN PRL-1	3.1.3.48
1XM4	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH PICLAMILAST	3.1.4.17 3.1.4.53
1XM5	CRYSTAL STRUCTURE OF METAL-DEPENDENT HYDROLASE YBEY FROM E. COLI, PFAM UPF0054	3.1
1XM6	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH (R)-MESOPRAM	3.1.4.17 3.1.4.53
1XM8	X-RAY STRUCTURE OF GLYOXALASE II FROM ARABIDOPSIS THALIANA GENE AT2G31350	3.1.2.6
1XMB	X-RAY STRUCTURE OF IAA-AMINOACID HYDROLASE FROM ARABIDOPSIS THALIANA GENE AT5G56660	3.5.1
1XMI	CRYSTAL STRUCTURE OF HUMAN F508A NBD1 DOMAIN WITH ATP	3.6.3.49 5.6.1.6
1XMJ	CRYSTAL STRUCTURE OF HUMAN DELTAF508 HUMAN NBD1 DOMAIN WITH ATP	3.6.3.49 5.6.1.6
1XMK	THE CRYSTAL STRUCTURE OF THE ZB DOMAIN FROM THE RNA EDITING ENZYME ADAR1	3.5.4 3.5.4.37
1XML	STRUCTURE OF HUMAN DCPS	3.6.1.59
1XMM	STRUCTURE OF HUMAN DCPS BOUND TO M7GDP	3.6.1.59
1XMN	CRYSTAL STRUCTURE OF THROMBIN BOUND TO HEPARIN	3.4.21.5
1XMU	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH ROFLUMILAST	3.1.4.17 3.1.4.53
1XMY	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH (R)-ROLIPRAM	3.1.4.17 3.1.4.53
1XN0	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH (R,S)-ROLIPRAM	3.1.4.17 3.1.4.53
1XN2	NEW SUBSTRATE BINDING POCKETS FOR BETA-SECRETASE.	3.4.23.46
1XN3	CRYSTAL STRUCTURE OF BETA-SECRETASE BOUND TO A LONG INHIBITOR WITH ADDITIONAL UPSTREAM RESIDUES.	3.4.23.46
1XNB	HIGH-RESOLUTION STRUCTURES OF XYLANASES FROM B. CIRCULANS AND T. HARZIANUM IDENTIFY A NEW FOLDING PATTERN AND IMPLICATIONS FOR THE ATOMIC BASIS OF THE CATALYSIS	3.2.1.8
1XNC	THERMOSTABILIZATION OF THE BACILLUS CIRCULANS XYLANASE, BY THE INTRODUCTION OF DISULFIDE BONDS	3.2.1.8
1XND	HIGH-RESOLUTION STRUCTURES OF XYLANASES FROM B. CIRCULANS AND T. HARZIANUM IDENTIFY A NEW FOLDING PATTERN AND IMPLICATIONS FOR THE ATOMIC BASIS OF THE CATALYSIS	3.2.1.8
1XNK	BETA-1,4-XYLANASE FROM CHAETOMIUM THERMOPHILUM COMPLEXED WITH METHYL THIOXYLOPENTOSIDE	3.2.1.8
1XNZ	CRYSTAL STRUCTURE OF MN(II) FORM OF E. COLI. METHIONINE AMINOPEPTIDASE IN COMPLEX WITH 5-(2-CHLOROPHENYL)FURAN-2-CARBOXYLIC ACID	3.4.11.18
1XO1	T5 5'-EXONUCLEASE MUTANT K83A	3.1.11.3 3.1.11
1XOE	N9 TERN INFLUENZA NEURAMINIDASE COMPLEXED WITH (2R,4R,5R)-5-(1-ACETYLAMINO-3-METHYL-BUTYL-PYRROLIDINE-2, 4-DICAROBYXYLIC ACID 4-METHYL ESTERDASE COMPLEXED WITH	3.2.1.18
1XOG	N9 TERN INFLUENZA NEURAMINIDASE COMPLEXED WITH A 2,5-DISUBSTITUTED TETRAHYDROFURAN-5-CARBOXYLIC ACID	3.2.1.18
1XOM	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4D IN COMPLEX WITH CILOMILAST	3.1.4.17 3.1.4.53
1XON	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4D IN COMPLEX WITH PICLAMILAST	3.1.4.17 3.1.4.53
1XOQ	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4D IN COMPLEX WITH ROFLUMILAST	3.1.4.17 3.1.4.53
1XOR	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4D IN COMPLEX WITH ZARDAVERINE	3.1.4.17 3.1.4.53
1XOS	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH SILDENAFIL	3.1.4.17 3.1.4.53
1XOT	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH VARDENAFIL	3.1.4.17 3.1.4.53
1XOV	THE CRYSTAL STRUCTURE OF THE LISTERIA MONOCYTOGENES BACTERIOPHAGE PSA ENDOLYSIN PLYPSA	3.5.1.28
1XOZ	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 5A IN COMPLEX WITH TADALAFIL	3.1.4.17 3.1.4.35
1XP0	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 5A IN COMPLEX WITH VARDENAFIL	3.1.4.17 3.1.4.35
1XP3	CRYSTAL STRUCTURE OF ENDONUCLEASE IV (BA4508) FROM BACILLUS ANTHRACIS AT 2.57A RESOLUTION.	3.1.21.2
1XP4	CRYSTAL STRUCTURE OF A PEPTIDOGLYCAN SYNTHESIS REGULATORY FACTOR (PBP3) FROM STREPTOCOCCUS PNEUMONIAE	3.4.16.4
1XPB	STRUCTURE OF BETA-LACTAMASE TEM1	3.5.2.6
1XPS	BOVINE RIBONUCLEASE A (PHOSPHATE-FREE) (93 % HUMIDITY)	3.1.27.5 4.6.1.18
1XPT	BOVINE RIBONUCLEASE A (PHOSPHATE-FREE)	3.1.27.5 4.6.1.18
1XQO	CRYSTAL STRUCTURE OF NATIVE PA-AGOG, 8-OXOGUANINE DNA GLYCOSYLASE FROM PYROBACULUM AEROPHILUM	3.2.2 4.2.99.18
1XQP	CRYSTAL STRUCTURE OF 8-OXOGUANOSINE COMPLEXED PA-AGOG, 8-OXOGUANINE DNA GLYCOSYLASE FROM PYROBACULUM AEROPHILUM	3.2.2 4.2.99.18
1XQV	CRYSTAL STRUCTURE OF INACTIVE F1-MUTANT G37A	3.4.11.5
1XQW	CRYSTAL STRUCTURE OF F1-MUTANT S105A COMPLEX WITH PHE-LEU	3.4.11.5
1XQX	CRYSTAL STRUCTURE OF F1-MUTANT S105A COMPLEX WITH PCK	3.4.11.5
1XQY	CRYSTAL STRUCTURE OF F1-MUTANT S105A COMPLEX WITH PRO-LEU-GLY-GLY	3.4.11.5
1XR5	CRYSTAL STRUCTURE OF THE RNA-DEPENDENT RNA POLYMERASE 3D FROM HUMAN RHINOVIRUS SEROTYPE 14	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
1XR6	CRYSTAL STRUCTURE OF RNA-DEPENDENT RNA POLYMERASE 3D FROM HUMAN RHINOVIRUS SEROTYPE 1B	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
1XR7	CRYSTAL STRUCTURE OF RNA-DEPENDENT RNA POLYMERASE 3D FROM HUMAN RHINOVIRUS SEROTYPE 16	2.7.7.48 3.4.22.29 3.6.1.15 3.4.22.28
1XRF	THE CRYSTAL STRUCTURE OF A NOVEL, LATENT DIHYDROOROTASE FROM AQUIFEX AEOLICUS AT 1.7 A RESOLUTION	3.5.2.3
1XRI	X-RAY STRUCTURE OF A PUTATIVE PHOSPHOPROTEIN PHOSPHATASE FROM ARABIDOPSIS THALIANA GENE AT1G05000	3.1.3.48
1XRL	CRYSTAL STRUCTURE OF ACTIVE SITE F1-MUTANT Y205F COMPLEX WITH INHIBITOR PCK	3.4.11.5
1XRM	CRYSTAL STRUCTURE OF ACTIVE SITE F1-MUTANT E213Q SOAKED WITH PEPTIDE ALA-PHE	3.4.11.5
1XRN	CRYSTAL STRUCTURE OF ACTIVE SITE F1-MUTANT E213Q SOAKED WITH PEPTIDE PHE-ALA	3.4.11.5
1XRO	CRYSTAL STRUCTURE OF ACTIVE SITE F1-MUTANT E213Q SOAKED WITH PEPTIDE PHE-LEU	3.4.11.5
1XRP	CRYSTAL STRUCTURE OF ACTIVE SITE F1-MUTANT E213Q SOAKED WITH PEPTIDE PRO-LEU-GLY-GLY	3.4.11.5
1XRQ	CRYSTAL STRUCTURE OF ACTIVE SITE F1-MUTANT E245Q SOAKED WITH PEPTIDE PHE-LEU	3.4.11.5
1XRR	CRYSTAL STRUCTURE OF ACTIVE SITE F1-MUTANT E245Q SOAKED WITH PEPTIDE PRO-PRO	3.4.11.5
1XRT	THE CRYSTAL STRUCTURE OF A NOVEL, LATENT DIHYDROOROTASE FROM AQUIFEX AEOLICUS AT 1.7 A RESOLUTION	3.5.2.3
1XRY	CRYSTAL STRUCTURE OF AEROMONAS PROTEOLYTICA AMINOPEPTIDASE IN COMPLEX WITH BESTATIN	3.4.11.10
1XS1	DCTP DEAMINASE FROM ESCHERICHIA COLI IN COMPLEX WITH DUTP	3.5.4.13
1XS4	DCTP DEAMINASE FROM ESCHERICHIA COLI- E138A MUTANT ENZYME IN COMPLEX WITH DCTP	3.5.4.13
1XS6	DCTP DEAMINASE FROM ESCHERICHIA COLI. E138A MUTANT ENZYME IN COMPLEX WITH DUTP	3.5.4.13
1XS7	CRYSTAL STRUCTURE OF A CYCLOAMIDE-URETHANE-DERIVED NOVEL INHIBITOR BOUND TO HUMAN BRAIN MEMAPSIN 2 (BETA-SECRETASE).	3.4.23.46
1XSA	STRUCTURE OF THE NUDIX ENZYME AP4A HYDROLASE FROM HOMO SAPIENS (E63A MUTANT)	3.6.1.17
1XSB	STRUCTURE OF THE NUDIX ENZYME AP4A HYDROLASE FROM HOMO SAPIENS (E63A MUTANT) IN COMPLEX WITH ATP. NO ATP RESTRAINTS INCLUDED	3.6.1.17
1XSC	STRUCTURE OF THE NUDIX ENZYME AP4A HYDROLASE FROM HOMO SAPIENS (E63A MUTANT) IN COMPLEX WITH ATP	3.6.1.17
1XSF	SOLUTION STRUCTURE OF A RESUSCITATION PROMOTING FACTOR DOMAIN FROM MYCOBACTERIUM TUBERCULOSIS	3
1XSQ	CRYSTAL STRUCTURE OF UREIDOGLYCOLATE HYDROLASE FROM E.COLI. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET ET81.	3.5.3.19 4.3.2.3
1XSR	X-RAY STRUCTURE OF NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET SFR7	3.5.3.19 4.3.2.3
1XT5	CRYSTAL STRUCTURE OF VCBP3, DOMAIN 1, FROM BRANCHIOSTOMA FLORIDAE	3.2.1.14
1XT9	CRYSTAL STRUCTURE OF DEN1 IN COMPLEX WITH NEDD8	3.4.22
1XTF	NEUROTOXIN BONT/A E224Q Y366F MUTANT	3.4.24.69
1XTI	STRUCTURE OF WILDTYPE HUMAN UAP56	3.6.4.13
1XTJ	STRUCTURE OF HUMAN UAP56 IN COMPLEX WITH ADP	3.6.4.13
1XTK	STRUCTURE OF DECD TO DEAD MUTATION OF HUMAN UAP56	3.6.4.13
1XTY	CRYSTAL STRUCTURE OF SULFOLOBUS SOLFATARICUS PEPTIDYL-TRNA HYDROLASE	3.1.1.29
1XUC	MATRIX METALLOPROTEINASE-13 COMPLEXED WITH NON-ZINC BINDING INHIBITOR	3.4.24
1XUD	MATRIX METALLOPROTEINASE-13 COMPLEXED WITH NON-ZINC BINDING INHIBITOR	3.4.24
1XUF	TRYPSIN-BABIM-ZN+2, PH 8.2	3.4.21.4
1XUG	TRYPSIN-BABIM-ZN+2, PH 8.2	3.4.21.4
1XUH	TRYPSIN-KETO-BABIM-CO+2, PH 8.2	3.4.21.4
1XUI	TRYPSIN-KETO-BABIM, ZN+2-FREE, PH 8.2	3.4.21.4
1XUJ	TRYPSIN-KETO-BABIM-ZN+2, PH 8.2	3.4.21.4
1XUK	TRYPSIN-BABIM-SULFATE, PH 5.9	3.4.21.4
1XUR	MATRIX METALLOPROTEINASE-13 COMPLEXED WITH NON-ZINC BINDING INHIBITOR	3.4.24
1XV8	CRYSTAL STRUCTURE OF HUMAN SALIVARY ALPHA-AMYLASE DIMER	3.2.1.1
1XVI	CRYSTAL STRUCTURE OF YEDP, PHOSPHATASE-LIKE DOMAIN PROTEIN FROM ESCHERICHIA COLI K12	3.1.3.70
1XVM	TRYPSIN FROM FUSARIUM OXYSPORUM- ROOM TEMPERATURE TO ATOMIC RESOLUTION	3.4.21.4
1XVO	TRYPSIN FROM FUSARIUM OXYSPORUM AT PH 6	3.4.21.4
1XW2	STRUCTURE OF A COLD-ADAPTED FAMILY 8 XYLANASE	3.2.1.8 3.2.1.4
1XW8	X-RAY STRUCTURE OF PUTATIVE LACTAM UTILIZATION PROTEIN YBGL. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET ET90.	3.5.2.9
1XWF	K185N MUTATED S-ADENOSYLHOMOCYSTEINE HYDROLASE	3.3.1.1
1XWI	CRYSTAL STRUCTURE OF VPS4B	3.6.4.6
1XWQ	STRUCTURE OF A COLD-ADAPTED FAMILY 8 XYLANASE	3.2.1.8 3.2.1.4
1XWT	STRUCTURE OF A COLD-ADAPTED FAMILY 8 XYLANASE	3.2.1.8 3.2.1.4
1XWW	CRYSTAL STRUCTURE OF HUMAN B-FORM LOW MOLECULAR WEIGHT PHOSPHOTYROSYL PHOSPHATASE AT 1.6 ANGSTROM RESOLUTION	3.1.3.48 3.1.3.2
1XWY	CRYSTAL STRUCTURE OF TATD DEOXYRIBONUCLEASE FROM ESCHERICHIA COLI K12 AT 2.0 A RESOLUTION	3.1.21 3.1.11 3.1.13
1XX2	REFINEMENT OF P99 BETA-LACTAMASE FROM ENTEROBACTER CLOACAE	3.5.2.6
1XX7	CONSERVED HYPOTHETICAL PROTEIN FROM PYROCOCCUS FURIOSUS PFU-403030-001	3.1.3.89
1XX9	CRYSTAL STRUCTURE OF THE FXIA CATALYTIC DOMAIN IN COMPLEX WITH ECOTINM84R	3.4.21.27
1XXD	CRYSTAL STRUCTURE OF THE FXIA CATALYTIC DOMAIN IN COMPLEX WITH MUTATED ECOTIN	3.4.21.27
1XXE	RDC REFINED SOLUTION STRUCTURE OF THE AALPXC/TU-514 COMPLEX	3.5.1 3.5.1.108
1XXF	CRYSTAL STRUCTURE OF THE FXIA CATALYTIC DOMAIN IN COMPLEX WITH ECOTIN MUTANT (ECOTINP)	3.4.21.27
1XXM	THE MODULAR ARCHITECTURE OF PROTEIN-PROTEIN BINDING SITE	3.5.2.6
1XXN	CRYSTAL STRUCTURE OF A MESOPHILIC XYLANASE A FROM BACILLUS SUBTILIS 1A1	3.2.1.8
1XXP	YERSINIA YOPH (RESIDUES 163-468) C403S BINDS PHOSPHOTYROSYL PEPTIDE AT TWO SITES	3.1.3.48
1XXS	STRUCTURAL INSIGHTS FOR FATTY ACID BINDING IN A LYS49 PHOSPHOLIPASE A2: CRYSTAL STRUCTURE OF MYOTOXIN II FROM BOTHROPS MOOJENI COMPLEXED WITH STEARIC ACID	3.1.1.4
1XXV	YERSINIA YOPH (RESIDUES 163-468) BINDS PHOSPHONODIFLUOROMETHYL-PHE CONTAINING HEXAPEPTIDE AT TWO SITES	3.1.3.48
1XXW	STRUCTURE OF ZINC INDUCED HETERODIMER OF TWO CALCIUM FREE ISOFORMS OF PHOSPHOLIPASE A2 FROM NAJA NAJA SAGITTIFERA AT 2.7A RESOLUTION	3.1.1.4
1XYF	ENDO-1,4-BETA-XYLANASE FROM STREPTOMYCES OLIVACEOVIRIDIS	3.2.1.8
1XYN	STRUCTURAL COMPARISON OF TWO MAJOR ENDO-1,4-BETA-XYLANASES FROM TRICHODREMA REESEI	3.2.1.8
1XYO	STRUCTURAL COMPARISON OF TWO MAJOR ENDO-1,4-BETA-XYLANASES FROM TRICHODREMA REESEI	3.2.1.8
1XYP	STRUCTURAL COMPARISON OF TWO MAJOR ENDO-1,4-BETA-XYLANASES FROM TRICHODREMA REESEI	3.2.1.8
1XYR	POLIOVIRUS 135S CELL ENTRY INTERMEDIATE	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1XYZ	A COMMON PROTEIN FOLD AND SIMILAR ACTIVE SITE IN TWO DISTINCT FAMILIES OF BETA-GLYCANASES	3.2.1.8
1XZA	FUSARIUM SOLANI CUTINASE MUTANT WITH SER 129 REPLACED BY CYS	3.1.1 3.1.1.74
1XZB	FUSARIUM SOLANI CUTINASE MUTANT WITH SER 129 REPLACED BY CYS COMPLEX WITH MERCURY ACETATE	3.1.1 3.1.1.74
1XZC	FUSARIUM SOLANI CUTINASE MUTANT WITH SER 129 REPLACED BY CYS COMPLEX WITH PARA-SULFUROUSPHENYL MERCURY	3.1.1 3.1.1.74
1XZD	FUSARIUM SOLANI CUTINASE MUTANT WITH SER 213 REPLACED BY CYS	3.1.1 3.1.1.74
1XZE	FUSARIUM SOLANI CUTINASE MUTANT WITH SER 92 REPLACED BY CYS	3.1.1 3.1.1.74
1XZF	FUSARIUM SOLANI CUTINASE MUTANT WITH THR 144 REPLACED BY CYS	3.1.1 3.1.1.74
1XZG	FUSARIUM SOLANI CUTINASE MUTANT WITH THR 45 REPLACED BY ALA	3.1.1 3.1.1.74
1XZH	FUSARIUM SOLANI CUTINASE MUTANT WITH THR 80 REPLACED BY PRO	3.1.1 3.1.1.74
1XZI	FUSARIUM SOLANI CUTINASE MUTANT WITH THR 119 REPLACED BY HIS	3.1.1 3.1.1.74
1XZJ	FUSARIUM SOLANI CUTINASE MUTANT WITH THR 38 REPLACED BY PHE	3.1.1 3.1.1.74
1XZK	FUSARIUM SOLANI CUTINASE COMPLEX WITH DI(ISOPROPYL)PHOSPHATE	3.1.1 3.1.1.74
1XZL	FUSARIUM SOLANI CUTINASE COMPLEX WITH N-HEXYLPHOSPHONATE ETHYL ESTER	3.1.1 3.1.1.74
1XZM	FUSARIUM SOLANI CUTINASE COMPLEX WITH N-UNDECYL O-METHYL CHLORO PHOSPHONATE ESTER	3.1.1 3.1.1.74
1XZP	STRUCTURE OF THE GTP-BINDING PROTEIN TRME FROM THERMOTOGA MARITIMA	3.6.5
1XZQ	STRUCTURE OF THE GTP-BINDING PROTEIN TRME FROM THERMOTOGA MARITIMA COMPLEXED WITH 5-FORMYL-THF	3.6.5
1XZW	SWEET POTATO PURPLE ACID PHOSPHATASE/PHOSPHATE COMPLEX	3.1.3.2
1Y0M	CRYSTAL STRUCTURE OF OF THE SH3 DOMAIN OF PHOSPHOLIPASE C GAMMA-1	3.1.4.11
1Y0R	CRYSTAL STRUCTURE OF THE TETRAHEDRAL AMINOPEPTIDASE FROM P. HORIKOSHII	3.4.11
1Y0Y	CRYSTAL STRUCTURE OF TETRAHEDRAL AMINOPEPTIDASE FROM P. HORIKOSHII IN COMPLEX WITH AMASTATIN	3.4.11
1Y1K	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 T58A MUTANT	3.4.21.62
1Y1N	IDENTIFICATION OF SH3 MOTIF IN M. TUBERCULOSIS METHIONINE AMINOPEPTIDASE SUGGESTS A MODE OF INTERACTION WITH THE RIBOSOME	3.4.11.18
1Y1O	X-RAY CRYSTAL STRUCTURE OF PENICILLIN-BINDING PROTEIN-RELATED FACTOR A FROM BACILLUS STEAROTHERMOPHILUS	3.1.22.4
1Y2B	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4D IN COMPLEX WITH 3,5-DIMETHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER	3.1.4.17 3.1.4.53
1Y2C	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4D IN COMPLEX WITH 3,5-DIMETHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER	3.1.4.17 3.1.4.53
1Y2D	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4D IN COMPLEX WITH 1-(4-METHOXY-PHENYL)-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER	3.1.4.17 3.1.4.53
1Y2E	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4D IN COMPLEX WITH 1-(4-AMINO-PHENYL)-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER	3.1.4.17 3.1.4.53
1Y2H	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH 1-(2-CHLORO-PHENYL)-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER	3.1.4.17 3.1.4.53
1Y2J	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4B IN COMPLEX WITH 3,5-DIMETHYL-1-(3-NITRO-PHENYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER	3.1.4.17 3.1.4.53
1Y2K	CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 4D IN COMPLEX WITH 3,5-DIMETHYL-1-(3-NITRO-PHENYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID ETHYL ESTER	3.1.4.17 3.1.4.53
1Y33	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 T58P MUTANT	3.4.21.62
1Y34	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 E60A MUTANT	3.4.21.62
1Y37	STRUCTURE OF FLUOROACETATE DEHALOGENASE FROM BURKHOLDERIA SP. FA1	3.8.1.3
1Y38	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 DIMER AND GLYCEROPHOSPHATE AT 2.4 A RESOLUTION	3.1.1.4
1Y3B	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 E60S MUTANT	3.4.21.62
1Y3C	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 R62A MUTANT	3.4.21.62
1Y3D	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 R67A MUTANT	3.4.21.62
1Y3F	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 F69A MUTANT	3.4.21.62
1Y3G	CRYSTAL STRUCTURE OF A SILANEDIOL PROTEASE INHIBITOR BOUND TO THERMOLYSIN	3.4.24.27
1Y3J	SOLUTION STRUCTURE OF THE COPPER(I) FORM OF THE FIFTH DOMAIN OF MENKES PROTEIN	3.6.3.4 7.2.2.8
1Y3K	SOLUTION STRUCTURE OF THE APO FORM OF THE FIFTH DOMAIN OF MENKES PROTEIN	3.6.3.4 7.2.2.8
1Y3U	TRYPSIN INHIBITOR COMPLEX	3.4.21.4
1Y3V	TRYPSIN INHIBITOR COMPLEX	3.4.21.4
1Y3W	TRYPSIN INHIBITOR COMPLEX	3.4.21.4
1Y3X	TRYPSIN INHIBITOR COMPLEX	3.4.21.4
1Y3Y	TRYPSIN INHIBITOR COMPLEX	3.4.21.4
1Y43	CRYSTAL STRUCTURE OF ASPERGILLOGLUTAMIC PEPTIDASE FROM ASPERGILLUS NIGER	3.4.23.19
1Y44	CRYSTAL STRUCTURE OF RNASE Z	3.1.26.11
1Y48	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 R65A MUTANT	3.4.21.62
1Y4A	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 M59R/E60S MUTANT	3.4.21.62
1Y4D	CRYSTAL STRUCTURE OF THE COMPLEX OF SUBTILISIN BPN' WITH CHYMOTRYPSIN INHIBITOR 2 M59R/E60S MUTANT	3.4.21.62
1Y4H	WILD TYPE STAPHOPAIN-STAPHOSTATIN COMPLEX	3.4.22
1Y4L	CRYSTAL STRUCTURE OF BOTHROPS ASPER MYOTOXIN II COMPLEXED WITH THE ANTI-TRYPANOSOMAL DRUG SURAMIN	3.1.1.4
1Y4W	CRYSTAL STRUCTURE OF EXO-INULINASE FROM ASPERGILLUS AWAMORI IN SPACEGROUP P21	3.2.1.80
1Y54	CRYSTAL STRUCTURE OF THE NATIVE CLASS C BETA-LACTAMASE FROM ENTEROBACTER CLOACAE 908R COMPLEXED WITH BRL42715	3.5.2.6
1Y59	DIANHYDROSUGAR-BASED BENZAMIDINE, FACTOR XA SPECIFIC INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN MUTANT	3.4.21.4
1Y5A	DIANHYDROSUGAR-BASED BENZAMIDINE, FACTOR XA SPECIFIC INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN MUTANT	3.4.21.4
1Y5B	DIANHYDROSUGAR-BASED BENZAMIDINE, FACTOR XA SPECIFIC INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN MUTANT	3.4.21.4
1Y5U	DIANHYDROSUGAR-BASED BENZAMIDINE, FACTOR XA SPECIFIC INHIBITOR IN COMPLEX WITH BOVINE TRYPSIN MUTANT	3.4.21.4
1Y65	CRYSTAL STRUCTURE OF BETA-HEXOSAMINIDASE FROM VIBRIO CHOLERAE IN COMPLEX WITH N-ACETYL-D-GLUCOSAMINE TO A RESOLUTION OF 1.85	3.2.1.52
1Y6H	CRYSTAL STRUCTURE OF LIPDF	3.5.1.88
1Y6O	CRYSTAL STRUCTURE OF DISULFIDE ENGINEERED PORCINE PANCREATIC PHOSPHOLIPASE A2 TO GROUP-X ISOZYME IN COMPLEX WITH INHIBITOR MJ33 AND PHOSPHATE IONS	3.1.1.4
1Y6P	CRYSTAL STRUCTURE OF DISULFIDE ENGINEERED PORCINE PANCRATIC PHOSPHOLIPASE A2 TO GROUP-X ISOZYME	3.1.1.4
1Y6Q	CYRSTAL STRUCTURE OF MTA/ADOHCY NUCLEOSIDASE COMPLEXED WITH MT-DADME-IMMA	3.2.2.16 3.2.2.9
1Y6R	CRYSTAL STRUCTURE OF MTA/ADOHCY NUCLEOSIDASE COMPLEXED WITH MT-IMMA.	3.2.2.16 3.2.2.9
1Y6V	STRUCTURE OF E. COLI ALKALINE PHOSPHATASE IN PRESENCE OF COBALT AT 1.60 A RESOLUTION	3.1.3.1
1Y6X	THE 1.25 A RESOLUTION STRUCTURE OF PHOSPHORIBOSYL-ATP PYROPHOSPHOHYDROLASE FROM MYCOBACTERIUM TUBERCULOSIS	3.6.1.31
1Y75	A NEW FORM OF CATALYTICALLY INACTIVE PHOSPHOLIPASE A2 WITH AN UNUSUAL DISULPHIDE BRIDGE CYS 32- CYS 49 REVEALS RECOGNITION FOR N-ACETYLGLUCOSMINE	3.1.1.4
1Y79	CRYSTAL STRUCTURE OF THE E.COLI DIPEPTIDYL CARBOXYPEPTIDASE DCP IN COMPLEX WITH A PEPTIDIC INHIBITOR	3.4.15.5
1Y7A	STRUCTURE OF D153H/K328W E. COLI ALKALINE PHOSPHATASE IN PRESENCE OF COBALT AT 1.77 A RESOLUTION	3.1.3.1
1Y7B	BETA-D-XYLOSIDASE, A FAMILY 43 GLYCOSIDE HYDROLASE	3.2.1.37
1Y7E	THE CRYSTAL STRUCTURE OF AMINOPEPTIDASE I FROM BORRELIA BURGDORFERI B31	3.4.11
1Y7H	STRUCTURAL AND BIOCHEMICAL STUDIES IDENTIFY TOBACCO SABP2 AS A METHYLSALICYLATE ESTERASE AND FURTHER IMPLICATE IT IN PLANT INNATE IMMUNITY, NORTHEAST STRUCTURAL GENOMICS TARGET AR2241	3.1.1
1Y7I	STRUCTURAL AND BIOCHEMICAL STUDIES IDENTIFY TOBACCO SABP2 AS A METHYLSALICYLATE ESTERASE AND FURTHER IMPLICATE IT IN PLANT INNATE IMMUNITY, NORTHEAST STRUCTURAL GENOMICS TARGET AR2241	3.1.1
1Y7O	THE STRUCTURE OF STREPTOCOCCUS PNEUMONIAE A153P CLPP	3.4.21.92
1Y7U	CRYSTAL STRUCTURE OF ACYL-COA HYDROLASE FROM BACILLUS CEREUS	3.1.2.20
1Y7V	X-RAY STRUCTURE OF HUMAN ACID-BETA-GLUCOSIDASE COVALENTLY BOUND TO CONDURITOL B EPOXIDE	3.2.1.45 2.4.1 3.2.1
1Y82	CONSERVED HYPOTHETICAL PROTEIN PFU-367848-001 FROM PYROCOCCUS FURIOSUS	3.1
1Y89	CRYSTAL STRUCTURE OF DEVB PROTEIN	3.1.1.31
1Y8J	CRYSTAL STRUCTURE OF HUMAN NEP COMPLEXED WITH AN IMIDAZO[4,5-C]PYRIDINE INHIBITOR	3.4.24.11
1Y8T	CRYSTAL STRUCTURE OF RV0983 FROM MYCOBACTERIUM TUBERCULOSIS- PROTEOLYTICALLY ACTIVE FORM	3.4.21.107
1Y92	CRYSTAL STRUCTURE OF THE P19A/N67D VARIANT OF BOVINE SEMINAL RIBONUCLEASE	3.1.27.5 4.6.1.18
1Y93	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN MMP12 COMPLEXED WITH ACETOHYDROXAMIC ACID AT ATOMIC RESOLUTION	3.4.24.65
1Y94	CRYSTAL STRUCTURE OF THE G16S/N17T/P19A/S20A/N67D VARIANT OF BOVINE SEMINAL RIBONUCLEASE	3.1.27.5 4.6.1.18
1Y97	THE HUMAN TREX2 3' EXONUCLEASE STRUCTURE SUGGESTS A MECHANISM FOR EFFICIENT NON-PROCESSIVE DNA CATALYSIS	3.1.11.2
1Y9G	CRYSTAL STRUCTURE OF EXO-INULINASE FROM ASPERGILLUS AWAMORI COMPLEXED WITH FRUCTOSE	3.2.1.80
1Y9M	CRYSTAL STRUCTURE OF EXO-INULINASE FROM ASPERGILLUS AWAMORI IN SPACEGROUP P212121	3.2.1.80
1Y9O	1H NMR STRUCTURE OF ACYLPHOSPHATASE FROM THE HYPERTHERMOPHILE SULFOLOBUS SOLFATARICUS	3.6.1.7
1Y9Z	CRYSTAL STRUCTURE OF PSYCHROPHILIC SUBTILISIN-LIKE SERINE PROTEASE FROM ANTARCTIC PSYCHROTROPH PSEUDOALTEROMONAS SP. AS-11 AT 0.14 NM RESOLUTION	3.4.21
1YA4	CRYSTAL STRUCTURE OF HUMAN LIVER CARBOXYLESTERASE 1 IN COMPLEX WITH TAMOXIFEN	3.1.1.1 3.1.1.13 3.1.1.56
1YA8	CRYSTAL STRUCTURE OF HUMAN LIVER CARBOXYLESTERASE IN COMPLEX WITH CLEAVAGE PRODUCTS OF MEVASTATIN	3.1.1.1 3.1.1.13 3.1.1.56
1YAF	STRUCTURE OF TENA FROM BACILLUS SUBTILIS	3.5.99.2
1YAH	CRYSTAL STRUCTURE OF HUMAN LIVER CARBOXYLESTERASE COMPLEXED TO ETYL ACETATE; A FATTY ACID ETHYL ESTER ANALOGUE	3.1.1.1 3.1.1.13 3.1.1.56
1YAK	COMPLEX OF BACILLUS SUBTILIS TENA WITH 4-AMINO-2-METHYL-5-HYDROXYMETHYLPYRIMIDINE	3.5.99.2
1YAL	CARICA PAPAYA CHYMOPAPAIN AT 1.7 ANGSTROMS RESOLUTION	3.4.22.6
1YAM	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: CALORIMETRIC STUDIES AND X-RAY STRUCTURAL ANALYSIS OF THE FIVE ISOLEUCINE TO VALINE MUTANTS	3.2.1.17
1YAN	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: CALORIMETRIC STUDIES AND X-RAY STRUCTURAL ANALYSIS OF THE FIVE ISOLEUCINE TO VALINE MUTANTS	3.2.1.17
1YAO	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: CALORIMETRIC STUDIES AND X-RAY STRUCTURAL ANALYSIS OF THE FIVE ISOLEUCINE TO VALINE MUTANTS	3.2.1.17
1YAP	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: CALORIMETRIC STUDIES AND X-RAY STRUCTURAL ANALYSIS OF THE FIVE ISOLEUCINE TO VALINE MUTANTS	3.2.1.17
1YAQ	CONTRIBUTION OF HYDROPHOBIC RESIDUES TO THE STABILITY OF HUMAN LYSOZYME: CALORIMETRIC STUDIES AND X-RAY STRUCTURAL ANALYSIS OF THE FIVE ISOLEUCINE TO VALINE MUTANTS	3.2.1.17
1YAX	CYSTAL STRUCTURE ANALYSIS OF S.TYPHIMURIUM PHOQ SENSOR DOMAIN WITH CALCIUM	2.7.3 2.7.13.3 3.1.3
1YBQ	CRYSTAL STRUCTURE OF ESCHERICHIA COLI ISOASPARTYL DIPEPTIDASE MUTANT D285N COMPLEXED WITH BETA-ASPARTYLHISTIDINE	3.4.19
1YBW	PROTEASE DOMAIN OF HGFA WITH NO INHIBITOR	3.4.21
1YC0	SHORT FORM HGFA WITH FIRST KUNITZ DOMAIN FROM HAI-1	3.4.21
1YC2	SIR2AF2-NAD-ADPRIBOSE-NICOTINAMIDE	3.5.1 2.3.1.286
1YC5	SIR2-P53 PEPTIDE-NICOTINAMIDE	3.5.1 2.3.1.286
1YCD	CRYSTAL STRUCTURE OF YEAST FSH1/YHR049W, A MEMBER OF THE SERINE HYDROLASE FAMILY	3.1
1YCL	CRYSTAL STRUCTURE OF B. SUBTILIS LUXS IN COMPLEX WITH A CATALYTIC 2-KETONE INTERMEDIATE	3.13.1 4.4.1.21
1YCM	SOLUTION STRUCTURE OF MATRIX METALLOPROTEINASE 12 (MMP12) IN THE PRESENCE OF N-ISOBUTYL-N-[4-METHOXYPHENYLSULFONYL]GLYCYL HYDROXAMIC ACID (NNGH)	3.4.24.65
1YDH	X-RAY STRUCTURE OF A LYSINE DECARBOXYLASE-LIKE PROTEIN FROM ARABIDOPSIS THALIANA GENE AT5G11950	3.2.2
1YDY	CRYSTAL STRUCTURE OF PERIPLASMIC GLYCEROPHOSPHODIESTER PHOSPHODIESTERASE FROM ESCHERICHIA COLI	3.1.4.46
1YE5	CRYSTAL STRUCTURE OF HYPOTHETICAL PROTEIN OF UNKNOWN FUNCTION FROM PYROCOCCUS HORIKOSHII OT3	3.1
1YE8	CRYSTAL STRUCTURE OF THEP1 FROM THE HYPERTHERMOPHILE AQUIFEX AEOLICUS	3.6.1.15
1YF4	CRYSTAL STRUCTURE OF TRYPSIN-VASOPRESSIN COMPLEX	3.4.21.4
1YF8	CRYSTAL STRUCTURE OF HIMALAYAN MISTLETOE RIP REVEALS THE PRESENCE OF A NATURAL INHIBITOR AND A NEW FUNCTIONALLY ACTIVE SUGAR-BINDING SITE	3.2.2.22
1YFI	CRYSTAL STRUCTURE OF RESTRICTION ENDONUCLEASE MSPI IN COMPLEX WITH ITS COGNATE DNA IN P212121 SPACE GROUP	3.1.21.4
1YFK	CRYSTAL STRUCTURE OF HUMAN B TYPE PHOSPHOGLYCERATE MUTASE	5.4.2.1 5.4.2.4 3.1.3.13 5.4.2.11
1YFO	RECEPTOR PROTEIN TYROSINE PHOSPHATASE ALPHA, DOMAIN 1 FROM MOUSE	3.1.3.48
1YG9	THE STRUCTURE OF MUTANT (N93Q) OF BLA G 2	3.4.23
1YGC	SHORT FACTOR VIIA WITH A SMALL MOLECULE INHIBITOR	3.4.21.21
1YGR	CRYSTAL STRUCTURE OF THE TANDEM PHOSPHATASE DOMAIN OF RPTP CD45	3.1.3.48
1YGU	CRYSTAL STRUCTURE OF THE TANDEM PHOSPHATASE DOMAINS OF RPTP CD45 WITH A PTYR PEPTIDE	3.1.3.48
1YGW	NMR STRUCTURE OF RIBONUCLEASE T1, 34 STRUCTURES	3.1.27.3 4.6.1.24
1YGZ	CRYSTAL STRUCTURE OF INORGANIC PYROPHOSPHATASE FROM HELICOBACTER PYLORI	3.6.1.1
1YH3	CRYSTAL STRUCTURE OF HUMAN CD38 EXTRACELLULAR DOMAIN	3.2.2.5 3.2.2.6 2.4.99.20
1YH8	CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS LPXC DEACETYLASE COMPLEXED WITH PALMITATE	3.5.1 3.5.1.108
1YHC	CRYSTAL STRUCTURE OF AQUIFEX AEOLICUS LPXC DEACETYLASE COMPLEXED WITH CACODYLATE	3.5.1 3.5.1.108
1YHT	CRYSTAL STRUCTURE ANALYSIS OF DISPERSIN B	3.2.1.52
1YI7	BETA-D-XYLOSIDASE (SELENOMETHIONINE) XYND FROM CLOSTRIDIUM ACETOBUTYLICUM	3.2.1.37
1YIF	CRYSTAL STRUCTURE OF BETA-1,4-XYLOSIDASE FROM BACILLUS SUBTILIS, NEW YORK STRUCTURAL GENOMICS CONSORTIUM	3.2.1.37
1YIK	STRUCTURE OF HEN EGG WHITE LYSOZYME SOAKED WITH CU-CYCLAM	3.2.1.17
1YIL	STRUCTURE OF HEN EGG WHITE LYSOZYME SOAKED WITH CU2-XYLYLBICYCLAM	3.2.1.17
1YIX	CRYSTAL STRUCTURE OF YCFH, TATD HOMOLOG FROM ESCHERICHIA COLI K12, AT 1.9 A RESOLUTION	3.1.21 3.1
1YJ3	CRYSTAL STRUCTURE ANALYSIS OF PRODUCT BOUND METHIONINE AMINOPEPTIDASE TYPE 1C FROM MYCOBACTERIUM TUBERCULOSIS	3.4.11.18
1YJ5	MOLECULAR ARCHITECTURE OF MAMMALIAN POLYNUCLEOTIDE KINASE, A DNA REPAIR ENZYME	2.7.1.78 3.1.3.32
1YJA	SUBTILISIN BPN' 8397+1 (E.C. 3.4.21.14) (MUTANT WITH MET 50 REPLACED BY PHE, ASN 76 REPLACED BY ASP, GLY 169 REPLACED BY ALA, GLN 206 REPLACED BY CYS, ASN 218 REPLACED BY SER AND LYS 256 REPLACED BY TYR) (M50F, N76D, G169A, Q206C, N218S, AND K256Y) IN 20% DIMETHYLFORMAMIDE	3.4.21.14 3.4.21.62
1YJB	SUBTILISIN BPN' 8397+1 (E.C. 3.4.21.14) (MUTANT WITH MET 50 REPLACED BY PHE, ASN 76 REPLACED BY ASP, GLY 169 REPLACED BY ALA, GLN 206 REPLACED BY CYS, ASN 218 REPLACED BY SER AND LYS 256 REPLACED BY TYR) (M50F, N76D, G169A, Q206C, N218S, AND K256Y) IN 35% DIMETHYLFORMAMIDE	3.4.21.14 3.4.21.62
1YJC	SUBTILISIN BPN' 8397+1 (E.C. 3.4.21.14) (MUTANT WITH MET 50 REPLACED BY PHE, ASN 76 REPLACED BY ASP, GLY 169 REPLACED BY ALA, GLN 206 REPLACED BY CYS, ASN 218 REPLACED BY SER AND LYS 256 REPLACED BY TYR) (M50F, N76D, G169A, Q206C, N218S, AND K256Y) IN 50% DIMETHYLFORMAMIDE	3.4.21.14 3.4.21.62
1YJM	CRYSTAL STRUCTURE OF THE FHA DOMAIN OF MOUSE POLYNUCLEOTIDE KINASE IN COMPLEX WITH AN XRCC4-DERIVED PHOSPHOPEPTIDE.	2.7.1.78 3.1.3.32
1YJR	SOLUTION STRUCTURE OF THE APO FORM OF THE SIXTH SOLUBLE DOMAIN A69P MUTANT OF MENKES PROTEIN	3.6.3.4 7.2.2.8
1YJT	SOLUTION STRUCTURE OF THE CU(I) FORM OF THE SIXTH SOLUBLE DOMAIN A69P MUTANT OF MENKES PROTEIN	3.6.3.4 7.2.2.8
1YJU	SOLUTION STRUCTURE OF THE APO FORM OF THE SIXTH SOLUBLE DOMAIN OF MENKES PROTEIN	3.6.3.4 7.2.2.8
1YJV	SOLUTION STRUCTURE OF THE CU(I) FORM OF THE SIXTH SOLUBLE DOMAIN OF MENKES PROTEIN	3.6.3.4 7.2.2.8
1YK8	CATHEPSIN K COMPLEXED WITH A CYANAMIDE-BASED INHIBITOR	3.4.22.38
1YKS	CRYSTAL STRUCTURE OF YELLOW FEVER VIRUS NS3 HELICASE	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
1YKX	EFFECT OF ALCOHOLS ON PROTEIN HYDRATION	3.2.1.17
1YKY	EFFECT OF ALCOHOLS ON PROTEIN HYDRATION	3.2.1.17
1YKZ	EFFECT OF ALCOHOLS ON PROTEIN HYDRATION	3.2.1.17
1YL0	EFFECT OF ALCOHOLS ON PROTEIN HYDRATION	3.2.1.17
1YL1	EFFECT OF ALCOHOLS ON PROTEIN HYDRATION	3.2.1.17
1YLI	CRYSTAL STRUCTURE OF HI0827, A HEXAMERIC BROAD SPECIFICITY ACYL-COENZYME A THIOESTERASE	3.1.2
1YLJ	ATOMIC RESOLUTION STRUCTURE OF CTX-M-9 BETA-LACTAMASE	3.5.2.6
1YLP	ATOMIC RESOLUTION STRUCTURE OF CTX-M-27 BETA-LACTAMASE	3.5.2.6
1YLT	ATOMIC RESOLUTION STRUCTURE OF CTX-M-14 BETA-LACTAMASE	3.5.2.6
1YLW	X-RAY STRUCTURE OF CTX-M-16 BETA-LACTAMASE	3.5.2.6
1YLY	X-RAY CRYSTALLOGRAPHIC STRUCTURE OF CTX-M-9 BETA-LACTAMASE COMPLEXED WITH CEFTAZIDIME-LIKE BORONIC ACID	3.5.2.6
1YLZ	X-RAY CRYSTALLOGRAPHIC STRUCTURE OF CTX-M-14 BETA-LACTAMASE COMPLEXED WITH CEFTAZIDIME-LIKE BORONIC ACID	3.5.2.6
1YM0	CRYSTAL STRUCTURE OF EARTHWORM FIBRINOLYTIC ENZYME COMPONENT B: A NOVEL, GLYCOSYLATED TWO-CHAINED TRYPSIN	3.4.21
1YM1	X-RAY CRYSTALLOGRAPHIC STRUCTURE OF CTX-M-9 BETA-LACTAMASE COMPLEXED WITH A BORONIC ACID INHIBITOR (SM2)	3.5.2.6
1YM2	CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE COMPLEXED WITH NVP-AUR200	3.4.23.46
1YM4	CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE COMPLEXED WITH NVP-AMK640	3.4.23.46
1YM9	CRYSTAL STRUCTURE OF THE CDC25B PHOSPHATASE CATALYTIC DOMAIN WITH THE ACTIVE SITE CYSTEINE IN THE SULFINIC FORM	3.1.3.48
1YMD	CRYSTAL STRUCTURE OF THE CDC25B PHOSPHATASE CATALYTIC DOMAIN WITH THE ACTIVE SITE CYSTEINE IN THE SULFONIC FORM	3.1.3.48
1YME	STRUCTURE OF CARBOXYPEPTIDASE	3.4.17.1
1YMK	CRYSTAL STRUCTURE OF THE CDC25B PHOSPHATASE CATALYTIC DOMAIN IN THE APO FORM	3.1.3.48
1YML	CRYSTAL STRUCTURE OF THE CDC25B PHOSPHATASE CATALYTIC DOMAIN WITH THE ACTIVE SITE CYSTEINE IN THE SULFENIC FORM	3.1.3.48
1YMN	THE STUDY OF REDUCTIVE UNFOLDING PATHWAYS OF RNASE A (Y92L MUTANT)	3.1.27.5 4.6.1.18
1YMR	THE STUDY OF REDUCTIVE UNFOLDING PATHWAYS OF RNASE A (Y92A MUTANT)	3.1.27.5 4.6.1.18
1YMS	X-RAY CRYSTALLOGRAPHIC STRUCTURE OF CTX-M-9 BETA-LACTAMASE COMPLEXED WITH NAFCININ-LIKE BORONIC ACID INHIBITOR	3.5.2.6
1YMW	THE STUDY OF REDUCTIVE UNFOLDING PATHWAYS OF RNASE A (Y92G MUTANT)	3.1.27.5 4.6.1.18
1YMX	X-RAY CRYSTALLOGRAPHIC STRUCTURE OF CTX-M-9 BETA-LACTAMASE COVALENTLY LINKED TO CEFOXITIN	3.5.2.6
1YMY	CRYSTAL STRUCTURE OF THE N-ACETYLGLUCOSAMINE-6-PHOSPHATE DEACETYLASE FROM ESCHERICHIA COLI K12	3.5.1.25
1YN9	CRYSTAL STRUCTURE OF BACULOVIRUS RNA 5'-PHOSPHATASE COMPLEXED WITH PHOSPHATE	3.1.3.33 3.1.3.48
1YNA	ENDO-1,4-BETA-XYLANASE, ROOM TEMPERATURE, PH 4.0	3.2.1.8
1YNB	CRYSTAL STRUCTURE OF GENOMICS APC5600	3.1.3.89
1YNH	CRYSTAL STRUCTURE OF N-SUCCINYLARGININE DIHYDROLASE, ASTB, BOUND TO SUBSTRATE AND PRODUCT, AN ENZYME FROM THE ARGININE CATABOLIC PATHWAY OF ESCHERICHIA COLI	3 3.5.3.23
1YNI	CRYSTAL STRUCTURE OF N-SUCCINYLARGININE DIHYDROLASE, ASTB, BOUND TO SUBSTRATE AND PRODUCT, AN ENZYME FROM THE ARGININE CATABOLIC PATHWAY OF ESCHERICHIA COLI	3 3.5.3.23
1YNM	CRYSTAL STRUCTURE OF RESTRICTION ENDONUCLEASE HINP1I	3.1.21.4
1YNS	CRYSTAL STRUCTURE OF HUMAN ENOLASE-PHOSPHATASE E1 AND ITS COMPLEX WITH A SUBSTRATE ANALOG	3.1.3.77
1YNV	ASP79 MAKES A LARGE, UNFAVORABLE CONTRIBUTION TO THE STABILITY OF RNASE SA	3.1.27.3 4.6.1.24
1YNY	MOLECULAR STRUCTURE OF D-HYDANTOINASE FROM A BACILLUS SP. AR9: EVIDENCE FOR MERCURY INHIBITION	3.5.2.2
1YOE	CRYSTAL STRUCTURE OF A THE E. COLI PYRIMIDINE NUCLEOSIDE HYDROLASE YBEK WITH BOUND RIBOSE	3.2.2.8 3.2
1YOU	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF MMP-13 COMPLEXED WITH A POTENT PYRIMIDINETRIONE INHIBITOR	3.4.24
1YOY	PREDICTED CODING REGION AF1432 FROM ARCHAEOGLOBUS FULGIDUS	3.1.3.89
1YP9	TRYPSIN INHIBITOR COMPLEX	3.4.21.4
1YPE	THROMBIN INHIBITOR COMPLEX	3.4.21.5
1YPG	THROMBIN INHIBITOR COMPLEX	3.4.21.5
1YPH	HIGH RESOLUTION STRUCTURE OF BOVINE ALPHA-CHYMOTRYPSIN	3.4.21.1
1YPJ	THROMBIN INHIBITOR COMPLEX	3.4.21.5
1YPK	THROMBIN INHIBITOR COMPLEX	3.4.21.5
1YPL	X-RAY CRYSTAL STRUCTURE OF THROMBIN INHIBITED BY SYNTHETIC CYANOPEPTIDE ANALOGUE RA-1008	3.4.21.5
1YPM	X-RAY CRYSTAL STRUCTURE OF THROMBIN INHIBITED BY SYNTHETIC CYANOPEPTIDE ANALOGUE RA-1014	3.4.21.5
1YPP	ACID ANHYDRIDE HYDROLASE	3.6.1.1
1YPT	CRYSTAL STRUCTURE OF YERSINIA PROTEIN TYROSINE PHOSPHATASE AT 2.5 ANGSTROMS AND THE COMPLEX WITH TUNGSTATE	3.1.3.48
1YQC	CRYSTAL STRUCTURE OF UREIDOGLYCOLATE HYDROLASE (ALLA) FROM ESCHERICHIA COLI O157:H7	3.5.3.19 4.3.2.3
1YQE	CRYSTAL STRUCTURE OF CONSERVED PROTEIN OF UNKNOWN FUNCTION AF0625	3.1.1.96
1YQK	HUMAN 8-OXOGUANINE GLYCOSYLASE CROSSLINKED WITH GUANINE CONTAINING DNA	3.2.2 4.2.99.18
1YQL	CATALYTICALLY INACTIVE HOGG1 CROSSLINKED WITH 7-DEAZA-8-AZAGUANINE CONTAINING DNA	3.2.2 4.2.99.18
1YQM	CATALYTICALLY INACTIVE HUMAN 8-OXOGUANINE GLYCOSYLASE CROSSLINKED TO 7-DEAZAGUANINE CONTAINING DNA	3.2.2 4.2.99.18
1YQR	CATALYTICALLY INACTIVE HUMAN 8-OXOGUANINE GLYCOSYLASE CROSSLINKED TO OXOG CONTAINING DNA	3.2.2 4.2.99.18
1YQS	INHIBITION OF THE R61 DD-PEPTIDASE BY N-BENZOYL-BETA-SULTAM	3.4.16.4
1YQY	STRUCTURE OF B. ANTHRAX LETHAL FACTOR IN COMPLEX WITH A HYDROXAMATE INHIBITOR	3.4.24.83
1YR2	STRUCTURAL AND MECHANISTIC ANALYSIS OF TWO PROLYL ENDOPEPTIDASES: ROLE OF INTER-DOMAIN DYNAMICS IN CATALYSIS AND SPECIFICITY	3.4.21.26
1YR6	PAB0955 CRYSTAL STRUCTURE : A GTPASE IN APO FORM FROM PYROCOCCUS ABYSSI	3.6.5
1YR7	PAB0955 CRYSTAL STRUCTURE : A GTPASE IN GTP-GAMMA-S BOUND FORM FROM PYROCOCCUS ABYSSI	3.6.5
1YR8	PAB0955 CRYSTAL STRUCTURE : A GTPASE IN GTP BOUND FORM FROM PYROCOCCUS ABYSSI	3.6.5
1YR9	PAB0955 CRYSTAL STRUCTURE : A GTPASE IN GDP AND PO4 BOUND FORM FROM PYROCOCCUS ABYSSI	3.6.5
1YRA	PAB0955 CRYSTAL STRUCTURE : A GTPASE IN GDP BOUND FORM FROM PYROCOCCUS ABYSSI	3.6.5
1YRB	PAB0955 CRYSTAL STRUCTURE : A GTPASE IN GDP AND MG BOUND FORM FROM PYROCOCCUS ABYSSI	3.6.5
1YRR	CRYSTAL STRUCTURE OF THE N-ACETYLGLUCOSAMINE-6-PHOSPHATE DEACETYLASE FROM ESCHERICHIA COLI K12 AT 2.0 A RESOLUTION	3.5.1.25
1YRZ	CRYSTAL STRUCTURE OF XYLAN BETA-1,4-XYLOSIDASE FROM BACILLUS HALODURANS C-125	3.2.1.37
1YS0	CRYSTAL STRUCTURE OF THE CDC25B PHOSPHATASE CATALYTIC DOMAIN WITH THE ACTIVE SITE CYSTEINE IN THE DISULFIDE FORM	3.1.3.48
1YS1	BURKHOLDERIA CEPACIA LIPASE COMPLEXED WITH HEXYLPHOSPHONIC ACID (R)-2-METHYL-3-PHENYLPROPYL ESTER	3.1.1.3
1YS2	BURKHOLDERIA CEPACIA LIPASE COMPLEXED WITH HEXYLPHOSPHONIC ACID (S) 2-METHYL-3-PHENYLPROPYL ESTER	3.1.1.3
1YSB	YEAST CYTOSINE DEAMINASE TRIPLE MUTANT	3.5.4.1
1YSC	2.8 ANGSTROMS STRUCTURE OF YEAST SERINE CARBOXYPEPTIDASE	3.4.16.5
1YSD	YEAST CYTOSINE DEAMINASE DOUBLE MUTANT	3.5.4.1
1YSJ	CRYSTAL STRUCTURE OF BACILLUS SUBTILIS YXEP PROTEIN (APC1829), A DINUCLEAR METAL BINDING PEPTIDASE FROM M20 FAMILY	3.5.1.14 3.5.1
1YSY	NMR STRUCTURE OF THE NONSTRUCTURAL PROTEIN 7 (NSP7) FROM THE SARS CORONAVIRUS	3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
1YT3	CRYSTAL STRUCTURE OF ESCHERICHIA COLI RNASE D, AN EXORIBONUCLEASE INVOLVED IN STRUCTURED RNA PROCESSING	3.1.26.3 3.1.13.5
1YT4	CRYSTAL STRUCTURE OF TEM-76 BETA-LACTAMASE AT 1.4 ANGSTROM RESOLUTION	3.5.2.6
1YT7	CATHEPSIN K COMPLEXED WITH A CONSTRAINED KETOAMIDE INHIBITOR	3.4.22.38
1YT9	HIV PROTEASE WITH OXIMINOARYLSULFONAMIDE BOUND	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1YTA	CRYSTAL STRUCTURE OF OLIGORIBONUCLEASE, THE LONE ESSENTIAL EXORIBONUCLEASE IN ESCHERICHIA COLI	3.1
1YTG	SIV PROTEASE CRYSTALLIZED WITH PEPTIDE PRODUCT	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1YTH	SIV PROTEASE CRYSTALLIZED WITH PEPTIDE PRODUCT	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1YTI	SIV PROTEASE CRYSTALLIZED WITH PEPTIDE PRODUCT	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1YTJ	SIV PROTEASE CRYSTALLIZED WITH PEPTIDE PRODUCT	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1YTN	HYDROLASE	3.1.3.48
1YTS	A LIGAND-INDUCED CONFORMATIONAL CHANGE IN THE YERSINIA PROTEIN TYROSINE PHOSPHATASE	3.1.3.48
1YTW	YERSINIA PTPASE COMPLEXED WITH TUNGSTATE	3.1.3.48
1YU6	CRYSTAL STRUCTURE OF THE SUBTILISIN CARLSBERG:OMTKY3 COMPLEX	3.4.21.62
1YUO	OPTIMISATION OF THE SURFACE ELECTROSTATICS AS A STRATEGY FOR COLD ADAPTATION OF URACIL-DNA N-GLYCOSYLASE (UNG)FROM ATLANTIC COD (GADUS MORHUA)	3.2.2.3 3.2.2.27
1YUY	HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE GENOTYPE 2A	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
1YV2	HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE GENOTYPE 2A	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
1YV4	X-RAY STRUCTURE OF M23L ONCONASE AT 100K	3.1.27
1YV6	X-RAY STRUCTURE OF M23L ONCONASE AT 298K	3.1.27
1YV7	X-RAY STRUCTURE OF (C87S,DES103-104) ONCONASE	3.1.27
1YV9	CRYSTAL STRUCTURE OF A HAD-LIKE PHOSPHATASE FROM ENTEROCOCCUS FAECALIS V583	3.1.3
1YVF	HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE COMPLEX WITH INHIBITOR PHA-00729145	2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13
1YVG	STRUCTURAL ANALYSIS OF THE CATALYTIC DOMAIN OF TETANUS NEUROTOXIN	3.4.24.68
1YVM	E. COLI METHIONINE AMINOPEPTIDASE IN COMPLEX WITH THIABENDAZOLE	3.4.11.18
1YVS	TRIMERIC DOMAIN SWAPPED BARNASE	3.1.27
1YVW	CRYSTAL STRUCTURE OF PHOSPHORIBOSYL-ATP PYROPHOSPHOHYDROLASE FROM BACILLUS CEREUS. NESGC TARGET BCR13.	3.6.1.31
1YVX	HEPATITIS C VIRUS RNA POLYMERASE GENOTYPE 2A IN COMPLEX WITH NON- NUCLEOSIDE ANALOGUE INHIBITOR	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
1YVZ	HEPATITIS C VIRUS RNA POLYMERASE GENOTYPE 2A IN COMPLEX WITH NON- NUCLEOSIDE ANALOGUE INHIBITOR	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
1YW4	CRYSTAL STRUCTURE OF THE SUCCINYLGLUTAMATE DESUCCINYLASE FROM CHROMOBACTERIUM VIOLACEUM, NORTHEAST STRUCTURAL GENOMICS TARGET CVR22.	3.1 3.5.1.96
1YW6	CRYSTAL STRUCTURE OF SUCCINYLGLUTAMATE DESUCCINYLASE FROM ESCHERICHIA COLI, NORTHEAST STRUCTURAL GENOMICS TARGET ET72.	3.1 3.5.1.96
1YW7	H-METAP2 COMPLEXED WITH A444148	3.4.11.18
1YW8	H-METAP2 COMPLEXED WITH A751277	3.4.11.18
1YW9	H-METAP2 COMPLEXED WITH A849519	3.4.11.18
1YWO	PHOSPHOLIPASE CGAMMA1 SH3 IN COMPLEX WITH A SLP-76 MOTIF	3.1.4.11
1YWP	PHOSPHOLIPASE CGAMMA1 SH3	3.1.4.11
1YX9	EFFECT OF DIMETHYL SULPHOXIDE ON THE CRYSTAL STRUCTURE OF PORCINE PEPSIN	3.4.23.1
1YXB	CRYSTAL STRUCTURE OF PHOSPHORIBOSYL-ATP PYROPHOSPHATASE FROM STREPTOMYCES COELICOLOR. NESG TARGET RR8.	3.6.1.31
1YXH	CRYSTAL STRUCTURE OF A NOVEL PHOSPHOLIPASE A2 FROM NAJA NAJA SAGITTIFERA WITH A STRONG ANTICOAGULANT ACTIVITY	3.1.1.4
1YXI	R-STATE AMP COMPLEX REVEALS INITIAL STEPS OF THE QUATERNARY TRANSITION OF FRUCTOSE-1,6-BISPHOSPHATASE	3.1.3.11
1YXL	CRYSTAL STRUCTURE OF A NOVEL PHOSPHOLIPASE A2 FROM NAJA NAJA SAGITTIFERA AT 1.5 A RESOLUTION	3.1.1.4
1YXR	NMR STRUCTURE OF VPS4A MIT DOMAIN	3.6.4.6
1YXW	A COMMON BINDING SITE FOR DISIALYLLACTOSE AND A TRI-PEPTIDE IN THE C-FRAGMENT OF TETANUS NEUROTOXIN	3.4.24.68
1YY6	THE CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF HAUSP/USP7 COMPLEXED WITH AN EBNA1 PEPTIDE	3.1.2.15 3.4.19.12
1YYK	CRYSTAL STRUCTURE OF RNASE III FROM AQUIFEX AEOLICUS COMPLEXED WITH DOUBLE-STRANDED RNA AT 2.5-ANGSTROM RESOLUTION	3.1.26.3
1YYN	A COMMON BINDING SITE FOR DISIALYLLACTOSE AND A TRI-PEPTIDE IN THE C-FRAGMENT OF TETANUS NEUROTOXIN	3.4.24.68
1YYO	CRYSTAL STRUCTURE OF RNASE III MUTANT E110K FROM AQUIFEX AEOLICUS COMPLEXED WITH DOUBLE-STRANDED RNA AT 2.9-ANGSTROM RESOLUTION	3.1.26.3
1YYW	CRYSTAL STRUCTURE OF RNASE III FROM AQUIFEX AEOLICUS COMPLEXED WITH DOUBLE STRANDED RNA AT 2.8-ANGSTROM RESOLUTION	3.1.26.3
1YYY	TRYPSIN INHIBITORS WITH RIGID TRIPEPTIDYL ALDEHYDES	3.4.21.4
1YYZ	R-STATE AMP COMPLEX REVEALS INITIAL STEPS OF THE QUATERNARY TRANSITION OF FRUCTOSE-1,6-BISPHOSPHATASE	3.1.3.11
1YZ0	R-STATE AMP COMPLEX REVEALS INITIAL STEPS OF THE QUATERNARY TRANSITION OF FRUCTOSE-1,6-BISPHOSPHATASE	3.1.3.11
1YZ4	CRYSTAL STRUCTURE OF DUSP15	3.1.3.48 3.1.3.16
1YZ9	CRYSTAL STRUCTURE OF RNASE III MUTANT E110Q FROM AQUIFEX AEOLICUS COMPLEXED WITH DOUBLE STRANDED RNA AT 2.1-ANGSTROM RESOLUTION	3.1.26.3
1YZB	SOLUTION STRUCTURE OF THE JOSEPHIN DOMAIN OF ATAXIN-3	3.4.19.12
1YZE	CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF USP7/HAUSP.	3.1.2.15 3.4.19.12
1Z0B	CRYSTAL STRUCTURE OF A. FULGIDUS LON PROTEOLYTIC DOMAIN E506A MUTANT	3.4.21.53 3.4.21
1Z0C	CRYSTAL STRUCTURE OF A. FULGIDUS LON PROTEOLYTIC DOMAIN D508A MUTANT	3.4.21.53 3.4.21
1Z0E	CRYSTAL STRUCTURE OF A. FULGIDUS LON PROTEOLYTIC DOMAIN	3.4.21.53 3.4.21
1Z0G	CRYSTAL STRUCTURE OF A. FULGIDUS LON PROTEOLYTIC DOMAIN	3.4.21.53 3.4.21
1Z0H	N-TERMINAL HELIX REORIENTS IN RECOMBINANT C-FRAGMENT OF CLOSTRIDIUM BOTULINUM TYPE B	3.4.24.69
1Z0T	CRYSTAL STRUCTURE OF A. FULGIDUS LON PROTEOLYTIC DOMAIN	3.4.21.53 3.4.21
1Z0V	CRYSTAL STRUCTURE OF A. FULGIDUS LON PROTEOLYTIC DOMAIN	3.4.21.53 3.4.21
1Z0W	CRYSTAL STRUCTURE OF A. FULGIDUS LON PROTEOLYTIC DOMAIN AT 1.2A RESOLUTION	3.4.21.53 3.4.21
1Z12	CRYSTAL STRUCTURE OF BOVINE LOW MOLECULAR WEIGHT PTPASE COMPLEXED WITH VANADATE	3.1.3.48 3.1.3.2
1Z13	CRYSTAL STRUCTURE OF BOVINE LOW MOLECULAR WEIGHT PTPASE COMPLEXED WITH MOLYBDATE	3.1.3.48 3.1.3.2
1Z19	CRYSTAL STRUCTURE OF A LAMBDA INTEGRASE(75-356) DIMER BOUND TO A COC' CORE SITE	2.7.7 3.1
1Z1B	CRYSTAL STRUCTURE OF A LAMBDA INTEGRASE DIMER BOUND TO A COC' CORE SITE	2.7.7 3.1
1Z1G	CRYSTAL STRUCTURE OF A LAMBDA INTEGRASE TETRAMER BOUND TO A HOLLIDAY JUNCTION	2.7.7 3.1
1Z1H	HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 3	3.4.23.16
1Z1I	CRYSTAL STRUCTURE OF NATIVE SARS CLPRO	3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
1Z1J	CRYSTAL STRUCTURE OF SARS 3CLPRO C145A MUTANT	3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
1Z1L	THE CRYSTAL STRUCTURE OF THE PHOSPHODIESTERASE 2A CATALYTIC DOMAIN	3.1.4.17
1Z1R	HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 2	3.4.23.16
1Z1W	CRYSTAL STRUCTURES OF THE TRICORN INTERACTING FACOR F3 FROM THERMOPLASMA ACIDOPHILUM, A ZINC AMINOPEPTIDASE IN THREE DIFFERENT CONFORMATIONS	3.4.11
1Z2L	CRYSTAL STRUCTURE OF ALLANTOATE-AMIDOHYDROLASE FROM E.COLI K12 IN COMPLEX WITH SUBSTRATE ALLANTOATE	3.5.3 3.5.3.9
1Z32	STRUCTURE-FUNCTION RELATIONSHIPS IN HUMAN SALIVARY ALPHA-AMYLASE: ROLE OF AROMATIC RESIDUES	3.2.1.1
1Z3A	CRYSTAL STRUCTURE OF TRNA ADENOSINE DEAMINASE TADA FROM ESCHERICHIA COLI	3.5.4 3.5.4.33
1Z3I	STRUCTURE OF THE SWI2/SNF2 CHROMATIN REMODELING DOMAIN OF EUKARYOTIC RAD54	3.6.4.12
1Z3J	SOLUTION STRUCTURE OF MMP12 IN THE PRESENCE OF N-ISOBUTYL-N-4-METHOXYPHENYLSULFONYL]GLYCYL HYDROXAMIC ACID (NNGH)	3.4.24.65
1Z3L	X-RAY CRYSTAL STRUCTURE OF A MUTANT RIBONUCLEASE S (F8ANB)	3.1.27.5 4.6.1.18
1Z3M	CRYSTAL STRUCTURE OF MUTANT RIBONUCLEASE S (F8NVA)	3.1.27.5 4.6.1.18
1Z3P	X-RAY CRYSTAL STRUCTURE OF A MUTANT RIBONUCLEASE S (M13NVA)	3.1.27.5 4.6.1.18
1Z3T	STRUCTURE OF PHANEROCHAETE CHRYSOSPORIUM CELLOBIOHYDROLASE CEL7D (CBH58) IN COMPLEX WITH CELLOBIOSE	3.2.1.91 3.2.1
1Z3V	STRUCTURE OF PHANEROCHAETE CHRYSOSPORIUM CELLOBIOHYDROLASE CEL7D (CBH58) IN COMPLEX WITH LACTOSE	3.2.1.91 3.2.1
1Z3W	STRUCTURE OF PHANEROCHAETE CHRYSOSPORIUM CELLOBIOHYDROLASE CEL7D (CBH58) IN COMPLEX WITH CELLOBIOIMIDAZOLE	3.2.1.91 3.2.1
1Z4I	STRUCTURE OF THE D41N VARIANT OF THE HUMAN MITOCHONDRIAL DEOXYRIBONUCLEOTIDASE IN COMPLEX WITH DEOXYRIBOURIDINE 5'-MONOPHOSPHATE	3.1.3
1Z4J	STRUCTURE OF THE D41N VARIANT OF THE HUMAN MITOCHONDRIAL DEOXYRIBONUCLEOTIDASE IN COMPLEX WITH URIDINE 2'-MONOPHOSPHATE	3.1.3
1Z4K	STRUCTURE OF THE D41N VARIANT OF THE HUMAN MITOCHONDRIAL DEOXYRIBONUCLEOTIDASE IN COMPLEX WITH THYMIDINE 3'-MONOPHOSPHATE	3.1.3
1Z4L	STRUCTURE OF THE D41N VARIANT OF THE HUMAN MITOCHONDRIAL DEOXYRIBONUCLEOTIDASE IN COMPLEX WITH THYMIDINE 5'-MONOPHOSPHATE	3.1.3
1Z4M	STRUCTURE OF THE D41N VARIANT OF THE HUMAN MITOCHONDRIAL DEOXYRIBONUCLEOTIDASE IN COMPLEX WITH URIDINE 5'-MONOPHOSPHATE	3.1.3
1Z4P	STRUCTURE OF THE D41N VARIANT OF THE HUMAN MITOCHONDRIAL DEOXYRIBONUCLEOTIDASE IN COMPLEX WITH DEOXYRIBOGUANOSINE 5'-MONOPHOSPHATE	3.1.3
1Z4Q	STRUCTURE OF THE D41N VARIANT OF THE HUMAN MITOCHONDRIAL DEOXYRIBONUCLEOTIDASE IN COMPLEX WITH 2',3'-DIDEOXY-2',3-DIDEHYDROTHYMIDINE 5'-MONOPHOSPHATE (D4T-MP)	3.1.3
1Z4U	HEPATITIS C VIRUS NS5B RNA-DEPENDENT RNA POLYMERASE COMPLEX WITH INHIBITOR PHA-00799585	2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13
1Z55	EFFECT OF ALCOHOLS ON PROTEIN HYDRATION	3.2.1.17
1Z5G	CRYSTAL STRUCTURE OF SALMONELLA TYPHIMURIUM APHA PROTEIN	3.1.3.2
1Z5N	CRYSTAL STRUCTURE OF MTA/ADOHCY NUCLEOSIDASE GLU12GLN MUTANT COMPLEXED WITH 5-METHYLTHIORIBOSE AND ADENINE	3.2.2.9
1Z5O	CRYSTAL STRUCTURE OF MTA/ADOHCY NUCLEOSIDASE ASP197ASN MUTANT COMPLEXED WITH 5'-METHYLTHIOADENOSINE	3.2.2.9
1Z5P	CRYSTAL STRUCTURE OF MTA/ADOHCY NUCLEOSIDASE WITH A LIGAND-FREE PURINE BINDING SITE	3.2.2.9
1Z5R	CRYSTAL STRUCTURE OF ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B	3.4.17.2
1Z5U	CRYSTAL STRUCTURE OF S. TYPHIMURIUM APHA COMPLEXED WITH CYCLIC-AMP	3.1.3.2
1Z66	NMR SOLUTION STRUCTURE OF DOMAIN III OF E-PROTEIN OF TICK-BORNE LANGAT FLAVIVIRUS (NO RDC RESTRAINTS)	3.4.21.91 3.6.1.15 3.6.4.13 2.1.1.56 2.1.1.57 2.7.7.48
1Z68	CRYSTAL STRUCTURE OF HUMAN FIBROBLAST ACTIVATION PROTEIN ALPHA	3.4.21 3.4.21.26 3.4.14.5
1Z6D	RIBONUCLEASE A- IMP COMPLEX	3.1.27.5 4.6.1.18
1Z6E	FACTOR XA IN COMPLEX WITH THE INHIBITOR 1-(3'-AMINO-1,2-BENZISOXAZOL-5'-YL)-N-(4-(2'-((DIMETHYLAMINO)METHYL)-1H-IMIDAZOL-1-YL)-2-FLUOROPHENYL)-3-(TRIFLUOROMETHYL)-1H-PYRAZOLE-5-CARBOXAMIDE (RAZAXABAN; DPC906; BMS-561389)	3.4.21.6
1Z6F	CRYSTAL STRUCTURE OF PENICILLIN-BINDING PROTEIN 5 FROM E. COLI IN COMPLEX WITH A BORONIC ACID INHIBITOR	3.4.16.4 3.5.2.6
1Z6J	CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF FACTOR VIIA/TISSUE FACTOR/PYRAZINONE INHIBITOR	3.4.21.21
1Z6S	RIBONUCLEASE A- AMP COMPLEX	3.1.27.5 4.6.1.18
1Z6V	HUMAN LACTOFERRICIN	3.4.21
1Z6W	HUMAN LACTOFERRICIN	3.4.21
1Z71	THROMBIN AND P2 PYRIDINE N-OXIDE INHIBITOR COMPLEX STRUCTURE	3.4.21.5
1Z72	STRUCTURE OF A PUTATIVE TRANSCRIPTIONAL REGULATOR FROM STREPTOCOCCUS PNEUMONIAE	3.5.99.2
1Z76	CRYSTAL STRUCTURE OF AN ACIDIC PHOSPHOLIPASE A2 (BTHA-I) FROM BOTHROPS JARARACUSSU VENOM COMPLEXED WITH P-BROMOPHENACYL BROMIDE	3.1.1.4
1Z7H	2.3 ANGSTROM CRYSTAL STRUCTURE OF TETANUS NEUROTOXIN LIGHT CHAIN	3.4.24.68
1Z7K	CRYSTAL STRUCTURE OF TRYPSIN- OVOMUCOID TURKEY EGG WHITE INHIBITOR COMPLEX	3.4.21.4
1Z7S	THE CRYSTAL STRUCTURE OF COXSACKIEVIRUS A21	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1Z7Z	CRYO-EM STRUCTURE OF HUMAN COXSACKIEVIRUS A21 COMPLEXED WITH FIVE DOMAIN ICAM-1KILIFI	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1Z88	CRYSTAL STRUCTURE OF LYS154ARG MUTANT OF MATURE APHA OF S. TYPHIMURIUM	3.1.3.2
1Z8C	CRYSTAL STRUCTURE OF THE COMPLEX OF MUTANT HIV-1 PROTEASE (L63P, A71V, V82T, I84V) WITH A HYDROXYETHYLAMINE PEPTIDOMIMETIC INHIBITOR BOC-PHE-PSI[R-CH(OH)CH2NH]-PHE-GLU-PHE-NH2	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1Z8G	CRYSTAL STRUCTURE OF THE EXTRACELLULAR REGION OF THE TRANSMEMBRANE SERINE PROTEASE HEPSIN WITH COVALENTLY BOUND PREFERRED SUBSTRATE.	3.4.21 3.4.21.106
1Z8I	CRYSTAL STRUCTURE OF THE THROMBIN MUTANT G193A BOUND TO PPACK	3.4.21.5
1Z8J	CRYSTAL STRUCTURE OF THE THROMBIN MUTANT G193P BOUND TO PPACK	3.4.21.5
1Z8R	2A CYSTEINE PROTEINASE FROM HUMAN COXSACKIEVIRUS B4 (STRAIN JVB / BENSCHOTEN / NEW YORK / 51)	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
1Z8T	STRUCTURE OF MUTANT PYRROLIDONE CARBOXYL PEPTIDASE (E192Q) FROM A HYPERTHERMOPHILE, PYROCOCCUS FURIOSUS	3.4.19.3
1Z8W	STRUCTURE OF MUTANT PYRROLIDONE CARBOXYL PEPTIDASE (E192I) FROM A HYPERTHERMOPHILE, PYROCOCCUS FURIOSUS	3.4.19.3
1Z8X	STRUCTURE OF MUTANT PYRROLIDONE CARBOXYL PEPTIDASE (E192V) FROM A HYPERTHERMOPHILE, PYROCOCCUS FURIOSUS	3.4.19.3
1Z96	CRYSTAL STRUCTURE OF THE MUD1 UBA DOMAIN	3.4.23
1Z9G	CRYSTAL STRUCTURE ANALYSIS OF THERMOLYSIN COMPLEXED WITH THE INHIBITOR (R)-RETRO-THIORPHAN	3.4.24.27
1Z9T	CRYSTAL STRUCTURE OF A PUTATIVE LACCASE (YFIH) FROM ESCHERICHIA COLI AT 1.54 A RESOLUTION	2.4.2.1 3.5.4.4 1.10.3 2.4.2.28
1ZAB	CRYSTAL STRUCTURE OF MOUSE CYTIDINE DEAMINASE COMPLEXED WITH 3-DEAZAURIDINE	3.5.4.5
1ZAP	SECRETED ASPARTIC PROTEASE FROM C. ALBICANS	3.4.23.24
1ZB7	CRYSTAL STRUCTURE OF BOTULINUM NEUROTOXIN TYPE G LIGHT CHAIN	3.4.24.69
1ZBA	FOOT-AND-MOUTH DISEASE VIRUS SEROTYPE A1061 COMPLEXED WITH OLIGOSACCHARIDE RECEPTOR.	3.4.22.46 3.6.1.15 3.4.22.28 2.7.7.48
1ZBE	FOOT-AND MOUTH DISEASE VIRUS SEROTYPE A1061	3.4.22.46 3.6.1.15 3.4.22.28 2.7.7.48
1ZBF	CRYSTAL STRUCTURE OF B. HALODURANS RNASE H CATALYTIC DOMAIN MUTANT D132N	3.1.26.4
1ZBG	CRYSTAL STRUCTURE OF A COMPLEX OF MUTANT HIV-1 PROTEASE (A71V, V82T, I84V) WITH A HYDROXYETHYLAMINE PEPTIDOMIMETIC INHIBITOR BOC-PHE-PSI[R-CH(OH)CH2NH]-PHE-GLU-PHE-NH2	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1ZBH	3'-END SPECIFIC RECOGNITION OF HISTONE MRNA STEM-LOOP BY 3'-EXONUCLEASE	3.1
1ZBI	BACILLUS HALODURANS RNASE H CATALYTIC DOMAIN MUTANT D132N IN COMPLEX WITH 12-MER RNA/DNA HYBRID	3.1.26.4
1ZBL	BACILLUS HALODURANS RNASE H CATALYTIC DOMAIN MUTANT D192N IN COMPLEX WITH 12-MER RNA/DNA HYBRID	3.1.26.4
1ZC0	CRYSTAL STRUCTURE OF HUMAN HEMATOPOIETIC TYROSINE PHOSPHATASE (HEPTP) CATALYTIC DOMAIN	3.1.3.48
1ZC2	CRYSTAL STRUCTURE OF PLASMID-ENCODED CLASS C BETA-LACTAMASE CMY-2 COMPLEXED WITH CITRATE MOLECULE	3.5.2.6
1ZC3	CRYSTAL STRUCTURE OF THE RAL-BINDING DOMAIN OF EXO84 IN COMPLEX WITH THE ACTIVE RALA	3.6.5.2
1ZC4	CRYSTAL STRUCTURE OF THE RAL-BINDING DOMAIN OF EXO84 IN COMPLEX WITH THE ACTIVE RALA	3.6.5.2
1ZCF	L-ASPARAGINASE FROM ERWINIA CAROTOVORA	3.5.1.1
1ZCK	NATIVE STRUCTURE PRL-1 (PTP4A1)	3.1.3.48
1ZCM	HUMAN CALPAIN PROTEASE CORE INHIBITED BY ZLLYCH2F	3.4.22.52
1ZCZ	CRYSTAL STRUCTURE OF PHOSPHORIBOSYLAMINOIMIDAZOLECARBOXAMIDE FORMYLTRANSFERASE / IMP CYCLOHYDROLASE (TM1249) FROM THERMOTOGA MARITIMA AT 1.88 A RESOLUTION	2.1.2.3 3.5.4.10
1ZD2	HUMAN SOLUBLE EPOXIDE HYDROLASE 4-(3-CYCLOHEXYLURIEDO)-ETHANOIC ACID COMPLEX	3.3.2.3 3.3.2.10 3.1.3.76
1ZD3	HUMAN SOLUBLE EPOXIDE HYDROLASE 4-(3-CYCLOHEXYLURIEDO)-BUTYRIC ACID COMPLEX	3.3.2.3 3.3.2.10 3.1.3.76
1ZD4	HUMAN SOLUBLE EPOXIDE HYDROLASE 4-(3-CYCLOHEXYLURIEDO)-HEXANOIC ACID COMPLEX	3.3.2.3 3.3.2.10 3.1.3.76
1ZD5	HUMAN SOLUBLE EPOXIDE HYDROLASE 4-(3-CYCLOHEXYLURIEDO)-HEPTANOIC ACID COMPLEX	3.3.2.3 3.3.2.10 3.1.3.76
1ZDP	CRYSTAL STRUCTURE ANALYSIS OF THERMOLYSIN COMPLEXED WITH THE INHIBITOR (S)-THIORPHAN	3.4.24.27
1ZEB	X-RAY STRUCTURE OF ALKALINE PHOSPHATASE FROM HUMAN PLACENTA IN COMPLEX WITH 5'-AMP	3.1.3.1
1ZED	ALKALINE PHOSPHATASE FROM HUMAN PLACENTA IN COMPLEX WITH P-NITROPHENYL-PHOSPHONATE	3.1.3.1
1ZEF	STRUCTURE OF ALKALINE PHOSPHATASE FROM HUMAN PLACENTA IN COMPLEX WITH ITS UNCOMPETITIVE INHIBITOR L-PHE	3.1.3.1
1ZG4	TEM1 BETA LACTAMASE	3.5.2.6
1ZG6	TEM1 BETA LACTAMASE MUTANT S70G	3.5.2.6
1ZG7	CRYSTAL STRUCTURE OF 2-(5-{[AMINO(IMINO)METHYL]AMINO}-2-CHLOROPHENYL)-3-SULFANYLPROPANOIC ACID BOUND TO ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B	3.4.17.2
1ZG8	CRYSTAL STRUCTURE OF (R)-2-(3-{[AMINO(IMINO)METHYL]AMINO}PHENYL)-3-SULFANYLPROPANOIC ACID BOUND TO ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B	3.4.17.2
1ZG9	CRYSTAL STRUCTURE OF 5-{[AMINO(IMINO)METHYL]AMINO}-2-(SULFANYLMETHYL)PENTANOIC ACID BOUND TO ACTIVATED PORCINE PANCREATIC CARBOXYPEPTIDASE B	3.4.17.2
1ZGB	CRYSTAL STRUCTURE OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE IN COMPLEX WITH AN (R)-TACRINE(10)-HUPYRIDONE INHIBITOR.	3.1.1.7
1ZGC	CRYSTAL STRUCTURE OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE IN COMPLEX WITH AN (RS)-TACRINE(10)-HUPYRIDONE INHIBITOR.	3.1.1.7
1ZGG	SOLUTION STRUCTURE OF A LOW MOLECULAR WEIGHT PROTEIN TYROSINE PHOSPHATASE FROM BACILLUS SUBTILIS	3.1.3.48 3.9.1.2
1ZGI	THROMBIN IN COMPLEX WITH AN OXAZOLOPYRIDINE INHIBITOR 21	3.4.21.5
1ZGV	THROMBIN IN COMPLEX WITH AN OXAZOLOPYRIDINE INHIBITOR 2	3.4.21.5
1ZGX	CRYSTAL STRUCTURE OF RIBONUCLEASE MUTANT	3.1.27.3 4.6.1.24
1ZH1	STRUCTURE OF THE ZINC-BINDING DOMAIN OF HCV NS5A	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
1ZHM	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF THE COAGULATION FACTOR XIA IN COMPLEX WITH BENZAMIDINE (S434A-T475A-K437 MUTANT)	3.4.21.27
1ZHP	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH BENZAMIDINE (S434A-T475A-K505 MUTANT)	3.4.21.27
1ZHQ	CRYSTAL STRUCTURE OF APO MVL	3.2.1
1ZHR	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH BENZAMIDINE (S434A-T475A-C482S-K437A MUTANT)	3.4.21.27
1ZHS	CRYSTAL STRUCTURE OF MVL BOUND TO MAN3GLCNAC2	3.2.1
1ZI6	CRYSTAL STRUCTURE ANALYSIS OF THE DIENELACTONE HYDROLASE (C123S) MUTANT- 1.7 A	3.1.1.45
1ZI8	CRYSTAL STRUCTURE ANALYSIS OF THE DIENELACTONE HYDROLASE MUTANT(E36D, C123S, A134S, S208G, A229V, K234R)- 1.4 A	3.1.1.45
1ZI9	CRYSTAL STRUCTURE ANALYSIS OF THE DIENELACTONE HYDROLASE (E36D, C123S) MUTANT- 1.5 A	3.1.1.45
1ZIC	CRYSTAL STRUCTURE ANALYSIS OF THE DIENELACTONE HYDROLASE (C123S, R206A) MUTANT- 1.7 A	3.1.1.45
1ZIV	CATALYTIC DOMAIN OF HUMAN CALPAIN-9	3.4.22
1ZIX	CRYSTAL STRUCTURE ANALYSIS OF THE DIENELACTONE HYDROLASE MUTANT (E36D, R105H, C123S, G211D, K234N)- 1.8 A	3.1.1.45
1ZIY	CRYSTAL STRUCTURE ANALYSIS OF THE DIENELACTONE HYDROLASE MUTANT (C123S) BOUND WITH THE PMS MOIETY OF THE PROTEASE INHIBITOR, PHENYLMETHYLSULFONYL FLUORIDE (PMSF)- 1.9 A	3.1.1.45
1ZJ4	CRYSTAL STRUCTURE ANALYSIS OF THE DIENELACTONE HYDROLASE MUTANT (E36D, C123S) BOUND WITH THE PMS MOIETY OF THE PROTEASE INHIBITOR, PHENYLMETHYLSULFONYL FLUORIDE (PMSF)- 1.7 A	3.1.1.45
1ZJ5	CRYSTAL STRUCTURE ANALYSIS OF THE DIENELACTONE HYDROLASE MUTANT (E36D, C123S, A134S, S208G, A229V, K234R) BOUND WITH THE PMS MOIETY OF THE PROTEASE INHIBITOR, PHENYLMETHYLSULFONYL FLUORIDE (PMSF)- 1.7 A	3.1.1.45
1ZJ7	CRYSTAL STRUCTURE OF A COMPLEX OF MUTANT HIV-1 PROTEASE (A71V, V82T, I84V) WITH A HYDROXYETHYLAMINE PEPTIDOMIMETIC INHIBITOR BOC-PHE-PSI[S-CH(OH)CH2NH]-PHE-GLU-PHE-NH2	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1ZJC	AMINOPEPTIDASE S FROM S. AUREUS	3.4.11
1ZJD	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH KUNITZ PROTEASE INHIBITOR DOMAIN OF PROTEASE NEXIN II	3.4.21.27
1ZJK	CRYSTAL STRUCTURE OF THE ZYMOGEN CATALYTIC REGION OF HUMAN MASP-2	3.4.21 3.4.21.104
1ZKJ	STRUCTURAL BASIS FOR THE EXTENDED SUBSTRATE SPECTRUM OF CMY-10, A PLASMID-ENCODED CLASS C BETA-LACTAMASE	3.5.2.6
1ZKL	MULTIPLE DETERMINANTS FOR INHIBITOR SELECTIVITY OF CYCLIC NUCLEOTIDE PHOSPHODIESTERASES	3.1.4.17 3.1.4.53
1ZKN	STRUCTURE OF PDE4D2-IBMX	3.1.4.17 3.1.4.53
1ZKW	CRYSTAL STRUCTURE OF ARG347ALA MUTANT OF BOTULINUM NEUROTOXIN E CATALYTIC DOMAIN	3.4.24.69
1ZKX	CRYSTAL STRUCTURE OF GLU158ALA/THR159ALA/ASN160ALA- A TRIPLE MUTANT OF CLOSTRIDIUM BOTULINUM NEUROTOXIN E CATALYTIC DOMAIN	3.4.24.69
1ZL0	STRUCTURE OF PROTEIN OF UNKNOWN FUNCTION PA5198 FROM PSEUDOMONAS AERUGINOSA	3.4.17.13
1ZL5	CRYSTAL STRUCTURE OF GLU335GLN MUTANT OF CLOSTRIDIUM BOTULINUM NEUROTOXIN E CATALYTIC DOMAIN	3.4.24.69
1ZL6	CRYSTAL STRUCTURE OF TYR350ALA MUTANT OF CLOSTRIDIUM BOTULINUM NEUROTOXIN E CATALYTIC DOMAIN	3.4.24.69
1ZL7	CRYSTAL STRUCTURE OF CATALYTICALLY-ACTIVE PHOSPHOLIPASE A2 WITH BOUND CALCIUM	3.1.1.4
1ZLB	CRYSTAL STRUCTURE OF CATALYTICALLY-ACTIVE PHOSPHOLIPASE A2 IN THE ABSENCE OF CALCIUM	3.1.1.4
1ZLF	CRYSTAL STRUCTURE OF A COMPLEX OF MUTANT HIV-1 PROTEASE (A71V, V82T, I84V) WITH A HYDROXYETHYLAMINE PEPTIDOMIMETIC INHIBITOR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1ZLH	CRYSTAL STRUCTURE OF THE TICK CARBOXYPEPTIDASE INHIBITOR IN COMPLEX WITH BOVINE CARBOXYPEPTIDASE A	3.4.17.1
1ZLI	CRYSTAL STRUCTURE OF THE TICK CARBOXYPEPTIDASE INHIBITOR IN COMPLEX WITH HUMAN CARBOXYPEPTIDASE B	3.4.17.2
1ZLP	PETAL DEATH PROTEIN PSR132 WITH CYSTEINE-LINKED GLUTARALDEHYDE FORMING A THIOHEMIACETAL ADDUCT	4.1.3 3.7.1.1 4.1.3.22
1ZLQ	CRYSTALLOGRAPHIC AND SPECTROSCOPIC EVIDENCE FOR HIGH AFFINITY BINDING OF FE EDTA (H2O)- TO THE PERIPLASMIC NICKEL TRANSPORTER NIKA	3.6.3.24
1ZLR	FACTOR XI CATALYTIC DOMAIN COMPLEXED WITH 2-GUANIDINO-1-(4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL)ETHYL NICOTINATE	3.4.21.27
1ZM1	CRYSTAL STRUCTURES OF COMPLEX F. SUCCINOGENES 1,3-1,4-BETA-D-GLUCANASE AND BETA-1,3-1,4-CELLOTRIOSE	3.2.1.73
1ZM6	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BEWEEN A GROUP I PHOSPHOLIPASE A2 AND DESIGNED PENTA PEPTIDE LEU-ALA-ILE-TYR-SER AT 2.6A RESOLUTION	3.1.1.4
1ZM8	APO CRYSTAL STRUCTURE OF NUCLEASE A FROM ANABAENA SP.	3.1.30
1ZMJ	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF FACTOR XI IN COMPLEX WITH 4-(GUANIDINOMETHYL)-PHENYLBORONIC ACID	3.4.21.27
1ZML	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF FACTOR XI IN COMPLEX WITH (R)-1-(4-(4-(HYDROXYMETHYL)-1,3,2-DIOXABOROLAN-2-YL)PHENETHYL)GUANIDINE	3.4.21.27
1ZMN	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH (R)-1-(4-(4-(HYDROXYMETHYL)-1,3,2-DIOXABOROLAN-2-YL)PHENYL)GUANIDINE	3.4.21.27
1ZN3	CRYSTAL STRUCTURE OF GLU335ALA MUTANT OF CLOSTRIDIUM BOTULINUM NEUROTOXIN TYPE E	3.4.24.69
1ZN6	X-RAY CRYSTAL STRUCTURE OF PROTEIN Q7WLM8 FROM BORDETELLA BRONCHISEPTICA. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET BOR19.	3.4
1ZNB	METALLO-BETA-LACTAMASE	3.5.2.6
1ZNO	CRYSTAL STRUCTURE OF VC702 FROM VIBRIO CHOLERAE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET: VCP1	3.6.1.73
1ZNS	CRYSTAL STRUCTURE OF N-COLE7/12-BP DNA/ZN COMPLEX	3.1
1ZOI	CRYSTAL STRUCTURE OF A STEREOSELECTIVE ESTERASE FROM PSEUDOMONAS PUTIDA IFO12996	3.1
1ZOM	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH A PEPTIDOMIMETIC INHIBITOR	3.4.21.27
1ZOS	STRUCTURE OF 5'-METHYLTHIONADENOSINE/S-ADENOSYLHOMOCYSTEINE NUCLEOSIDASE FROM S. PNEUMONIAE WITH A TRANSITION-STATE INHIBITOR MT-IMMA	3.2.2.16 3.2.2.9
1ZP5	CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MMP-8 AND A N-HYDROXYUREA INHIBITOR	3.4.24.34
1ZP7	THE STRUCTURE OF BACILLUS SUBTILIS RECU HOLLIDAY JUNCTION RESOLVASE AND ITS ROLE IN SUBSTRATE SELECTION AND SEQUENCE SPECIFIC CLEAVAGE.	3.1.22.4
1ZP8	HIV PROTEASE WITH INHIBITOR AB-2	3.4.23.16
1ZPA	HIV PROTEASE WITH SCRIPPS AB-3 INHIBITOR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1ZPB	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH 4-METHYL-PENTANOIC ACID {1-[4-GUANIDINO-1-(THIAZOLE-2-CARBONYL)-BUTYLCARBAMOYL]-2-METHYL-PROPYL}-AMIDE	3.4.21.27
1ZPC	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH 2-[2-(3-CHLORO-PHENYL)-2-HYDROXY-ACETYLAMINO]-N-[4-GUANIDINO-1-(THIAZOLE-2-CARBONYL)-BUTYL]-3-METHYL-BUTYRAMIDE	3.4.21.27
1ZPE	ARGINASE I COVALENTLY MODIFIED WITH BUTYLAMINE AT Q19C	3.5.3.1
1ZPG	ARGINASE I COVALENTLY MODIFIED WITH PROPYLAMINE AT Q19C	3.5.3.1
1ZPK	CRYSTAL STRUCTURE OF THE COMPLEX OF MUTANT HIV-1 PROTEASE (A71V, V82T, I84V) WITH A HYDROXYETHYLAMINE PEPTIDOMIMETIC INHIBITOR BOC-PHE-PSI[R-CH(OH)CH2NH]-PHE-GLU-PHE-NH2	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1ZPS	CRYSTAL STRUCTURE OF METHANOBACTERIUM THERMOAUTOTROPHICUM PHOSPHORIBOSYL-AMP CYCLOHYDROLASE HISI	3.5.4.19
1ZPW	CRYSTAL STRUCTURE OF A HYPOTHETICAL PROTEIN TT1823 FROM THERMUS THERMOPHILUS	3.1
1ZPZ	FACTOR XI CATALYTIC DOMAIN COMPLEXED WITH N-((R)-1-(4-BROMOPHENYL)ETHYL)UREA-ASN-VAL-ARG-ALPHA-KETOTHIAZOLE	3.4.21.27
1ZR0	CRYSTAL STRUCTURE OF KUNITZ DOMAIN 1 OF TISSUE FACTOR PATHWAY INHIBITOR-2 WITH BOVINE TRYPSIN	3.4.21.4
1ZR8	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN GROUP II PHOSPHOLIPASE A2 AND A PLANT ALKALOID AJMALINE AT 2.0A RESOLUTION	3.1.1.4
1ZRB	THROMBIN IN COMPLEX WITH AN AZAFLUORENYL INHIBITOR 23B	3.4.21.5
1ZRK	FACTOR XI COMPLEXED WITH 3-HYDROXYPROPYL 3-(7-AMIDINONAPHTHALENE-1-CARBOXAMIDO)BENZENESULFONATE	3.4.21.27
1ZRM	CRYSTAL STRUCTURE OF THE REACTION INTERMEDIATE OF L-2-HALOACID DEHALOGENASE WITH 2-CHLORO-N-BUTYRATE	3.8.1.2
1ZRN	INTERMEDIATE STRUCTURE OF L-2-HALOACID DEHALOGENASE WITH MONOCHLOROACETATE	3.8.1.2
1ZRS	WILD-TYPE LD-CARBOXYPEPTIDASE	3.4.17.13
1ZS0	CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MMP-8 AND A PHOSPHONATE INHIBITOR (S-ENANTIOMER)	3.4.24.34
1ZS9	CRYSTAL STRUCTURE OF HUMAN ENOLASE-PHOSPHATASE E1	3.1.3.77
1ZSF	CRYSTAL STRUCTURE OF COMPLEX OF A HYDROXYETHYLAMINE INHIBITOR WITH HIV-1 PROTEASE AT 2.0A RESOLUTION	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1ZSJ	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH N-(7-CARBAMIMIDOYL-NAPHTHALEN-1-YL)-3-HYDROXY-2-METHYL-BENZAMIDE	3.4.21.27
1ZSK	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH 6-CARBAMIMIDOYL-4-(3-HYDROXY-2-METHYL-BENZOYLAMINO)-NAPHTHALENE-2-CARBOXYLIC ACID METHYL ESTER	3.4.21.27
1ZSL	FACTOR XI COMPLEXED WITH A PYRIMIDINONE INHIBITOR	3.4.21.27
1ZSR	CRYSTAL STRUCTURE OF WILD TYPE HIV-1 PROTEASE (BRU ISOLATE) WITH A HYDROXYETHYLAMINE PEPTIDOMIMETIC INHIBITOR BOC-PHE-PSI[S-CH(OH)CH2NH]-PHE-GLU-PHE-NH2	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1ZTJ	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH 2-(5-BENZYLAMINO-2-METHYLSULFANYL-6-OXO-6H-PYRIMIDIN-1-YL)-N-[4-GUANIDINO-1-(THIAZOLE-2-CARBONYL)-BUTYL]-ACETAMIDE	3.4.21.27
1ZTK	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH 2-(5-AMINO-6-OXO-2-M-TOLYL-6H-PYRIMIDIN-1-YL)-N-[4-GUANIDINO-1-(THIAZOLE-2-CARBONYL)-BUTYL]-ACETAMIDE	3.4.21.27
1ZTL	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF COAGULATION FACTOR XI IN COMPLEX WITH N-[4-GUANIDINO-1-(THIAZOLE-2-CARBONYL)-BUTYL]-2-{6-OXO-5-[(QUINOLIN-8-YLMETHYL)-AMINO]-2-M-TOLYL-6H-PYRIMIDIN-1-YL}-ACETAMIDE	3.4.21.27
1ZTQ	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF MMP-13 COMPLEXED WITH WAY-033	3.4.24
1ZTT	NETROPSIN BOUND TO D(CTTAATTCGAATTAAG) IN COMPLEX WITH MMLV RT CATALYTIC FRAGMENT	2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1
1ZTW	D(CTTAATTCGAATTAAG) COMPLEXED WITH MOLONEY MURINE LEUKEMIA VIRUS REVERSE TRANSCRIPTASE CATALYTIC FRAGMENT	2.7.7.49 3.4.23 2.7.7.7 3.1.26.4 2.7.7 3.1
1ZTZ	CRYSTAL STRUCTURE OF HIV PROTEASE- METALLACARBORANE COMPLEX	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
1ZUR	CRYSTAL STRUCTURE OF SPIN LABELED T4 LYSOZYME (V131R1F)	3.2.1.17
1ZVM	CRYSTAL STRUCTURE OF HUMAN CD38: CYCLIC-ADP-RIBOSYL SYNTHETASE/NAD+ GLYCOHYDROLASE	3.2.2.5 3.2.2.6 2.4.99.20
1ZVQ	STRUCTURE OF THE Q61G MUTANT OF RAS IN THE GDP-BOUND FORM	3.6.5.2
1ZVR	CRYSTAL STRUCTURE OF MTMR2 IN COMPLEX WITH PHOSPHATIDYLINOSITOL 3,5-BISPHOSPHATE	3.1.3 3.1.3.95 3.1.3.64
1ZVX	CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN MMP-8 AND A PHOSPHONATE INHIBITOR (R-ENANTIOMER)	3.4.24.34
1ZW6	CRYSTAL STRUCTURE OF THE GTP-BOUND FORM OF RASQ61G	3.6.5.2
1ZWN	CRYSTAL STRUCTURE OF SPIN LABELED T4 LYSOZYME (V131R1B)	3.2.1.17
1ZWP	THE ATOMIC RESOLUTION CRYSTAL STRUCTURE OF THE PHOSPHOLIPASE A2 (PLA2) COMPLEX WITH NIMESULIDE REVEALS ITS WEAKER BINDING TO PLA2	3.1.1.4
1ZWX	CRYSTAL STRUCTURE OF SMCL	3.1.4.12
1ZWY	CRYSTAL STRUCTURE OF PROTEIN VC0702 FROM VIBRIO CHOLERAE	3.6.1.73
1ZXC	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TNF-ALPHA CONVERTING ENZYME (TACE) WITH INHIBITOR	3.4.24.86
1ZXV	X-RAY CRYSTAL STRUCTURE OF THE ANTHRAX LETHAL FACTOR BOUND TO A SMALL MOLECULE INHIBITOR, BI-MFM3, 3-{5-[5-(4-CHLORO-PHENYL)-FURAN-2-YLMETHYLENE]-4-OXO-2-THIOXO-THIAZOLIDIN-3-YL}-PROPIONIC ACID.	3.4.24.83
1ZXZ	X-RAY STRUCTURE OF PEPTIDE DEFORMYLASE FROM ARABIDOPSIS THALIANA (ATPDF1A); CRYSTALS GROWN IN PEG-5000 MME AS PRECIPITANT	3.5.1.88
1ZY0	X-RAY STRUCTURE OF PEPTIDE DEFORMYLASE FROM ARABIDOPSIS THALIANA (ATPDF1A); CRYSTALS GROWN IN PEG-6000	3.5.1.88
1ZY1	X-RAY STRUCTURE OF PEPTIDE DEFORMYLASE FROM ARABIDOPSIS THALIANA (ATPDF1A) IN COMPLEX WITH MET-ALA-SER	3.5.1.88
1ZY7	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF AN ADENOSINE DEAMINASE THAT ACTS ON RNA (HADAR2) BOUND TO INOSITOL HEXAKISPHOSPHATE (IHP)	3.5.4.37
1ZY9	CRYSTAL STRUCTURE OF ALPHA-GALACTOSIDASE (EC 3.2.1.22) (MELIBIASE) (TM1192) FROM THERMOTOGA MARITIMA AT 2.34 A RESOLUTION	3.2.1.22
1ZYO	CRYSTAL STRUCTURE OF THE SERINE PROTEASE DOMAIN OF SESBANIA MOSAIC VIRUS POLYPROTEIN	3.4.21.19
1ZYQ	T7 DNA POLYMERASE IN COMPLEX WITH 8OG AND INCOMING DDATP	2.7.7.7 3.1.11
1ZYT	CRYSTAL STRUCTURE OF SPIN LABELED T4 LYSOZYME (A82R1)	3.2.1.17
1ZYX	CRYSTAL STRUCTURE OF THE COMPLEX OF A GROUP IIA PHOSPHOLIPASE A2 WITH A SYNTHETIC ANTI-INFLAMMATORY AGENT LICOFELONE AT 1.9A RESOLUTION	3.1.1.4
1ZZ0	CRYSTAL STRUCTURE OF A HDAC-LIKE PROTEIN WITH ACETATE BOUND	3.5.1
1ZZ1	CRYSTAL STRUCTURE OF A HDAC-LIKE PROTEIN WITH SAHA BOUND	3.5.1
1ZZ3	CRYSTAL STRUCTURE OF A HDAC-LIKE PROTEIN WITH CYPX BOUND	3.5.1
1ZZM	CRYSTAL STRUCTURE OF YJJV, TATD HOMOLOG FROM ESCHERICHIA COLI K12, AT 1.8 A RESOLUTION	3.1.21 3.1
1ZZW	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN MAP KINASE PHOSPHATASE 5	3.1.3.48 3.1.3.16
1ZZZ	TRYPSIN INHIBITORS WITH RIGID TRIPEPTIDYL ALDEHYDES	3.4.21.4
200L	THERMODYNAMIC AND STRUCTURAL COMPENSATION IN SIZE-SWITCH" CORE-REPACKING VARIANTS OF T4 LYSOZYME"	3.2.1.17
201L	HOW AMINO-ACID INSERTIONS ARE ALLOWED IN AN ALPHA-HELIX OF T4 LYSOZYME	3.2.1.17
205L	HOW AMINO-ACID INSERTIONS ARE ALLOWED IN AN ALPHA-HELIX OF T4 LYSOZYME	3.2.1.17
206L	PHAGE T4 LYSOZYME	3.2.1.17
207L	MUTANT HUMAN LYSOZYME C77A	3.2.1.17
208L	MUTANT HUMAN LYSOZYME C77A	3.2.1.17
209L	PROTEIN STRUCTURE PLASTICITY EXEMPLIFIED BY INSERTION AND DELETION MUTANTS IN T4 LYSOZYME	3.2.1.17
210L	PROTEIN STRUCTURE PLASTICITY EXEMPLIFIED BY INSERTION AND DELETION MUTANTS IN T4 LYSOZYME	3.2.1.17
211L	PROTEIN STRUCTURE PLASTICITY EXEMPLIFIED BY INSERTION AND DELETION MUTANTS IN T4 LYSOZYME	3.2.1.17
212L	PROTEIN STRUCTURE PLASTICITY EXEMPLIFIED BY INSERTION AND DELETION MUTANTS IN T4 LYSOZYME	3.2.1.17
213L	PROTEIN STRUCTURE PLASTICITY EXEMPLIFIED BY INSERTION AND DELETION MUTANTS IN T4 LYSOZYME	3.2.1.17
214L	PROTEIN STRUCTURE PLASTICITY EXEMPLIFIED BY INSERTION AND DELETION MUTANTS IN T4 LYSOZYME	3.2.1.17
215L	PROTEIN STRUCTURE PLASTICITY EXEMPLIFIED BY INSERTION AND DELETION MUTANTS IN T4 LYSOZYME	3.2.1.17
216L	STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME	3.2.1.17
217L	STRUCTURAL BASIS OF ALPHA-HELIX PROPENSITY AT TWO SITES IN T4 LYSOZYME	3.2.1.17
218L	PROTEIN STRUCTURE PLASTICITY EXEMPLIFIED BY INSERTION AND DELETION MUTANTS IN T4 LYSOZYME	3.2.1.17
219L	PROTEIN STRUCTURE PLASTICITY EXEMPLIFIED BY INSERTION AND DELETION MUTANTS IN T4 LYSOZYME	3.2.1.17
220L	GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS	3.2.1.17
221L	THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME	3.2.1.17
221P	THREE-DIMENSIONAL STRUCTURES OF H-RAS P21 MUTANTS: MOLECULAR BASIS FOR THEIR INABILITY TO FUNCTION AS SIGNAL SWITCH MOLECULES	3.6.5.2
222L	GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS	3.2.1.17
223L	GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS	3.2.1.17
224L	THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME	3.2.1.17
225L	GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS	3.2.1.17
226L	GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS	3.2.1.17
227L	GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS	3.2.1.17
228L	GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS	3.2.1.17
229L	GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS	3.2.1.17
230L	T4 LYSOZYME MUTANT M6L	3.2.1.17
231L	T4 LYSOZYME MUTANT M106K	3.2.1.17
232L	T4 LYSOZYME MUTANT M120K	3.2.1.17
233L	T4 LYSOZYME MUTANT M120L	3.2.1.17
234L	T4 LYSOZYME MUTANT M106L	3.2.1.17
235L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
236L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
237L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
238L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
239L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
240L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
241L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
242L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
243L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
244L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
245L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
246L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
247L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
248L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
249L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
250L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
251L	THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT	3.2.1.17
252L	GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS	3.2.1.17
253L	LYSOZYME	3.2.1.17
254L	LYSOZYME	3.2.1.17
255L	HYDROLASE	3.2.1.17
256L	BACTERIOPHAGE T4 LYSOZYME	3.2.1.17
257L	AN ADAPTABLE METAL-BINDING SITE ENGINEERED INTO T4 LYSOZYME	3.2.1.17
258L	AN ADAPTABLE METAL-BINDING SITE ENGINEERED INTO T4 LYSOZYME	3.2.1.17
259L	AN ADAPTABLE METAL-BINDING SITE ENGINEERED INTO T4 LYSOZYME	3.2.1.17
260L	AN ADAPTABLE METAL-BINDING SITE ENGINEERED INTO T4 LYSOZYME	3.2.1.17
261L	STRUCTURAL CHARACTERISATION OF AN ENGINEERED TANDEM REPEAT CONTRASTS THE IMPORTANCE OF CONTEXT AND SEQUENCE IN PROTEIN FOLDING	3.2.1.17
262L	STRUCTURAL CHARACTERISATION OF AN ENGINEERED TANDEM REPEAT CONTRASTS THE IMPORTANCE OF CONTEXT AND SEQUENCE IN PROTEIN FOLDING	3.2.1.17
2A00	THE SOLUTION STRUCTURE OF THE AMP-PNP BOUND NUCLEOTIDE BINDING DOMAIN OF KDPB	3.6.3.12 7.2.2.6
2A0I	F FACTOR TRAI RELAXASE DOMAIN BOUND TO F ORIT SINGLE-STRANDED DNA	3.6.1 5.6.2.1 3.6.4.12
2A0M	ARGINASE SUPERFAMILY PROTEIN FROM TRYPANOSOMA CRUZI	3.5.3.8
2A0Q	STRUCTURE OF THROMBIN IN 400 MM POTASSIUM CHLORIDE	3.4.21.5
2A11	CRYSTAL STRUCTURE OF NUCLEASE DOMAIN OF RIBONUCLASE III FROM MYCOBACTERIUM TUBERCULOSIS	3.1.26.3
2A1D	STAPHYLOCOAGULASE BOUND TO BOVINE THROMBIN	3.4.21.5
2A1E	HIGH RESOLUTION STRUCTURE OF HIV-1 PR WITH TS-126	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2A1J	CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THE C-TERMINAL DOMAINS OF HUMAN XPF AND ERCC1	3.1
2A1R	CRYSTAL STRUCTURE OF PARN NUCLEASE DOMAIN	3.1.13.4
2A1S	CRYSTAL STRUCTURE OF NATIVE PARN NUCLEASE DOMAIN	3.1.13.4
2A29	THE SOLUTION STRUCTURE OF THE AMP-PNP BOUND NUCLEOTIDE BINDING DOMAIN OF KDPB	3.6.3.12 7.2.2.6
2A2K	CRYSTAL STRUCTURE OF AN ACTIVE SITE MUTANT, C473S, OF CDC25B PHOSPHATASE CATALYTIC DOMAIN	3.1.3.48
2A2Q	COMPLEX OF ACTIVE-SITE INHIBITED HUMAN COAGULATION FACTOR VIIA WITH HUMAN SOLUBLE TISSUE FACTOR IN THE PRESENCE OF CA2+, MG2+, NA+, AND ZN2+	3.4.21.21
2A2X	ORALLY ACTIVE THROMBIN INHIBITORS IN COMPLEX WITH THROMBIN INH12	3.4.21.5
2A31	TRYPSIN IN COMPLEX WITH BORATE	3.4.21.4
2A32	TRYPSIN IN COMPLEX WITH BENZENE BORONIC ACID	3.4.21.4
2A33	X-RAY STRUCTURE OF A LYSINE DECARBOXYLASE-LIKE PROTEIN FROM ARABIDOPSIS THALIANA GENE AT2G37210	3.2.2
2A39	HUMICOLA INSOLENS ENDOCELLULASE EGI NATIVE STRUCTURE	3.2.1.4
2A3A	CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS CHITINASE B1 IN COMPLEX WITH THEOPHYLLINE	3.2.1.14
2A3B	CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS CHITINASE B1 IN COMPLEX WITH CAFFEINE	3.2.1.14
2A3C	CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS CHITINASE B1 IN COMPLEX WITH PENTOXIFYLLINE	3.2.1.14
2A3E	CRYSTAL STRUCTURE OF ASPERGILLUS FUMIGATUS CHITINASE B1 IN COMPLEX WITH ALLOSAMIDIN	3.2.1.14
2A3H	CELLOBIOSE COMPLEX OF THE ENDOGLUCANASE CEL5A FROM BACILLUS AGARADHERANS AT 2.0 A RESOLUTION	3.2.1.4
2A3K	CRYSTAL STRUCTURE OF THE HUMAN PROTEIN TYROSINE PHOSPHATASE, PTPN7 (HEPTP, HEMATOPOIETIC PROTEIN TYROSINE PHOSPHATASE)	3.1.3.48
2A3L	X-RAY STRUCTURE OF ADENOSINE 5'-MONOPHOSPHATE DEAMINASE FROM ARABIDOPSIS THALIANA IN COMPLEX WITH COFORMYCIN 5'-PHOSPHATE	3.5.4.6
2A3Q	X-RAY STRUCTURE OF PROTEIN FROM MUS MUSCULUS MM.29898	3.6.1.12
2A3U	CRYSTAL STRUCTURE OF SULBACTAM BOUND TO E166A VARIANT OF SHV-1 BETA-LACTAMASE	3.5.2.6
2A45	CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THROMBIN AND THE CENTRAL E" REGION OF FIBRIN"	3.4.21.5
2A49	CRYSTAL STRUCTURE OF CLAVULANIC ACID BOUND TO E166A VARIANT OF SHV-1 BETA-LACTAMASE	3.5.2.6
2A4F	SYNTHESIS AND ACTIVITY OF N-AXYL AZACYCLIC UREA HIV-1 PROTEASE INHIBITORS WITH HIGH POTENCY AGAINST MULTIPLE DRUG RESISTANT VIRAL STRAINS.	3.4.23.16
2A4G	HEPATITIS C PROTEASE NS3-4A SERINE PROTEASE WITH KETOAMIDE INHIBITOR SCH225724 BOUND	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
2A4O	DUAL MODES OF MODIFICATION OF HEPATITIS A VIRUS 3C PROTEASE BY A SERINE DERIVED BETA-LACTONE: SELECTIVE CRYTSTALLIZATION AND HIGH RESOLUTION STRUCTURE OF THE HIS102 ADDUCT	3.4.22.28 3.6.1.15 2.7.7.48
2A4R	HCV NS3 PROTEASE DOMAIN WITH A KETOAMIDE INHIBITOR COVALENTLY BOUND.	3.4.22 3.4.21.98 3.6.1.15 3.6.4.13 2.7.7.48
2A4T	CRYSTAL STRUCTURE OF SPIN LABELED T4 LYSOZYME (V131R7)	3.2.1.17
2A5A	CRYSTAL STRUCTURE OF UNBOUND SARS CORONAVIRUS MAIN PEPTIDASE IN THE SPACE GROUP C2	3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2A5I	CRYSTAL STRUCTURES OF SARS CORONAVIRUS MAIN PEPTIDASE INHIBITED BY AN AZA-PEPTIDE EPOXIDE IN THE SPACE GROUP C2	3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2A5K	CRYSTAL STRUCTURES OF SARS CORONAVIRUS MAIN PEPTIDASE INHIBITED BY AN AZA-PEPTIDE EPOXIDE IN SPACE GROUP P212121	3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2A6B	CRYSTAL STRUCTURE OF A PUTATIVE TRANSCRIPTIONAL REGULATOR OF THE TENA FAMILY (SPR0628) FROM STREPTOCOCCUS PNEUMONIAE R6 AT 1.70 A RESOLUTION	3.5.99.2
2A6R	CRYSTAL STRUCTURE OF YOEB UNDER PEG CONDITION	3.1
2A6S	CRYSTAL STRUCTURE OF YOEB UNDER ISOPROPANOL CONDITION	3.1
2A6T	CRYSTAL STRUCTURE OF S.POMBE MRNA DECAPPING ENZYME DCP2P	3
2A6U	PH EVOLUTION OF TETRAGONAL HEWL AT 4 DEGREES CELCIUS.	3.2.1.17
2A75	TRYPANOSOMA RANGELI SIALIDASE IN COMPLEX WITH 2,3- DIFLUOROSIALIC ACID (COVALENT INTERMEDIATE)	3.2.1.18
2A78	CRYSTAL STRUCTURE OF THE C3BOT-RALA COMPLEX REVEALS A NOVEL TYPE OF ACTION OF A BACTERIAL EXOENZYME	3.6.5.2
2A7C	ON THE ROUTINE USE OF SOFT X-RAYS IN MACROMOLECULAR CRYSTALLOGRAPHY, PART III- THE OPTIMAL DATA COLLECTION WAVELENGTH	3.4.21.36
2A7D	ON THE ROUTINE USE OF SOFT X-RAYS IN MACROMOLECULAR CRYSTALLOGRAPHY, PART III- THE OPTIMAL DATA COLLECTION WAVELENGTH	3.2.1.17
2A7F	ON THE ROUTINE USE OF SOFT X-RAYS IN MACROMOLECULAR CRYSTALLOGRAPHY, PART III- THE OPTIMAL DATA COLLECTION WAVELENGTH	3.2.1.17
2A7G	ON THE ROUTINE USE OF SOFT X-RAYS IN MACROMOLECULAR CRYSTALLOGRAPHY, PART III- THE OPTIMAL DATA COLLECTION WAVELENGTH	2.2.1.2 3.4.24.27
2A7H	ON THE ROUTINE USE OF SOFT X-RAYS IN MACROMOLECULAR CRYSTALLOGRAPHY, PART III- THE OPTIMAL DATA COLLECTION WAVELENGTH	3.4.21.4
2A7J	ON THE ROUTINE USE OF SOFT X-RAYS IN MACROMOLECULAR CRYSTALLOGRAPHY, PART III- THE OPTIMAL DATA COLLECTION WAVELENGTH	3.4.21.36
2A7M	1.6 ANGSTROM RESOLUTION STRUCTURE OF THE QUORUM-QUENCHING N-ACYL HOMOSERINE LACTONE HYDROLASE OF BACILLUS THURINGIENSIS	3.1.1 3.1.1.81
2A7U	NMR SOLUTION STRUCTURE OF THE E.COLI F-ATPASE DELTA SUBUNIT N-TERMINAL DOMAIN IN COMPLEX WITH ALPHA SUBUNIT N-TERMINAL 22 RESIDUES	3.6.3.14
2A7W	CRYSTAL STRUCTURE OF PHOSPHORIBOSYL-ATP PYROPHOSPHATASE FROM CHROMOBACTERIUM VIOLACEUM (ATCC 12472). NESG TARGET CVR7	3.6.1.31
2A8A	CRYSTAL STRUCTURE OF CLOSTRIDIUM BOTULINUM NEUROTOXIN SEROTYPE F LIGHT CHAIN	3.4.24.69
2A8B	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN TYROSINE PHOSPHATASE RECEPTOR, TYPE R	3.1.3.48
2A8H	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF TACE WITH THIOMORPHOLINE SULFONAMIDE HYDROXAMATE INHIBITOR	3.4.24.86
2A8I	CRYSTAL STRUCTURE OF HUMAN TASPASE1	3.4.25
2A8J	CRYSTAL STRUCTURE OF HUMAN TASPASE1 (ACIVATED FORM)	3.4.25
2A8K	STRUCTURAL AND MUTATIONAL STUDIES OF THE CATALYTIC DOMAIN OF COLICIN E5A TRNA-SPECIFIC RIBONUCLEASE	3.1
2A8L	CRYSTAL STRUCTURE OF HUMAN TASPASE1 (T234A MUTANT)	3.4.25
2A8M	CRYSTAL STRUCTURE OF HUMAN TASPASE1 (T234S MUTANT)	3.4.25
2A8N	BIOCHEMICAL AND STRUCTURAL STUDIES OF A-TO-I EDITING BY TRNA:A34 DEAMINASES AT THE WOBBLE POSITION OF TRANSFER RNA	3.5.4.33
2A8P	2.7 ANGSTROM CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THE NUCLEAR SNORNA DECAPPING NUDIX HYDROLASE X29 AND MANGANESE	3.6.1 3.6.1.62 3.6.1.64
2A8Q	2.6 ANGSTROM CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THE NUCLEAR SNORNA DECAPPING NUDIX HYDROLASE X29 AND MANGANESE IN THE PRESENCE OF 7-METHYL-GDP	3.6.1 3.6.1.62 3.6.1.64
2A8R	2.45 ANGSTROM CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THE NUCLEAR SNORNA DECAPPING NUDIX HYDROLASE X29 AND MANGANESE IN THE PRESENCE OF 7-METHYL-GTP	3.6.1 3.6.1.62 3.6.1.64
2A8S	2.45 ANGSTROM CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THE NUCLEAR SNORNA DECAPPING NUDIX HYDROLASE X29, MANGANESE AND GTP	3.6.1 3.6.1.62 3.6.1.64
2A8T	2.1 ANGSTROM CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THE NUCLEAR U8 SNORNA DECAPPING NUDIX HYDROLASE X29, MANGANESE AND M7G-PPP-A	3.6.1 3.6.1.62 3.6.1.64
2A8Z	STRUCTURE OF A COLD-ADAPTED FAMILY 8 XYLANASE	3.2.1.8 3.2.1.4
2A96	CRYSTAL STRUCTURE OF PHOSPHATE TETHERED PHON OF S. TYPHIMURIUM	3.1.3.2
2A97	CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF CLOSTRIDIUM BOTULINUM NEUROTOXIN SEROTYPE F	3.4.24.69
2A9G	STRUCTURE OF C406A ARGININE DEIMINASE IN COMPLEX WITH L-ARGININE	3.5.3.6
2A9K	CRYSTAL STRUCTURE OF THE C3BOT-NAD-RALA COMPLEX REVEALS A NOVEL TYPE OF ACTION OF A BACTERIAL EXOENZYME	3.6.5.2
2A9U	STRUCTURE OF THE N-TERMINAL DOMAIN OF HUMAN UBIQUITIN CARBOXYL-TERMINAL HYDROLASE 8 (USP8)	3.1.2.15 3.4.19.12
2AAA	CALCIUM BINDING IN ALPHA-AMYLASES: AN X-RAY DIFFRACTION STUDY AT 2.1 ANGSTROMS RESOLUTION OF TWO ENZYMES FROM ASPERGILLUS	3.2.1.1
2AAD	THE ROLE OF HISTIDINE-40 IN RIBONUCLEASE T1 CATALYSIS: THREE-DIMENSIONAL STRUCTURES OF THE PARTIALLY ACTIVE HIS40LYS MUTANT	3.1.27.3 4.6.1.24
2AAE	THE ROLE OF HISTIDINE-40 IN RIBONUCLEASE T1 CATALYSIS: THREE-DIMENSIONAL STRUCTURES OF THE PARTIALLY ACTIVE HIS40LYS MUTANT	3.1.27.3 4.6.1.24
2AAF	STRUCTURE OF H278A ARGININE DEIMINASE WITH L-ARGININE FORMING A S-ALKYLTHIOURONIUM REACTION INTERMEDIATE	3.5.3.6
2AAI	CRYSTALLOGRAPHIC REFINEMENT OF RICIN TO 2.5 ANGSTROMS	3.2.2.22
2AAS	HIGH-RESOLUTION THREE-DIMENSIONAL STRUCTURE OF RIBONUCLEASE A IN SOLUTION BY NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY	3.1.27.5 4.6.1.18
2AB0	CRYSTAL STRUCTURE OF E. COLI PROTEIN YAJL (THIJ)	3.1.2 3.5.1 3.5.1.124
2ABR	STRUCTURE OF D280A ARGININE DEIMINASE WITH L-ARGININE FORMING A S-ALKYLTHIOURONIUM REACTION INTERMEDIATE	3.5.3.6
2ABW	GLUTAMINASE SUBUNIT OF THE PLASMODIAL PLP SYNTHASE (VITAMIN B6 BIOSYNTHESIS)	2.6 4.3.3.6 3.5.1.2
2ABZ	CRYSTAL STRUCTURE OF C19A/C43A MUTANT OF LEECH CARBOXYPEPTIDASE INHIBITOR IN COMPLEX WITH BOVINE CARBOXYPEPTIDASE A	3.4.17.1
2AC1	CRYSTAL STRUCTURE OF A CELL-WALL INVERTASE FROM ARABIDOPSIS THALIANA	3.2.1.26
2ACE	NATIVE ACETYLCHOLINESTERASE (E.C. 3.1.1.7) FROM TORPEDO CALIFORNICA	3.1.1.7
2ACF	NMR STRUCTURE OF SARS-COV NON-STRUCTURAL PROTEIN NSP3A (SARS1) FROM SARS CORONAVIRUS	3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2ACI	STRUCTURE OF D166A ARGININE DEIMINASE	3.5.3.6
2ACJ	CRYSTAL STRUCTURE OF THE B/Z JUNCTION CONTAINING DNA BOUND TO Z-DNA BINDING PROTEINS	3.5.4 3.5.4.37
2ACK	ACETYLCHOLINESTERASE COMPLEXED WITH EDROPHONIUM, MONOCHROMATIC DATA	3.1.1.7
2ACT	CRYSTALLOGRAPHIC REFINEMENT OF THE STRUCTURE OF ACTINIDIN AT 1.7 ANGSTROMS RESOLUTION BY FAST FOURIER LEAST-SQUARES METHODS	3.4.22.14
2ACY	ACYL-PHOSPHATASE (COMMON TYPE) FROM BOVINE TESTIS	3.6.1.7
2ADA	ATOMIC STRUCTURE OF ADENOSINE DEAMINASE COMPLEXED WITH A TRANSITION-STATE ANALOG: UNDERSTANDING CATALYSIS AND IMMUNODEFICIENCY MUTATIONS	3.5.4.4
2ADD	CRYSTAL STRUCTURE OF FRUCTAN 1-EXOHYDROLASE IIA FROM CICHORIUM INTYBUS IN COMPLEX WITH SUCROSE	3.2.1.153 3.2.1.80
2ADE	CRYSTAL STRUCTURE OF FRUCTAN 1-EXOHYDROLASE IIA FROM CICHORIUM INTYBUS IN COMPLEX WITH FRUCTOSE	3.2.1.153 3.2.1.80
2ADU	HUMAN METHIONINE AMINOPEPTIDASE COMPLEX WITH 4-ARYL-1,2,3-TRIAZOLE INHIBITOR	3.4.11.18
2AE0	CRYSTAL STRUCTURE OF MLTA FROM ESCHERICHIA COLI REVEALS A UNIQUE LYTIC TRANSGLYCOSYLASE FOLD	3.2.1 4.2.2
2AE5	GLUTARYL 7-AMINOCEPHALOSPORANIC ACID ACYLASE: MUTATIONAL STUDY OF ACTIVATION MECHANISM	3.5.1.11 3.5.1.93
2AEB	CRYSTAL STRUCTURE OF HUMAN ARGINASE I AT 1.29 A RESOLUTION AND EXPLORATION OF INHIBITION IN IMMUNE RESPONSE.	3.5.3.1
2AEG	X-RAY CRYSTAL STRUCTURE OF PROTEIN ATU5096 FROM AGROBACTERIUM TUMEFACIENS. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET ATR63.	3.4
2AEI	CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF FACTOR VIIA/TISSUE FACTOR AND 2-[[6-[3-(AMINOIMINOMETHYL)PHENOXY]-3,5-DIFLURO-4-[(1-METHYL-3-PHENYLPROPYL)AMINO]-2-PYRIDINYL]OXY]-BENZOIC ACID	3.4.21.21
2AEP	AN EPIDEMIOLOGICALLY SIGNIFICANT EPITOPE OF A 1998 INFLUENZA VIRUS NEURAMINIDASE FORMS A HIGHLY HYDRATED INTERFACE IN THE NA-ANTIBODY COMPLEX.	3.2.1.18
2AEQ	AN EPIDEMIOLOGICALLY SIGNIFICANT EPITOPE OF A 1998 INFLUENZA VIRUS NEURAMINIDASE FORMS A HIGHLY HYDRATED INTERFACE IN THE NA-ANTIBODY COMPLEX.	3.2.1 3.2.1.18
2AER	CRYSTAL STRUCTURE OF BENZAMIDINE-FACTOR VIIA/SOLUBLE TISSUE FACTOR COMPLEX.	3.4.21.21
2AEY	CRYSTAL STRUCTURE OF FRUCTAN 1-EXOHYDROLASE IIA FROM CICHORIUM INTYBUS IN COMPLEX WITH 2,5 DIDEOXY-2,5-IMMINO-D-MANNITOL	3.2.1.153 3.2.1.80
2AEZ	CRYSTAL STRUCTURE OF FRUCTAN 1-EXOHYDROLASE IIA (E201Q) FROM CICHORIUM INTYBUS IN COMPLEX WITH 1-KESTOSE	3.2.1.153 3.2.1.80
2AFQ	1.9 ANGSTROM CRYSTAL STRUCTURE OF WILD-TYPE HUMAN THROMBIN IN THE SODIUM FREE STATE	3.4.21.5
2AGA	DE-UBIQUITINATING FUNCTION OF ATAXIN-3: INSIGHTS FROM THE SOLUTION STRUCTURE OF THE JOSEPHIN DOMAIN	3.4.19.12
2AGS	TRYPANOSOMA RANGELI SIALIDASE IN COMPLEX WITH 2-KETO-3-DEOXY-D-GLYCERO-D-GALACTO-2,3-DIFLUORO-NONONIC ACID (2,3-DIFLUORO-KDN)	3.2.1.18
2AGV	CRYSTAL STRUCTURE OF THE SR CA2+-ATPASE WITH BHQ AND TG	3.6.3.8 7.2.2.10
2AH2	TRYPANOSOMA CRUZI TRANS-SIALIDASE IN COMPLEX WITH 2,3-DIFLUOROSIALIC ACID (COVALENT INTERMEDIATE)	3.2.1.18
2AH4	GUANIDINOBENZOYL-TRYPSIN ACYL-ENZYME AT 1.13 A RESOLUTION	3.4.21.4
2AHD	THE APO STRUCTURE OF METHANOCOCCUS JANNASCHII PHOSPHODIESTERASE MJ0936	3.1.4
2AHF	UNSATURATED GLUCURONYL HYDROLASE MUTANT D88N	3.2.1 3.2.1.179
2AHM	CRYSTAL STRUCTURE OF SARS-COV SUPER COMPLEX OF NON-STRUCTURAL PROTEINS: THE HEXADECAMER	3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2AHN	HIGH RESOLUTION STRUCTURE OF A CHERRY ALLERGEN PRU AV 2	3.2.1.39
2AHO	STRUCTURE OF THE ARCHAEAL INITIATION FACTOR EIF2 ALPHA-GAMMA HETERODIMER FROM SULFOLOBUS SOLFATARICUS COMPLEXED WITH GDPNP	3.6.5.3
2AHS	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN TYROSINE RECEPTOR PHOSPHATASE BETA	3.1.3.48
2AI6	SOLUTION STRUCTURE OF HUMAN PHOSPHOHISTIDINE PHOSPHATASE 1	3.1.3 3.9.1.3
2AI7	S.PNEUMONIAE POLYPEPTIDE DEFORMYLASE COMPLEXED WITH SB-485345	3.5.1.88
2AI8	E.COLI POLYPEPTIDE DEFORMYLASE COMPLEXED WITH SB-485343	3.5.1.88
2AI9	S.AUREUS POLYPEPTIDE DEFORMYLASE	3.5.1.88
2AIA	S.PNEUMONIAE PDF COMPLEXED WITH SB-543668	3.5.1.88
2AID	STRUCTURE OF A NON-PEPTIDE INHIBITOR COMPLEXED WITH HIV-1 PROTEASE: DEVELOPING A CYCLE OF STRUCTURE-BASED DRUG DESIGN	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AIE	S.PNEUMONIAE POLYPEPTIDE DEFORMYLASE COMPLEXED WITH SB-505684	3.5.1.88
2AIG	ADAMALYSIN II WITH PEPTIDOMIMETIC INHIBITOR POL647	3.4.24.46
2AIM	CRUZAIN INHIBITED WITH BENZOYL-ARGININE-ALANINE-FLUOROMETHYLKETONE	3.4.22 3.4.22.51
2AIO	METALLO BETA LACTAMASE L1 FROM STENOTROPHOMONAS MALTOPHILIA COMPLEXED WITH HYDROLYZED MOXALACTAM	3.5.2.6
2AIP	CRYSTAL STRUCTURE OF NATIVE PROTEIN C ACTIVATOR FROM THE VENOM OF COPPERHEAD SNAKE AGKISTRODON CONTORTRIX CONTORTRIX	3.4.21.74 3.4.21
2AIQ	CRYSTAL STRUCTURE OF BENZAMIDINE-INHIBITED PROTEIN C ACTIVATOR FROM THE VENOM OF COPPERHEAD SNAKE AGKISTRODON CONTORTRIX CONTORTRIX	3.4.21.74 3.4.21
2AJ0	SOLUTION STRUCTURE OF APOCADA	3.6.3.3 7.2.2.21
2AJ1	SOLUTION STRUCTURE OF APOCADA	3.6.3.3 7.2.2.21
2AJB	PORCINE DIPEPTIDYL PEPTIDASE IV (CD26) IN COMPLEX WITH THE TRIPEPTIDE TERT-BUTYL-GLY-L-PRO-L-ILE (TBU-GPI)	3.4.14.5
2AJD	PORCINE DIPEPTIDYL PEPTIDASE IV (CD26) IN COMPLEX WITH L-PRO-BORO-L-PRO (BOROPRO)	3.4.14.5
2AJF	STRUCTURE OF SARS CORONAVIRUS SPIKE RECEPTOR-BINDING DOMAIN COMPLEXED WITH ITS RECEPTOR	3.4.17 3.4.17.23
2AJQ	STRUCTURE OF REPLICATIVE DNA POLYMERASE PROVIDES INSIGTS INTO THE MECHANISMS FOR PROCESSIVITY, FRAMESHIFTING AND EDITING	2.7.7.7 3.1.11
2AKC	CRYSTAL STRUCTURE OF TUNGSTATE COMPLEX OF THE PHON PROTEIN FROM S. TYPHIMURIUM	3.1.3.2
2ALA	CRYSTAL STRUCTURE OF THE SEMLIKI FOREST VIRUS ENVELOPE PROTEIN E1 IN ITS MONOMERIC CONFORMATION.	3.4.21.90
2ALP	REFINED STRUCTURE OF ALPHA-LYTIC PROTEASE AT 1.7 ANGSTROMS RESOLUTION. ANALYSIS OF HYDROGEN BONDING AND SOLVENT STRUCTURE	3.4.21.12
2ALU	DETECTION OF NEW BINDING SITE IN THE C-TERMINAL LOBE OF LACTOFERRIN:CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN BOVINE LACTOFERRIN AND A TETRASACCHARIDE AT 2.1A RESOLUTION	3.4.21
2ALV	X-RAY STRUCTURAL ANALYSIS OF SARS CORONAVIRUS 3CL PROTEINASE IN COMPLEX WITH DESIGNED ANTI-VIRAL INHIBITORS	3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2ALW	GOLGI ALPHA-MANNOSIDASE II COMPLEX WITH NOEUROMYCIN	3.2.1.114
2AMD	CRYSTAL STRUCTURE OF SARS_COV MPRO IN COMPLEX WITH AN INHIBITOR N9	3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2AMG	STRUCTURE OF HYDROLASE (GLYCOSIDASE)	3.2.1.60
2AMP	CRYSTAL STRUCTURE OF PORCINE TRANSMISSIBLE GASTROENTERITIS VIRUS MPRO IN COMPLEX WITH AN INHIBITOR N1	3.4.22 3.4.19.12 2.7.7.48 3.6.4.12 3.6.4.13 3.1.13 3.1 2.1.1
2AMQ	CRYSTAL STRUCTURE OF SARS_COV MPRO IN COMPLEX WITH AN INHIBITOR N3	3.4.22 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2AMX	CRYSTAL STRUCTURE OF PLASMODIUM YOELII ADENOSINE DEAMINASE (PY02076)	3.5.4.4
2ANE	CRYSTAL STRUCTURE OF N-TERMINAL DOMAIN OF E.COLI LON PROTEASE	3.4.21.53
2ANG	CRYSTAL STRUCTURE OF HUMAN ANGIOGENIN OF THE MET(-1) FORM	3.1.27
2ANH	ALKALINE PHOSPHATASE (D153H)	3.1.3.1
2ANK	ORALLY ACTIVE THROMBIN INHIBITORS IN COMPLEX WITH THROMBIN AND AN EXOSITE DECAPEPTIDE	3.4.21.5
2ANM	TERNARY COMPLEX OF AN ORALLY ACTIVE THROMBIN INHIBITOR WITH HUMAN THROMBIN AND A C-TERMINAL HIRUDIN DERIVED EXO-SIT INHIBITOR	3.4.21.5
2ANP	FUNCTIONAL GLUTAMATE 151 TO HISTIDINE MUTANT OF THE AMINOPEPTIDASE FROM AEROMONAS PROTEOLYTICA.	3.4.11.10
2ANV	CRYSTAL STRUCTURE OF P22 LYSOZYME MUTANT L86M	3.2.1.17
2ANW	EXPRESSION, CRYSTALLIZATION AND THREE-DIMENSIONAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN PLASMA KALLIKREIN: IMPLICATIONS FOR STRUCTURE-BASED DESIGN OF PROTEASE INHIBITORS	3.4.21.34
2ANX	CRYSTAL STRUCTURE OF BACTERIOPHAGE P22 LYSOZYME MUTANT L87M	3.2.1.17
2ANY	EXPRESSION, CRYSTALLIZATION AND THE THREE-DIMENSIONAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN PLASMA KALLIKREIN: IMPLICATIONS FOR STRUCTURE-BASED DESIGN OF PROTEASE INHIBITORS	3.4.21.34
2AO7	ADAM10 DISINTEGRIN AND CYSTEINE- RICH DOMAIN	3.4.24.81
2AOC	CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE MUTANT I84V WITH A SUBSTRATE ANALOG P2-NC	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AOD	CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE WITH A SUBSTRATE ANALOG P2-NC	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AOE	CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE MUTANT V82A WITH A SUBSTRATE ANALOG CA-P2	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AOF	CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE MUTANT V82A WITH A SUBSTRATE ANALOG P1-P6	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AOG	CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE MUTANT V82A WITH A SUBSTRATE ANALOG P2-NC	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AOH	CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE MUTANT V82A WITH A SUBSTRATE ANALOG P6-PR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AOI	CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE WITH A SUBSTRATE ANALOG P1-P6	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AOJ	CRYSTAL STRUCTURE ANALYSIS OF HIV-1 PROTEASE WITH A SUBSTRATE ANALOG P6-PR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2APJ	X-RAY STRUCTURE OF PROTEIN FROM ARABIDOPSIS THALIANA AT4G34215 AT 1.6 ANGSTROM RESOLUTION	3.1
2APQ	CRYSTAL STRUCTURE OF AN ACTIVE SITE MUTANT OF BOVINE PANCREATIC RIBONUCLEASE A (H119A-RNASE A) WITH A 10-GLUTAMINE EXPANSION IN THE C-TERMINAL HINGE-LOOP.	3.1.27.5 4.6.1.18
2APR	STRUCTURE AND REFINEMENT AT 1.8 ANGSTROMS RESOLUTION OF THE ASPARTIC PROTEINASE FROM RHIZOPUS CHINENSIS	3.4.23.6 3.4.23.21
2AQ0	SOLUTION STRUCTURE OF THE HUMAN HOMODIMERIC DNA REPAIR PROTEIN XPF	3.1
2AQO	CRYSTAL STRUCTURE OF E. COLI ISOASPARTYL DIPEPTIDASE MUTANT E77Q	3.4.19
2AQU	STRUCTURE OF HIV-1 PROTEASE BOUND TO ATAZANAVIR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AQV	CRYSTAL STRUCTURE OF E. COLI ISOASPARTYL DIPEPTIDASE MUTANT Y137F	3.4.19
2AR3	E90A MUTANT STRUCTURE OF PLYL	3.5.1.28
2AR9	CRYSTAL STRUCTURE OF A DIMERIC CASPASE-9	3.4.22 3.4.22.62
2ARF	SOLUTION STRUCTURE OF THE WILSON ATPASE N-DOMAIN IN THE PRESENCE OF ATP	3.6.3.4 7.2.2.8
2ARM	CRYSTAL STRUCTURE OF THE COMPLEX OF PHOSPHOLIPASE A2 WITH A NATURAL COMPOUND ATROPINE AT 1.2 A RESOLUTION	3.1.1.4
2ARY	CATALYTIC DOMAIN OF HUMAN CALPAIN-1	3.4.22.52
2AS8	CRYSTAL STRUCTURE OF MATURE AND FULLY ACTIVE DER P 1 ALLERGEN	3.4.22 3.4.22.65
2AS9	FUNCTIONAL AND STRUCTURAL CHARACTERIZATION OF SPL PROTEASES FROM STAPHYLOCOCCUS AUREUS	3.4.21
2ASE	NMR STRUCTURE OF THE F28L MUTANT OF CDC42HS	3.6.5.2
2ASI	ASPARTIC PROTEINASE	3.4.23.23
2ATM	CRYSTAL STRUCTURE OF THE RECOMBINANT ALLERGEN VES V 2	3.2.1.35
2ATO	CRYSTAL STRUCTURE OF HUMAN CATHEPSIN K IN COMPLEX WITH MYOCRISIN	3.4.22.38
2ATQ	RB69 SINGLE-STRANDED DNA BINDING PROTEIN-DNA POLYMERASE FUSION	2.7.7.7 3.1.11
2ATV	THE CRYSTAL STRUCTURE OF HUMAN RERG IN THE GDP BOUND STATE	3.6.5.2
2ATX	CRYSTAL STRUCTURE OF THE TC10 GPPNHP COMPLEX	3.6.5.2
2AU6	CRYSTAL STRUCTURE OF CATALYTIC INTERMEDIATE OF INORGANIC PYROPHOSPHATASE	3.6.1.1
2AU7	THE R43Q ACTIVE SITE VARIANT OF E.COLI INORGANIC PYROPHOSPHATASE	3.6.1.1
2AU8	CATALYTIC INTERMEDIATE STRUCTURE OF INORGANIC PYROPHOSPHATASE	3.6.1.1
2AU9	INORGANIC PYROPHOSPHATASE COMPLEXED WITH SUBSTRATE	3.6.1.1
2AUB	LYSOZYME STRUCTURE DERIVED FROM THIN-FILM-BASED CRYSTALS	3.2.1.17
2AUD	UNLIGANDED HINCII	3.1.21.4
2AUM	ACTIVE SITE SER115ALA MUTANT OF LD-CARBOXYPEPTIDASE	3.4.17.13
2AUN	ACTIVE SITE HIS285ALA MUTANT OF LD-CARBOXYPEPTIDASE	3.4.17.13
2AUT	CRYSTAL STRUCTURE OF LYS154ASN MUTANT OF MATURE APHA OF S. TYPHIMURIUM	3.1.3.2
2AUU	INORGANIC PYROPHOSPHATASE COMPLEXED WITH MAGNESIUM PYROPHOSPHATE AND FLUORIDE	3.6.1.1
2AUX	CATHEPSIN K COMPLEXED WITH A SEMICARBAZONE INHIBITOR	3.4.22.38
2AUZ	CATHEPSIN K COMPLEXED WITH A SEMICARBAZONE INHIBITOR	3.4.22.38
2AV5	CRYSTAL STRUCTURE OF PYROCOCCUS FURIOSUS POP5, AN ARCHAEAL RIBONUCLEASE P PROTEIN	3.1.26.5
2AVM	KINETICS, STABILITY, AND STRUCTURAL CHANGES IN HIGH RESOLUTION CRYSTAL STRUCTURES OF HIV-1 PROTEASE WITH DRUG RESISTANT MUTATIONS L24I, I50V, AND G73S	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AVO	KINETICS, STABILITY, AND STRUCTURAL CHANGES IN HIGH RESOLUTION CRYSTAL STRUCTURES OF HIV-1 PROTEASE WITH DRUG RESISTANT MUTATIONS L24I, I50V, AND G73S	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AVQ	KINETICS, STABILITY, AND STRUCTURAL CHANGES IN HIGH RESOLUTION CRYSTAL STRUCTURES OF HIV-1 PROTEASE WITH DRUG RESISTANT MUTATIONS L24I, I50V, AND G73S	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AVS	KINETICS, STABILITY, AND STRUCTURAL CHANGES IN HIGH RESOLUTION CRYSTAL STRUCTURES OF HIV-1 PROTEASE WITH DRUG RESISTANT MUTATIONS L24I, I50V, AND G73S	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AVV	KINETICS, STABILITY, AND STRUCTURAL CHANGES IN HIGH RESOLUTION CRYSTAL STRUCTURES OF HIV-1 PROTEASE WITH DRUG RESISTANT MUTATIONS L24I, I50V, AND G73S	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AWN	CRYSTAL STRUCTURE OF THE ADP-MG-BOUND E. COLI MALK (CRYSTALLIZED WITH ATP-MG)	3.6.3.19 7.5.2.1
2AWO	CRYSTAL STRUCTURE OF THE ADP-MG-BOUND E. COLI MALK (CRYSTALLIZED WITH ADP-MG)	3.6.3.19 7.5.2.1
2AWZ	HEPATITIS C VIRUS NS5B RNA POLYMERASE IN COMPLEX WITH A COVALENT INHIBITOR (5H)	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
2AX0	HEPATITIS C VIRUS NS5B RNA POLYMERASE IN COMPLEX WITH A COVALENT INHIBITOR (5X)	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
2AX1	HEPATITIS C VIRUS NS5B RNA POLYMERASE IN COMPLEX WITH A COVALENT INHIBITOR (5EE)	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
2AXC	CRYSTAL STRUCTURE OF COLE7 TRANSLOCATION DOMAIN	3.1
2AXE	IODINATED COMPLEX OF ACETYL XYLAN ESTERASE AT 1.80 ANGSTROMS	3.1.1.6 3.1.1.72
2AXL	SOLUTION STRUCTURE OF A MULTIFUNCTIONAL DNA- AND PROTEIN-BINDING DOMAIN OF HUMAN WERNER SYNDROME PROTEIN	3.6.4.12 3.1
2AXN	CRYSTAL STRUCTURE OF THE HUMAN INDUCIBLE FORM 6-PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE	2.7.1.105 3.1.3.46
2AYH	CRYSTAL AND MOLECULAR STRUCTURE AT 1.6 ANGSTROMS RESOLUTION OF THE HYBRID BACILLUS ENDO-1,3-1,4-BETA-D-GLUCAN 4-GLUCANOHYDROLASE H(A16-M)	3.2.1.73
2AYI	WILD-TYPE AMPT FROM THERMUS THERMOPHILUS	3.4.11
2AYK	INHIBITOR-FREE CATALYTIC FRAGMENT OF HUMAN FIBROBLAST COLLAGENASE, NMR, MINIMIZED AVERAGE STRUCTURE	3.4.24.7
2AYN	STRUCTURE OF USP14, A PROTEASOME-ASSOCIATED DEUBIQUITINATING ENZYME	3.1.2.15 3.4.19.12
2AYO	STRUCTURE OF USP14 BOUND TO UBQUITIN ALDEHYDE	3.1.2.15 3.4.19.12
2AYS	A CONSERVED NON-METALLIC BINDING SITE IN THE C-TERMINAL LOBE OF LACTOFERRIN: STRUCTURE OF THE COMPLEX OF C-TERMINAL LOBE OF BOVINE LACTOFERRIN WITH N-ACETYL GALACTOSAMINE AT 1.86 A RESOLUTION	3.4.21
2AYW	CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN TRYPSIN AND A DESIGNED SYNTHETIC HIGHLY POTENT INHIBITOR IN THE PRESENCE OF BENZAMIDINE AT 0.97 A RESOLUTION	3.4.21.4
2AZ8	HIV-1 PROTEASE NL4-3 IN COMPLEX WITH INHIBITOR, TL-3	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AZ9	HIV-1 PROTEASE NL4-3 1X MUTANT	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AZB	HIV-1 PROTEASE NL4-3 3X MUTANT IN COMPLEX WITH INHIBITOR, TL-3	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AZC	HIV-1 PROTEASE NL4-3 6X MUTANT	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2AZR	CRYSTAL STRUCTURE OF PTP1B WITH BICYCLIC THIOPHENE INHIBITOR	3.1.3.48
2AZY	CRYSTAL STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2 IN COMPLEX WITH CHOLATE	3.1.1.4
2AZZ	CRYSTAL STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2 IN COMPLEX WITH TAUROCHOLATE	3.1.1.4
2B00	CRYSTAL STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2 IN COMPLEX WITH GLYCOCHOLATE	3.1.1.4
2B01	CRYSTAL STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2 IN COMPLEX WITH TAUROCHENODEOXYCHOLATE	3.1.1.4
2B03	CRYSTAL STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2 IN COMPLEX WITH TAUROCHENODEOXYCHOLATE	3.1.1.4
2B04	CRYSTAL STRUCTURE OF PORCINE PANCREATIC PHOSPHOLIPASE A2 IN COMPLEX WITH GLYCOCHENODEOXYCHOLATE	3.1.1.4
2B07	CRYSTAL STRUCTURE OF PTP1B WITH TRICYCLIC THIOPHENE INHIBITOR.	3.1.3.48
2B0C	THE CRYSTAL STRUCTURE OF THE PUTATIVE PHOSPHATASE FROM ESCHERICHIA COLI	3.1.3.10
2B0D	ECORV RESTRICTION ENDONUCLEASE/GAATTC/CA2+	3.1.21.4
2B0E	ECORV RESTRICTION ENDONUCLEASE/GAAUTC/CA2+	3.1.21.4
2B0F	NMR STRUCTURE OF THE HUMAN RHINOVIRUS 3C PROTEASE (SEROTYPE 14) WITH COVALENTLY BOUND ACE-LEALFQ-ETHYLPROPIONATE INHIBITOR	3.4.22.28 3.4.22.29 3.6.1.15 2.7.7.48
2B0P	TRUNCATED S. AUREUS LYTM, P212121 CRYSTAL FORM	3.4.24.75
2B0V	NUDIX HYDROLASE FROM NITROSOMONAS EUROPAEA.	3.6.1
2B13	TRUNCATED S. AUREUS LYTM, P41 CRYSTAL FORM	3.4.24.75
2B17	SPECIFIC BINDING OF NON-STEROIDAL ANTI-INFLAMMATORY DRUGS (NSAIDS) TO PHOSPHOLIPASE A2: CRYSTAL STRUCTURE OF THE COMPLEX FORMED BETWEEN PHOSPHOLIPASE A2 AND DICLOFENAC AT 2.7 A RESOLUTION:	3.1.1.4
2B1G	CRYSTAL STRUCTURES OF TRANSITION STATE ANALOGUE INHIBITORS OF INOSINE MONOPHOSPHATE CYCLOHYDROLASE	3.5.4.10 2.1.2.3
2B1I	CRYSTAL STRUCTURES OF TRANSITION STATE ANALOGUE INHIBITORS OF INOSINE MONOPHOSPHATE CYCLOHYDROLASE	3.5.4.10 2.1.2.3
2B1Q	X-RAY STRUCTURE OF THE SUCROSE-PHOSPHATASE (SPP) FROM SYNECHOCYSTIS SP.PCC6803 IN COMPLEX WITH TREHALOSE	3.1.3.24
2B1R	X-RAY STRUCTURE OF THE SUCROSE-PHOSPHATASE (SPP) FROM SYNECHOCYSTIS SP.PCC6803 IN COMPLEX WITH CELLOBIOSE	3.1.3.24
2B2N	STRUCTURE OF TRANSCRIPTION-REPAIR COUPLING FACTOR	3.6.4
2B2T	TANDEM CHROMODOMAINS OF HUMAN CHD1 COMPLEXED WITH HISTONE H3 TAIL CONTAINING TRIMETHYLLYSINE 4 AND PHOSPHOTHREONINE 3	3.6.4.12
2B2U	TANDEM CHROMODOMAINS OF HUMAN CHD1 COMPLEXED WITH HISTONE H3 TAIL CONTAINING TRIMETHYLLYSINE 4 AND DIMETHYLARGININE 2	3.6.4.12
2B2V	CRYSTAL STRUCTURE ANALYSIS OF HUMAN CHD1 CHROMODOMAINS 1 AND 2 BOUND TO HISTONE H3 RESI 1-15 MEK4	3.6.4.12
2B2W	TANDEM CHROMODOMAINS OF HUMAN CHD1 COMPLEXED WITH HISTONE H3 TAIL CONTAINING TRIMETHYLLYSINE 4	3.6.4.12
2B2Y	TANDEM CHROMODOMAINS OF HUMAN CHD1	3.6.4.12
2B3H	CRYSTAL STRUCTURE OF HUMAN METHIONINE AMINOPEPTIDASE TYPE I WITH A THIRD COBALT IN THE ACTIVE SITE	3.4.11.18
2B3J	CRYSTAL STRUCTURE OF STAPHYLOCOCCUS AUREUS TRNA ADENOSINE DEAMINASE, TADA, IN COMPLEX WITH RNA	3.5.4 3.5.4.33
2B3K	CRYSTAL STRUCTURE OF HUMAN METHIONINE AMINOPEPTIDASE TYPE I IN THE HOLO FORM	3.4.11.18
2B3L	CRYSTAL STRUCTURE OF TYPE I HUMAN METHIONINE AMINOPEPTIDASE IN THE APO FORM	3.4.11.18
2B3O	CRYSTAL STRUCTURE OF HUMAN TYROSINE PHOSPHATASE SHP-1	3.1.3.48
2B3W	NMR STRUCTURE OF THE E.COLI PROTEIN YBIA, NORTHEAST STRUCTURAL GENOMICS TARGET ET24.	3.2.2
2B3Z	CRYSTAL STRUCTURE OF A BIFUNCTIONAL DEAMINASE AND REDUCTASE INVOLVED IN RIBOFLAVIN BIOSYNTHESIS	3.5.4.26 1.1.1.193
2B43	CRYSTAL STRUCTURE OF THE NORWALK VIRUS RNA DEPENDENT RNA POLYMERASE FROM STRAIN HU/NLV/DRESDEN174/1997/GE	2.7.7.48 3.4.22.66 3.6.1.15
2B44	TRUNCATED S. AUREUS LYTM, P 32 2 1 CRYSTAL FORM	3.4.24.75
2B45	CRYSTAL STRUCTURE OF AN ENGINEERED UNINHIBITED BACILLUS SUBTILIS XYLANASE IN FREE STATE	3.2.1.8
2B46	CRYSTAL STRUCTURE OF AN ENGINEERED UNINHIBITED BACILLUS SUBTILIS XYLANASE IN SUBSTRATE BOUND STATE	3.2.1.8
2B49	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF PROTEIN TYROSINE PHOSPHATASE, NON-RECEPTOR TYPE 3	3.1.3.48
2B4F	STRUCTURE OF A COLD-ADAPTED FAMILY 8 XYLANASE IN COMPLEX WITH SUBSTRATE	3.2.1.8 3.2.1.4
2B4J	STRUCTURAL BASIS FOR THE RECOGNITION BETWEEN HIV-1 INTEGRASE AND LEDGF/P75	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2B4K	ACETOBACTER TURBIDANS ALPHA-AMINO ACID ESTER HYDROLASE COMPLEXED WITH PHENYLGLYCINE	3.1.1.43
2B4O	STRUCTURE OF THE R258K MUTANT OF SELENOMONAS RUMINANTIUM PTP-LIKE PHYTASE	3.1.3.72
2B4P	STRUCTURE OF THE D223N MUTANT OF SELENOMONAS RUMINANTIUM PTP-LIKE PHYTASE	3.1.3.72
2B4S	CRYSTAL STRUCTURE OF A COMPLEX BETWEEN PTP1B AND THE INSULIN RECEPTOR TYROSINE KINASE	3.1.3.48
2B4U	STRUCTURE OF THE C252S MUTANT OF SELENOMONAS RUMINANTIUM PTP-LIKE PHYTASE	3.1.3.72
2B4Y	CRYSTAL STRUCTURE OF HUMAN SIRTUIN HOMOLOG 5	3.5.1 2.3.1
2B5D	CRYSTAL STRUCTURE OF THE NOVEL ALPHA-AMYLASE AMYC FROM THERMOTOGA MARITIMA	3.2.1.1
2B5J	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH JANSSEN-R165481	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2B5R	1B LACTAMASE / B LACTAMASE INHIBITOR	3.5.2.6
2B5T	2.1 ANGSTROM STRUCTURE OF A NONPRODUCTIVE COMPLEX BETWEEN ANTITHROMBIN, SYNTHETIC HEPARIN MIMETIC SR123781 AND TWO S195A THROMBIN MOLECULES	3.4.21.5
2B5U	CRYSTAL STRUCTURE OF COLICIN E3 V206C MUTANT IN COMPLEX WITH ITS IMMUNITY PROTEIN	3.1
2B5Z	HEN LYSOZYME CHEMICALLY GLYCOSYLATED	3.2.1.17
2B65	CRYSTAL STRUCTURE OF THE COMPLEX OF C-LOBE OF BOVINE LACTOFERRIN WITH MALTOSE AT 1.5A RESOLUTION	3.4.21
2B6A	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH THR-50	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2B6B	CRYO EM STRUCTURE OF DENGUE COMPLEXED WITH CRD OF DC-SIGN	3.4.21.91 3.6.1.15 3.6.4.13
2B6E	X-RAY CRYSTAL STRUCTURE OF PROTEIN HI1161 FROM HAEMOPHILUS INFLUENZAE. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET IR63.	3.1.2
2B6N	THE 1.8 A CRYSTAL STRUCTURE OF A PROTEINASE K LIKE ENZYME FROM A PSYCHROTROPH SERRATIA SPECIES	3.4.21
2B6T	T4 LYSOZYME MUTANT L99A AT 200 MPA	3.2.1.17
2B6W	T4 LYSOZYME MUTANT L99A AT 200 MPA	3.2.1.17
2B6X	T4 LYSOZYME MUTANT L99A AT 200 MPA	3.2.1.17
2B6Y	T4 LYSOZYME MUTANT L99A AT AMBIENT PRESSURE	3.2.1.17
2B6Z	T4 LYSOZYME MUTANT L99A AT AMBIENT PRESSURE	3.2.1.17
2B70	T4 LYSOZYME MUTANT L99A AT AMBIENT PRESSURE	3.2.1.17
2B72	T4 LYSOZYME MUTANT L99A AT 100 MPA	3.2.1.17
2B73	T4 LYSOZYME MUTANT L99A AT 100 MPA	3.2.1.17
2B74	T4 LYSOZYME MUTANT L99A AT 100 MPA	3.2.1.17
2B75	T4 LYSOZYME MUTANT L99A AT 150 MPA	3.2.1.17
2B7D	FACTOR VIIA INHIBITORS: CHEMICAL OPTIMIZATION, PRECLINICAL PHARMACOKINETICS, PHARMACODYNAMICS, AND EFFICACY IN A BABOON THROMBOSIS MODEL	3.4.21.21
2B7F	CRYSTAL STRUCTURE OF HUMAN T-CELL LEUKEMIA VIRUS PROTEASE, A NOVEL TARGET FOR ANTI-CANCER DESIGN	3.4.23 2.7.7.49 2.7.7.7 3.1.26.4 2.7.7 3.1
2B7T	STRUCTURE OF ADAR2 DSRBM1	3.5 3.5.4.37
2B7U	RIBOSOME INACTIVATING PROTEIN TYPE 1 FROM CHARYBDIS MARITIMA AGG	3.2.2.22
2B7V	STRUCTURE OF ADAR2 DSRBM2	3.5 3.5.4.37
2B7X	SEQUENTIAL REORGANIZATION OF BETA-SHEET TOPOLOGY BY INSERTION OF A SINGLE STRAND	3.2.1.17
2B7Z	STRUCTURE OF HIV-1 PROTEASE MUTANT BOUND TO INDINAVIR	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2B82	CRYSTAL STRUCTURE OF APHA CLASS B ACID PHOSPHATASE/PHOSPHOTRANSFERASE TERNARY COMPLEX WITH ADENOSINE AND PHOSPHATE BOUND TO THE CATALYTIC METAL AT 1.2 A RESOLUTION	3.1.3.2
2B8H	A/NWS/WHALE/MAINE/1/84 (H1N9) REASSORTANT INFLUENZA VIRUS NEURAMINIDASE	3.2.1.18
2B8J	CRYSTAL STRUCTURE OF APHA CLASS B ACID PHOSPHATASE/PHOSPHOTRANSFERASE TERNARY COMPLEX WITH ADENOSINE AND PHOSPHATE AT 2 A RESOLUTION	3.1.3.2
2B8L	CRYSTAL STRUCTURE OF HUMAN BETA SECRETASE COMPLEXED WITH INHIBITOR	3.4.23.46
2B8O	CRYSTAL STRUCTURE OF GLU-GLY-ARG-CHLOROMETHYL KETONE-FACTOR VIIA/SOLUBLE TISSUE FACTOR COMPLEX	3.4.21.21
2B8V	CRYSTAL STRUCTURE OF HUMAN BETA-SECRETASE COMPLEXED WITH L-L000430,469	3.4.23.46
2B8W	CRYSTAL-STRUCTURE OF THE N-TERMINAL LARGE GTPASE DOMAIN OF HUMAN GUANYLATE BINDING PROTEIN 1 (HGBP1) IN COMPLEX WITH GMP/ALF4	3.6.5
2B92	CRYSTAL-STRUCTURE OF THE N-TERMINAL LARGE GTPASE DOMAIN OF HUMAN GUANYLATE BINDING PROTEIN 1 (HGBP1) IN COMPLEX WITH GDP/ALF3	3.6.5
2B96	THIRD CALCIUM ION FOUND IN AN INHIBITOR BOUND PHOSPHOLIPASE A2	3.1.1.4
2BAA	THE REFINED CRYSTAL STRUCTURE OF AN ENDOCHITINASE FROM HORDEUM VULGARE L. SEEDS TO 1.8 ANGSTROMS RESOLUTION	3.2.1.14
2BAG	3D STRUCTURE OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE COMPLEXED WITH GANSTIGMINE	3.1.1.7
2BAM	RESTRICTION ENDONUCLEASE BAMHI COMPLEX WITH DNA AND CALCIUM IONS (PRE-REACTIVE COMPLEX).	3.1.21.4
2BAN	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH JANSSEN-R157208	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2BAT	THE STRUCTURE OF THE COMPLEX BETWEEN INFLUENZA VIRUS NEURAMINIDASE AND SIALIC ACID, THE VIRAL RECEPTOR	3.2.1.18
2BAX	ATOMIC RESOLUTION STRUCTURE OF THE DOUBLE MUTANT (K53,56M) OF BOVINE PANCREATIC PHOSPHOLIPASE A2	3.1.1.4
2BAZ	STRUCTURE OF YOSS, A PUTATIVE DUTPASE FROM BACILLUS SUBTILIS	3.6.1.23
2BB0	STRUCTURE OF IMIDAZOLONEPROPIONASE FROM BACILLUS SUBTILIS	3.5.2.7
2BB4	PORCINE PANCREATIC ELASTASE COMPLEXED WITH BETA-CASOMORPHIN-7 AND ASP-PHE AT PH 5.0	3.4.21.36
2BB7	MN FORM OF E. COLI METHIONINE AMINOPEPTIDASE IN COMPLEX WITH A QUINOLINYL SULFONAMIDE INHIBITOR	3.4.11.18
2BB9	STRUCTURE OF HIV1 PROTEASE AND AKC4P_133A COMPLEX.	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2BBB	STRUCTURE OF HIV1 PROTEASE AND HH1_173_3A COMPLEX.	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2BBV	THE REFINED THREE-DIMENSIONAL STRUCTURE OF AN INSECT VIRUS AT 2.8 ANGSTROMS RESOLUTION	3.4.23.44
2BBY	DNA-BINDING DOMAIN FROM HUMAN RAP30, NMR, 30 STRUCTURES	3.6.4.12
2BC2	METALLO BETA-LACTAMASE II FROM BACILLUS CEREUS 569/H/9 AT PH 6.0, TRIGONAL CRYSTAL FORM	3.5.2.6
2BC9	CRYSTAL-STRUCTURE OF THE N-TERMINAL LARGE GTPASE DOMAIN OF HUMAN GUANYLATE BINDING PROTEIN 1 (HGBP1) IN COMPLEX WITH NON-HYDROLYSABLE GTP ANALOGUE GPPNHP	3.6.5
2BCD	X-RAY CRYSTAL STRUCTURE OF PROTEIN PHOSPHATASE-1 WITH THE MARINE TOXIN MOTUPORIN BOUND	3.1.3.16
2BCE	CHOLESTEROL ESTERASE FROM BOS TAURUS	3.1.1.13 3.1.1.3 3.1.1.6
2BCH	A POSSIBLE OF SECOND CALCIUM ION IN INTERFACIAL BINDING: ATOMIC AND MEDIUM RESOLUTION CRYSTAL STRUCTURES OF THE QUADRUPLE MUTANT OF PHOSPHOLIPASE A2	3.1.1.4
2BCO	X-RAY STRUCTURE OF SUCCINYLGLUTAMATE DESUCCINALASE FROM VIBRIO PARAHAEMOLYTICUS (RIMD 2210633) AT THE RESOLUTION 2.3 A, NORTHEAST STRUCTURAL GENOMICS TARGET VPR14	3.1 3.5.1.96
2BD1	A POSSIBLE ROLE OF THE SECOND CALCIUM ION IN INTERFACIAL BINDING: ATOMIC AND MEDIUM RESOLUTION CRYSTAL STRUCTURES OF THE QUADRUPLE MUTANT OF PHOSPHOLIPASE A2	3.1.1.4
2BD2	PORCINE PANCREATIC ELASTASE COMPLEXED WITH BETA-CASOMORPHIN-7 AND ARG-PHE AT PH 5.0	3.4.21.36
2BD3	PORCINE PANCREATIC ELASTASE COMPLEXED WITH BETA-CASOMORPHIN-7 AND LYS-ALA-NH2 AT PH 5.0	3.4.21.36
2BD4	PORCINE PANCREATIC ELASTASE COMPLEXED WITH BETA-CASOMORPHIN-7 AND LYS-SER AT PH 5.0	3.4.21.36
2BD5	PORCINE PANCREATIC ELASTASE COMPLEXED WITH BETA-CASOMORPHIN-7 AND LYS-SER AT PH 5 AND IMMERSED IN PH 9 BUFFER FOR 30 SECONDS	3.4.21.36
2BD7	PORCINE PANCREATIC ELASTASE COMPLEXED WITH BETA-CASOMORPHIN-7 AND ARG-PHE AT PH 5.0 (50 MIN SOAK)	3.4.21.36
2BD8	PORCINE PANCREATIC ELASTASE COMPLEXED WITH BETA-CASOMORPHIN-7 AND ARG-PHE AT PH 5.0 (50 MIN SOAK) AND IMMERSED IN PH 9 BUFFER FOR 30 SECONDS	3.4.21.36
2BD9	PORCINE PANCREATIC ELASTASE COMPLEXED WITH BETA-CASOMORPHIN-7 AND ARG-PHE AT PH 5.0 (50 MIN SOAK) AND IMMERSED IN PH 9 BUFFER FOR 28 SECONDS (2ND PH JUMP)	3.4.21.36
2BDA	PORCINE PANCREATIC ELASTASE COMPLEXED WITH N-ACETYL-NPI AND ALA-ALA AT PH 5.0	3.4.21.36
2BDB	PORCINE PANCREATIC ELASTASE COMPLEXED WITH ASN-PRO-ILE AND ALA-ALA AT PH 5.0	3.4.21.36
2BDC	PORCINE PANCREATIC ELASTASE COMPLEXED WITH ASN-PRO-ILE AT PH 5.0	3.4.21.36
2BDG	HUMAN KALLIKREIN 4 COMPLEX WITH NICKEL AND P-AMINOBENZAMIDINE	3.4.21
2BDH	HUMAN KALLIKREIN 4 COMPLEX WITH ZINC AND P-AMINOBENZAMIDINE	3.4.21
2BDL	CATHEPSIN K COMPLEXED WITH A PYRROLIDINE KETOAMIDE-BASED INHIBITOR	3.4.22.38
2BDR	CRYSTAL STRUCTURE OF THE PUTATIVE UREIDOGLYCOLATE HYDROLASE PP4288 FROM PSEUDOMONAS PUTIDA, NORTHEAST STRUCTURAL GENOMICS TARGET PPR49	3.5.3.19 4.3.2.3
2BDU	X-RAY STRUCTURE OF A CYTOSOLIC 5'-NUCLEOTIDASE III FROM MUS MUSCULUS MM.158936	3.1.3.5 3.1.3.91
2BDV	X-RAY CRYSTAL STRUCTURE OF PHAGE-RELATED PROTEIN BB2244 FROM BORDETELLA BRONCHISEPTICA. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET BOR24.	3.4
2BDX	X-RAY CRYSTAL STRUCTURE OF DIHYDROMICROCYSTIN-LA BOUND TO PROTEIN PHOSPHATASE-1	3.1.3.16
2BDY	THROMBIN IN COMPLEX WITH INHIBITOR	3.4.21.5
2BDZ	MEXICAIN FROM JACARATIA MEXICANA	3.4.22
2BE1	STRUCTURE OF THE COMPACT LUMENAL DOMAIN OF YEAST IRE1	2.7.11.1 3.1.26
2BE2	CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE (RT) IN COMPLEX WITH R221239	2.7.7.49 3.4.23.16 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2BEJ	STRUCTURE OF THE BACTERIAL CHROMOSOME SEGREGATION PROTEIN SOJ	3.6
2BEK	STRUCTURE OF THE BACTERIAL CHROMOSOME SEGREGATION PROTEIN SOJ	3.6
2BER	Y370G ACTIVE SITE MUTANT OF THE SIALIDASE FROM MICROMONOSPORA VIRIDIFACIENS IN COMPLEX WITH BETA-NEU5AC (SIALIC ACID).	3.2.1.18
2BF6	ATOMIC RESOLUTION STRUCTURE OF THE BACTERIAL SIALIDASE NANI FROM CLOSTRIDIUM PERFRINGENS IN COMPLEX WITH ALPHA-SIALIC ACID (NEU5AC).	3.2.1.18
2BFK	BACILLUS CEREUS METALLO-BETA-LACTAMASE (BCII) ARG (121) CYS MUTANT. SOLVED AT PH7 USING 20MM ZNSO4 IN BUFFER. 1MM DTT WAS USED AS A REDUCING AGENT	3.5.2.6
2BFL	BACILLUS CEREUS METALLO-BETA-LACTAMASE (BCII) ARG (121) CYS MUTANT. SOLVED AT PH5 USING 20MM ZNSO4 IN BUFFER. 1MM DTT WAS USED AS A REDUCING AGENT.	3.5.2.6
2BFN	THE CRYSTAL STRUCTURE OF THE COMPLEX OF THE HALOALKANE DEHALOGENASE LINB WITH THE PRODUCT OF DEHALOGENATION REACTION 1,2-DICHLOROPROPANE.	3.8.1.5
2BFQ	MACRO DOMAINS ARE ADP-RIBOSE BINDING MOLECULES	3.2.2
2BFR	THE MACRO DOMAIN IS AN ADP-RIBOSE BINDING MODULE	3.2.2
2BFZ	BACILLUS CEREUS METALLO-BETA-LACTAMASE (BCII) ARG (121) CYS MUTANT. SOLVED AT PH4.5 USING 20MM ZNSO4 IN BUFFER. 1MM DTT WAS USED AS A REDUCING AGENT. CYS221 IS OXIDIZED.	3.5.2.6
2BG1	ACTIVE SITE RESTRUCTURING REGULATES LIGAND RECOGNITION IN CLASSA PENICILLIN-BINDING PROTEINS (PBPS)	2.4.1.129 3.4.16.4
2BG2	BACILLUS CEREUS METALLO-BETA-LACTAMASE (BCII) ARG (121) CYS MUTANT. SOLVED AT PH4.5 USING 20MM ZNSO4 IN THE BUFFER. 1MM DTT AND 1MM TCEP- HCL WERE USED AS REDUCING AGENTS. CYS221 IS REDUCED.	3.5.2.6
2BG6	BACILLUS CEREUS METALLO-BETA-LACTAMASE (BCII) ARG (121) CYS MUTANT. SOLVED AT PH5 USING 20 MICROMOLAR ZNSO4 IN THE BUFFER. 1MM DTT WAS USED AS A REDUCING AGENT. CYS221 IS OXIDIZED.	3.5.2.6
2BG7	BACILLUS CEREUS METALLO-BETA-LACTAMASE (BCII) ARG (121) CYS MUTANT. SOLVED AT PH4.5 USING 20 MICROMOLAR ZNSO4 IN THE BUFFER. 1MM DTT WAS USED AS A REDUCING AGENT. CYS221 IS OXIDIZED.	3.5.2.6
2BG8	BACILLUS CEREUS METALLO-BETA-LACTAMASE (BCII) ARG (121) CYS MUTANT. SOLVED AT PH4.5 USING 20 MICROMOLAR ZNSO4 IN THE BUFFER. 1MM DTT AND 1MM TCEP-HCL WERE USED AS REDUCING AGENTS.	3.5.2.6
2BGA	BACILLUS CEREUS METALLO-BETA-LACTAMASE (BCII) ARG (121) CYS MUTANT. SOLVED AT PH7 USING 20 MICROMOLAR ZNSO4 IN THE BUFFER. 1MM DTT WAS USED AS A REDUCING AGENT. CYS221 IS OXIDIZED.	3.5.2.6
2BGD	STRUCTURE-BASED DESIGN OF PROTEIN TYROSINE PHOSPHATASE-1B INHIBITORS	3.1.3.48
2BGE	STRUCTURE-BASED DESIGN OF PROTEIN TYROSINE PHOSPHATASE-1B INHIBITORS	3.1.3.48
2BGN	HIV-1 TAT PROTEIN DERIVED N-TERMINAL NONAPEPTIDE TRP2-TAT(1-9) BOUND TO THE ACTIVE SITE OF DIPEPTIDYL PEPTIDASE IV (CD26)	3.4.14.5
2BGR	CRYSTAL STRUCTURE OF HIV-1 TAT DERIVED NONAPEPTIDES TAT(1-9) BOUND TO THE ACTIVE SITE OF DIPEPTIDYL PEPTIDASE IV (CD26)	3.4.14.5
2BH3	ZN SUBSTITUTED E. COLI AMINOPEPTIDASE P IN COMPLEX WITH PRODUCT	3.4.11.9
2BH7	CRYSTAL STRUCTURE OF A SEMET DERIVATIVE OF AMID AT 2.2 ANGSTROMS	3.5.1.28
2BHA	E. COLI AMINOPEPTIDASE P IN COMPLEX WITH SUBSTRATE	3.4.11.9
2BHB	ZN SUBSTITUTED E. COLI AMINOPEPTIDASE P	3.4.11.9
2BHC	NA SUBSTITUTED E. COLI AMINOPEPTIDASE P	3.4.11.9
2BHD	MG SUBSTITUTED E. COLI AMINOPEPTIDASE P IN COMPLEX WITH PRODUCT	3.4.11.9
2BHG	3C PROTEASE FROM TYPE A10(61) FOOT-AND-MOUTH DISEASE VIRUS	3.4.22.28 3.4.22.46 3.6.1.15 2.7.7.48
2BHR	DENGUE VIRUS RNA HELICASE	3.4.21.91 3.6.1.15 3.6.4.13
2BHU	CRYSTAL STRUCTURE OF DEINOCOCCUS RADIODURANS MALTOOLIGOSYLTREHALOSE TREHALOHYDROLASE	3.2.1.1 3.2.1.141
2BHY	CRYSTAL STRUCTURE OF DEINOCOCCUS RADIODURANS MALTOOLIGOSYLTREHALOSE TREHALOHYDROLASE IN COMPLEX WITH TREHALOSE	3.2.1.1 3.2.1.141
2BHZ	CRYSTAL STRUCTURE OF DEINOCOCCUS RADIODURANS MALTOOLIGOSYLTREHALOSE TREHALOHYDROLASE IN COMPLEX WITH MALTOSE	3.2.1.1 3.2.1.141
2BIF	6-PHOSPHOFRUCTO-2-KINASE/FRUCTOSE-2,6-BISPHOSPHATASE H256A MUTANT WITH F6P IN PHOSPHATASE ACTIVE SITE	2.7.1.105 3.1.3.46
2BIJ	CRYSTAL STRUCTURE OF THE HUMAN PROTEIN TYROSINE PHOSPHATASE PTPN5 (STEP, STRIATUM ENRICHED ENRICHED PHOSPHATASE)	3.1.3.48
2BJD	SULFOLOBUS SOLFATARICUS ACYLPHOSPHATASE. TRICLINIC SPACE GROUP	3.6.1.7
2BJE	ACYLPHOSPHATASE FROM SULFOLOBUS SOLFATARICUS. MONCLINIC P21 SPACE GROUP	3.6.1.7
2BJF	CRYSTAL STRUCTURE OF CONJUGATED BILE ACID HYDROLASE FROM CLOSTRIDIUM PERFRINGENS IN COMPLEX WITH REACTION PRODUCTS TAURINE AND DEOXYCHOLATE	3.5.1.24 3.5.1
2BJG	CRYSTAL STRUCTURE OF CONJUGATED BILE ACID HYDROLASE FROM CLOSTRIDIUM PERFRINGENS IN COMPLEX WITH REACTION PRODUCTS TAURINE AND DEOXYCHOLATE	3.5.1.24 3.5.1
2BJH	CRYSTAL STRUCTURE OF S133A ANFAEA-FERULIC ACID COMPLEX	3.1.1.73
2BJI	HIGH RESOLUTION STRUCTURE OF MYO-INOSITOL MONOPHOSPHATASE, THE TARGET OF LITHIUM THERAPY	3.1.3.25 3.1.3.94
2BJJ	STRUCTURE OF RECOMBINANT HUMAN LACTOFERRIN PRODUCED IN THE MILK OF TRANSGENIC COWS	3.4.21
2BJU	PLASMEPSIN II COMPLEXED WITH A HIGHLY ACTIVE ACHIRAL INHIBITOR	3.4.23.39
2BKL	STRUCTURAL AND MECHANISTIC ANALYSIS OF TWO PROLYL ENDOPEPTIDASES: ROLE OF INTER-DOMAIN DYNAMICS IN CATALYSIS AND SPECIFICITY	3.4.21.26
2BKQ	NEDD8 PROTEASE	3.4.22
2BKR	NEDD8 NEDP1 COMPLEX	3.4.22
2BKS	CRYSTAL STRUCTURE OF RENIN-PF00074777 COMPLEX	3.4.23.15
2BKT	CRYSTAL STRUCTURE OF RENIN-PF00257567 COMPLEX	3.4.23.15
2BKV	STRUCTURE AND KINETICS OF A MONOMERIC GLUCOSAMINE-6-PHOSPHATE DEAMINASE: MISSING LINK OF THE NAGB SUPERFAMILY	3.5.99.6
2BKX	STRUCTURE AND KINETICS OF A MONOMERIC GLUCOSAMINE-6-PHOSPHATE DEAMINASE: MISSING LINK OF THE NAGB SUPERFAMILY	3.5.99.6
2BL2	THE MEMBRANE ROTOR OF THE V-TYPE ATPASE FROM ENTEROCOCCUS HIRAE	3.6.3.14
2BLO	ELASTASE BEFORE A HIGH DOSE X-RAY BURN""	3.4.21.36
2BLP	RNASE BEFORE UNATTENUATED X-RAY BURN	3.1.27.5 4.6.1.18
2BLQ	ELASTASE AFTER A HIGH DOSE X-RAY BURN""	3.4.21.36
2BLS	AMPC BETA-LACTAMASE FROM ESCHERICHIA COLI	3.5.2.6
2BLV	TRYPSIN BEFORE A HIGH DOSE X-RAY BURN""	3.4.21.4
2BLW	TRYPSIN AFTER A HIGH DOSE X-RAY BURN""	3.4.21.4
2BLX	HEWL BEFORE A HIGH DOSE X-RAY BURN""	3.2.1.17
2BLY	HEWL AFTER A HIGH DOSE X-RAY BURN""	3.2.1.17
2BLZ	RNASE AFTER A HIGH DOSE X-RAY BURN""	3.1.27.5 4.6.1.18
2BM2	HUMAN BETA-II TRYPTASE IN COMPLEX WITH 4-(3-AMINOMETHYL-PHENYL)- PIPERIDIN-1-YL-(5-PHENETHYL- PYRIDIN-3-YL)-METHANONE	3.4.21.59
2BMD	HIGH RESOLUTION STRUCTURE OF GDP-BOUND HUMAN RAB4A	3.6.5.2
2BME	HIGH RESOLUTION STRUCTURE OF GPPNHP-BOUND HUMAN RAB4A	3.6.5.2
2BMF	DENGUE VIRUS RNA HELICASE AT 2.4A	3.4.21.91 3.6.1.15 3.6.4.13
2BMG	CRYSTAL STRUCTURE OF FACTOR XA IN COMPLEX WITH 50	3.4.21.6
2BMI	METALLO-BETA-LACTAMASE	3.5.2.6
2BML	OFLOXACIN-LIKE ANTIBIOTICS INHIBIT PNEUMOCOCCAL CELL WALL DEGRADING VIRULENCE FACTORS	3.5.1.28
2BN7	MN SUBSTITUTED E. COLI AMINOPEPTIDASE P IN COMPLEX WITH PRODUCT AND ZN	3.4.11.9
2BNG	STRUCTURE OF AN M.TUBERCULOSIS LEH-LIKE EPOXIDE HYDROLASE	3.3.2.8 3.3.2.10 3.3.2.11
2BNJ	THE XYLANASE TA FROM THERMOASCUS AURANTIACUS UTILIZES ARABINOSE DECORATIONS OF XYLAN AS SIGNIFICANT SUBSTRATE SPECIFICITY DETERMINANTS.	3.2.1.8
2BO5	BOVINE OLIGOMYCIN SENSITIVITY CONFERRAL PROTEIN N-TERMINAL DOMAIN	3.6.3.14
2BO9	HUMAN CARBOXYPEPTIDASE A4 IN COMPLEX WITH HUMAN LATEXIN.	3.4.17
2BOA	HUMAN PROCARBOXYPEPTIDASE A4.	3.4.17
2BOD	CATALYTIC DOMAIN OF ENDO-1,4-GLUCANASE CEL6A FROM THERMOBIFIDA FUSCA IN COMPLEX WITH METHYL CELLOBIOSYL-4-THIO-BETA-CELLOBIOSIDE	3.2.1.4
2BOE	CATALYTIC DOMAIN OF ENDO-1,4-GLUCANASE CEL6A MUTANT Y73S FROM THERMOBIFIDA FUSCA	3.2.1.4
2BOF	CATALYTIC DOMAIN OF ENDO-1,4-GLUCANASE CEL6A MUTANT Y73S FROM THERMOBIFIDA FUSCA IN COMPLEX WITH CELLOTETROSE	3.2.1.4
2BOG	CATALYTIC DOMAIN OF ENDO-1,4-GLUCANASE CEL6A MUTANT Y73S FROM THERMOBIFIDA FUSCA IN COMPLEX WITH METHYL CELLOBIOSYL-4-THIO-BETA- CELLOBIOSIDE	3.2.1.4
2BOH	CRYSTAL STRUCTURE OF FACTOR XA IN COMPLEX WITH COMPOUND 1""	3.4.21.6
2BOK	FACTOR XA - CATION	3.4.21.6
2BOO	THE CRYSTAL STRUCTURE OF URACIL-DNA N-GLYCOSYLASE (UNG) FROM DEINOCOCCUS RADIODURANS.	3.2.2.3 3.2.2.27
2BOV	MOLECULAR RECOGNITION OF AN ADP-RIBOSYLATING CLOSTRIDIUM BOTULINUM C3 EXOENZYME BY RALA GTPASE	3.6.5.2
2BP2	THE STRUCTURE OF BOVINE PANCREATIC PROPHOSPHOLIPASE A2 AT 3.0 ANGSTROMS RESOLUTION	3.1.1.4
2BPP	PHOSPHOLIPASE A2 ENGINEERING. X-RAY STRUCTURAL AND FUNCTIONAL EVIDENCE FOR THE INTERACTION OF LYSINE-56 WITH SUBSTRATES	3.1.1.4
2BPU	THE KEDGE HOLMIUM DERIVATIVE OF HEN EGG-WHITE LYSOZYME AT HIGH RESOLUTION FROM SINGLE WAVELENGTH ANOMALOUS DIFFRACTION	3.2.1.17
2BPV	HIV-1 PROTEASE-INHIBITOR COMPLEX	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2BPW	HIV-1 PROTEASE-INHIBITOR COMPLEX	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2BPX	HIV-1 PROTEASE-INHIBITOR COMPLEX	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2BPY	HIV-1 PROTEASE-INHIBITOR COMPLEX	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2BPZ	HIV-1 PROTEASE-INHIBITOR COMPLEX	3.4.23.16 2.7.7.49 2.7.7.7 3.1.26.13 3.1.13.2 2.7.7 3.1
2BQ6	CRYSTAL STRUCTURE OF FACTOR XA IN COMPLEX WITH 21	3.4.21.6
2BQ7	CRYSTAL STRUCTURE OF FACTOR XA IN COMPLEX WITH 43	3.4.21.6
2BQ8	CRYSTAL STRUCTURE OF HUMAN PURPLE ACID PHOSPHATASE WITH AN INHIBITORY CONFORMATION OF THE REPRESSION LOOP	3.1.3.2
2BQA	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQB	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQC	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQD	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQE	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQF	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQG	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQH	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQI	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQJ	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQK	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQL	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQM	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQN	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQO	CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME	3.2.1.17
2BQV	HIV-1 PROTEASE IN COMPLEX WITH INHIBITOR AHA455	3.4.23.16
2BQW	CRYSTAL STRUCTURE OF FACTOR XA IN COMPLEX WITH COMPOUND 45	3.4.21.6
2BQX	INORGANIC PYROPHOSPHATASE FROM THE PATHOGENIC BACTERIUM HELICOBACTER PYLORI-KINETIC AND STRUCTURAL PROPERTIES	3.6.1.1
2BQY	INORGANIC PYROPHOSPHATASE FROM THE PATHOGENIC BACTERIUM HELICOBACTER PYLORI-KINETIC AND STRUCTURAL PROPERTIES	3.6.1.1
2BR6	CRYSTAL STRUCTURE OF QUORUM-QUENCHING N-ACYL HOMOSERINE LACTONE LACTONASE	3.1.1.81
2BRF	CRYSTAL STRUCTURE OF THE FHA DOMAIN OF HUMAN POLYNUCLEOTIDE KINASE 3' PHOSPHATASE	3.1.3.32 2.7.1.78
2BRK	CRYSTAL STRUCTURE OF HEPATITIS C VIRUS POLYMERASE IN COMPLEX WITH AN ALLOSTERIC INHIBITOR (COMPOUND 1)	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
2BRL	CRYSTAL STRUCTURE OF HEPATITIS C VIRUS POLYMERASE IN COMPLEX WITH AN ALLOSTERIC INHIBITOR (COMPOUND 2)	2.7.7.48 3.4.22 3.4.21.98 3.6.1.15 3.6.4.13
2BSQ	FITAB BOUND TO DNA	3.1
2BSY	EPSTEIN BARR VIRUS DUTPASE	3.6.1.23
2BT1	EPSTEIN BARR VIRUS DUTPASE IN COMPLEX WITH A,B-IMINO DUTP	3.6.1.23
2BTC	BOVINE TRYPSIN IN COMPLEX WITH SQUASH SEED INHIBITOR (CUCURBITA PEPO TRYPSIN INHIBITOR II)	3.4.21.4
2BTN	CRYSTAL STRUCTURE AND CATALYTIC MECHANISM OF THE QUORUM-QUENCHING N- ACYL HOMOSERINE LACTONE HYDROLASE	3.1.1.81
2BU4	RIBONUCLEASE T1 COMPLEX WITH 2'GMP	3.1.27.3 4.6.1.24
2BUB	CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE IV (CD26) IN COMPLEX WITH A REVERSED AMIDE INHIBITOR	3.4.14.5
2BUG	SOLUTION STRUCTURE OF THE TPR DOMAIN FROM PROTEIN PHOSPHATASE 5 IN COMPLEX WITH HSP90 DERIVED PEPTIDE	3.1.3.16
2BV5	CRYSTAL STRUCTURE OF THE HUMAN PROTEIN TYROSINE PHOSPHATASE PTPN5 AT 1.8A RESOLUTION	3.1.3.48
2BV9	HOW FAMILY 26 GLYCOSIDE HYDROLASES ORCHESTRATE CATALYSIS ON DIFFERENT POLYSACCHARIDES. STRUCTURE AND ACTIVITY OF A CLOSTRIDIUM THERMOCELLUM LICHENASE, CTLIC26A	3.2.1.4
2BVD	HOW FAMILY 26 GLYCOSIDE HYDROLASES ORCHESTRATE CATALYSIS ON DIFFERENT POLYSACCHARIDES. STRUCTURE AND ACTIVITY OF A CLOSTRIDIUM THERMOCELLUM LICHENASE, CTLIC26A	3.2.1.4
2BVL	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF TOXIN B FROM CLOSTRIDIUM DIFFICILE IN COMPLEX WITH UDP, GLC AND MANGANESE ION	2.4.1 3.4.22
2BVM	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF TOXIN B FROM CLOSTRIDIUM DIFFICILE IN COMPLEX WITH UDP, GLC AND MANGANESE ION	2.4.1 3.4.22
2BVN	E. COLI EF-TU:GDPNP IN COMPLEX WITH THE ANTIBIOTIC ENACYLOXIN IIA	3.6.1.48
2BVR	HUMAN THROMBIN COMPLEXED WITH FRAGMENT-BASED SMALL MOLECULES OCCUPYING THE S1 POCKET	3.4.21.5
2BVS	HUMAN THROMBIN COMPLEXED WITH FRAGMENT-BASED SMALL MOLECULES OCCUPYING THE S1 POCKET	3.4.21.5
2BVT	THE STRUCTURE OF A MODULAR ENDO-BETA-1,4-MANNANASE FROM CELLULOMONAS FIMI EXPLAINS THE PRODUCT SPECIFICITY OF GLYCOSIDE HYDROLASE FAMILY 26 MANNANASES.	3.2.1.78
2BVV	SUGAR RING DISTORTION IN THE GLYCOSYL-ENZYME INTERMEDIATE OF A FAMILY G/11 XYLANASE.	3.2.1.8
2BVW	CELLOBIOHYDROLASE II (CEL6A) FROM HUMICOLA INSOLENS IN COMPLEX WITH GLUCOSE AND CELLOTETRAOSE	3.2.1.91
2BVX	DESIGN AND DISCOVERY OF NOVEL, POTENT THROMBIN INHIBITORS WITH A SOLUBILIZING CATIONIC P1-P2-LINKER	3.4.21.5
2BVY	THE STRUCTURE AND CHARACTERIZATION OF A MODULAR ENDO-BETA-1,4-MANNANASE FROM CELLULOMONAS FIMI	3.2.1.78
2BW8	NATIVE STRUCTURE OF ENDOGLUCANASE 12A (CEL12A) FROM RHODOTHERMUS MARINUS	3.2.1.4
2BWA	STRUCTURE OF ENDOGLUCANASE 12A (CEL12A) FROM RHODOTHERMUS MARINUS IN COMPLEX WITH CELLOPENTAOSE, 20 MINUTE SOAK.	3.2.1.4
2BWC	STRUCTURE OF ENDOGLUCANASE 12A (CEL12A) FROM RHODOTHERMUS MARINUS IN COMPLEX WITH CELLOPENTAOSE (5 MINUTE SOAK)	3.2.1.4
2BWK	MURINE ANGIOGENIN, SULPHATE COMPLEX	3.1.27.5 3.1.27
2BWL	MURINE ANGIOGENIN, PHOSPHATE COMPLEX	3.1.27.5 3.1.27
2BWS	HIS243ALA ESCHERICHIA COLI AMINOPEPTIDASE P	3.4.11.9
2BWT	ASP260ALA ESCHERICHIA COLI AMINOPEPTIDASE P	3.4.11.9
2BWU	ASP271ALA ESCHERICHIA COLI AMINOPEPTIDASE P	3.4.11.9
2BWV	HIS361ALA ESCHERICHIA COLI AMINOPEPTIDASE P	3.4.11.9
2BWW	HIS350ALA ESCHERICHIA COLI AMINOPEPTIDASE P	3.4.11.9
2BWX	HIS354ALA ESCHERICHIA COLI AMINOPEPTIDASE P	3.4.11.9
2BWY	GLU383ALA ESCHERICHIA COLI AMINOPEPTIDASE P	3.4.11.9
2BX2	CATALYTIC DOMAIN OF E. COLI RNASE E	3.1.4 3.1.26.12
2BX3	CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (P43212)	3.4.24 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2BX4	CRYSTAL STRUCTURE OF SARS CORONAVIRUS MAIN PROTEINASE (P21212)	3.4.22 3.4.24 3.4.19.12 3.4.22.69 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2BXT	DESIGN AND DISCOVERY OF NOVEL, POTENT THROMBIN INHIBITORS WITH A SOLUBILIZING CATIONIC P1-P2-LINKER	3.4.21.5
2BXU	DESIGN AND DISCOVERY OF NOVEL, POTENT THROMBIN INHIBITORS WITH A SOLUBILIZING CATIONIC P1-P2-LINKER	3.4.21.5
2BXY	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.2.1.1 3.2.1.141
2BXZ	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.2.1.1 3.2.1.141
2BY0	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.2.1.1 3.2.1.141
2BY1	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.2.1.1 3.2.1.141
2BY2	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.2.1.1 3.2.1.141
2BY3	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.2.1.1 3.2.1.141
2BY4	SR CA(2+)-ATPASE IN THE HNE2 STATE COMPLEXED WITH THE THAPSIGARGIN DERIVATIVE BOC-12ADT.	3.6.3.8 7.2.2.10
2BY5	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.4.21.4
2BY6	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.4.21.4
2BY7	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.4.21.4
2BY8	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.4.21.4
2BY9	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.4.21.4
2BYA	IS RADIATION DAMAGE DEPENDENT ON THE DOSE-RATE USED DURING MACROMOLECULAR CRYSTALLOGRAPHY DATA COLLECTION	3.4.21.4
2BYE	NMR SOLUTION STRUCTURE OF PHOSPHOLIPASE C EPSILON RA 1 DOMAIN	3.1.4.11
2BYF	NMR SOLUTION STRUCTURE OF PHOSPHOLIPASE C EPSILON RA 2 DOMAIN	3.1.4.11
2BZ1	CRYSTAL STRUCTURE OF APO E. COLI GTP CYCLOHYDROLASE II	3.5.4.25
2BZ6	ORALLY AVAILABLE FACTOR7A INHIBITOR	3.4.21.21
2BZA	BOVINE PANCREAS BETA-TRYPSIN IN COMPLEX WITH BENZYLAMINE	3.4.21.4
2BZD	GALACTOSE RECOGNITION BY THE CARBOHYDRATE-BINDING MODULE OF A BACTERIAL SIALIDASE.	3.2.1.18
2BZL	CRYSTAL STRUCTURE OF THE HUMAN PROTEIN TYROSINE PHOSPHATASE N14 AT 1. 65 A RESOLUTION	3.1.3.48
2BZZ	CRYSTAL STRUCTURES OF EOSINOPHIL-DERIVED NEUROTOXIN IN COMPLEX WITH THE INHIBITORS 5'-ATP, AP3A, AP4A AND AP5A	3.1.27.5 4.6.1.18
2C01	CRYSTAL STRUCTURES OF EOSINOPHIL-DERIVED NEUROTOXIN IN COMPLEX WITH THE INHIBITORS 5'-ATP, AP3A, AP4A AND AP5A	3.1.27.5 4.6.1.18
2C02	CRYSTAL STRUCTURES OF EOSINOPHIL-DERIVED NEUROTOXIN IN COMPLEX WITH THE INHIBITORS 5'-ATP, AP3A, AP4A AND AP5A	3.1.27.5 4.6.1.18
2C05	CRYSTAL STRUCTURES OF EOSINOPHIL-DERIVED NEUROTOXIN IN COMPLEX WITH THE INHIBITORS 5'-ATP, AP3A, AP4A AND AP5A	3.1.27.5 4.6.1.18
2C06	NMR-BASED MODEL OF THE COMPLEX OF THE TOXIN KID AND A 5-NUCLEOTIDE SUBSTRATE RNA FRAGMENT (AUACA)	3.1
2C0B	CATALYTIC DOMAIN OF E. COLI RNASE E IN COMPLEX WITH 13-MER RNA	3.1.4 3.1.26.12
2C0H	X-RAY STRUCTURE OF BETA-MANNANASE FROM BLUE MUSSEL MYTILUS EDULIS	3.2.1.78
2C0P	AGED FORM OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY TABUN	3.1.1.7
2C0Q	NON-AGED FORM OF MOUSE ACETYLCHOLINESTERASE INHIBITED BY TABUN	3.1.1.7
2C0Y	THE CRYSTAL STRUCTURE OF A CYS25ALA MUTANT OF HUMAN PROCATHEPSIN S	3.4.22.27
2C1C	STRUCTURAL BASIS OF THE RESISTANCE OF AN INSECT CARBOXYPEPTIDASE TO PLANT PROTEASE INHIBITORS	3.4.17.2
2C1E	CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE MICHAEL ACCEPTOR INHIBITORS.	3.4.22 3.4.22.56
2C1F	THE STRUCTURE OF THE FAMILY 11 XYLANASE FROM NEOCALLIMASTIX PATRICIARUM	3.2.1.8
2C1G	STRUCTURE OF STREPTOCOCCUS PNEUMONIAE PEPTIDOGLYCAN DEACETYLASE (SPPGDA)	3.5.1.33 3.5.1.104
2C1I	STRUCTURE OF STREPTOCOCCUS PNEUMONIAE PEPTIDOGLYCAN DEACETYLASE (SPPGDA) D 275 N MUTANT.	3.5.1.33 3.5.1.104
2C1L	STRUCTURE OF THE BFII RESTRICTION ENDONUCLEASE	3.1.21.4
2C1W	THE STRUCTURE OF XENDOU: A SPLICING INDEPENDENT SNORNA PROCESSING ENDORIBONUCLEASE	3.1
2C2H	CRYSTAL STRUCTURE OF THE HUMAN RAC3 IN COMPLEX WITH GDP	3.6.5.2
2C2K	CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE MICHAEL ACCEPTOR INHIBITORS.	3.4.22 3.4.22.56
2C2M	CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE MICHAEL ACCEPTOR INHIBITORS.	3.4.22 3.4.22.56
2C2O	CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE MICHAEL ACCEPTOR INHIBITORS.	3.4.22 3.4.22.56
2C2P	THE CRYSTAL STRUCTURE OF MISMATCH SPECIFIC URACIL-DNA GLYCOSYLASE (MUG) FROM DEINOCOCCUS RADIODURANS	3.2.2
2C2Q	THE CRYSTAL STRUCTURE OF MISMATCH SPECIFIC URACIL-DNA GLYCOSYLASE (MUG) FROM DEINOCOCCUS RADIODURANS. INACTIVE MUTANT ASP93ALA.	3.2.2
2C2X	THREE DIMENSIONAL STRUCTURE OF BIFUNCTIONAL METHYLENETETRAHYDROFOLATE DEHYDROGENASE-CYCLOHYDROLASE FROM MYCOBACTERIUM TUBERCULOSIS	1.5.1.5 3.5.4.9
2C2Y	THREE DIMENSIONAL STRUCTURE OF BIFUNCTIONAL METHYLENETETRAHYDROFOLATE DEHYDROGENASE-CYCLOHYDROLASE FROM MYCOBACTERIUM TUBERCULOSIS	1.5.1.5 3.5.4.9
2C2Z	CRYSTAL STRUCTURE OF CASPASE-8 IN COMPLEX WITH AZA-PEPTIDE MICHAEL ACCEPTOR INHIBITOR	3.4.22 3.4.22.61
2C3S	STRUCTURE OF SARS COV MAIN PROTEINASE AT 1.9 A (PH6.5)	3.4.24 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2C40	CRYSTAL STRUCTURE OF INOSINE-URIDINE PREFERRING NUCLEOSIDE HYDROLASE FROM BACILLUS ANTHRACIS AT 2.2A RESOLUTION	3.2.2.1
2C46	CRYSTAL STRUCTURE OF THE HUMAN RNA GUANYLYLTRANSFERASE AND 5'- PHOSPHATASE	2.7.7.50 3.1.3.33
2C4A	STRUCTURE OF NEURAMINIDASE SUBTYPE N9 COMPLEXED WITH 30 MM SIALIC ACID (NANA, NEU5AC), CRYSTAL SOAKED FOR 3 HOURS AT 291 K.	3.2.1.18
2C4B	INHIBITOR CYSTINE KNOT PROTEIN MCOEETI FUSED TO THE CATALYTICALLY INACTIVE BARNASE MUTANT H102A	3.1.27.3 3.1.27
2C4F	CRYSTAL STRUCTURE OF FACTOR VII.STF COMPLEXED WITH PD0297121	3.4.21.21
2C4H	TORPEDO CALIFORNICA ACETYLCHOLINESTERASE IN COMPLEX WITH 500MM ACETYLTHIOCHOLINE	3.1.1.7
2C4L	STRUCTURE OF NEURAMINIDASE SUBTYPE N9 COMPLEXED WITH 30 MM SIALIC ACID (NANA, NEU5AC), CRYSTAL SOAKED FOR 24 HOURS AT 291 K AND FINALLY BACKSOAKED FOR 30 MIN IN A CRYOPROTECTANT SOLUTION WHICH DID NOT CONTAIN NEU5AC	3.2.1.18
2C4N	NAGD FROM E.COLI K-12 STRAIN	3.1.3.5
2C4R	CATALYTIC DOMAIN OF E. COLI RNASE E	3.1.4 3.1.26.12
2C53	A COMPARATIVE STUDY OF URACIL DNA GLYCOSYLASES FROM HUMAN AND HERPES SIMPLEX VIRUS TYPE 1	3.2.2.3 3.2.2.27
2C56	A COMPARATIVE STUDY OF URACIL DNA GLYCOSYLASES FROM HUMAN AND HERPES SIMPLEX VIRUS TYPE 1	3.2.2.3 3.2.2.27
2C58	TORPEDO CALIFORNICA ACETYLCHOLINESTERASE IN COMPLEX WITH 20MM ACETYLTHIOCHOLINE	3.1.1.7
2C5F	TORPEDO CALIFORNICA ACETYLCHOLINESTERASE IN COMPLEX WITH A NON HYDROLYSABLE SUBSTRATE ANALOGUE, 4-OXO-N,N,N-TRIMETHYLPENTANAMINIUM	3.1.1.7
2C5G	TORPEDO CALIFORNICA ACETYLCHOLINESTERASE IN COMPLEX WITH 20MM THIOCHOLINE	3.1.1.7
2C5L	STRUCTURE OF PLC EPSILON RAS ASSOCIATION DOMAIN WITH HRAS	3.6.5.2
2C5W	PENICILLIN-BINDING PROTEIN 1A (PBP-1A) ACYL-ENZYME COMPLEX (CEFOTAXIME) FROM STREPTOCOCCUS PNEUMONIAE	2.4.1.129 3.4.16.4
2C61	CRYSTAL STRUCTURE OF THE NON-CATALYTIC B SUBUNIT OF A-TYPE ATPASE FROM M. MAZEI GO1	3.6.3.14
2C6C	MEMBRANE-BOUND GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN COMPLEX WITH GPI-18431 (S)-2-(4-IODOBENZYLPHOSPHONOMETHYL)-PENTANEDIOIC ACID	3.4.17.21
2C6G	MEMBRANE-BOUND GLUTAMATE CARBOXYPEPTIDASE II (GCPII) WITH BOUND GLUTAMATE	3.4.17.21
2C6P	MEMBRANE-BOUND GLUTAMATE CARBOXYPEPTIDASE II (GCPII) IN COMPLEX WITH PHOSPHATE ANION	3.4.17.21
2C6W	PENICILLIN-BINDING PROTEIN 1A (PBP-1A) FROM STREPTOCOCCUS PNEUMONIAE	2.4.1.129 3.4.16.4
2C6Z	CRYSTAL STRUCTURE OF DIMETHYLARGININE DIMETHYLAMINOHYDROLASE I IN COMPLEX WITH CITRULLINE	3.5.3.18
2C71	THE STRUCTURE OF A FAMILY 4 ACETYL XYLAN ESTERASE FROM CLOSTRIDIUM THERMOCELLUM IN COMPLEX WITH A MAGNESIUM ION.	3.1.1.72 3.2.1.8
2C77	EF-TU COMPLEXED WITH A GTP ANALOG AND THE ANTIBIOTIC GE2270 A	3.1.5.1
2C78	EF-TU COMPLEXED WITH A GTP ANALOG AND THE ANTIBIOTIC PULVOMYCIN	3.1.5.1
2C79	THE STRUCTURE OF A FAMILY 4 ACETYL XYLAN ESTERASE FROM CLOSTRIDIUM THERMOCELLUM IN COMPLEX WITH A COLBALT ION.	3.1.1.72 3.2.1.8
2C7B	THE CRYSTAL STRUCTURE OF ESTE1, A NEW THERMOPHILIC AND THERMOSTABLE CARBOXYLESTERASE CLONED FROM A METAGENOMIC LIBRARY	3.1.1.1
2C7S	CRYSTAL STRUCTURE OF HUMAN PROTEIN TYROSINE PHOSPHATASE KAPPA AT 1.95A RESOLUTION	3.1.3.48
2C88	CRYSTAL STRUCTURE OF (SR) CALCIUM-ATPASE E2(TG):AMPPCP FORM	3.6.3.8 7.2.2.10
2C8I	COMPLEX OF ECHOVIRUS TYPE 12 WITH DOMAINS 1, 2, 3 AND 4 OF ITS RECEPTOR DECAY ACCELERATING FACTOR (CD55) BY CRYO ELECTRON MICROSCOPY AT 16 A	3.4.22.29 3.6.1.15 3.4.22.28 2.7.7.48
2C8K	CRYSTAL STRUCTURE OF (SR) CALCIUM-ATPASE E2(TG) WITH PARTIALLY OCCUPIED AMPPCP SITE	3.6.3.8 7.2.2.10
2C8L	CRYSTAL STRUCTURE OF (SR) CALCIUM-ATPASE E2(TG) FORM	3.6.3.8 7.2.2.10
2C8O	LYSOZYME (1SEC) AND UV LASR EXCITED FLUORESCENCE	3.2.1.17
2C8P	LYSOZYME (60SEC) AND UV LASER EXCITED FLUORESCENCE	3.2.1.17
2C8T	THE 3.0 A RESOLUTION STRUCTURE OF CASEINOLYTIC CLP PROTEASE 1 FROM MYCOBACTERIUM TUBERCULOSIS	3.4.21.92
2C8W	THROMBIN INHIBITORS	3.4.21.5
2C8X	THROMBIN INHIBITORS	3.4.21.5
2C8Y	THROMBIN INHIBITORS	3.4.21.5
2C8Z	THROMBIN INHIBITORS	3.4.21.5
2C90	THROMBIN INHIBITORS	3.4.21.5
2C93	THROMBIN INHIBITORS	3.4.21.5
2C9A	CRYSTAL STRUCTURE OF THE MAM-IG MODULE OF RECEPTOR PROTEIN TYROSINE PHOSPHATASE MU	3.1.3.48
2C9M	STRUCTURE OF (SR) CALCIUM-ATPASE IN THE CA2E1 STATE SOLVED IN A P1 CRYSTAL FORM.	3.6.3.8 7.2.2.10
2C9O	3D STRUCTURE OF THE HUMAN RUVB-LIKE HELICASE RUVBL1	3.6.1 3.6.4.12
2CAR	CRYSTAL STRUCTURE OF HUMAN INOSINE TRIPHOSPHATASE	3.6.1.19 3.6.1.9
2CB5	HUMAN BLEOMYCIN HYDROLASE, C73S/DELE455 MUTANT	3.4.22 3.4.22.40
2CBH	DETERMINATION OF THE THREE-DIMENSIONAL STRUCTURE OF THE C-TERMINAL DOMAIN OF CELLOBIOHYDROLASE I FROM TRICHODERMA REESEI. A STUDY USING NUCLEAR MAGNETIC RESONANCE AND HYBRID DISTANCE GEOMETRY-DYNAMICAL SIMULATED ANNEALING	3.2.1.91
2CBI	STRUCTURE OF THE CLOSTRIDIUM PERFRINGENS NAGJ FAMILY 84 GLYCOSIDE HYDROLASE, A HOMOLOGUE OF HUMAN O-GLCNACASE	3.2.1.35 3.2.1.169
2CBJ	STRUCTURE OF THE CLOSTRIDIUM PERFRINGENS NAGJ FAMILY 84 GLYCOSIDE HYDROLASE, A HOMOLOGUE OF HUMAN O-GLCNACASE IN COMPLEX WITH PUGNAC	3.2.1.35 3.2.1.169
2CBN	CRYSTAL STRUCTURE OF ZIPD FROM ESCHERICHIA COLI	3.1.26.11 3.1
2CBU	BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH CASTANOSPERMINE	3.2.1.21
2CBV	BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH CALYSTEGINE B2	3.2.1.21
2CBY	CRYSTAL STRUCTURE OF THE ATP-DEPENDENT CLP PROTEASE PROTEOLYTIC SUBUNIT 1 (CLPP1) FROM MYCOBACTERIUM TUBERCULOSIS	3.4.21.92
2CC0	FAMILY 4 CARBOHYDRATE ESTERASE FROM STREPTOMYCES LIVIDANS IN COMPLEX WITH ACETATE	3.1.1.72
2CC1	CRYSTAL STRUCTURE OF THE CLASS A BETA-LACTAMASE FROM MYCOBACTERIUM FORTUITUM	3.5.2.6
2CCQ	THE PUB DOMAIN FUNCTIONS AS A P97 BINDING MODULE IN HUMAN PEPTIDE N-GLYCANASE.	3.5.1.52
2CCR	STRUCTURE OF BETA-1,4-GALACTANASE	3.2.1.89
2CDR	CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE EPOXIDE INHIBITORS.	3.4.22 3.4.22.56
2CDS	LYSOZYME	3.2.1.17
2CE2	CRYSTAL STRUCTURE ANALYSIS OF A FLUORESCENT FORM OF H-RAS P21 IN COMPLEX WITH GDP	3.6.5.2
2CE3	CRYSTAL STRUCTURE OF THE ATP-DEPENDENT CLP PROTEASE PROTEOLYTIC SUBUNIT 1 (CLPP1) FROM MYCOBACTERIUM TUBERCULOSIS	3.4.21.92
2CE7	EDTA TREATED	3.4.24
2CEJ	P1' EXTENDED HIV-1 PROTEASE INHIBITORS ENCOMPASSING A TERTIARY ALCOHOL IN THE TRANSITION-STATE MIMICKING SCAFFOLD	3.4.23.16
2CEK	CONFORMATIONAL FLEXIBILITY IN THE PERIPHERAL SITE OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE REVEALED BY THE COMPLEX STRUCTURE WITH A BIFUNCTIONAL INHIBITOR	3.1.1.7
2CEL	ACTIVE-SITE MUTANT E212Q DETERMINED AT PH 6.0 WITH NO LIGAND BOUND IN THE ACTIVE SITE	3.2.1.91
2CEM	P1' EXTENDED HIV-1 PROTEASE INHIBITORS ENCOMPASSING A TERTIARY ALCOHOL IN THE TRANSITION-STATE MIMICKING SCAFFOLD	3.4.23.16
2CEN	P1' EXTENDED HIV-1 PROTEASE INHIBITORS ENCOMPASSING A TERTIARY ALCOHOL IN THE TRANSITION-STATE MIMICKING SCAFFOLD	3.4.23.16
2CEQ	BETA-GLYCOSIDASE FROM SULFOLOBUS SOLFATARICUS IN COMPLEX WITH GLUCOIMIDAZOLE	3.2.1.23
2CER	BETA-GLYCOSIDASE FROM SULFOLOBUS SOLFATARICUS IN COMPLEX WITH PHENETHYL-SUBSTITUTED GLUCOIMIDAZOLE	3.2.1.21 3.2.1.23
2CES	BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH GLUCOIMIDAZOLE	3.2.1.21
2CET	BETA-GLUCOSIDASE FROM THERMOTOGA MARITIMA IN COMPLEX WITH PHENETHYL- SUBSTITUTED GLUCOIMIDAZOLE	3.2.1.21
2CEV	ARGINASE FROM BACILLUS CALDEVELOX, NATIVE STRUCTURE AT PH 8.5	3.5.3.1
2CF4	PYROCOCCUS HORIKOSHII TET1 PEPTIDASE CAN ASSEMBLE INTO A TETRAHEDRON OR A LARGE OCTAHEDRAL SHELL	3.4.11
2CF8	COMPLEX OF RECOMBINANT HUMAN THROMBIN WITH AN INHIBITOR	3.4.21.5
2CF9	COMPLEX OF RECOMBINANT HUMAN THROMBIN WITH AN INHIBITOR	3.4.21.5
2CFR	CRYSTAL STRUCTURE OF HUMAN PYRIDOXAL 5'-PHOSPHATE PHOSPHATASE	3.1.3.74 3.1.3.3
2CFS	CRYSTAL STRUCTURE OF HUMAN PYRIDOXAL 5'-PHOSPHATE PHOSPHATASE	3.1.3.74 3.1.3.3
2CFT	CRYSTAL STRUCTURE OF HUMAN PYRIDOXAL 5'-PHOSPHATE PHOSPHATASE WITH ITS SUBSTRATE	3.1.3.74 3.1.3.3
2CFV	CRYSTAL STRUCTURE OF HUMAN PROTEIN TYROSINE PHOSPHATASE RECEPTOR TYPE J	3.1.3.48
2CGA	BOVINE CHYMOTRYPSINOGEN A. X-RAY CRYSTAL STRUCTURE ANALYSIS AND REFINEMENT OF A NEW CRYSTAL FORM AT 1.8 ANGSTROMS RESOLUTION	3.4.21.1
2CGI	SIRAS STRUCTURE OF TETRAGONAL LYSOZYME USING DERIVATIVE DATA COLLECTED AT THE HIGH ENERGY REMOTE HOLMIUM KEDGE	3.2.1.17
2CHA	THE STRUCTURE OF CRYSTALLINE ALPHA-CHYMOTRYPSIN, $V.THE ATOMIC STRUCTURE OF TOSYL-ALPHA-CHYMOTRYPSIN AT 2 ANGSTROMS RESOLUTION	3.4.21.1
2CHM	CRYSTAL STRUCTURE OF N2 SUBSTITUTED PYRAZOLO PYRIMIDINONES - A FLIPPED BINDING MODE IN PDE5	3.1.4.17 3.1.4.35 3.1.4.53
2CHN	BACTEROIDES THETAIOTAOMICRON HEXOSAMINIDASE WITH O-GLCNACASE ACTIVITY- NAG-THIAZOLINE COMPLEX	3.2.1.52 3.2.1.169
2CHO	BACTEROIDES THETAIOTAOMICRON HEXOSAMINIDASE WITH O-GLCNACASE ACTIVITY	3.2.1.52 3.2.1.169
2CI1	CRYSTAL STRUCTURE OF DIMETHYLARGININE DIMETHYLAMINOHYDROLASE I IN COMPLEX WITH S-NITROSO-LHOMOCYSTEINE	3.5.3.18
2CI3	CRYSTAL STRUCTURE OF DIMETHYLARGININE DIMETHYLAMINOHYDROLASE CRYSTAL FORM I	3.5.3.18
2CI4	CRYSTAL STRUCTURE OF DIMETHYLARGININE DIMETHYLAMINOHYDROLASE I CRYSTAL FORM II	3.5.3.18
2CI5	CRYSTAL STRUCTURE OF DIMETHYLARGININE DIMETHYLAMINOHYDROLASE I IN COMPLEX WITH L-HOMOCYSTEINE	3.5.3.18
2CI6	CRYSTAL STRUCTURE OF DIMETHYLARGININE DIMETHYLAMINOHYDROLASE I BOUND WITH ZINC LOW PH	3.5.3.18
2CI7	CRYSTAL STRUCTURE OF DIMETHYLARGININE DIMETHYLAMINOHYDROLASE I IN COMPLEX WITH ZINC, HIGH PH	3.5.3.18
2CIC	THE CRYSTAL STRUCTURE OF A COMPLEX OF CAMPYLOBACTER JEJUNI DUTPASE WITH SUBSTRATE ANALOGUE DUPNHPP	3.6.1.23
2CIJ	MEMBRANE-BOUND GLUTAMATE CARBOXYPEPTIDASE II (GCPII) WITH BOUND METHIONINE	3.4.17.21
2CIO	THE HIGH RESOLUTION X-RAY STRUCTURE OF PAPAIN COMPLEXED WITH FRAGMENTS OF THE TRYPANOSOMA BRUCEI CYSTEINE PROTEASE INHIBITOR ICP.	3.4.22.2
2CIP	STRUCTURE OF THE MICHAELIS COMPLEX OF A FAMILY 26 LICHENASE	3.2.1.4
2CIT	STRUCTURE OF THE COVALENT INTERMEDIATE OF A FAMILY 26 LICHENASE	3.2.1.4
2CJE	THE CRYSTAL STRUCTURE OF A COMPLEX OF LEISHMANIA MAJOR DUTPASE WITH SUBSTRATE ANALOGUE DUPNHP	3.6.1.23
2CJI	CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX	3.4.21.6
2CJL	CRYSTAL STRUCTURE AND ENZYMATIC PROPERTIES OF A BACTERIAL FAMILY 19 CHITINASE REVEAL DIFFERENCES WITH PLANT ENZYMES	3.2.1.14
2CJP	STRUCTURE OF POTATO (SOLANUM TUBEROSUM) EPOXIDE HYDROLASE I (STEH1)	3.3.2.3
2CJQ	BOVINE VIRAL DIARRHEA VIRUS CP7-R12 RNA-DEPENDENT RNA POLYMERASE	2.7.7.48 3.4.22 3.4.21.113 3.6.1.15 3.6.4.13
2CJX	EXTENDED SUBSTRATE RECOGNITION IN CASPASE-3 REVEALED BY HIGH RESOLUTION X-RAY STRUCTURE ANALYSIS	3.4.22.56
2CJY	EXTENDED SUBSTRATE RECOGNITION IN CASPASE-3 REVEALED BY HIGH RESOLUTION X-RAY STRUCTURE ANALYSIS	3.4.22.56
2CJZ	CRYSTAL STRUCTURE OF THE C472S MUTANT OF HUMAN PROTEIN TYROSINE PHOSPHATASE PTPN5 (STEP, STRIATUM ENRICHED PHOSPHATASE) IN COMPLEX WITH PHOSPHOTYROSINE	3.1.3.48
2CK3	AZIDE INHIBITED BOVINE F1-ATPASE	3.6.3.14
2CKA	SOLUTION STRUCTURES OF THE BRK DOMAINS OF THE HUMAN CHROMO HELICASE DOMAIN 7 AND 8, REVEALS STRUCTURAL SIMILARITY WITH GYF DOMAIN SUGGESTING A ROLE IN PROTEIN INTERACTION	3.6.1 3.6.4.12
2CKC	SOLUTION STRUCTURES OF THE BRK DOMAINS OF THE HUMAN CHROMO HELICASE DOMAIN 7 AND 8, REVEALS STRUCTURAL SIMILARITY WITH GYF DOMAIN SUGGESTING A ROLE IN PROTEIN INTERACTION	3.6.4.12
2CKG	THE STRUCTURE OF SENP1 SUMO-2 CO-COMPLEX SUGGESTS A STRUCTURAL BASIS FOR DISCRIMINATION BETWEEN SUMO PARALOGUES DURING PROCESSING	3.4.22
2CKH	SENP1-SUMO2 COMPLEX	3.4.22
2CKI	STRUCTURE OF ULILYSIN, A MEMBER OF THE PAPPALYSIN FAMILY OF METZINCIN METALLOENDOPEPTIDASES.	3.4.24
2CKM	TORPEDO CALIFORNICA ACETYLCHOLINESTERASE COMPLEXED WITH ALKYLENE- LINKED BIS-TACRINE DIMER (7 CARBON LINKER)	3.1.1.7
2CKR	X-RAY CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF THERMOBIFIDA FUSCA ENDOGLUCANASE CEL5A (E5) E355Q IN COMPLEX WITH CELLOTETRAOSE	3.2.1.4
2CKS	X-RAY CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF THERMOBIFIDA FUSCA ENDOGLUCANASE CEL5A (E5)	3.2.1.4
2CKW	THE 2.3 A RESOLUTION STRUCTURE OF THE SAPPORO VIRUS RNA DEPENDANT RNA POLYMERASE.	2.7.7.48 3.6.1.15 3.4.22.66
2CL0	CRYSTAL STRUCTURE ANALYSIS OF A FLUORESCENT FORM OF H-RAS P21 IN COMPLEX WITH GPPNHP	3.6.5.2
2CL2	ENDO-1,3(4)-BETA-GLUCANASE FROM PHANEROCHAETE CHRYSOSPORIUM, SOLVED USING NATIVE SULFUR SAD, EXHIBITING INTACT HEPTASACCHARIDE GLYCOSYLATION	3.2.1.6
2CL6	CRYSTAL STRUCTURE ANALYSIS OF A FLUORESCENT FORM OF H-RAS P21 IN COMPLEX WITH S-CAGED GTP	3.6.5.2
2CL7	CRYSTAL STRUCTURE ANALYSIS OF A FLUORESCENT FORM OF H-RAS P21 IN COMPLEX WITH GTP	3.6.5.2
2CLC	CRYSTAL STRUCTURE ANALYSIS OF A FLUORESCENT FORM OF H-RAS P21 IN COMPLEX WITH GTP (2)	3.6.5.2
2CLD	CRYSTAL STRUCTURE ANALYSIS OF A FLUORESCENT FORM OF H-RAS P21 IN COMPLEX WITH GDP (2)	3.6.5.2
2CLT	CRYSTAL STRUCTURE OF THE ACTIVE FORM (FULL-LENGTH) OF HUMAN FIBROBLAST COLLAGENASE.	3.4.24.7
2CLY	SUBCOMPLEX OF THE STATOR OF BOVINE MITOCHONDRIAL ATP SYNTHASE	3.6.3.14
2CM0	THE PUB DOMAIN FUNCTIONS AS A P97 BINDING MODULE IN HUMAN PEPTIDE N-GLYCANASE.	3.5.1.52
2CM1	CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF SERINE THREONINE PROTEIN PHOSPHATASE PSTP IN COMPLEX WITH 2 MANGANESE IONS.	3.1.3.16
2CM2	STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B (P212121)	3.1.3.48
2CM3	STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B (C2)	3.1.3.48
2CM7	STRUCTURAL BASIS FOR INHIBITION OF PROTEIN TYROSINE PHOSPHATASE 1B BY ISOTHIAZOLIDINONE HETEROCYCLIC PHOSPHONATE MIMETICS	3.1.3.48
2CM8	STRUCTURAL BASIS FOR INHIBITION OF PROTEIN TYROSINE PHOSPHATASE 1B BY ISOTHIAZOLIDINONE HETEROCYCLIC PHOSPHONATE MIMETICS	3.1.3.48
2CMA	STRUCTURAL BASIS FOR INHIBITION OF PROTEIN TYROSINE PHOSPHATASE 1B BY ISOTHIAZOLIDINONE HETEROCYCLIC PHOSPHONATE MIMETICS	3.1.3.48
2CMB	STRUCTURAL BASIS FOR INHIBITION OF PROTEIN TYROSINE PHOSPHATASE 1B BY ISOTHIAZOLIDINONE HETEROCYCLIC PHOSPHONATE MIMETICS	3.1.3.48
2CMC	STRUCTURAL BASIS FOR INHIBITION OF PROTEIN TYROSINE PHOSPHATASE 1B BY ISOTHIAZOLIDINONE HETEROCYCLIC PHOSPHONATE MIMETICS	3.1.3.48
2CMF	TORPEDO CALIFORNICA ACETYLCHOLINESTERASE COMPLEXED WITH ALKYLENE- LINKED BIS-TACRINE DIMER (5 CARBON LINKER)	3.1.1.7
2CML	STRUCTURE OF NEURAMINIDASE FROM ENGLISH DUCK SUBTYPE N6 COMPLEXED WITH 30 MM ZANAMIVIR, CRYSTAL SOAKED FOR 3 HOURS AT 291 K.	3.2.1.18
2CMU	CRYSTAL STRUCTURE OF A PUTATIVE PEPTIDYL-ARGININE DEIMINASE	3.5.3.6
2CMY	CRYSTAL COMPLEX BETWEEN BOVINE TRYPSIN AND VERONICA HEDERIFOLIA TRYPSIN INHIBITOR	3.4.21.4
2CN0	COMPLEX OF RECOMBINANT HUMAN THROMBIN WITH A DESIGNED INHIBITOR	3.4.21.5
2CN1	CRYSTAL STRUCTURE OF HUMAN CYTOSOLIC 5'-NUCLEOTIDASE III (NT5C3)(CASP TARGET)	3.1.3.5 3.1.3.91
2CN3	CRYSTAL STRUCTURES OF CLOSTRIDIUM THERMOCELLUM XYLOGLUCANASE	3.2.1.151 3.2.1
2CNC	FAMILY 10 XYLANASE	3.2.1.8
2CNE	STRUCTURAL INSIGHTS INTO THE DESIGN OF NONPEPTIDIC ISOTHIAZOLIDINONE- CONTAINING INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
2CNF	STRUCTURAL INSIGHTS INTO THE DESIGN OF NONPEPTIDIC ISOTHIAZOLIDINONE- CONTAINING INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
2CNG	STRUCTURAL INSIGHTS INTO THE DESIGN OF NONPEPTIDIC ISOTHIAZOLIDINONE- CONTAINING INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
2CNH	STRUCTURAL INSIGHTS INTO THE DESIGN OF NONPEPTIDIC ISOTHIAZOLIDINONE- CONTAINING INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
2CNI	STRUCTURAL INSIGHTS INTO THE DESIGN OF NONPEPTIDIC ISOTHIAZOLIDINONE- CONTAINING INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE 1B	3.1.3.48
2CNK	CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE EPOXIDE INHIBITORS.	3.4.22 3.4.22.56
2CNL	CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE EPOXIDE INHIBITORS.	3.4.22 3.4.22.56
2CNN	CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE EPOXIDE INHIBITORS.	3.4.22 3.4.22.56
2CNO	CRYSTAL STRUCTURES OF CASPASE-3 IN COMPLEX WITH AZA-PEPTIDE EPOXIDE INHIBITORS.	3.4.22 3.4.22.56
2CON	SOLUTION STRUCTURE OF RSGI RUH-035, A ZN-RIBBON MODULE IN MOUSE CDNA	3.1
2COV	CRYSTAL STRUCTURE OF CBM31 FROM BETA-1,3-XYLANASE	3.2.1.32
2CPR	SOLUTION STRUCTURE OF THE HRDC DOMAIN OF HUMAN EXOSOME COMPONENT 10	3.1.13
2CPT	SOLUTION STRUCTURE OF MIT DOMAIN FROM HUMAN SKD1	3.6.4.6
2CPU	SUBSITE MAPPING OF THE ACTIVE SITE OF HUMAN PANCREATIC ALPHA-AMYLASE USING SUBSTRATES, THE PHARMACOLOGICAL INHIBITOR ACARBOSE, AND AN ACTIVE SITE VARIANT	3.2.1.1
2CPW	SOLUTION STRUCTURE OF RSGI RUH-031, A UBA DOMAIN FROM HUMAN CDNA	3.1.3.48
2CQA	SOLUTION STRUCTURE OF RSGI RUH-039, A FRAGMENT OF C-TERMINAL DOMAIN OF RUVB-LIKE 2 FROM HUMAN CDNA	3.6.1 3.6.4.12
2CQZ	CRYSTAL STRUCTURE OF PH0347 PROTEIN FROM PYROCOCCUS HORIKOSHII OT3	3.1.3.89
2CS5	SOLUTION STRUCTURE OF PDZ DOMAIN OF PROTEIN TYROSINE PHOSPHATASE, NON-RECEPTOR TYPE 4	3.1.3.48
2CTB	THE HIGH RESOLUTION CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN CARBOXYPEPTIDASE A AND L-PHENYL LACTATE	3.4.17.1
2CTC	THE HIGH RESOLUTION CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN CARBOXYPEPTIDASE A AND L-PHENYL LACTATE	3.4.17.1
2CU7	SOLUTION STRUCTURE OF THE SANT DOMAIN OF HUMAN KIAA1915 PROTEIN	3.4.19
2CUT	CUTINASE, A LIPOLYTIC ENZYME WITH A PREFORMED OXYANION HOLE	3.1.1 3.1.1.74
2CUU	CRYSTAL STRUCTURE OF SPIN LABELED T4 LYSOZYME (V131R1)	3.2.1.17
2CV3	CRYSTAL STRUCTURE OF PORCINE PANCREATIC ELASTASE COMPLEXED WITH A MACROCLYCLIC PEPTIDE INHIBITOR	3.4.21.36
2CV8	CRYSTAL STRUCTURE OF TRNA-INTRON ENDONUCLEASE FROM SULFOLOBUS TOKODAII	3.1.27.9 4.6.1.16
2CVR	NMR SOLUTION STRUCTURE OF SSO7D MUTANT, K12L, 12 CONFORMERS	3.1.27
2CW7	CRYSTAL STRUCTURE OF INTEIN HOMING ENDONUCLEASE II	3.1 2.7.7.7
2CW8	CRYSTAL STRUCTURE OF INTEIN HOMING ENDONUCLEASE II	3.1 2.7.7.7
2CWI	X-RAY CRYSTAL STRUCTURE ANALYSIS OF RECOMBINANT WILD-TYPE CANINE MILK LYSOZYME (APO-TYPE)	3.2.1.17
2CWJ	CRYSTAL STRUCTURE OF APE1501, A PUTATIVE ENDONUCLEASE FROM AEROPYRUM PERNIX	3.1
2CWR	CRYSTAL STRUCTURE OF CHITIN BIDING DOMAIN OF CHITINASE FROM PYROCOCCUS FURIOSUS	3.2.1.14
2CXV	DUAL MODES OF MODIFICATION OF HEPATITIS A VIRUS 3C PROTEASE BY A SERINE-DERIVED BETALACTONE: SELECTIVE CRYSTALLIZATION AND HIGH-RESOLUTION STRUCTURE OF THE HIS-102 ADDUCT	3.4.22.28 3.6.1.15 2.7.7.48
2CY7	THE CRYSTAL STRUCTURE OF HUMAN ATG4B	3.4.22
2CY9	CRYSTAL STRUCTURE OF THIOESTERASE SUPERFAMILY MEMBER2 FROM MUS MUSCULUS	3.1.2 3.1.2.2
2CYD	CRYSTAL STRUCTURE OF LITHIUM BOUND ROTOR RING OF THE V-ATPASE FROM ENTEROCOCCUS HIRAE	3.6.3.14
2CYE	CRYSTAL STRUCTURE OF THIOESTERASE COMPLEXED WITH COENZYME A AND ZN FROM THERMUS THERMOPHILUS HB8	3.1.2
2CYG	CRYSTAL STRUCTURE AT 1.45- RESOLUTION OF THE MAJOR ALLERGEN ENDO-BETA-1,3-GLUCANASE OF BANANA AS A MOLECULAR BASIS FOR THE LATEX-FRUIT SYNDROME	3.2.1.39
2CZH	CRYSTAL STRUCTURE OF HUMAN MYO-INOSITOL MONOPHOSPHATASE 2 (IMPA2) WITH PHOSPHATE ION (ORTHORHOMBIC FORM)	3.1.3.25
2CZI	CRYSTAL STRUCTURE OF HUMAN MYO-INOSITOL MONOPHOSPHATASE 2 (IMPA2) WITH CALCIUM AND PHOSPHATE IONS	3.1.3.25
2CZK	CRYSTAL STRUCTURE OF HUMAN MYO-INOSITOL MONOPHOSPHATASE 2 (IMPA2) (TRIGONAL FORM)	3.1.3.25
2CZN	SOLUTION STRUCTURE OF THE CHITIN-BINDING DOMAIN OF HYPERTHERMOPHILIC CHITINASE FROM PYROCOCCUS FURIOSUS	3.2.1.14
2CZQ	A NOVEL CUTINASE-LIKE PROTEIN FROM CRYPTOCOCCUS SP.	3.1.1
2CZV	CRYSTAL STRUCTURE OF ARCHEAL RNASE P PROTEIN PH1481P IN COMPLEX WITH PH1877P	3.1.26.5
2D00	SUBUNIT F OF V-TYPE ATPASE/SYNTHASE	3.6.3.14
2D05	CHITOSANASE FROM BACILLUS CIRCULANS MUTANT K218P	3.2.1.132
2D07	CRYSTAL STRUCTURE OF SUMO-3-MODIFIED THYMINE-DNA GLYCOSYLASE	3.2.2 3.2.2.29
2D0A	CRYSTAL STRUCTURE OF BST-RNASE HIII	3.1.26.4
2D0B	CRYSTAL STRUCTURE OF BST-RNASE HIII IN COMPLEX WITH MG2+	3.1.26.4
2D0C	CRYSTAL STRUCTURE OF BST-RNASE HIII IN COMPLEX WITH MN2+	3.1.26.4
2D0D	CRYSTAL STRUCTURE OF A META-CLEAVAGE PRODUCT HYDROLASE (CUMD) A129V MUTANT	3.7.1.9
2D0F	CRYSTAL STRUCTURE OF THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE 1 (TVAI) MUTANT D356N COMPLEXED WITH P2, A PULLULAN MODEL OLIGOSACCHARIDE	3.2.1.1 3.2.1.135
2D0G	CRYSTAL STRUCTURE OF THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE 1 (TVAI) MUTANT D356N/E396Q COMPLEXED WITH P5, A PULLULAN MODEL OLIGOSACCHARIDE	3.2.1.1 3.2.1.135
2D0H	CRYSTAL STRUCTURE OF THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE 1 (TVAI) MUTANT D356N/E396Q COMPLEXED WITH P2, A PULLULAN MODEL OLIGOSACCHARIDE	3.2.1.1 3.2.1.135
2D1G	STRUCTURE OF FRANCISELLA TULARENSIS ACID PHOSPHATASE A (ACPA) BOUND TO ORTHOVANADATE	3.1.3.2
2D1I	STRUCTURE OF HUMAN ATG4B	3.4.22
2D1J	FACTOR XA IN COMPLEX WITH THE INHIBITOR 2-[[4-[(5-CHLOROINDOL-2-YL)SULFONYL]PIPERAZIN-1-YL] CARBONYL]THIENO[3,2-B]PYRIDINE N-OXIDE	3.4.21.6
2D1N	COLLAGENASE-3 (MMP-13) COMPLEXED TO A HYDROXAMIC ACID INHIBITOR	3.4.24
2D1O	STROMELYSIN-1 (MMP-3) COMPLEXED TO A HYDROXAMIC ACID INHIBITOR	3.4.24.17
2D1Z	CRYSTAL STRUCTURE OF CATALYTIC-SITE MUTANT XYLANASE FROM STREPTOMYCES OLIVACEOVIRIDIS E-86	3.2.1.8
2D20	CRYSTAL STRUCTURE OF MICHAELIS COMPLEX OF CATALYTIC-SITE MUTANT XYLANASE FROM STREPTOMYCES OLIVACEOVIRIDIS E-86	3.2.1.8
2D22	CRYSTAL STRUCTURE OF COVALENT GLYCOSYL-ENZYME INTERMEDIATE OF CATALYTIC-SITE MUTANT XYLANASE FROM STREPTOMYCES OLIVACEOVIRIDIS E-86	3.2.1.8
2D23	CRYSTAL STRUCTURE OF EP COMPLEX OF CATALYTIC-SITE MUTANT XYLANASE FROM STREPTOMYCES OLIVACEOVIRIDIS E-86	3.2.1.8
2D24	CRYSTAL STRUCTURE OF ES COMPLEX OF CATALYTIC-SITE MUTANT XYLANASE FROM STREPTOMYCES OLIVACEOVIRIDIS E-86	3.2.1.8
2D2D	CRYSTAL STRUCTURE OF SARS-COV MPRO IN COMPLEX WITH AN INHIBITOR I2	3.4.24 3.4.19.12 3.4.22.69 3.4.22 2.7.7.48 3.6.4.12 3.6.4.13 2.1.1 3.1.13 3.1
2D2G	OPDA FROM AGROBACTERIUM RADIOBACTER WITH BOUND PRODUCT DIMETHYLTHIOPHOSPHATE	3.1.8.1
2D2H	OPDA FROM AGROBACTERIUM RADIOBACTER WITH BOUND INHIBITOR TRIMETHYL PHOSPHATE AT 1.8 A RESOLUTION	3.1.8.1
2D2J	OPDA FROM AGROBACTERIUM RADIOBACTER WITHOUT INHIBITOR/PRODUCT PRESENT AT 1.75 A RESOLUTION	3.1.8.1
2D2O	STRUCTURE OF A COMPLEX OF THERMOACTINOMYCES VULGARIS R-47 ALPHA-AMYLASE 2 WITH MALTOHEXAOSE DEMONSTRATES THE IMPORTANT ROLE OF AROMATIC RESIDUES AT THE REDUCING END OF THE SUBSTRATE BINDING CLEFT	3.2.1.135
2D2V	X-RAY STRUCTURE OF THE SUCROSE-PHOSPHATASE (SPP) FROM SYNECHOCYSTIS SP.PCC6803 IN COMPLEX WITH MALTOSE	3.1.3.24
2D30	CRYSTAL STRUCTURE OF CYTIDINE DEAMINASE CDD-2 (BA4525) FROM BACILLUS ANTHRACIS AT 2.40A RESOLUTION	3.5.4.5
2D3K	STRUCTURAL STUDY ON PROJECT ID PH1539 FROM PYROCOCCUS HORIKOSHII OT3	3.1.1.29
2D3L	CRYSTAL STRUCTURE OF MALTOHEXAOSE-PRODUCING AMYLASE FROM BACILLUS SP.707 COMPLEXED WITH MALTOPENTAOSE.	3.2.1.98
2D3N	CRYSTAL STRUCTURE OF MALTOHEXAOSE-PRODUCING AMYLASE FROM BACILLUS SP.707 COMPLEXED WITH MALTOHEXAOSE	3.2.1.98
2D3U	X-RAY CRYSTAL STRUCTURE OF HEPATITIS C VIRUS RNA DEPENDENT RNA POLYMERASE IN COMPLEX WITH NON-NUCLEOSIDE ANALOGUE INHIBITOR	2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13
2D3Y	CRYSTAL STRUCTURE OF URACIL-DNA GLYCOSYLASE FROM THERMUS THERMOPHILUS HB8	3.2.2
2D3Z	X-RAY CRYSTAL STRUCTURE OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE IN COMPLEX WITH NON-NUCLEOSIDE ANALOGUE INHIBITOR	2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13
2D41	X-RAY CRYSTAL STRUCTURE OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE IN COMPLEX WITH NON-NUCLEOSIDE INHIBITOR	2.7.7.48 3.4.21.98 3.6.1.15 3.6.4.13
2D43	CRYSTAL STRUCTURE OF ARABINOFURANOSIDASE COMPLEXED WITH ARABINOTRIOSE	3.2.1.55
2D44	CRYSTAL STRUCTURE OF ARABINOFURANOSIDASE COMPLEXED WITH ARABINOFURANOSYL-ALPHA-1,2-XYLOBIOSE	3.2.1.55
2D49	SOLUTION STRUCTURE OF THE CHITIN-BINDING DOMAIN OF STREPTOMYCES GRISEUS CHITINASE C	3.2.1.14
2D4G	STRUCTURE OF YJCG PROTEIN, A PUTATIVE 2'-5' RNA LIGASE FROM BACILLUS SUBTILIS	3.1
2D4H	CRYSTAL-STRUCTURE OF THE N-TERMINAL LARGE GTPASE DOMAIN OF HUMAN GUANYLATE BINDING PROTEIN 1 (HGBP1) IN COMPLEX WITH GMP	3.6.5
2D4I	MONOCLINIC HEN EGG-WHITE LYSOZYME CRYSTALLIZED AT PH4.5 FORM HEAVY WATER SOLUTION	3.2.1.17
2D4J	TRANSFORMED MONOCLINIC CRYSTAL OF HEN EGG-WHITE LYSOZYME FROM A HEAVY WATER SOLUTION	3.2.1.17
2D4K	MONOCLINIC HEN EGG-WHITE LYSOZYME CRYSTALLIZED AT 313K	3.2.1.17
2D4L	CRYSTAL STRUCTURE OF TRUNCATED IN C-TERMINAL M-PMV DUTPASE	3.6.1.23 3.4.23
2D4M	CRYSTAL STRUCTURE OF APO M-PMV DUTPASE	3.6.1.23 3.4.23
2D4N	CRYSTAL STRUCTURE OF M-PMV DUTPASE COMPLEXED WITH DUPNPP, SUBSTRATE ANALOGUE	3.6.1.23 3.4.23
2D5J	UNSATURATED GLUCURONYL HYDROLASE TRIGGERS HYDRATION OF VINYL ETHER GROUP BUT NOT OF GLYCOSIDIC BOND	3.2.1 3.2.1.179
2D5L	CRYSTAL STRUCTURE OF PROLYL TRIPEPTIDYL AMINOPEPTIDASE FROM PORPHYROMONAS GINGIVALIS	3.4.14 3.4.14.12
2D5N	CRYSTAL STRUCTURE OF A BIFUNCTIONAL DEAMINASE AND REDUCTASE INVOLVED IN RIBOFLAVIN BIOSYNTHESIS	3.5.4.26 1.1.1.193
2D5R	CRYSTAL STRUCTURE OF A TOB-HCAF1 COMPLEX	3.1.13.4
2D5U	SOLUTION STRUCTURE OF THE N-TERMINAL PORTION OF THE PUB DOMAIN OF MOUSE PEPTIDE:N-GLYCANASE	3.5.1.52
2D6B	NOVEL BROMATE SPECIES TRAPPED WITHIN A PROTEIN CRYSTAL	3.2.1.17
2D73	CRYSTAL STRUCTURE ANALYSIS OF SUSB	3.2.1.20 3.2.1.3
2D74	CRYSTAL STRUCTURE OF TRANSLATION INITIATION FACTOR AIF2BETAGAMMA HETERODIMER	3.6.5.3
2D7D	STRUCTURAL INSIGHTS INTO THE CRYPTIC DNA DEPENDENT ATP-ASE ACTIVITY OF UVRB	3.1
2D7E	CRYSTAL STRUCTURE OF N-TERMINAL DOMAIN OF PRIA FROM E.COLI	3.6.1 3.6.4
2D7G	CRYSTAL STRUCTURE OF THE AA COMPLEX OF THE N-TERMINAL DOMAIN OF PRIA	3.6.4
2D7H	CRYSTAL STRUCTURE OF THE CCC COMPLEX OF THE N-TERMINAL DOMAIN OF PRIA	3.6.4
2D7S	FOOT AND MOUTH DISEASE VIRUS RNA-DEPENDENT RNA POLYMERASE IN COMPLEX WITH VPG PROTEIN	2.7.7.48 3.4.22.28 3.4.22.46 3.6.1.15
2D80	CRYSTAL STRUCTURE OF PHB DEPOLYMERASE FROM PENICILLIUM FUNICULOSUM	3.1.1.75
2D81	PHB DEPOLYMERASE (S39A) COMPLEXED WITH R3HB TRIMER	3.1.1.75
2D8L	CRYSTAL STRUCTURE OF UNSATURATED RHAMNOGALACTURONYL HYDROLASE IN COMPLEX WITH DGLCA-GALNAC	3.2.1 3.2.1.172
2D8W	STRUCTURE OF HYPER-VIL-TRYPSIN	3.4.21.4
2D91	STRUCTURE OF HYPER-VIL-LYSOZYME	3.2.1.17
2D97	STRUCTURE OF VIL-XYLANASE	3.2.1.8
2D98	STRUCTURE OF VIL (EXTRA KI/I2 ADDED)-XYLANASE	3.2.1.8
2D9I	SOLUTION STRUCTURE OF THE SMR DOMAIN OF NEDD4-BINDING PROTEIN 2	3
2DAG	SOLUTION STRUCTURE OF THE FIRST UBA DOMAIN IN THE HUMAN UBIQUITIN SPECIFIC PROTEASE 5 (ISOPEPTIDASE 5)	3.1.2.15 3.4.19.12
2DAK	SOLUTION STRUCTURE OF THE SECOND UBA DOMAIN IN THE HUMAN UBIQUITIN SPECIFIC PROTEASE 5 (ISOPEPTIDASE 5)	3.1.2.15 3.4.19.12
2DAT	SOLUTION STRUCTURE OF THE BROMODOMAIN OF HUMAN SWI/SNF RELATED MATRIX ASSOCIATED ACTIN DEPENDENT REGULATOR OF CROMATIN SUBFAMILY A MEMBER 2	3.6.4
2DB2	SOLUTION STRUCTURE OF THE DOUBLE-STRANDED RNA BINDING DOMAIN IN KIAA0890 PROTEIN	3.6.4.13
2DB3	STRUCTURAL BASIS FOR RNA UNWINDING BY THE DEAD-BOX PROTEIN DROSOPHILA VASA	3.6.1.3 3.6.4.13
2DB4	CRYSTAL STRUCTURE OF ROTOR RING WITH DCCD OF THE V- ATPASE FROM ENTEROCOCCUS HIRAE	3.6.3.14
2DBO	CRYSTAL STRUCTURE OF D-TYR-TRNA(TYR) DEACYLASE FROM AQUIFEX AEOLICUS	3.1 3.1.1.96
2DBT	CRYSTAL STRUCTURE OF CHITINASE C FROM STREPTOMYCES GRISEUS HUT6037	3.2.1.14
2DBU	CRYSTAL STRUCTURE OF GAMMA-GLUTAMYLTRANSPEPTIDASE FROM ESCHERICHIA COLI	2.3.2.2 3.4.19.13
2DBW	CRYSTAL STRUCTURE OF GAMMA-GLUTAMYLTRANSPEPTIDASE FROM ESCHERICHIA COLI ACYL-ENZYME INTERMEDIATE	2.3.2.2 3.4.19.13
2DBX	CRYSTAL STRUCTURE OF GAMMA-GLUTAMYLTRANSPEPTIDASE FROM ESCHERICHIA COLI COMPLEXED WITH L-GLUTAMATE	2.3.2.2 3.4.19.13
2DC6	X-RAY CRYSTAL STRUCTURE ANALYSIS OF BOVINE SPLEEN CATHEPSIN B-CA073 COMPLEX	3.4.22.1
2DC7	X-RAY CRYSTAL STRUCTURE ANALYSIS OF BOVINE SPLEEN CATHEPSIN B-CA042 COMPLEX	3.4.22.1
2DC8	X-RAY CRYSTAL STRUCTURE ANALYSIS OF BOVINE SPLEEN CATHEPSIN B-CA059 COMPLEX	3.4.22.1
2DC9	X-RAY CRYSTAL STRUCTURE ANALYSIS OF BOVINE SPLEEN CATHEPSIN B-CA074ME COMPLEX	3.4.22.1
2DCA	X-RAY CRYSTAL STRUCTURE ANALYSIS OF BOVINE SPLEEN CATHEPSIN B-CA075 COMPLEX	3.4.22.1
2DCB	X-RAY CRYSTAL STRUCTURE ANALYSIS OF BOVINE SPLEEN CATHEPSIN B-CA076 COMPLEX	3.4.22.1
2DCC	X-RAY CRYSTAL STRUCTURE ANALYSIS OF BOVINE SPLEEN CATHEPSIN B-CA077 COMPLEX	3.4.22.1
2DCD	X-RAY CRYSTAL STRUCTURE ANALYSIS OF BOVINE SPLEEN CATHEPSIN B-CA078 COMPLEX	3.4.22.1
2DCE	SOLUTION STRUCTURE OF THE SWIRM DOMAIN OF HUMAN KIAA1915 PROTEIN	3.4.19
2DCF	CRYSTAL STRUCTURE OF 6-AMINOHEXANOATE-DIMER HYDROLASE S112A/G181D/H266N MUTANT WITH SUBSTRATE	3.5.1.46
2DCH	CRYSTAL STRUCTURE OF ARCHAEAL INTRON-ENCODED HOMING ENDONUCLEASE I-TSP061I	3.1
2DCJ	A TWO-DOMAIN STRUCTURE OF ALKALIPHILIC XYNJ FROM BACILLUS SP. 41M-1	3.2.1.8
2DCK	A TETRAGONAL-LATTICE STRUCTURE OF ALKALIPHILIC XYNJ FROM BACILLUS SP. 41M-1	3.2.1.8
2DCM	THE CRYSTAL STRUCTURE OF S603A MUTATED PROLYL TRIPEPTIDYL AMINOPEPTIDASE COMPLEXED WITH SUBSTRATE	3.4.14 3.4.14.12
2DCU	CRYSTAL STRUCTURE OF TRANSLATION INITIATION FACTOR AIF2BETAGAMMA HETERODIMER WITH GDP	3.6.5.3
2DCY	CRYSTAL STRUCTURE OF BACILLUS SUBTILIS FAMILY-11 XYLANASE	3.2.1.8
2DCZ	THERMAL STABILIZATION OF BACILLUS SUBTILIS FAMILY-11 XYLANASE BY DIRECTED EVOLUTION	3.2.1.8
2DD4	THIOCYANATE HYDROLASE (SCNASE) FROM THIOBACILLUS THIOPARUS RECOMBINANT APO-ENZYME	3.5.5.8
2DD5	THIOCYANATE HYDROLASE (SCNASE) FROM THIOBACILLUS THIOPARUS NATIVE HOLO-ENZYME	3.5.5.8
2DDF	CRYSTAL STRUCTURE OF TACE IN COMPLEX WITH TAPI-2	3.4.24.86
2DDG	CRYSTAL STRUCTURE OF URACIL-DNA GLYCOSYLASE IN COMPLEX WITH AP:G CONTAINING DNA	3.2.2
2DDK	CRYSTAL STRUCTURE OF HUMAN MYO-INOSITOL MONOPHOSPHATASE 2 (IMPA2) (ORTHORHOMBIC FORM)	3.1.3.25
2DDR	CRYSTAL STRUCTURE OF SPHINGOMYELINASE FROM BACILLUS CEREUS WITH CALCIUM ION	3.1.4.12
2DDS	CRYSTAL STRUCTURE OF SPHINGOMYELINASE FROM BACILLUS CEREUS WITH COBALT ION	3.1.4.12
2DDT	CRYSTAL STRUCTURE OF SPHINGOMYELINASE FROM BACILLUS CEREUS WITH MAGNESIUM ION	3.1.4.12
2DDU	CRYSTAL STRUCTURE OF THE THIRD REPEAT DOMAIN OF REELIN	3.4.21
2DDX	CRYSTAL STRUCTURE OF BETA-1,3-XYLANASE FROM VIBRIO SP. AX-4	3.2.1 3.2.1.32
2DDY	SOLUTION STRUCTURE OF MATRILYSIN (MMP-7) COMPLEXED TO CONSTRAINT CONFORMATIONAL SULFONAMIDE INHIBITOR	3.4.24.23
2DE2	CRYSTAL STRUCTURE OF DESULFURIZATION ENZYME DSZB	3.13.1.3
2DE3	CRYSTAL STRUCTURE OF DSZB C27S MUTANT IN COMPLEX WITH 2'-HYDROXYBIPHENYL-2-SULFINIC ACID	3.13.1.3
2DE4	CRYSTAL STRUCTURE OF DSZB C27S MUTANT IN COMPLEX WITH BIPHENYL-2-SULFINIC ACID	3.13.1.3
2DE8	CRYSTAL STRUCTURE OF PORCINE PANCREATIC ELASTASE WITH A UNIQUE CONFORMATION INDUCED BY TRIS	3.4.21.36
2DE9	CRYSTAL STRUCTURE OF PORCINE PANCREATIC ELASTASE COMPLEXED WITH TRIS AFTER SOAKING A TRIS-FREE SOLUTION	3.4.21.36
2DEA	CRYSTAL STRUCTURE OF THE AMINOPEPTIDASE OF AEROMONAS PROTEOLYTICA AT PH 4.7	3.4.11.10
2DEF	PEPTIDE DEFORMYLASE CATALYTIC CORE (RESIDUES 1-147), NMR, 20 STRUCTURES	3.5.1.31 3.5.1.88
2DEM	CRYSTAL STRUCTURE OF URACIL-DNA GLYCOSYLASE IN COMPLEX WITH AP:A CONTAINING DNA	3.2.2
2DEO	1510-N MEMBRANE PROTEASE SPECIFIC FOR A STOMATIN HOMOLOG FROM PYROCOCCUS HORIKOSHII	3.4.21
2DEP	CRYSTAL STRUCTURE OF XYLANASE B FROM CLOSTRIDIUM STERCORARIUM F9	3.2.1.4 3.2.1.8
2DF5	CRYSTAL STRUCTURE OF PF-PCP(1-204)-C	3.4.19.3
2DFA	CRYSTAL STRUCTURE OF LACTAM UTILIZATION PROTEIN FROM THERMUS THERMOPHILUS HB8	3.5.2.9
2DFB	XYLANASE II FROM TRICODERMA REESEI AT 100K	3.2.1.8
2DFC	XYLANASE II FROM TRICODERMA REESEI AT 293K	3.2.1.8
2DFE	CRYSTAL STRUCTURE OF TK-RNASE HII(1-200)-C	3.1.26.4
2DFF	CRYSTAL STRUCTURE OF TK-RNASE HII(1-204)-C	3.1.26.4
2DFH	CRYSTAL STRUCTURE OF TK-RNASE HII(1-212)-C	3.1.26.4
2DFI	CRYSTAL STRUCTURE OF PF-MAP(1-292)-C	3.4.11.18
2DFJ	CRYSTAL STRUCTURE OF THE DIADENOSINE TETRAPHOSPHATE HYDROLASE FROM SHIGELLA FLEXNERI 2A	3.6.1.41
2DFP	X-RAY STRUCTURE OF AGED DI-ISOPROPYL-PHOSPHORO-FLUORIDATE (DFP) BOUND TO ACETYLCHOLINESTERASE	3.1.1.7
2DFX	CRYSTAL STRUCTURE OF THE CARBOXY TERMINAL DOMAIN OF COLICIN E5 COMPLEXED WITH ITS INHIBITOR	3.1
2DG0	CRYSTAL STRUCTURE OF DRP35, A 35KDA DRUG RESPONSIVE PROTEIN FROM STAPHYLOCOCCUS AUREUS	3.1.1.25 3.1.1
2DG1	CRYSTAL STRUCTURE OF DRP35, A 35KDA DRUG RESPONSIVE PROTEIN FROM STAPHYLOCOCCUS AUREUS, COMPLEXED WITH CA2+	3.1.1.25 3.1.1
2DG5	CRYSTAL STRUCTURE OF GAMMA-GLUTAMYL TRANSPEPTIDASE FROM ESCHERICHIA COLI IN COMPLEX WITH HYDROLYZED GLUTATHIONE	2.3.2.2 3.4.19.13
2DGA	CRYSTAL STRUCTURE OF HEXAMERIC BETA-GLUCOSIDASE IN WHEAT	3.2.1.21 3.2.1.182
2DGZ	SOLUTION STRUCTURE OF THE HELICASE AND RNASE D C-TERMINAL DOMAIN IN WERNER SYNDROME ATP-DEPENDENT HELICASE	3.6.1 3.6.4.12 3.1
2DHC	CRYSTALLOGRAPHIC ANALYSIS OF THE CATALYTIC MECHANISM OF HALOALKANE DEHALOGENASE	3.8.1.5
2DHD	CRYSTALLOGRAPHIC ANALYSIS OF THE CATALYTIC MECHANISM OF HALOALKANE DEHALOGENASE	3.8.1.5
2DHE	CRYSTALLOGRAPHIC ANALYSIS OF THE CATALYTIC MECHANISM OF HALOALKANE DEHALOGENASE	3.8.1.5
2DHR	WHOLE CYTOSOLIC REGION OF ATP-DEPENDENT METALLOPROTEASE FTSH (G399L)	3.4.24
2DI4	CRYSTAL STRUCTURE OF THE FTSH PROTEASE DOMAIN	3.4.24
2DIE	ALKALINE ALPHA-AMYLASE AMYK FROM BACILLUS SP. KSM-1378	3.2.1.1
2DJF	CRYSTAL STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE I (CATHEPSIN C) IN COMPLEX WITH THE INHIBITOR GLY-PHE-CHN2	3.4.14.1
2DJG	RE-DETERMINATION OF THE NATIVE STRUCTURE OF HUMAN DIPEPTIDYL PEPTIDASE I (CATHEPSIN C)	3.4.14.1
2DJH	CRYSTAL STRUCTURE OF THE CARBOXY-TERMINAL RIBONUCLEASE DOMAIN OF COLICIN E5	3.1
2DJM	SOLUTION STRUCTURE OF N-TERMINAL STARCH-BINDING DOMAIN OF GLUCOAMYLASE FROM RHIZOPUS ORYZAE	3.2.1.3
2DJU	SOLUTION STRUCTURES OF THE FN3 DOMAIN OF HUMAN RECEPTOR-TYPE TYROSINE-PROTEIN PHOSPHATASE F	3.1.3.48
2DKF	CRYSTAL STRUCTURE OF TTHA0252 FROM THERMUS THERMOPHILUS HB8, A RNA DEGRADATION PROTEIN OF THE METALLO-BETA-LACTAMASE SUPERFAMILY	3.1
2DKO	EXTENDED SUBSTRATE RECOGNITION IN CASPASE-3 REVEALED BY HIGH RESOLUTION X-RAY STRUCTURE ANALYSIS	3.4.22 3.4.22.56
2DKQ	SOLUTION STRUCTURE OF THE PTB DOMAIN OF KIAA1075 PROTEIN FROM HUMAN	3.1.3.48
2DKV	CRYSTAL STRUCTURE OF CLASS I CHITINASE FROM ORYZA SATIVA L. JAPONICA	3.2.1.14
2DL6	SOLUTION STRUCTURE OF THE FIRST BRK DOMAIN FROM HUMAN CHROMODOMAIN-HELICASE-DNA-BINDING PROTEIN 8	3.6.4.12
2DLE	SOLUTION STRUCTURE OF THE FOURTH FN3 DOMAIN OF HUMAN RECEPTOR-TYPE TYROSINE-PROTEIN PHOSPHATASE ETA	3.1.3.48