1ATP

2.2 angstrom refined crystal structure of the catalytic subunit of camp-dependent protein kinase complexed with mnatp and a peptide inhibitor

• Total interactions analyzed: 1
• Total true interactions: 1
• Strongest Interaction:
  • Chains: E-I
  • Int. Res.: 91
  • Norm. En. per Res.: -5.5524
• Hub Node: E(1)

All Interactions

Chains	Hydro. Bond Ener. (kJ/mol)	Elec. Ener. (kJ/mol)	VDW. Ener. (kJ/mol)	Tot. Stab. Ener. (kJ/mol)	#int. res.	# Short cont.	#Hydr. int.	#VDW pairs	#salt bridges	#Pot. fav. elec. int	#Pot. unfav. elec. int
E-I	-68.9289	-126.5159	-309.826	-505.2709	91	19	4	10924	11	34	21

Interface residues

• E-I: ALA12I, ALA21I, ALA233E, ALA240E, ALA8I, ARG133E, ARG134E, ARG137E, ARG15I, ARG165E, ARG18I, ARG19I, ARG256E, ARG56E, ASN171E, ASN20I, ASP166E, ASP184E, ASP241E, ASP24I, ASP328E, ASP9I, CYS199E, GLN242E, GLN245E, GLN84E, GLU127E, GLU170E, GLU203E, GLU230E, GLY136E, GLY14I, GLY17I, GLY186E, GLY200E, GLY234E, GLY50E, GLY52E, HIS23I, HIS260E, HIS87E, ILE11I, ILE135E, ILE209E, ILE210E, ILE22I, ILE246E, LEU132E, LEU167E, LEU173E, LEU198E, LEU205E, LEU227E, LEU49E, LEU82E, LYS168E, LYS78E, LYS81E, LYS83E, PHE10I, PHE129E, PHE187E, PHE238E, PHE239E, PHE257E, PHE327E, PHE54E, PRO169E, PRO202E, PRO236E, PRO237E, PRO243E, PRO258E, SER130E, SER13I, SER259E, SER53E, THR16I, THR201E, THR51E, THR5I, THR6I, TYR204E, TYR215E, TYR229E, TYR235E, TYR247E, TYR330E, TYR7I, VAL226E, VAL57E