2HNI

crystal structure of biotin protein ligase from pyrococcus horikoshii ot3, k111a mutation

• Total interactions analyzed: 1
• Total true interactions: 1
• Strongest Interaction:
  • Chains: A-B
  • Int. Res.: 96
  • Norm. En. per Res.: -5.0517
• Hub Node: A(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
A-B	-127.5843	-16.3854	-340.998	-484.9678	96	16	5	12440	3	18	9

Interface residues

• A-B: ALA39A, ALA39B, ARG11A, ARG11B, ARG12A, ARG12B, ARG158A, ARG158B, ASP165A, ASP165B, ASP40A, ASP40B, GLN17A, GLN17B, GLU18A, GLU18B, GLU32A, GLU32B, GLU57A, GLU57B, GLY10A, GLY10B, GLY34A, GLY34B, GLY3A, GLY3B, GLY58A, GLY58B, GLY59A, GLY59B, ILE14A, ILE14B, ILE161A, ILE161B, ILE19A, ILE19B, ILE37A, ILE37B, ILE8A, ILE8B, ILE9A, ILE9B, LEU153A, LEU153B, LEU154A, LEU154B, LEU2A, LEU2B, LEU31A, LEU31B, LEU4A, LEU4B, LEU60A, LEU60B, LEU62A, LEU62B, LYS41A, LYS41B, LYS5A, LYS5B, MET1A, MET1B, PHE157A, PHE157B, PHE16A, PHE16B, PHE25A, PHE25B, PRO152A, PRO152B, SER155A, SER155B, SER29A, SER29B, SER7A, SER7B, THR20A, THR20B, THR35A, THR35B, THR6A, THR6B, TRP61A, TRP61B, TYR15A, TYR15B, VAL132A, VAL132B, VAL13A, VAL13B, VAL156A, VAL156B, VAL36A, VAL36B, VAL38A, VAL38B