Structure of PDB 5n55 Chain C Binding Site BS02

Receptor Information
>5n55 Chain C (length=228) Species: 573 (Klebsiella pneumoniae) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
EYPTVEIPVGEVRLYQIADGVWSHIATQSFDGAVYPSNGLIVRDGDELLL
IDTAWGAKNTAALLAEIEKQIGLPVTRAVSTHFHDDRVGGVDVLRKAGVA
TYASPSTRRLAEAEGNEIPTHSLEGLSSSGDAVRFGPVELFYPGAAHSTD
NLVVYVPSANVLYGGCAVLALSRTSAGNVADADLAEWPTSVERIQKHYPE
AEVVIPGHGLPGGLDLLQHTANVVTAHK
Ligand information
Ligand ID8NN
InChIInChI=1S/C21H16ClN3O4/c22-19-14-7-2-1-6-13(14)18(26)17(25-19)20(27)24-16(21(28)29)9-11-10-23-15-8-4-3-5-12(11)15/h1-8,10,16,23,26H,9H2,(H,24,27)(H,28,29)/t16-/m0/s1
InChIKeyPVDFWPDMZYPBMH-INIZCTEOSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 2.0.6c1ccc2c(c1)c(c(nc2Cl)C(=O)N[C@@H](Cc3c[nH]c4c3cccc4)C(=O)O)O
OpenEye OEToolkits 2.0.6c1ccc2c(c1)c(c(nc2Cl)C(=O)NC(Cc3c[nH]c4c3cccc4)C(=O)O)O
CACTVS 3.385OC(=O)[CH](Cc1c[nH]c2ccccc12)NC(=O)c3nc(Cl)c4ccccc4c3O
CACTVS 3.385OC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)c3nc(Cl)c4ccccc4c3O
FormulaC21 H16 Cl N3 O4
Name(1-chloro-4-hydroxyisoquinoline-3-carbonyl)-L-tryptophan
ChEMBLCHEMBL2419266
DrugBank
ZINCZINC000096910827
PDB chain5n55 Chain C Residue 502 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB5n55 Crystallographic analyses of isoquinoline complexes reveal a new mode of metallo-beta-lactamase inhibition.
Resolution1.99 Å
Binding residue
(original residue number in PDB)
F62 Y67 P68 W87 H116 D117 D118 R205 G209 N210 H240
Binding residue
(residue number reindexed from 1)
F30 Y35 P36 W55 H84 D85 D86 R173 G177 N178 H208
Annotation score1
Binding affinityMOAD: Kd=1.03uM
Enzymatic activity
Catalytic site (original residue number in PDB) H114 H116 D118 H179 C198 L201 N210 H240
Catalytic site (residue number reindexed from 1) H82 H84 D86 H147 C166 L169 N178 H208
Enzyme Commision number 3.5.2.6: beta-lactamase.
External links