Structure of PDB 2vqx Chain A Binding Site BS01

Receptor Information
>2vqx Chain A (length=322) Species: 28151 (Serratia proteamaculans) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
ARSVIPPYMLRRIIEHGSLPQRDCALHTLNHVKTSTGGEVIRDIYDAENS
TQLPGKQVRNEGQASNHDVAVDEAYDYLGVTYDFFWQAFKRNSLDNQGLP
LTGSVHYGKEYQNAFWNGQQMVFGDGDGEIFNRFTIAIDVVGHALAHGVT
ESEAGLIYFQQAGALNESLSDVFGSLVKQFHLKQTADKADWLIGEGLLAK
GINGKGLRSMSAPGTAYDDPLLGKDPQPASMKDYIQTKEDNGGVHLNSGI
PNRAFYLAATALGGYAWEKAGYIWYDTLCDKALPQDADFATFARTTVKHA
EQRFDSKVAQKVQQAWHQVGVA
Ligand information
Ligand IDZN
InChIInChI=1S/Zn/q+2
InChIKeyPTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
SoftwareSMILES
CACTVS 3.341[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
FormulaZn
NameZINC ION
ChEMBLCHEMBL1236970
DrugBankDB14532
ZINC
PDB chain2vqx Chain A Residue 1342 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2vqx Crystal Structure of the Protealysin Precursor: Insights Into Propeptide Function.
Resolution1.821 Å
Binding residue
(original residue number in PDB)
H162 H166 E186
Binding residue
(residue number reindexed from 1)
H143 H147 E167
Annotation score4
Enzymatic activity
Catalytic site (original residue number in PDB) H162 A163 H166 Y177 E186 D259 H264
Catalytic site (residue number reindexed from 1) H143 A144 H147 Y158 E167 D240 H245
Enzyme Commision number 3.4.24.-
Gene Ontology
Molecular Function
GO:0004222 metalloendopeptidase activity
GO:0008237 metallopeptidase activity
GO:0046872 metal ion binding
Biological Process
GO:0006508 proteolysis
Cellular Component
GO:0005576 extracellular region

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Molecular Function

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Cellular Component
External links
PDB RCSB:2vqx, PDBe:2vqx, PDBj:2vqx
PDBsum2vqx
PubMed19915005
UniProtQ5MJ80

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