Structure of PDB 2vqx Chain A Binding Site BS01
Receptor Information
>2vqx Chain A (length=322) Species:
28151
(Serratia proteamaculans) [
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ARSVIPPYMLRRIIEHGSLPQRDCALHTLNHVKTSTGGEVIRDIYDAENS
TQLPGKQVRNEGQASNHDVAVDEAYDYLGVTYDFFWQAFKRNSLDNQGLP
LTGSVHYGKEYQNAFWNGQQMVFGDGDGEIFNRFTIAIDVVGHALAHGVT
ESEAGLIYFQQAGALNESLSDVFGSLVKQFHLKQTADKADWLIGEGLLAK
GINGKGLRSMSAPGTAYDDPLLGKDPQPASMKDYIQTKEDNGGVHLNSGI
PNRAFYLAATALGGYAWEKAGYIWYDTLCDKALPQDADFATFARTTVKHA
EQRFDSKVAQKVQQAWHQVGVA
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
2vqx Chain A Residue 1342 [
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Receptor-Ligand Complex Structure
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PDB
2vqx
Crystal Structure of the Protealysin Precursor: Insights Into Propeptide Function.
Resolution
1.821 Å
Binding residue
(original residue number in PDB)
H162 H166 E186
Binding residue
(residue number reindexed from 1)
H143 H147 E167
Annotation score
4
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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Biological Process
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Cellular Component
External links
PDB
RCSB:2vqx
,
PDBe:2vqx
,
PDBj:2vqx
PDBsum
2vqx
PubMed
19915005
UniProt
Q5MJ80
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