Structure of PDB 1xry Chain A Binding Site BS02
Receptor Information
>1xry Chain A (length=291) Species:
671
(Vibrio proteolyticus) [
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MPPITQQATVTAWLPQVDASQITGTISSLESFTNRFYTTTSGAQASDWIA
SEWQALSASLPNASVKQVSHSGYNQKSVVMTITGSEAPDEWIVIGGHLDS
TIGSHTNEQSVAPGADDDASGIAAVTEVIRVLSENNFQPKRSIAFMAYAA
EEVGLRGSQDLANQYKSEGKNVVSALQLDMTNYKGSAQDVVFITDYTDSN
FTQYLTQLMDEYLPSLTYGFDTCGYACSDHASWHNAGYPAAMPFESKFND
YNPRIHTTQDTLANSDPTGSHAKKFTQLGLAYAIEMGSATG
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
1xry Chain A Residue 1002 [
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Receptor-Ligand Complex Structure
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PDB
1xry
Interactions of Streptomyces griseus Aminopeptidase and Aeromonas proteolytica Aminopeptidase with Bestatin. Structural analysis of homologous enzymes with different binding modes.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
H97 D117 D179
Binding residue
(residue number reindexed from 1)
H97 D117 D179
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H97 D117 E151 E152 D179 H256
Catalytic site (residue number reindexed from 1)
H97 D117 E151 E152 D179 H256
Enzyme Commision number
3.4.11.10
: bacterial leucyl aminopeptidase.
Gene Ontology
Molecular Function
GO:0008235
metalloexopeptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:1xry
,
PDBe:1xry
,
PDBj:1xry
PDBsum
1xry
PubMed
UniProt
Q01693
|AMPX_VIBPR Bacterial leucyl aminopeptidase
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