Structure of PDB 7wxx Chain A Binding Site BS04
Receptor Information
>7wxx Chain A (length=164) Species:
9606
(Homo sapiens) [
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GYSLFPNSPKWTSKVVTYRIVSYTRDLPHITVDRLVSKALNMWGKEIPLH
FRKVVWGTADIMIGFARGAHGDSYPFDGPGNTLAHAFAPGTGLGGDAHFD
EDERWTDGSSLGINFLYAATHQLGHSLGMGHSSDPNAVMYPTYQNFKLSQ
DDIKGIQKLYGKRS
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
7wxx Chain A Residue 303 [
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Receptor-Ligand Complex Structure
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PDB
7wxx
Discovery of Highly Potent and Selective Matrix Metalloproteinase-7 Inhibitors by Hybridizing the S1' Subsite Binder with Short Peptides.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
H163 D165 H178 H191
Binding residue
(residue number reindexed from 1)
H70 D72 H85 H98
Annotation score
4
Enzymatic activity
Enzyme Commision number
3.4.24.23
: matrilysin.
Gene Ontology
Molecular Function
GO:0004222
metalloendopeptidase activity
GO:0008237
metallopeptidase activity
GO:0008270
zinc ion binding
Biological Process
GO:0006508
proteolysis
Cellular Component
GO:0031012
extracellular matrix
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7wxx
,
PDBe:7wxx
,
PDBj:7wxx
PDBsum
7wxx
PubMed
36137271
UniProt
P09237
|MMP7_HUMAN Matrilysin (Gene Name=MMP7)
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