Structure of PDB 456c Chain B Binding Site BS02
Receptor Information
>456c Chain B (length=159) Species:
9606
(Homo sapiens) [
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LKWSKMNLTYRIVNYTPDMTHSEVEKAFKKAFKVWSDVTPLNFTRLHDGI
ADIMISFGIKEHGDFYPFDGPSGLLAHAFPPGPNYGGDAHFDDDETWTSS
SKGYNLFLVAAHEFGHSLGLDHSKDPGALMFPIYTYTGKSHFMLPDDDVQ
GIQSLYGPG
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
456c Chain B Residue 273 [
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Receptor-Ligand Complex Structure
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PDB
456c
Crystal structures of MMP-1 and -13 reveal the structural basis for selectivity of collagenase inhibitors.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
H172 D174 H187 H200
Binding residue
(residue number reindexed from 1)
H62 D64 H77 H90
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H222 E223 H226 H232
Catalytic site (residue number reindexed from 1)
H112 E113 H116 H122
Enzyme Commision number
3.4.24.-
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
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:456c
,
PDBe:456c
,
PDBj:456c
PDBsum
456c
PubMed
10074939
UniProt
P45452
|MMP13_HUMAN Collagenase 3 (Gene Name=MMP13)
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