Structure of PDB 456c Chain B Binding Site BS04
Receptor Information
>456c Chain B (length=159) Species:
9606
(Homo sapiens) [
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LKWSKMNLTYRIVNYTPDMTHSEVEKAFKKAFKVWSDVTPLNFTRLHDGI
ADIMISFGIKEHGDFYPFDGPSGLLAHAFPPGPNYGGDAHFDDDETWTSS
SKGYNLFLVAAHEFGHSLGLDHSKDPGALMFPIYTYTGKSHFMLPDDDVQ
GIQSLYGPG
Ligand information
Ligand ID
CBP
InChI
InChI=1S/C19H20ClNO6S/c20-14-1-3-15(4-2-14)27-16-5-7-17(8-6-16)28(24,25)19(13-18(22)21-23)9-11-26-12-10-19/h1-8,23H,9-13H2,(H,21,22)
InChIKey
QOPFTBAEAJQKSY-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
ONC(=O)CC1(CCOCC1)[S](=O)(=O)c2ccc(Oc3ccc(Cl)cc3)cc2
ACDLabs 10.04
O=S(=O)(c2ccc(Oc1ccc(Cl)cc1)cc2)C3(CC(=O)NO)CCOCC3
OpenEye OEToolkits 1.5.0
c1cc(ccc1Oc2ccc(cc2)Cl)S(=O)(=O)C3(CCOCC3)CC(=O)NO
Formula
C19 H20 Cl N O6 S
Name
2-{4-[4-(4-CHLORO-PHENOXY)-BENZENESULFONYL]-TETRAHYDRO-PYRAN-4-YL}-N-HYDROXY-ACETAMIDE
ChEMBL
CHEMBL93687
DrugBank
DB02049
ZINC
ZINC000003821624
PDB chain
456c Chain B Residue 1 [
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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)
A186 L218 H222 E223 H226 H232 L239 F241 P242 I243 Y244 T245
Binding residue
(residue number reindexed from 1)
A76 L108 H112 E113 H116 H122 L129 F131 P132 I133 Y134 T135
Annotation score
1
Binding affinity
MOAD
: Ki=0.17nM
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
View graph for
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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