Structure of PDB 4dpe Chain B Binding Site BS07
Receptor Information
>4dpe Chain B (length=167) Species:
9606
(Homo sapiens) [
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IPKWRKTHLTYRIVNYTPDLPKDAVDSAVEKALKVWEEVTPLTFSRLYEG
EADIMISFAVREHGDFYPFDGPGNVLAHAYAPGPGINGDAHFDDDEQWTK
DTTGTNLFLVAAHEIGHSLGLFHSANTEALMYPLYHSLTDLTRFRLSQDD
INGIQSLYGPPPDSPET
Ligand information
Ligand ID
NGH
InChI
InChI=1S/C13H20N2O5S/c1-10(2)8-15(9-13(16)14-17)21(18,19)12-6-4-11(20-3)5-7-12/h4-7,10,17H,8-9H2,1-3H3,(H,14,16)
InChIKey
JIRXORZYIXSWOB-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(C)C[N@](CC(=O)NO)S(=O)(=O)c1ccc(cc1)OC
CACTVS 3.341
COc1ccc(cc1)[S](=O)(=O)N(CC(C)C)CC(=O)NO
ACDLabs 10.04
O=C(NO)CN(S(=O)(=O)c1ccc(OC)cc1)CC(C)C
OpenEye OEToolkits 1.5.0
CC(C)CN(CC(=O)NO)S(=O)(=O)c1ccc(cc1)OC
Formula
C13 H20 N2 O5 S
Name
N-ISOBUTYL-N-[4-METHOXYPHENYLSULFONYL]GLYCYL HYDROXAMIC ACID
ChEMBL
CHEMBL311932
DrugBank
DB08271
ZINC
ZINC000003818629
PDB chain
4dpe Chain B Residue 313 [
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Receptor-Ligand Complex Structure
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PDB
4dpe
Structure of matrix metalloproteinase-3 with a platinum-based inhibitor.
Resolution
1.96 Å
Binding residue
(original residue number in PDB)
V163 L164 A165 H201 E202 H205 H211 Y223
Binding residue
(residue number reindexed from 1)
V75 L76 A77 H113 E114 H117 H123 Y135
Annotation score
1
Binding affinity
BindingDB: Ki=132nM,IC50=6500nM
Enzymatic activity
Catalytic site (original residue number in PDB)
H201 E202 H205 H211
Catalytic site (residue number reindexed from 1)
H113 E114 H117 H123
Enzyme Commision number
3.4.24.17
: stromelysin 1.
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:4dpe
,
PDBe:4dpe
,
PDBj:4dpe
PDBsum
4dpe
PubMed
23660647
UniProt
P08254
|MMP3_HUMAN Stromelysin-1 (Gene Name=MMP3)
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