Structure of PDB 1umt Chain A Binding Site BS03
Receptor Information
>1umt Chain A (length=166) Species:
9606
(Homo sapiens) [
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FRTFPGIPKWRKTHLTYRIVNYTPDLPKDAVDSAVEKALKVWEEVTPLTF
SRLYEGEADIMISFAVREHGDFYPFDGPGNVLAHAYAPGPGINGDAHFDD
DEQWTKDTTGTNLFLVAAHEIGHSLGLFHSANTEALMYPLYHSLTDLTRF
RLSQDDINGIQSLYGP
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
1umt Chain A Residue 3 [
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Receptor-Ligand Complex Structure
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PDB
1umt
Solution structure of the catalytic domain of human stromelysin complexed with a hydrophobic inhibitor.
Resolution
N/A
Binding residue
(original residue number in PDB)
D158 G159 G161 N162 V163 L164 D181 E184
Binding residue
(residue number reindexed from 1)
D76 G77 G79 N80 V81 L82 D99 E102
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H201 E202 H205 H211
Catalytic site (residue number reindexed from 1)
H119 E120 H123 H129
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:1umt
,
PDBe:1umt
,
PDBj:1umt
PDBsum
1umt
PubMed
8580839
UniProt
P08254
|MMP3_HUMAN Stromelysin-1 (Gene Name=MMP3)
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