Structure of PDB 2w0d Chain A Binding Site BS03
Receptor Information
>2w0d Chain A (length=158) Species:
9606
(Homo sapiens) [
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GPVWRKHYITYRINNYTPDMNREDVDYAIRKAFQVWSNVTPLKFSKINTG
MADILVVFARGAHGDFHAFDGKGGILAHAFGPGSGIGGDAHFDEDEFWTT
HSGGTNLFLTAVHAIGHSLGLGHSSDPKAVMFPTYKYVDINTFRLSADDI
RGIQSLYG
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
2w0d Chain A Residue 1266 [
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Receptor-Ligand Complex Structure
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PDB
2w0d
Does a Fast Nuclear Magnetic Resonance Spectroscopy- and X-Ray Crystallography Hybrid Approach Provide Reliable Structural Information of Ligand-Protein Complexes? a Case Study of Metalloproteinases.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D175 G176 G178 I180 D198 E201
Binding residue
(residue number reindexed from 1)
D70 G71 G73 I75 D93 E96
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H218 A219 H222 H228
Catalytic site (residue number reindexed from 1)
H113 A114 H117 H123
Enzyme Commision number
3.4.24.65
: macrophage elastase.
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:2w0d
,
PDBe:2w0d
,
PDBj:2w0d
PDBsum
2w0d
PubMed
19239231
UniProt
P39900
|MMP12_HUMAN Macrophage metalloelastase (Gene Name=MMP12)
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