Structure of PDB 2d1n Chain B Binding Site BS03
Receptor Information
>2d1n Chain B (length=166) Species:
9606
(Homo sapiens) [
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YNVFPRTLKWSKMNLTYRIVNYTPDMTHSEVEKAFKKAFKVWSDVTPLNF
TRLHDGIADIMISFGIKEHGDFYPFDGPSGLLAHAFPPGPNYGGDAHFDD
DETWTSSSKGYNLFLVAAHEFGHSLGLDHSKDPGALMFPIYTYTGKSHFM
LPDDDVQGIQSLYGPG
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
2d1n Chain B Residue 282 [
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Receptor-Ligand Complex Structure
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PDB
2d1n
Crystal structures of the catalytic domain of human stromelysin-1 (MMP-3) and collagenase-3 (MMP-13) with a hydroxamic acid inhibitor SM-25453
Resolution
2.37 Å
Binding residue
(original residue number in PDB)
D179 G180 S182 L184 D202 E205
Binding residue
(residue number reindexed from 1)
D76 G77 S79 L81 D99 E102
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H222 E223 H226 H232
Catalytic site (residue number reindexed from 1)
H119 E120 H123 H129
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2d1n
,
PDBe:2d1n
,
PDBj:2d1n
PDBsum
2d1n
PubMed
16603129
UniProt
P45452
|MMP13_HUMAN Collagenase 3 (Gene Name=MMP13)
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