Structure of PDB 2clt Chain A Binding Site BS02
Receptor Information
>2clt Chain A (length=367) Species:
9606
(Homo sapiens) [
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FVLTEGNPRWEQTHLTYRIENYTPDLPRADVDHAIEKAFQLWSNVTPLTF
TKVSEGQADIMISFVRGDHRDNSPFDGPGGNLAHAFQPGPGIGGDAHFDE
DERWTNNFREYNLHRVAAHALGHSLGLSHSTDIGALMYPSYTFSGDVQLA
QDDIDGIQAIYGRSQNPVQPIGPQTPKACDSKLTFDAITTIRGEVMFFKD
RFYMRTNPFYPEVELNFISVFWPQLPNGLEAAYEFADRDEVRFFKGNKYW
AVQGQNVLHGYPKDIYSSFGFPRTVKHIDAALSEENTGKTYFFVANKYWR
YDEYKRSMDPGYPKMIAHDFPGIGHKVDAVFMKDGFFYFFHGTRQYKFDP
KTKRILTLQKANSWFNC
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
2clt Chain A Residue 1102 [
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Receptor-Ligand Complex Structure
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PDB
2clt
Crystal Structure of an Active Form of Human Mmp-1.
Resolution
2.67 Å
Binding residue
(original residue number in PDB)
D266 E310 D359 D408
Binding residue
(residue number reindexed from 1)
D186 E230 D279 D328
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H199 A200 H203 H209
Catalytic site (residue number reindexed from 1)
H119 A120 H123 H129
Enzyme Commision number
3.4.24.7
: interstitial collagenase.
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:2clt
,
PDBe:2clt
,
PDBj:2clt
PDBsum
2clt
PubMed
16890240
UniProt
P03956
|MMP1_HUMAN Interstitial collagenase (Gene Name=MMP1)
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