Structure of PDB 2erq Chain B Binding Site BS03
Receptor Information
>2erq Chain B (length=423) Species:
8730
(Crotalus atrox) [
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LTPEQQRYLNAKKYVKLFLVADYIMYLKYGRNLTAVRTRMYDIVNVITPI
YHRMNIHVALVGLEIWSNTDKIIVQSSADVTLDLFAKWRATDLLSRKSHD
NAQLLTGINFNGPTAGLGYLGGICNTMYSAGIVQDHSKIHHLVAIAMAHE
MGHNLGMDHDKDTCTCGTRPCVMAGALSCEASFLFSDCSQKDHREFLIKN
MPQCILKKPLKTDVVSPAVCGNYFVEVGEECDCGSPRTCRDPCCDATTCK
LRQGAQCAEGLCCDQCRFKGAGTECRAAKDECDMADVCTGRSAECTDRFQ
RNGQPCKNNNGYCYNGKCPIMADQCIALFGPGATVSQDACFQFNREGNHY
GYCRKEQNTKIACEPQDVKCGRLYCFPNSPENKNPCNIYYSPNDEDKGMV
LPGTKCADRKACSNGQCVDVTTP
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
2erq Chain B Residue 702 [
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Receptor-Ligand Complex Structure
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PDB
2erq
Crystal structures of VAP1 reveal ADAMs' MDC domain architecture and its unique C-shaped scaffold
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
D469 M470 D472 D483 R484
Binding residue
(residue number reindexed from 1)
D283 M284 D286 D297 R298
Annotation score
4
Enzymatic activity
Enzyme Commision number
3.4.24.-
Gene Ontology
Molecular Function
GO:0004222
metalloendopeptidase activity
GO:0008237
metallopeptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:2erq
,
PDBe:2erq
,
PDBj:2erq
PDBsum
2erq
PubMed
16688218
UniProt
Q9DGB9
|VM3V1_CROAT Zinc metalloproteinase-disintegrin-like VAP1
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