Structure of PDB 2vrj Chain B Binding Site BS02
Receptor Information
>2vrj Chain B (length=443) Species:
2336
(Thermotoga maritima) [
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VKKFPEGFLWGVATASYQIEGSPLADGAGMSIWHTFSHTPGNVKNGDTGD
VACDHYNRWKEDIEIIEKLGVKAYRFSISWPRILPEGTGRVNQKGLDFYN
RIIDTLLEKGITPFVTIYHWDLPFALQLKGGWANREIADWFAEYSRVLFE
NFGDRVKNWITLNEPWVVAIVGHLYGVHAPGMRDIYVAFRAVHNLLRAHA
RAVKVFRETVKDGKIGIVFNNGYFEPASEKEEDIRAVRFMHQFNNYPLFL
NPIYRGDYPELVLEFAREYLPENYKDDMSEIQEKIDFVGLNYYSGHLVKF
DPDAPAKVSFVERDLPKTAMGWEIVPEGIYWILKKVKEEYNPPEVYITEN
GAAFDDVVSEDGRVHDQNRIDYLKAHIGQAWKAIQEGVPLKGYFVWSLLD
NFEWAEGYSKRFGIVYVDYSTQKRIVKDSGYWYSNVVKNNGLE
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
2vrj Chain B Residue 1447 [
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Receptor-Ligand Complex Structure
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PDB
2vrj
Molecular Basis for Beta-Glucosidase Inhibition by Ring-Modified Calystegine Analogues.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
D278 E282
Binding residue
(residue number reindexed from 1)
D276 E280
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
R77 H121 E166 V169 N293 Y295 E351
Catalytic site (residue number reindexed from 1)
R75 H119 E164 V167 N291 Y293 E349
Enzyme Commision number
3.2.1.21
: beta-glucosidase.
Gene Ontology
Molecular Function
GO:0004553
hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0008422
beta-glucosidase activity
GO:0016798
hydrolase activity, acting on glycosyl bonds
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0030245
cellulose catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:2vrj
,
PDBe:2vrj
,
PDBj:2vrj
PDBsum
2vrj
PubMed
18833549
UniProt
Q08638
|BGLA_THEMA Beta-glucosidase A (Gene Name=bglA)
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