Structure of PDB 2cbu Chain B Binding Site BS02
Receptor Information
>2cbu Chain B (length=441) Species:
2336
(Thermotoga maritima) [
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NVKKFPEGFLWGVATASYQIEGSPLADGAGMSIWHTFSHTPGNVKNGDTG
DVACDHYNRWKEDIEIIEKLGVKAYRFSISWPRILPEGTGRVNQKGLDFY
NRIIDTLLEKGITPFVTIYHWDLPFALQLKGGWANREIADWFAEYSRVLF
ENFGDRVKNWITLNEPWVVAIVGHLYGVHAPGMRDIYVAFRAVHNLLRAH
ARAVKVFRETVKDGKIGIVFNNGYFEPASEKEEDIRAVRFMHQFNNYPLF
LNPIYRGDYPELVLEFAREYLPENYKDDMSEIQEKIDFVGLNYYSGHLVK
FDPDAKVSFVERDLPKTAMGWEIVPEGIYWILKKVKEEYNPPEVYITENG
AAFDDVVSEDGRVHDQNRIDYLKAHIGQAWKAIQEGVPLKGYFVWSLLDN
FEWAEGYSKRFGIVYVDYSTQKRIVKDSGYWYSNVVKNNGL
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
2cbu Chain B Residue 1446 [
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Receptor-Ligand Complex Structure
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PDB
2cbu
Dissection of Conformationally Restricted Inhibitors Binding to a Beta-Glucosidase.
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
D278 E282
Binding residue
(residue number reindexed from 1)
D277 E281
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)
R76 H120 E165 V168 N292 Y294 E348
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:2cbu
,
PDBe:2cbu
,
PDBj:2cbu
PDBsum
2cbu
PubMed
16628756
UniProt
Q08638
|BGLA_THEMA Beta-glucosidase A (Gene Name=bglA)
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