Structure of PDB 2bwa Chain A Binding Site BS01

Receptor Information
>2bwa Chain A (length=226) Species: 29549 (Rhodothermus marinus) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
TVELCGRWDARDVAGGRYRVINNVWGAETAQCIEVGLETGNFTITRADHD
NGNNVAAYPAIYFGCHWGACTSNSGLPRRVQELSDVRTSWTLTPITTGRW
NAAYDIWFSPVTNSGNGYSGGAELMIWLNWNGGVMPGGSRVATVELAGAT
WEVWYADWDWNYIAYRRTTPTTSVSELDLKAFIDDAVARGYIRPEWYLHA
VETGFELWEGGAGLRSADFSVTVQKL
Ligand information
Ligand IDGLC
InChIInChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1
InChIKeyWQZGKKKJIJFFOK-DVKNGEFBSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.5.0C(C1C(C(C(C(O1)O)O)O)O)O
OpenEye OEToolkits 1.5.0C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O)O)O)O)O
CACTVS 3.341OC[CH]1O[CH](O)[CH](O)[CH](O)[CH]1O
CACTVS 3.341OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
ACDLabs 10.04OC1C(O)C(OC(O)C1O)CO
FormulaC6 H12 O6
Namealpha-D-glucopyranose;
alpha-D-glucose;
D-glucose;
glucose
ChEMBLCHEMBL423707
DrugBank
ZINCZINC000003861213
PDB chain2bwa Chain C Residue 1 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2bwa Dimerisation and an increase in active site aromatic groups as adaptations to high temperatures: X-ray solution scattering and substrate-bound crystal structures of Rhodothermus marinus endoglucanase Cel12A.
Resolution1.68 Å
Binding residue
(original residue number in PDB)
W26 Y59 D106 E124 M126 E207
Binding residue
(residue number reindexed from 1)
W25 Y58 D105 E123 M125 E206
Annotation score4
Enzymatic activity
Catalytic site (original residue number in PDB) E124 E207
Catalytic site (residue number reindexed from 1) E123 E206
Enzyme Commision number 3.2.1.4: cellulase.
Gene Ontology
Molecular Function
GO:0004553 hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0008810 cellulase activity
Biological Process
GO:0000272 polysaccharide catabolic process

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Molecular Function

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Biological Process
External links
PDB RCSB:2bwa, PDBe:2bwa, PDBj:2bwa
PDBsum2bwa
PubMed16343530
UniProtO33897

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