Structure of PDB 1w3l Chain A Binding Site BS01
Receptor Information
>1w3l Chain A (length=300) Species:
76935
(Salipaludibacillus agaradhaerens) [
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SVVEEHGQLSISNGELVNERGEQVQLKGMSSHGLQWYGQFVNYESMKWLR
DDWGINVFRAAMYTSSGGYIDDPSVKEKVKEAVEAAIDLDIYVIIDWHIL
SDNDPNIYKEEAKDFFDEMSELYGDYPNVIYEIANEPNGSDVTWGNQIKP
YAEEVIPIIRNNDPNNIIIVGTGTWSQDVHHAADNQLADPNVMYAFHFYA
GTHGQNLRDQVDYALDQGAAIFVSEWGTSAATGDGGVFLDEAQVWIDFMD
ERNLSWANWSLTHKDESSAALMPGANPTGGWTEAELSPSGTFVREKIRES
Ligand information
Ligand ID
BGC
InChI
InChI=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
InChIKey
WQZGKKKJIJFFOK-VFUOTHLCSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
C(C1C(C(C(C(O1)O)O)O)O)O
CACTVS 3.370
OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O
CACTVS 3.370
OC[CH]1O[CH](O)[CH](O)[CH](O)[CH]1O
OpenEye OEToolkits 1.7.6
C([C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)O)O)O)O
ACDLabs 12.01
OC1C(O)C(OC(O)C1O)CO
Formula
C6 H12 O6
Name
beta-D-glucopyranose;
beta-D-glucose;
D-glucose;
glucose
ChEMBL
CHEMBL1614854
DrugBank
DB02379
ZINC
ZINC000003833800
PDB chain
1w3l Chain B Residue 1 [
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Receptor-Ligand Complex Structure
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PDB
1w3l
Structural, Thermodynamic, and Kinetic Analyses of Tetrahydrooxazine-Derived Inhibitors Bound to {Beta}-Glucosidases
Resolution
1.04 Å
Binding residue
(original residue number in PDB)
H35 W39 Y66 W262 K267 E269
Binding residue
(residue number reindexed from 1)
H32 W36 Y63 W259 K264 E266
Annotation score
4
Binding affinity
PDBbind-CN
: -logKd/Ki=6.28,Ki=0.52uM
Enzymatic activity
Enzyme Commision number
3.2.1.4
: cellulase.
Gene Ontology
Molecular Function
GO:0004553
hydrolase activity, hydrolyzing O-glycosyl compounds
Biological Process
GO:0000272
polysaccharide catabolic process
GO:0005975
carbohydrate metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1w3l
,
PDBe:1w3l
,
PDBj:1w3l
PDBsum
1w3l
PubMed
15356002
UniProt
O85465
|GUN5_SALAG Endoglucanase 5A (Gene Name=cel5A)
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