Structure of PDB 1lq2 Chain A Binding Site BS01

Receptor Information
>1lq2 Chain A (length=602) Species: 4513 (Hordeum vulgare) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
DYVLYKDATKPVEDRVADLLGRMTLAEKIGQMTQIERLVATPDVLRDNFI
GSLLSGGGSVPRKGATAKEWQDMVDGFQKACMSTRLGIPMIYGIDAVHGQ
NNVYGATIFPHNVGLGATRDPYLVKRIGEATALEVRATGIQYAFAPCIAV
CRDPRWGRCYESYSEDRRIVQSMTELIPGLQGDVPKDFTSGMPFVAGKNK
VAACAKHFVGDGGTVDGINENNTIINREGLMNIHMPAYKNAMDKGVSTVM
ISYSSWNGVKMHANQDLVTGYLKDTLKFKGFVISDWEGIDRITTPAGSDY
SYSVKASILAGLDMIMVPNKYQQFISILTGHVNGGVIPMSRIDDAVTRIL
RVKFTMGLFENPYADPAMAEQLGKQEHRDLAREAARKSLVLLKNGKTSTD
APLLPLPKKAPKILVAGSHADNLGYQCGGWTIEWQGDTGRTTVGTTILEA
VKAAVDPSTVVVFAENPDAEFVKSGGFSYAIVAVGEHPYTETKGDNLNLT
IPEPGLSTVQAVCGGVRCATVLISGRPVVVQPLLAASDALVAAWLPGSEG
QGVTDALFGDFGFTGRLPRTWFKSVDQLPMNVGDAHYDPLFRLGYGLTTN
AT
Ligand information
Ligand IDIDD
InChIInChI=1S/C14H16N2O4/c17-7-10-11(18)12(19)13(20)14-15-9(6-16(10)14)8-4-2-1-3-5-8/h1-6,10-13,17-20H,7H2/t10-,11-,12+,13-/m1/s1
InChIKeyDLVNFMROYKHANV-FVCCEPFGSA-N
SMILES
SoftwareSMILES
CACTVS 3.341OC[CH]1[CH](O)[CH](O)[CH](O)c2nc(cn12)c3ccccc3
OpenEye OEToolkits 1.5.0c1ccc(cc1)c2cn3c(n2)C(C(C(C3CO)O)O)O
OpenEye OEToolkits 1.5.0c1ccc(cc1)c2cn3c(n2)[C@@H]([C@H]([C@@H]([C@H]3CO)O)O)O
CACTVS 3.341OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)c2nc(cn12)c3ccccc3
ACDLabs 10.04OC2c1nc(cn1C(C(O)C2O)CO)c3ccccc3
FormulaC14 H16 N2 O4
Name(5R,6R,7S,8S)-5-(HYDROXYMETHYL)-2-PHENYL-5,6,7,8-TETRAHYDROIMIDAZO[1,2-A]PYRIDINE-6,7,8-TRIOL;
GLUCO-PHENYLIMIDAZOLE
ChEMBL
DrugBankDB02862
ZINCZINC000033821368
PDB chain1lq2 Chain A Residue 621 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB1lq2 Three-dimensional Structure of the Barley {beta}-D-Glucan Glucohydrolase in Complex with a Transition State Mimic.
Resolution2.7 Å
Binding residue
(original residue number in PDB)
D95 R158 K206 H207 M250 D285 W286 W434 E491
Binding residue
(residue number reindexed from 1)
D95 R158 K206 H207 M250 D285 W286 W434 E491
Annotation score1
Binding affinityPDBbind-CN: -logKd/Ki=8.77,Ki=1.7nM
Enzymatic activity
Catalytic site (original residue number in PDB) D285 E491
Catalytic site (residue number reindexed from 1) D285 E491
Enzyme Commision number 3.2.1.21: beta-glucosidase.
Gene Ontology
Molecular Function
GO:0004553 hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0016798 hydrolase activity, acting on glycosyl bonds
Biological Process
GO:0005975 carbohydrate metabolic process
Cellular Component
GO:0005576 extracellular region

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:1lq2, PDBe:1lq2, PDBj:1lq2
PDBsum1lq2
PubMed14597633
UniProtQ9XEI3

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