Structure of PDB 5xxo Chain B Binding Site BS04

Receptor Information
>5xxo Chain B (length=732) Species: 226186 (Bacteroides thetaiotaomicron VPI-5482) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
DMDRFIDALMKKMTVEEKIGQLNLPVDIAAKIKRGEVGGLFNLKGVEKIR
DVQKQAVEQSRLGIPLLFGMDVIHGYETMFPIPLGLSCTWDMTAIEESAR
IAAIEASADGISWTFSPMVDISRDPRWGRVSEGSGEDPFLGAMIAEAMVL
GYQGKDMQRNDEIMACVKHFALYGAGEGGRDYNTVDMSRQRMFNEYMLPY
EAAVEAGVGSVMASFNEVDGVPATANKWLMTDVLRGQWGFNGFVVTNYTG
ISEMIDHGIGDLQTVSARAINAGVDMDMVSEGFVSTLKKSIQEGKVSMET
LNTACRRILEAKYKLGLFDNPYKYCDLKRPARDIFTKAHRDAARRIAAES
FVLLKNDNVTLRPGTPAEPLLPFNPKGNIAVIGPLADSRTNMPGTWSVAA
VLDRCPSLVEGLKEMTAGKANILYAKGSNLISDASYEERATMFGRSLNRD
NRTDEQLLNEALTVANQSDIIIAALGESSEMSGESSSRTDLNIPDVQQNL
LKELLKTGKPVVLVLFTGRPLTLTWEQEHVPAILNVWFGGSEAAYAIGDA
LFGYVNPGGKLTMSFPKNVGQIPLYYAHKNTGRPLAQGKWFEKFRSNYLD
VDNEPLYPFGYGLSYTTFSYGDIDLSRSTIDMTGELTAAVMVTNTGTWPG
SEVVQLYIRDLVGSTTRPVKELKGFQKIFLEPGQSEIVRFKIAPEMLRYY
NYDLQLVAEPGEFEVMIGTNSRDVKSARFTLK
Ligand information
Ligand IDMG
InChIInChI=1S/Mg/q+2
InChIKeyJLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341[Mg++]
FormulaMg
NameMAGNESIUM ION
ChEMBL
DrugBankDB01378
ZINC
PDB chain5xxo Chain B Residue 801 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB5xxo Function and structure relationships of a beta-1,2-glucooligosaccharide-degrading beta-glucosidase.
Resolution2.02 Å
Binding residue
(original residue number in PDB)
D699 V701
Binding residue
(residue number reindexed from 1)
D660 V662
Annotation score4
Enzymatic activity
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
GO:0046872 metal ion binding
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0009251 glucan catabolic process

View graph for
Molecular Function

View graph for
Biological Process
External links
PDB RCSB:5xxo, PDBe:5xxo, PDBj:5xxo
PDBsum5xxo
PubMed29131329
UniProtQ8A1U1

[Back to BioLiP]