Structure of PDB 5xc0 Chain A Binding Site BS01

Receptor Information
>5xc0 Chain A (length=353) Species: 65673 (Bacillus sp. NG-27) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
VQPFAAQVASLADRYEESFDIGAAVEPHQLNGRQGKVLKHHYNSIVAENA
MKPISLQPEEGVFTWDGADAIVEFARKNNMNLRFHTLVWHNQVPDWFFLD
EEGNPMVEETNEAKRQANKELLLERLETHIKTVVERYKDDVTAWDVVNEV
VDDGTPERGLRESVWYQITGDEYIRVAFETARKYAGEDAKLFINDYNTEV
TPKRDHLYNLVQDLLADGVPIDGVGHQAHIQIDWPTIDEIRTSMEMFAGL
GLDNQVTELDVSLYGWPPRPAFPTYDAIPQERFQAQADRYNQLFELYEEL
DADLSSVTFWGIADNHTWLDDRAREYNDGVGKDAPFVFDPNYRVKPAFWR
IID
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 chain5xc0 Chain A Residue 401 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB5xc0 Small Glycols Discover Cryptic Pockets on Proteins for Fragment-Based Approaches.
Resolution2.32 Å
Binding residue
(original residue number in PDB)
N292 R351 D354
Binding residue
(residue number reindexed from 1)
N291 R350 D353
Annotation score4
Enzymatic activity
Catalytic site (original residue number in PDB) E149 N195 H230 E259 D261
Catalytic site (residue number reindexed from 1) E149 N194 H229 E258 D260
Enzyme Commision number 3.2.1.8: endo-1,4-beta-xylanase.
Gene Ontology
Molecular Function
GO:0004553 hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0016798 hydrolase activity, acting on glycosyl bonds
GO:0031176 endo-1,4-beta-xylanase activity
GO:0046872 metal ion binding
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0045493 xylan catabolic process

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Molecular Function

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Biological Process
External links
PDB RCSB:5xc0, PDBe:5xc0, PDBj:5xc0
PDBsum5xc0
PubMed33570386
UniProtO30700

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