Structure of PDB 5efd Chain A Binding Site BS01
Receptor Information
>5efd Chain A (length=354) Species:
65673
(Bacillus sp. NG-27) [
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VQPFAAQVASLADRYEESFDIGAAVEPHQLNGRQGKVLKHHYNSIVAENA
MKPISLQPEEGVFTWDGADAIVEFARKNNMNLRFHTLVWHNQVPDWFFLD
EEGNPMVEETNEAKRQANKELLLERLETHIKTVVERYKDDVTAWDVVNEV
VDDGTPNERGLRESVWYQITGDEYIRVAFETARKYAGEDAKLFINDYNTE
VTPKRDHLYNLVQDLLADGVPIDGVGHQAHIQIDWPTIDEIRTSMEMFAG
LGLDNQVTELDVSLYGWPPRPAFPTYDAIPQERFQAQADRYNQLFELYEE
LDADLSSVTFWGIADNHTWLDDRAREYNDGVGKDAPFVFDPNYRVKPAFW
RIID
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
5efd Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
5efd
Small Glycols Discover Cryptic Pockets on Proteins for Fragment-Based Approaches.
Resolution
1.674 Å
Binding residue
(original residue number in PDB)
N292 R351 D354
Binding residue
(residue number reindexed from 1)
N292 R351 D354
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
E149 N195 H230 E259 D261
Catalytic site (residue number reindexed from 1)
E149 N195 H230 E259 D261
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
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:5efd
,
PDBe:5efd
,
PDBj:5efd
PDBsum
5efd
PubMed
33570386
UniProt
O30700
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