Structure of PDB 2dcj Chain A Binding Site BS01

Receptor Information
>2dcj Chain A (length=327) Species: 98930 (Bacillus sp. 41M-1) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
AITSNEIGTHDGYDYEFWKDSGGSGSMTLNSGGTFSAQWSNVNNILFRKG
KKFDETQTHQQIGNMSINYGATYNPNGNSYLTVYGWTVDPLVEFYIVDSW
GTWRPPGGTPKGTINVDGGTYQIYETTRYNQPSIKGTATFQQYWSVRTSK
RTSGTISVSEHFRAWESLGMNMGNMYEVALTVEGYQSSGSANVYSNTLTI
GGQSGGEQATRVEAESMTKGGPYTSNITSPFNGVALYANGDNVSFNHSFT
KANSSFSLRGASNNSNMARVDLRIGGQNRGTFYFGDQYPAVYTINNINHG
IGNQLVELIVTADDGTWDAYLDYLEIR
Ligand information
Ligand IDCA
InChIInChI=1S/Ca/q+2
InChIKeyBHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
SoftwareSMILES
CACTVS 3.341[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
FormulaCa
NameCALCIUM ION
ChEMBL
DrugBankDB14577
ZINC
PDB chain2dcj Chain A Residue 1001 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2dcj A two-domain structure of alkaliphilic XynJ from Bacillus sp. 41M-1
Resolution2.24 Å
Binding residue
(original residue number in PDB)
E213 E215 N232 D322
Binding residue
(residue number reindexed from 1)
E213 E215 N232 D322
Annotation score4
Enzymatic activity
Catalytic site (original residue number in PDB) N44 Y84 E93 Y95 E183
Catalytic site (residue number reindexed from 1) N44 Y84 E93 Y95 E183
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:0030246 carbohydrate binding
Biological Process
GO:0005975 carbohydrate metabolic process

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Molecular Function

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Biological Process
External links
PDB RCSB:2dcj, PDBe:2dcj, PDBj:2dcj
PDBsum2dcj
PubMed
UniProtQ9RC94

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