Structure of PDB 1v0m Chain A Binding Site BS01
Receptor Information
>1v0m Chain A (length=302) Species:
1916
(Streptomyces lividans) [
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AESTLGAAAAQSGRYFGTAIASGRLSDSTYTSIAGREFNMVTAENEMKID
ATEPQRGQFNFSSADRVYNWAVQNGKQVRGHTLAWHSQQPGWMQSLSGSA
LRQAMIDHINGVMAHYKGKIVQWDVVNEAFADGSSGARRDSNLQRSGNDW
IEVAFRTARAADPSAKLCYNDYNVENWTWAKTQAMYNMVRDFKQRGVPID
CVGFQSHFNSGSPYNSNFRTTLQNFAALGVDVAITELDIQGAPASTYANV
TNDCLAVSRCLGITVWGVRDSDSWRSEQTPLLFNNDGSKKAAYTAVLDAL
NG
Ligand information
Ligand ID
XDN
InChI
InChI=1S/C5H11NO3/c7-3-1-6-2-4(8)5(3)9/h3-9H,1-2H2/t3-,4+,5+
InChIKey
RMCNETIHECSPMZ-SCDXWVJYSA-N
SMILES
Software
SMILES
CACTVS 3.370
O[C@H]1CNC[C@@H](O)[C@@H]1O
ACDLabs 12.01
OC1CNCC(O)C1O
CACTVS 3.370
O[CH]1CNC[CH](O)[CH]1O
OpenEye OEToolkits 1.7.6
C1[C@H](C([C@H](CN1)O)O)O
OpenEye OEToolkits 1.7.6
C1C(C(C(CN1)O)O)O
Formula
C5 H11 N O3
Name
PIPERIDINE-3,4,5-TRIOL;
XYLOSE-DERIVED 1-DEOXY-NOJIRIMYCIN
ChEMBL
CHEMBL110830
DrugBank
ZINC
ZINC000100872034
PDB chain
1v0m Chain A Residue 1303 [
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Receptor-Ligand Complex Structure
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PDB
1v0m
Atomic Resolution Analyses of the Binding of Xylobiose-Derived Deoxynojirimycin and Isofagomine to Xylanase Xyn10A
Resolution
1.07 Å
Binding residue
(original residue number in PDB)
K48 H81 W85 N127 Q205 E236 W266 W274 G302
Binding residue
(residue number reindexed from 1)
K48 H81 W85 N127 Q205 E236 W266 W274 G302
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=5.10,Ki=8uM
Enzymatic activity
Catalytic site (original residue number in PDB)
E128 N170 H207 E236 D238
Catalytic site (residue number reindexed from 1)
E128 N170 H207 E236 D238
Enzyme Commision number
3.2.1.8
: endo-1,4-beta-xylanase.
Gene Ontology
Molecular Function
GO:0004553
hydrolase activity, hydrolyzing O-glycosyl compounds
Biological Process
GO:0005975
carbohydrate metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1v0m
,
PDBe:1v0m
,
PDBj:1v0m
PDBsum
1v0m
PubMed
15306887
UniProt
P26514
|XYNA_STRLI Endo-1,4-beta-xylanase A (Gene Name=xlnA)
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