Structure of PDB 1ur2 Chain A Binding Site BS03
Receptor Information
>1ur2 Chain A (length=351) Species:
39650
(Cellvibrio mixtus) [
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TGLKSAYKDNFLIGAALNATIASGADERLNTLIAKEFNSITPENCMKWGV
LRDAQGQWNWKDADAFVAFGTKHNLHMVGHTLVWHSQIHDEVFKNADGSY
ISKAALQKKMEEHITTLAGRYKGKLAAWDVVNEAVGDDLKMRDSHWYKIM
GDDFIYNAFTLANEVDPKAHLMYNDYNIERTGKREATVEMIERLQKRGMP
IHGLGIQGHLGIDTPPIAEIEKSIIAFAKLGLRVHFTSLDVDVLPSVWEL
PVAEVSTRFEYKPERDPYTKGLPQEMQDKLAKRYEDLFKLFIKHSDKIDR
ATFWGVSDDASWLNGFPIPGRTNYPLLFDRKLQPKDAYFRLLDLKRLEHH
H
Ligand information
Ligand ID
XYS
InChI
InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3+,4-,5+/m1/s1
InChIKey
SRBFZHDQGSBBOR-LECHCGJUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1C(C(C(C(O1)O)O)O)O
CACTVS 3.341
O[CH]1CO[CH](O)[CH](O)[CH]1O
OpenEye OEToolkits 1.5.0
C1[C@H]([C@@H]([C@H]([C@H](O1)O)O)O)O
CACTVS 3.341
O[C@@H]1CO[C@H](O)[C@H](O)[C@H]1O
ACDLabs 10.04
OC1C(O)COC(O)C1O
Formula
C5 H10 O5
Name
alpha-D-xylopyranose;
alpha-D-xylose;
D-xylose;
xylose;
XYLOPYRANOSE
ChEMBL
DrugBank
DB03389
ZINC
ZINC000001529214
PDB chain
1ur2 Chain C Residue 1 [
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Receptor-Ligand Complex Structure
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PDB
1ur2
The Mechanisms by which Family 10 Glycoside Hydrolases Bind Decorated Substrates
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
K71 H104 Q231 H233 S262 W328 W336
Binding residue
(residue number reindexed from 1)
K47 H80 Q207 H209 S238 W304 W312
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
E157 N198 H233 S262 D264
Catalytic site (residue number reindexed from 1)
E133 N174 H209 S238 D240
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
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0045493
xylan catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1ur2
,
PDBe:1ur2
,
PDBj:1ur2
PDBsum
1ur2
PubMed
14668328
UniProt
O68541
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