Structure of PDB 4oeh Chain E Binding Site BS01
Receptor Information
>4oeh Chain E (length=251) Species:
243277
(Vibrio cholerae O1 biovar El Tor str. N16961) [
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KTVFHLGVTEADLNGATLAIIPGDPARVQKIAELMDNPVFLASHREYTVY
RAELDGQSVVVCSTGIGGPSTSIAVEELAQLGVRTFLRVGTTGAIQPHVN
VGDMIVTTGSVRLDGASLHFAPMEFPAVPDFDVATAMKAAAQESGATVHM
GVTASSDTFYPGQERYDTFTGRVVRRFQGSMKEWQDMGVLNFEMESATLL
TMCASSGLKAGCVAGVIINRTQKEIPDHATLKETEARSIKVVVEAARKML
K
Ligand information
Ligand ID
URA
InChI
InChI=1S/C4H4N2O2/c7-3-1-2-5-4(8)6-3/h1-2H,(H2,5,6,7,8)
InChIKey
ISAKRJDGNUQOIC-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
O=C1NC=CC(=O)N1
ACDLabs 10.04
O=C1C=CNC(=O)N1
OpenEye OEToolkits 1.5.0
C1=CNC(=O)NC1=O
Formula
C4 H4 N2 O2
Name
URACIL
ChEMBL
CHEMBL566
DrugBank
DB03419
ZINC
ZINC000000895045
PDB chain
4oeh Chain E Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4oeh
X-ray structures of uridine phosphorylase from Vibrio cholerae in complexes with uridine, thymidine, uracil, thymine, and phosphate anion: Substrate specificity of bacterial uridine phosphorylases.
Resolution
1.91 Å
Binding residue
(original residue number in PDB)
T93 T94 G95 F161 Q165
Binding residue
(residue number reindexed from 1)
T91 T92 G93 F159 Q163
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
H7 G25 R29 R47 E79 R90 T93 R167 I219 I220 R222 L233
Catalytic site (residue number reindexed from 1)
H5 G23 R27 R45 E77 R88 T91 R165 I217 I218 R220 L231
Enzyme Commision number
2.4.2.3
: uridine phosphorylase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004850
uridine phosphorylase activity
GO:0016757
glycosyltransferase activity
GO:0016763
pentosyltransferase activity
GO:0046872
metal ion binding
GO:0047847
deoxyuridine phosphorylase activity
Biological Process
GO:0009116
nucleoside metabolic process
GO:0009164
nucleoside catabolic process
GO:0009166
nucleotide catabolic process
GO:0044206
UMP salvage
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4oeh
,
PDBe:4oeh
,
PDBj:4oeh
PDBsum
4oeh
PubMed
UniProt
Q9K4U1
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