Structure of PDB 4df1 Chain B Binding Site BS02
Receptor Information
>4df1 Chain B (length=199) Species:
444157
(Pyrobaculum neutrophilum V24Sta) [
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NLPLVVALDTEVLKAIDVAKRLKGAVAGFKVGWDLIFEGGISIVGEIARY
GNVIVDLKIADVPHVASRVVEKLVNRGACCVIVHGFLHPSLPRGQHVYVL
VKMTAPTIYDEMWEKLLNSVQDVRGFVLPGNQPEVVAQARKRIGCSYRII
SPGIGPQGGRPGAAIEAGADFEIVGRYVLEDPARISQWAQYRPTCFETP
Ligand information
Ligand ID
BMP
InChI
InChI=1S/C9H13N2O10P/c12-4-1-5(13)11(9(16)10-4)8-7(15)6(14)3(21-8)2-20-22(17,18)19/h1,3,6-8,13-15H,2H2,(H,10,12,16)(H2,17,18,19)/t3-,6-,7-,8-/m1/s1
InChIKey
UDOBICLZEKUKCV-YXZULKJRSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1=C(N(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O)O
OpenEye OEToolkits 1.5.0
C1=C(N(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)O)O)O)O
CACTVS 3.341
O[CH]1[CH](O)[CH](O[CH]1CO[P](O)(O)=O)N2C(=O)NC(=O)C=C2O
CACTVS 3.341
O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CO[P](O)(O)=O)N2C(=O)NC(=O)C=C2O
ACDLabs 10.04
O=C1NC(=O)N(C(O)=C1)C2OC(C(O)C2O)COP(=O)(O)O
Formula
C9 H13 N2 O10 P
Name
6-HYDROXYURIDINE-5'-PHOSPHATE
ChEMBL
CHEMBL383923
DrugBank
DB02890
ZINC
ZINC000024479522
PDB chain
4df1 Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4df1
Crystal structure of orotidine 5'-monophosphate decarboxylase from Thermoproteus neutrophilus complexed with inhibitor BMP
Resolution
1.899 Å
Binding residue
(original residue number in PDB)
D12 K33 K61 M106 T107 P155 Q160 G178 R179
Binding residue
(residue number reindexed from 1)
D9 K30 K58 M103 T104 P152 Q157 G175 R176
Annotation score
3
Enzymatic activity
Enzyme Commision number
4.1.1.23
: orotidine-5'-phosphate decarboxylase.
Gene Ontology
Molecular Function
GO:0004590
orotidine-5'-phosphate decarboxylase activity
GO:0016831
carboxy-lyase activity
Biological Process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0006221
pyrimidine nucleotide biosynthetic process
GO:0044205
'de novo' UMP biosynthetic process
Cellular Component
GO:0005829
cytosol
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External links
PDB
RCSB:4df1
,
PDBe:4df1
,
PDBj:4df1
PDBsum
4df1
PubMed
UniProt
B1Y9Q9
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