Structure of PDB 1dvj Chain C Binding Site BS01
Receptor Information
>1dvj Chain C (length=236) Species:
145262
(Methanothermobacter thermautotrophicus) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
MDVMNRLILAMDLMNRDDALRVTGEVREYIDTVKIGYPLVLSEGMDIIAE
FRKRFGCRIIADFKVADIPETNEKICRATFKAGADAIIVHGFPGADSVRA
CLNVAEEMGREVFLLTEMSHPGAEMFIQGAADEIARMGVDLGVKNYVGPS
TRPERLSRLREIIGQDSFLISPGVGAQGGDPGETLRFADAIIVGRSIYLA
DNPAAAAAGIIESIKDLLIPEDPAANKARKEAELAA
Ligand information
Ligand ID
UP6
InChI
InChI=1S/C8H12N3O9P/c12-4-1-9-11(8(15)10-4)7-6(14)5(13)3(20-7)2-19-21(16,17)18/h1,3,5-7,13-14H,2H2,(H,10,12,15)(H2,16,17,18)/t3-,5-,6-,7-/m1/s1
InChIKey
LRVZOSYMNMNQFR-SHUUEZRQSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1=NN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)O)O)O
CACTVS 3.341
O[CH]1[CH](O)[CH](O[CH]1CO[P](O)(O)=O)N2N=CC(=O)NC2=O
CACTVS 3.341
O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CO[P](O)(O)=O)N2N=CC(=O)NC2=O
OpenEye OEToolkits 1.5.0
C1=NN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O
ACDLabs 10.04
O=C1N(N=CC(=O)N1)C2OC(C(O)C2O)COP(=O)(O)O
Formula
C8 H12 N3 O9 P
Name
6-AZA URIDINE 5'-MONOPHOSPHATE;
6-AZA-UMP
ChEMBL
CHEMBL463480
DrugBank
DB03718
ZINC
ZINC000012503861
PDB chain
1dvj Chain C Residue 5003 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
1dvj
Electrostatic stress in catalysis: structure and mechanism of the enzyme orotidine monophosphate decarboxylase.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
D20 K42 K72 M126 S127 P180 G202 R203
Binding residue
(residue number reindexed from 1)
D12 K34 K64 M118 S119 P172 G194 R195
Annotation score
2
Binding affinity
MOAD
: Ki=0.51mM
BindingDB: Ki=12400nM
Enzymatic activity
Catalytic site (original residue number in PDB)
K42 D70 K72 D75
Catalytic site (residue number reindexed from 1)
K34 D62 K64 D67
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
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1dvj
,
PDBe:1dvj
,
PDBj:1dvj
PDBsum
1dvj
PubMed
10681441
UniProt
O26232
|PYRF_METTH Orotidine 5'-phosphate decarboxylase (Gene Name=pyrF)
[
Back to BioLiP
]