Structure of PDB 3s9y Chain D Binding Site BS02
Receptor Information
>3s9y Chain D (length=320) Species:
36329
(Plasmodium falciparum 3D7) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
GFKVKLEKRRNAINTCLCIGLDPDEKDIENFMKNEKENNYNNIKKNLKEK
YINNVSIKKDILLKAPDNIIREEKSEEFFYFFNHFCFYIINETNKYALTF
KMNFAFYIPYGSVGIDVLKNVFDYLYELNIPTILDMKINDIGNTVKNYRK
FIFEYLKSDSCTVNIYMGTNMLKDICYDEEKNKYYSAFVLVKTTNPDSAI
FQKNLSLDNKQAYVIMAQEALNMSSYLNLEQNNEFIGFVVGANSYDEMNY
IRTYFPNCYILSPGIGAQNGDLHKTLTNGYHKSYEKILINIGRAITKNPY
PQKAAQMYYDQINAILKQNM
Ligand information
Ligand ID
FNU
InChI
InChI=1S/C9H13FN3O9P/c10-3-6(11)13(9(17)12-7(3)16)8-5(15)4(14)2(22-8)1-21-23(18,19)20/h2,4-5,8,14-15H,1,11H2,(H,12,16,17)(H2,18,19,20)/t2-,4-,5-,8-/m1/s1
InChIKey
OLBMCLUPWOAIRA-UMMCILCDSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=P(O)(O)OCC2OC(N1C(=O)NC(=O)C(F)=C1N)C(O)C2O
CACTVS 3.370
NC1=C(F)C(=O)NC(=O)N1[CH]2O[CH](CO[P](O)(O)=O)[CH](O)[CH]2O
CACTVS 3.370
NC1=C(F)C(=O)NC(=O)N1[C@@H]2O[C@H](CO[P](O)(O)=O)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.7.0
C(C1C(C(C(O1)N2C(=C(C(=O)NC2=O)F)N)O)O)OP(=O)(O)O
OpenEye OEToolkits 1.7.0
C([C@@H]1[C@H]([C@H]([C@@H](O1)N2C(=C(C(=O)NC2=O)F)N)O)O)OP(=O)(O)O
Formula
C9 H13 F N3 O9 P
Name
6-amino-5-fluorouridine 5'-(dihydrogen phosphate)
ChEMBL
CHEMBL474165
DrugBank
ZINC
ZINC000040406933
PDB chain
3s9y Chain D Residue 324 [
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
3s9y
Structure-activity relationships of orotidine-5'-monophosphate decarboxylase inhibitors as anticancer agents.
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
D23 K102 N104 D136 K138 T194 T195 P264 Q269 G293 R294
Binding residue
(residue number reindexed from 1)
D22 K101 N103 D135 K137 T193 T194 P263 Q268 G292 R293
Annotation score
2
Binding affinity
MOAD
: Ki=16.6uM
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:0005515
protein binding
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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3s9y
,
PDBe:3s9y
,
PDBj:3s9y
PDBsum
3s9y
PubMed
19260677
UniProt
Q8IJH3
[
Back to BioLiP
]