Structure of PDB 1fxo Chain D Binding Site BS02
Receptor Information
>1fxo Chain D (length=292) Species:
287
(Pseudomonas aeruginosa) [
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KRKGIILAGGSGTRLHPATLAISKQLLPVYDKPMIYYPLSTLMLAGIREI
LIISTPQDTPRFQQLLGDGSNWGLDLQYAVQPSPDGLAQAFLIGESFIGN
DLSALVLGDNLYYGHDFHELLGSASQRQTGASVFAYHVLDPERYGVVEFD
QGGKAISLEEKPLEPKSNYAVTGLYFYDQQVVDIARDLKPSPRGELEITD
VNRAYLERGQLSVEIMGRGYAWLDTGTHDSLLEAGQFIATLENRQGLKVA
CPEEIAYRQKWIDAAQLEKLAAPLAKNGYGQYLKRLLTETVY
Ligand information
Ligand ID
TMP
InChI
InChI=1S/C10H15N2O8P/c1-5-3-12(10(15)11-9(5)14)8-2-6(13)7(20-8)4-19-21(16,17)18/h3,6-8,13H,2,4H2,1H3,(H,11,14,15)(H2,16,17,18)/t6-,7+,8+/m0/s1
InChIKey
GYOZYWVXFNDGLU-XLPZGREQSA-N
SMILES
Software
SMILES
CACTVS 3.341
CC1=CN([CH]2C[CH](O)[CH](CO[P](O)(O)=O)O2)C(=O)NC1=O
OpenEye OEToolkits 1.5.0
CC1=CN(C(=O)NC1=O)C2CC(C(O2)COP(=O)(O)O)O
OpenEye OEToolkits 1.5.0
CC1=CN(C(=O)NC1=O)[C@H]2C[C@@H]([C@H](O2)COP(=O)(O)O)O
CACTVS 3.341
CC1=CN([C@H]2C[C@H](O)[C@@H](CO[P](O)(O)=O)O2)C(=O)NC1=O
ACDLabs 10.04
O=C1NC(=O)N(C=C1C)C2OC(C(O)C2)COP(=O)(O)O
Formula
C10 H15 N2 O8 P
Name
THYMIDINE-5'-PHOSPHATE
ChEMBL
CHEMBL394429
DrugBank
DB01643
ZINC
ZINC000001678872
PDB chain
1fxo Chain D Residue 9502 [
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Receptor-Ligand Complex Structure
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PDB
1fxo
The structural basis of the catalytic mechanism and regulation of glucose-1-phosphate thymidylyltransferase (RmlA).
Resolution
1.66 Å
Binding residue
(original residue number in PDB)
L8 G10 G11 Q26 Q82 P85 G87 L88 D110
Binding residue
(residue number reindexed from 1)
L7 G9 G10 Q25 Q81 P84 G86 L87 D109
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.7.7.24
: glucose-1-phosphate thymidylyltransferase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0008879
glucose-1-phosphate thymidylyltransferase activity
GO:0016779
nucleotidyltransferase activity
GO:0046872
metal ion binding
Biological Process
GO:0009058
biosynthetic process
GO:0009244
lipopolysaccharide core region biosynthetic process
GO:0019305
dTDP-rhamnose biosynthetic process
GO:0045226
extracellular polysaccharide biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:1fxo
,
PDBe:1fxo
,
PDBj:1fxo
PDBsum
1fxo
PubMed
11118200
UniProt
Q9HU22
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