Structure of PDB 1fxo Chain G Binding Site BS03
Receptor Information
>1fxo Chain G (length=293) Species:
287
(Pseudomonas aeruginosa) [
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MKRKGIILAGGSGTRLHPATLAISKQLLPVYDKPMIYYPLSTLMLAGIRE
ILIISTPQDTPRFQQLLGDGSNWGLDLQYAVQPSPDGLAQAFLIGESFIG
NDLSALVLGDNLYYGHDFHELLGSASQRQTGASVFAYHVLDPERYGVVEF
DQGGKAISLEEKPLEPKSNYAVTGLYFYDQQVVDIARDLKPSPRGELEIT
DVNRAYLERGQLSVEIMGRGYAWLDTGTHDSLLEAGQFIATLENRQGLKV
ACPEEIAYRQKWIDAAQLEKLAAPLAKNGYGQYLKRLLTETVY
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 G Residue 9513 [
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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)
Y114 G115 H116 D117 E255 I256
Binding residue
(residue number reindexed from 1)
Y114 G115 H116 D117 E255 I256
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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