Structure of PDB 1lqp Chain A Binding Site BS03
Receptor Information
>1lqp Chain A (length=134) Species:
287
(Pseudomonas aeruginosa) [
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MLTGLNHLTLAVADLPASIAFYRDLLGFRLEARWDQGAYLELGSLWLCLS
REPQYGGPAADYTHYAFGIAAADFARFAAQLRAHGVREWKQNRSEGDSFY
FLDPDGHRLEAHVGDLRSRLAACRQAPYAGMRFA
Ligand information
Ligand ID
FCN
InChI
InChI=1S/C3H7O4P/c1-2-3(7-2)8(4,5)6/h2-3H,1H3,(H2,4,5,6)/t2-,3+/m0/s1
InChIKey
YMDXZJFXQJVXBF-STHAYSLISA-N
SMILES
Software
SMILES
CACTVS 3.341
C[C@@H]1O[C@@H]1[P](O)(O)=O
OpenEye OEToolkits 1.5.0
C[C@H]1[C@H](O1)P(=O)(O)O
ACDLabs 10.04
O=P(O)(O)C1OC1C
OpenEye OEToolkits 1.5.0
CC1C(O1)P(=O)(O)O
CACTVS 3.341
C[CH]1O[CH]1[P](O)(O)=O
Formula
C3 H7 O4 P
Name
FOSFOMYCIN;
1,2-EPOXYPROPYLPHOSPHONIC ACID
ChEMBL
CHEMBL1757
DrugBank
DB00828
ZINC
ZINC000001530427
PDB chain
1lqp Chain A Residue 4004 [
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Receptor-Ligand Complex Structure
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PDB
1lqp
Crystal structure of a genomically encoded fosfomycin resistance protein (FosA) at 1.19 A resolution by MAD phasing off the L-III edge of Tl(+)
Resolution
1.19 Å
Binding residue
(original residue number in PDB)
Y62 K90 R93
Binding residue
(residue number reindexed from 1)
Y62 K90 R93
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.5.1.18
: glutathione transferase.
Gene Ontology
Molecular Function
GO:0004364
glutathione transferase activity
GO:0016740
transferase activity
GO:0046872
metal ion binding
Biological Process
GO:0046677
response to antibiotic
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1lqp
,
PDBe:1lqp
,
PDBj:1lqp
PDBsum
1lqp
PubMed
12224946
UniProt
Q9I4K6
|FOSA_PSEAE Glutathione transferase FosA (Gene Name=fosA)
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