Structure of PDB 1m32 Chain E Binding Site BS01
Receptor Information
>1m32 Chain E (length=361) [
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YLLLTPGPLTTSRTVKEAMLFDSCTWDDDYNIGVVEQIRQQLTALATASE
GYTSVLLQGSGSYAVEAVLGSALGPQDKVLIVSNGAYGARMVEMAGLMGI
AHHAYDCGEVARPDVQAIDAILNADPTISHIAMVHSETTTGMLNPIDEVG
ALAHRYGKTYIVDAMSSFGGIPMDIAALHIDYLISSANKCIQGVPGFAFV
IAREQKLAACKGHSRSLSLDLYAQWRCMEDNHGKWRFTSPTHTVLAFAQA
LKELAKEGGVAARHQRYQQNQRSLVAGMRALGFNTLLDDELHSPIITAFY
SPEDPQYRFSEFYRRLKEQGFVIYPGKVSQSDCFRIGNIGEVYAADITAL
LTAIRTAMYWT
Ligand information
Ligand ID
PO4
InChI
InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKey
NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
[O-][P]([O-])([O-])=O
ACDLabs 10.04
[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0
[O-]P(=O)([O-])[O-]
Formula
O4 P
Name
PHOSPHATE ION
ChEMBL
DrugBank
DB14523
ZINC
PDB chain
1m32 Chain E Residue 4605 [
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Receptor-Ligand Complex Structure
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PDB
1m32
Degradation Pathway of the Phosphonate Ciliatine: Crystal Structure of 2-Aminoethylphosphonate Transaminase
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
Y91 Y328
Binding residue
(residue number reindexed from 1)
Y87 Y324
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.6.1.37
: 2-aminoethylphosphonate--pyruvate transaminase.
Gene Ontology
Molecular Function
GO:0008483
transaminase activity
GO:0047304
2-aminoethylphosphonate-pyruvate transaminase activity
Biological Process
GO:0019700
organic phosphonate catabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:1m32
,
PDBe:1m32
,
PDBj:1m32
PDBsum
1m32
PubMed
12403617
UniProt
P96060
|PHNW_SALTY 2-aminoethylphosphonate--pyruvate transaminase (Gene Name=phnW)
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