Structure of PDB 6oog Chain A Binding Site BS01
Receptor Information
>6oog Chain A (length=252) Species:
6204
(Taenia solium) [
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PHMTRKLFVGGNWKMNGSYSHINTFFDTLQKADTDPNADIVIGVPACYLK
YAQDKAPKGIKIAAENCYKVGSGAFTGEISTEMIKDCGCEWVILGHSERR
HIFGESNELIGEKVKHALDSGLNVIPCIGELLSEREAGKTNDVCFAQMDA
IAKNVPSKEAWDKVVIAYEPVWAIGTGKTATPAQAQEVHKVVRDWIRKHV
DAGIADKVRILYGGSVTASNAKDLGTQPDVDGFLVGGASLKPDFITIINA
RR
Ligand information
Ligand ID
PGA
InChI
InChI=1S/C2H5O6P/c3-2(4)1-8-9(5,6)7/h1H2,(H,3,4)(H2,5,6,7)
InChIKey
ASCFNMCAHFUBCO-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
OC(=O)CO[P](O)(O)=O
OpenEye OEToolkits 1.5.0
C(C(=O)O)OP(=O)(O)O
ACDLabs 10.04
O=P(O)(O)OCC(=O)O
Formula
C2 H5 O6 P
Name
2-PHOSPHOGLYCOLIC ACID
ChEMBL
CHEMBL47181
DrugBank
DB02726
ZINC
ZINC000003869735
PDB chain
6oog Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
6oog
Crystal structures of Triosephosphate Isomerases from Taenia solium and Schistosoma mansoni provide insights for vaccine rationale and drug design against helminth parasites.
Resolution
2.02 Å
Binding residue
(original residue number in PDB)
K12 H94 E167 I172 G173 S213 G234 G235
Binding residue
(residue number reindexed from 1)
K14 H96 E169 I174 G175 S215 G236 G237
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
N10 K12 H94 E96 E167 G173 S213
Catalytic site (residue number reindexed from 1)
N12 K14 H96 E98 E169 G175 S215
Enzyme Commision number
5.3.1.1
: triose-phosphate isomerase.
Gene Ontology
Molecular Function
GO:0004807
triose-phosphate isomerase activity
GO:0016853
isomerase activity
Biological Process
GO:0006094
gluconeogenesis
GO:0006096
glycolytic process
GO:0019563
glycerol catabolic process
GO:0046166
glyceraldehyde-3-phosphate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6oog
,
PDBe:6oog
,
PDBj:6oog
PDBsum
6oog
PubMed
31923219
UniProt
Q9GTX8
|TPIS_TAESO Triosephosphate isomerase
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