Structure of PDB 5gzp Chain B Binding Site BS01
Receptor Information
>5gzp Chain B (length=246) Species:
5833
(Plasmodium falciparum) [
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ARKYFVAANWKCNGTLESIKSLTNSFNNLDFDPSKLDVVVFPVSVHYDHT
RKLLQSKFSTGIQNVSKFNGSCTGEVSAEIAKDLNIEYVIIGHFERRKYF
HETDEDVREKLQASLKNNLKAVVCFGESLEQREQNKTIEVITKQVKAFVD
LIDNFDNVILVYEPLWAIGTGKTATPEQAQLVHKEIRKIVKDTCGEKQAN
QIRILYGGSVNTENCSSLIQQEDIDGFLVGNASLKESFVDIIKSAM
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
5gzp Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5gzp
Y74COX MUTANT OF PLASMODIUM FALCIPARUM TRIOSEPHOSPHATE ISOMERASE
Resolution
2.03 Å
Binding residue
(original residue number in PDB)
K12 H95 E165 I170 G171 G210 S211 L230 G232 N233
Binding residue
(residue number reindexed from 1)
K11 H93 E163 I168 G169 G208 S209 L228 G230 N231
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
N10 K12 H95 E97 E165 G171 S211
Catalytic site (residue number reindexed from 1)
N9 K11 H93 E95 E163 G169 S209
Enzyme Commision number
5.3.1.1
: triose-phosphate isomerase.
Gene Ontology
Molecular Function
GO:0004807
triose-phosphate isomerase activity
GO:0016853
isomerase activity
GO:0042802
identical protein binding
Biological Process
GO:0006094
gluconeogenesis
GO:0006096
glycolytic process
GO:0019563
glycerol catabolic process
GO:0046166
glyceraldehyde-3-phosphate biosynthetic process
Cellular Component
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:5gzp
,
PDBe:5gzp
,
PDBj:5gzp
PDBsum
5gzp
PubMed
UniProt
Q07412
|TPIS_PLAFA Triosephosphate isomerase (Gene Name=TPI)
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