Structure of PDB 1aw1 Chain J Binding Site BS01
Receptor Information
>1aw1 Chain J (length=255) Species:
90736
(Moritella marina) [
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RHPVVMGNWKLNGSKEMVVDLLNGLNAELEGVTGVDVAVAPPALFVDLAE
RTLTEAGSAIILGAQNTDLNNSGAFTGDMSPAMLKEFGATHIIIGHSERR
EYHAESDEFVAKKFAFLKENGLTPVLCIGESDAQNEAGETMAVCARQLDA
VINTQGVEALEGAIIAYEPIWAIGTGKAATAEDAQRIHAQIRAHIAEKSE
AVAKNVVIQYGGSVKPENAAAYFAQPDIDGALVGGAALDAKSFAAIAKAA
AEAKA
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
1aw1 Chain J Residue 290 [
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Receptor-Ligand Complex Structure
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PDB
1aw1
Triose-phosphate isomerase (TIM) of the psychrophilic bacterium Vibrio marinus. Kinetic and structural properties.
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
K11 H97 E169 L233 G235 G236
Binding residue
(residue number reindexed from 1)
K10 H96 E168 L232 G234 G235
Annotation score
2
Enzymatic activity
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:1aw1
,
PDBe:1aw1
,
PDBj:1aw1
PDBsum
1aw1
PubMed
9442062
UniProt
P50921
|TPIS_MORMI Triosephosphate isomerase (Gene Name=tpiA)
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