Structure of PDB 1ml1 Chain C Binding Site BS01
Receptor Information
>1ml1 Chain C (length=241) Species:
5702
(Trypanosoma brucei brucei) [
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SKPQPIAAANWKSGSPDSLSELIDLFNSTSINHDVQCVVASTFVHLAMTK
ERLSHPKFVIAAQNAGNADALASLKDFGVNWIVLGHSERRWYYGETNEIV
ADKVAAAVASGFMVIACIGETLQERESGRTAVVVLTQIAAIAKKLKKADW
AKVVIAYEPVWAIGTGKVATPQQAQEAHALIRSWVSSKIGADVAGELRIL
YGGSVNGKNARTLYQQRDVNGFLVGGASLKPEFVDIIKATQ
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
1ml1 Chain C Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
1ml1
Protein engineering with monomeric triosephosphate isomerase (monoTIM): the modelling and structure verification of a seven-residue loop.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
N11 K13 H95 E167 I172 G173 S213 G234 G235
Binding residue
(residue number reindexed from 1)
N10 K12 H86 E158 I163 G164 S204 G225 G226
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
N11 K13 H95 E97 E167 G173 S213
Catalytic site (residue number reindexed from 1)
N10 K12 H86 E88 E158 G164 S204
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
GO:0020015
glycosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1ml1
,
PDBe:1ml1
,
PDBj:1ml1
PDBsum
1ml1
PubMed
9089815
UniProt
P04789
|TPIS_TRYBB Triosephosphate isomerase, glycosomal
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