Structure of PDB 2x1s Chain B Binding Site BS01
Receptor Information
>2x1s Chain B (length=237) Species:
5702
(Trypanosoma brucei brucei) [
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SKPQPIAAANWKSSPDSLSELIDLFNSTSINHDVQCVVASTFVHLAMTKE
RLSHPKFVIAAQNAGNADALASLKDFGVNWIVLGHSERRWYYGETNEIVA
DKVAAAVASGFMVIACIGETLQERESGRTAVVVLTQIAAIAKKLKKADWA
KVVIAYEPVWAIGTGKVATPQQAQEAHALIRSWVSSKIGADVAGELRILY
GGSVNGKNARTLYQQRDVNGFLAGLKPEFVDIIKATQ
Ligand information
Ligand ID
X1S
InChI
InChI=1S/C3H6O5S/c4-3(5)1-2-9(6,7)8/h1-2H2,(H,4,5)(H,6,7,8)
InChIKey
OURSFPZPOXNNKX-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.352
OC(=O)CC[S](O)(=O)=O
OpenEye OEToolkits 1.6.1
C(CS(=O)(=O)O)C(=O)O
ACDLabs 10.04
O=C(O)CCS(=O)(=O)O
Formula
C3 H6 O5 S
Name
3-SULFOPROPANOIC ACID
ChEMBL
DrugBank
ZINC
ZINC000001848385
PDB chain
2x1s Chain B Residue 1252 [
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Receptor-Ligand Complex Structure
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PDB
2x1s
Crystallographic Binding Studies with an Engineered Monomeric Variant of Triosephosphate Isomerase
Resolution
1.93 Å
Binding residue
(original residue number in PDB)
H95 E167 I172 G212 S213
Binding residue
(residue number reindexed from 1)
H85 E157 I162 G202 S203
Annotation score
1
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 H85 E87 E157 G163 S203
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:2x1s
,
PDBe:2x1s
,
PDBj:2x1s
PDBsum
2x1s
PubMed
20693693
UniProt
P04789
|TPIS_TRYBB Triosephosphate isomerase, glycosomal
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