Structure of PDB 1usl Chain A Binding Site BS01
Receptor Information
>1usl Chain A (length=156) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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GMRVYLGADHAGYELKQRIIEHLKQTGHEPIDCGALRYDADDDYPAFCIA
AATRTVADPGSLGIVLGGSGNGEQIAANKVPGARCALAWSVQTAALAREH
NNAQLIGIGGRMHTVAEALAIVDAFVTTPWSKAQRHQRRIDILAEYERTH
EAPPVP
Ligand information
Ligand ID
PO4
InChI
InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKey
NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
[O-][P]([O-])([O-])=O
ACDLabs 10.04
[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0
[O-]P(=O)([O-])[O-]
Formula
O4 P
Name
PHOSPHATE ION
ChEMBL
DrugBank
DB14523
ZINC
PDB chain
1usl Chain A Residue 1159 [
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Receptor-Ligand Complex Structure
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PDB
1usl
Mycobacterium Tuberculosis Ribose-5-Phosphate Isomerase Has a Known Fold, But a Novel Active Site
Resolution
1.88 Å
Binding residue
(original residue number in PDB)
R137 R141
Binding residue
(residue number reindexed from 1)
R135 R139
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D11 G69 S71 H102 H138
Catalytic site (residue number reindexed from 1)
D9 G67 S69 H100 H136
Enzyme Commision number
5.3.1.6
: ribose-5-phosphate isomerase.
Gene Ontology
Molecular Function
GO:0004751
ribose-5-phosphate isomerase activity
GO:0005515
protein binding
GO:0016853
isomerase activity
GO:0016861
intramolecular oxidoreductase activity, interconverting aldoses and ketoses
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006098
pentose-phosphate shunt
GO:0009052
pentose-phosphate shunt, non-oxidative branch
GO:0019316
D-allose catabolic process
Cellular Component
GO:0005576
extracellular region
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1usl
,
PDBe:1usl
,
PDBj:1usl
PDBsum
1usl
PubMed
14687575
UniProt
P9WKD7
|RPIB_MYCTU Ribose-5-phosphate isomerase B (Gene Name=rpiB)
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