Structure of PDB 5tsq Chain A Binding Site BS01
Receptor Information
>5tsq Chain A (length=312) Species:
1448350
(Leishmania braziliensis braziliensis) [
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PRKIILDCDPGIDDAVAILLAYGNPEIELLAITTVVGNQTLEKVTRNAQL
VADVAGIVGVPIAAGCCKPLVRKVRTAPQIHGETGLGTVSYPSEFKTKLD
KRHAVHLIIELIMSHEPKSITLVPTGGLTNIAMAARLEPRIVERVKEVVL
MGGSCCIGNASPVAEFNIFVDPEAAHIVFNESWDVTMVGLDLTSQALATP
EVLQRVKEVRTKPADFILKILEFYTKVYETQRNTYAKVHDPCAVAYVIDP
TVMTTNRVPVNIELNGELTAGMTVTDFRYPRPEQCHTQVASKLDFSKYWD
LVIDALQRIGDP
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
5tsq Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
5tsq
Crystal structure of IUnH from Leishmania braziliensis in complex with D-Ribose
Resolution
1.53 Å
Binding residue
(original residue number in PDB)
D10 D15 T126 D241
Binding residue
(residue number reindexed from 1)
D9 D14 T125 D240
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D10 D15 N39 V75 T126 F167 N168 H240 D241
Catalytic site (residue number reindexed from 1)
D9 D14 N38 V74 T125 F166 N167 H239 D240
Enzyme Commision number
3.2.2.1
: purine nucleosidase.
Gene Ontology
Molecular Function
GO:0008477
purine nucleosidase activity
GO:0016798
hydrolase activity, acting on glycosyl bonds
GO:0016799
hydrolase activity, hydrolyzing N-glycosyl compounds
GO:0045437
uridine nucleosidase activity
GO:0046872
metal ion binding
Biological Process
GO:0006139
nucleobase-containing compound metabolic process
GO:0006152
purine nucleoside catabolic 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:5tsq
,
PDBe:5tsq
,
PDBj:5tsq
PDBsum
5tsq
PubMed
UniProt
A4H9Q9
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