Structure of PDB 4i72 Chain B Binding Site BS01
Receptor Information
>4i72 Chain B (length=328) [
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GSHMAKTVILDHDGNKDDFVAMILLLSNPKKVNLIGCICTDADCFVENGF
DVTGKIMCAMHRLIKTPLFPIGKSTATAVNAFPTEWRFSAKNLDDMPFLN
IVEDVALWEKLKPENEAHNGQQLLADLVMKSKEKVTVCVTGPLSNMAWCI
EKYGEAFTSKVEECVIMGGAVDVGGNVFLPTTDGSAEWNIYWDPPAAKKV
LCCPNIRCVLFSLDATNTVPVRSVDVKGFGAQNQYLLSQMVGTMWAMSTH
EEILRDGDAYYAWDALTAAYILEPTIATLEPVALDVDVSKGKSEGRTPRA
SGKPCVHVARNPSKQMFHDLVFASTRVC
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
4i72 Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4i72
Structures of purine nucleosidase from Trypanosoma brucei bound to isozyme-specific trypanocidals and a novel metalorganic inhibitor
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
D10 D15 T137 D261
Binding residue
(residue number reindexed from 1)
D13 D18 T140 D264
Annotation score
1
Enzymatic activity
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:0016810
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds
GO:0046872
metal ion binding
Biological Process
GO:0006139
nucleobase-containing compound metabolic process
GO:0006152
purine nucleoside catabolic process
GO:0006166
purine ribonucleoside salvage
Cellular Component
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:4i72
,
PDBe:4i72
,
PDBj:4i72
PDBsum
4i72
PubMed
23897478
UniProt
Q57ZL6
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