Structure of PDB 6rmw Chain F Binding Site BS02
Receptor Information
>6rmw Chain F (length=378) Species:
36329
(Plasmodium falciparum 3D7) [
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IVQWNSRYSYNQLKNKDSLIMFLVEIFRSLFVSNCIDKNIDNVLLSIEEM
FIDHYYNPQHSRLKYLIDDVGIFFTKLPITKAFHTYNKKYRITKRLYAPP
TFNEVRHILNLAQILSLEEGLDLLTFDANETLYPDGHDFNDEVLASYISC
LLKKMNIAIVTAASYNNDAEKYQKRLENLLKYFSKHNIKDGSYKNFYVMG
GESNYLFKCNEEATLYSVPENEWRHYKKFVDYDTVQEILNISEKCLEKVI
KDFGLCAQIQRKEKSIGLVPNKINYMIKYEVLEEAVIRIKKEIIKNKITA
PYCAFNGGQDLWVDVGNKAEGLLILQKLLKIQKKKCCHIGDQFLHSGNDF
PTRFCSLTLWVSNPQETKACLKSIMHLN
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
6rmw Chain F Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
6rmw
Structure and catalytic regulation of Plasmodium falciparum IMP specific nucleotidase.
Resolution
3.5 Å
Binding residue
(original residue number in PDB)
D170 N172 D394
Binding residue
(residue number reindexed from 1)
D127 N129 D341
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.1.3.99
: IMP-specific 5'-nucleotidase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0005524
ATP binding
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
GO:0050483
IMP 5'-nucleotidase activity
Biological Process
GO:0006190
inosine salvage
GO:0006204
IMP catabolic process
GO:0009117
nucleotide metabolic process
GO:0071590
nicotinamide riboside biosynthetic process
GO:0071592
nicotinic acid riboside biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6rmw
,
PDBe:6rmw
,
PDBj:6rmw
PDBsum
6rmw
PubMed
32591529
UniProt
A0A144A134
|ISN1_PLAF7 IMP-specific 5'-nucleotidase 1 (Gene Name=ISN1)
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