Structure of PDB 2qx0 Chain B Binding Site BS02
Receptor Information
>2qx0 Chain B (length=159) Species:
632
(Yersinia pestis) [
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MIRVYIALGSNLAMPLQQVSAAREALAHLPRSRLVACSPLYRTKPLGPQD
QPDFLNAVVALDTSLPPEQLLDHTQAIERNQGRVRKEQRWGPRTLDLDIM
LYGDQVIKTDRLTIPHYGLKAREFMLYPLADIAPDLIFPDGESLSECLKR
VDKNGLVLW
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
2qx0 Chain B Residue 164 [
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Receptor-Ligand Complex Structure
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PDB
2qx0
Structure and activity of Yersinia pestis 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase as a novel target for the development of antiplague therapeutics.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
D96 D98
Binding residue
(residue number reindexed from 1)
D96 D98
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R83 R93 D96 D98
Catalytic site (residue number reindexed from 1)
R83 R93 D96 D98
Enzyme Commision number
2.7.6.3
: 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase.
Gene Ontology
Molecular Function
GO:0003848
2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0046872
metal ion binding
Biological Process
GO:0009396
folic acid-containing compound biosynthetic process
GO:0016310
phosphorylation
GO:0046654
tetrahydrofolate biosynthetic process
GO:0046656
folic acid biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:2qx0
,
PDBe:2qx0
,
PDBj:2qx0
PDBsum
2qx0
PubMed
18007032
UniProt
A0A5P8YCA3
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