Structure of PDB 4m5n Chain B Binding Site BS04
Receptor Information
>4m5n Chain B (length=160) Species:
83333
(Escherichia coli K-12) [
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HMTVAYIAIGSNLASPLEQVNAALKALGDIPESHILTVSSFYRTPPLGPQ
DQPDYLNAAVALETSLAPEELLNHTQRIELQQGRVRKAERWGPRTLDLDI
MLFGNEVINTERLTVPHYDMKNRGFMLWPLFEIAPELVFPDGEMLRQILH
TRAFDKLNKW
Ligand information
Ligand ID
YH7
InChI
InChI=1S/C5H5N5S/c6-3-2-4(8-1-7-2)10-5(11)9-3/h1H,(H4,6,7,8,9,10,11)
InChIKey
LQJZZLRZEPKRRQ-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
C1=NC2=C(NC(=S)N=C2N1)N
CACTVS 3.370
NC1=C2N=CNC2=NC(=S)N1
ACDLabs 12.01
S=C2N=C1C(N=CN1)=C(N2)N
Formula
C5 H5 N5 S
Name
6-amino-1,9-dihydro-2H-purine-2-thione
ChEMBL
DrugBank
ZINC
ZINC000004353400
PDB chain
4m5n Chain B Residue 204 [
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Receptor-Ligand Complex Structure
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PDB
4m5n
The identification, analysis and structure-based development of novel inhibitors of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
T42 P44 L45 Y53 N55 D95 F123
Binding residue
(residue number reindexed from 1)
T44 P46 L47 Y55 N57 D97 F125
Annotation score
1
Binding affinity
MOAD
: Kd=7.5uM
Enzymatic activity
Catalytic site (original residue number in PDB)
R82 R92 D95 D97
Catalytic site (residue number reindexed from 1)
R84 R94 D97 D99
Enzyme Commision number
2.7.6.3
: 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003848
2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
Biological Process
GO:0009396
folic acid-containing compound biosynthetic process
GO:0016310
phosphorylation
GO:0046654
tetrahydrofolate biosynthetic process
GO:0046656
folic acid biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4m5n
,
PDBe:4m5n
,
PDBj:4m5n
PDBsum
4m5n
PubMed
24613625
UniProt
P26281
|HPPK_ECOLI 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase (Gene Name=folK)
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