Structure of PDB 4my1 Chain G Binding Site BS02
Receptor Information
>4my1 Chain G (length=347) Species:
198094
(Bacillus anthracis str. Ames) [
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NAMWESKFVKEGLTFDDVLLVPAKSDVLPREVSVKTVLSESLQLNIPLIS
AGMDTVTEADMAIAMARQGGLGIIHKNMSIEQQAEQVDKVKRSGGLLVGA
AVGVTADAMTRIDALVKASVDAIVLDTAHGHSQGVIDKVKEVRAKYPSLN
IIAGNVATAEATKALIEAGANVVKVGIGPGSICTTRVVAGVGVPQLTAVY
DCATEARKHGIPVIADGGIKYSGDMVKALAAGAHVVMLGSMFAGVAESPG
ETEIYQGRQFKVYRGMGSVGAMELVPEGIEGRVPYKGPLADTVHQLVGGL
RAGMGYCGAQDLEFLRENAQFIRMSGAGLLESHPHHVQITKEAPNYS
Ligand information
Ligand ID
P68
InChI
InChI=1S/C18H20BrN3O2/c1-12(22-24)13-5-4-6-14(11-13)18(2,3)21-17(23)20-16-9-7-15(19)8-10-16/h4-11,24H,1-3H3,(H2,20,21,23)/b22-12+
InChIKey
DSTKQECXQMKQLN-WSDLNYQXSA-N
SMILES
Software
SMILES
ACDLabs 12.01
Brc2ccc(NC(=O)NC(c1cccc(\C(=N\O)C)c1)(C)C)cc2
OpenEye OEToolkits 1.7.6
C/C(=N\O)/c1cccc(c1)C(C)(C)NC(=O)Nc2ccc(cc2)Br
CACTVS 3.385
CC(=N\O)/c1cccc(c1)C(C)(C)NC(=O)Nc2ccc(Br)cc2
OpenEye OEToolkits 1.7.6
CC(=NO)c1cccc(c1)C(C)(C)NC(=O)Nc2ccc(cc2)Br
CACTVS 3.385
CC(=NO)c1cccc(c1)C(C)(C)NC(=O)Nc2ccc(Br)cc2
Formula
C18 H20 Br N3 O2
Name
1-(4-bromophenyl)-3-(2-{3-[(1E)-N-hydroxyethanimidoyl]phenyl}propan-2-yl)urea
ChEMBL
CHEMBL3329562
DrugBank
ZINC
ZINC000095920528
PDB chain
4my1 Chain G Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
4my1
Crystal Structure of the Inosine 5'-monophosphate Dehydrogenase, with a Internal Deletion of CBS Domain from Bacillus anthracis str. Ames complexed with P68
Resolution
2.5997 Å
Binding residue
(original residue number in PDB)
H254 G392 M397 E416
Binding residue
(residue number reindexed from 1)
H129 G267 M272 E277
Annotation score
1
Binding affinity
BindingDB: IC50=4.0nM,Ki=48nM
Enzymatic activity
Enzyme Commision number
1.1.1.205
: IMP dehydrogenase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0003938
IMP dehydrogenase activity
GO:0016491
oxidoreductase activity
Biological Process
GO:0006164
purine nucleotide biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:4my1
,
PDBe:4my1
,
PDBj:4my1
PDBsum
4my1
PubMed
UniProt
A0A6L8P2U9
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