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TargetHPr kinase/phosphorylase
LigandBDBM50137122
Substrate/Competitorn/a
Meas. Tech.ChEMBL_81577 (CHEMBL689337)
pH7±n/a
IC50 17000±n/a nM
Commentsextracted
Citation Bunyapaiboonsri, TRamström, HRamström, OHaiech, JLehn, JM Generation of bis-cationic heterocyclic inhibitors of Bacillus subtilis HPr kinase/phosphatase from a ditopic dynamic combinatorial library. J Med Chem46:5803-11 (2003) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
HPr kinase/phosphorylase
Name:HPr kinase/phosphorylase
Synonyms:HPRK_BACSU | HPr kinase | hprK | ptsK | yvoB
Type:PROTEIN
Mol. Mass.:34693.07
Organism:Bacillus subtilis
Description:ChEMBL_81578
Residue:310
Sequence:
MAKVRTKDVMEQFNLELISGEEGINRPITMSDLSRPGIEIAGYFTYYPRERVQLLGKTEL
SFFEQLPEEEKKQRMDSLCTDVTPAIILSRDMPIPQELIDASEKNGVPVLRSPLKTTRLS
SRLTNFLESRLAPTTAIHGVLVDIYGVGVLITGKSGVGKSETALELVKRGHRLVADDCVE
IRQEDQDTLVGNAPELIEHLLEIRGLGIINVMTLFGAGAVRSNKRITIVMNLELWEQGKQ
YDRLGLEEETMKIIDTEITKLTIPVRPGRNLAVIIEVAAMNFRLKRMGLNAAEQFTNKLA
DVIEDGEQEE
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  Blast E-value cutoff:
BDBM50137122
n/a
NameBDBM50137122
Synonyms:(3-Benzyl-2-imino-2,3-dihydro-benzoimidazol-1-yl)-acetic acid [1-(4-{[2-(3-benzyl-2-imino-2,3-dihydro-benzoimidazol-1-yl)-acetyl]-hydrazonomethyl}-phenyl)-meth-(E)-ylidene]-hydrazide; dihydrobromide | CHEMBL552627
TypeSmall organic molecule
Emp. Form.C40H36N10O2
Mol. Mass.688.7796
SMILESN=c1n(CC(=O)N\N=C\c2ccc(\C=N\NC(=O)Cn3c4ccccc4n(Cc4ccccc4)c3=N)cc2)c2ccccc2n1Cc1ccccc1
Structure
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