Target
HPr kinase/phosphorylase
Ligand
BDBM50144924
Substrate
n/a
Meas. Tech.
ChEMBL_87254 (CHEMBL699244)
EC50
20000±n/a nM
Citation
 Ramström, HBourotte, MPhilippe, CSchmitt, MHaiech, JBourguignon, JJ Heterocyclic bis-cations as starting hits for design of inhibitors of the bifunctional enzyme histidine-containing protein kinase/phosphatase from Bacillus subtilis. J Med Chem 47:2264-75 (2004) [PubMed]  Article 
Target
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:
MAKVRTKDVMEQFNLELISGEEGINRPITMSDLSRPGIEIAGYFTYYPRERVQLLGKTELSFFEQLPEEEKKQRMDSLCTDVTPAIILSRDMPIPQELIDASEKNGVPVLRSPLKTTRLSSRLTNFLESRLAPTTAIHGVLVDIYGVGVLITGKSGVGKSETALELVKRGHRLVADDCVEIRQEDQDTLVGNAPELIEHLLEIRGLGIINVMTLFGAGAVRSNKRITIVMNLELWEQGKQYDRLGLEEETMKIIDTEITKLTIPVRPGRNLAVIIEVAAMNFRLKRMGLNAAEQFTNKLADVIEDGEQEE
  
Inhibitor
Name:
BDBM50144924
Synonyms:
3-[8-(2-amino-1-benzyl-1H-benzo[d]imidazol-3-ium-3-yl)octyl]-1-benzyl-1H-benzo[d]imidazol-3-ium-2-amine | CHEMBL306844
Type:
Small organic molecule
Emp. Form.:
C36H42N6
Mol. Mass.:
558.7578
SMILES:
[NH2+]=c1n(CCCCCCCCn2c3ccccc3n(Cc3ccccc3)c2=[NH2+])c2ccccc2n1Cc1ccccc1
Structure:
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