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8Q5L

PqsR coinducer binding domain of Pseudomonas aeruginosa with ligand 2f: 2-(4-(3-((6-chloro-1-isopropyl-1H-benzo[d]imidazol-2-yl)amino)-2-hydroxypropoxy)phenyl)acetonitrile

Summary for 8Q5L
Entry DOI10.2210/pdb8q5l/pdb
Related8Q5K
DescriptorTranscriptional regulator MvfR, 2-[4-[(2~{S})-3-[(6-chloranyl-1-propan-2-yl-benzimidazol-2-yl)amino]-2-oxidanyl-propoxy]phenyl]ethanenitrile (3 entities in total)
Functional Keywordstranscriptional regulator, transcription
Biological sourcePseudomonas aeruginosa UCBPP-PA14
Total number of polymer chains1
Total formula weight24687.36
Authors
Markham-Lee, Z.J.,Emsley, J. (deposition date: 2023-08-09, release date: 2024-01-17, Last modification date: 2024-02-07)
Primary citationSoukarieh, F.,Mashabi, A.,Richardson, W.,Oton, E.V.,Romero, M.,Dubern, J.F.,Robertson, S.N.,Lucanto, S.,Markham-Lee, Z.,Sou, T.,Kukavica-Ibrulj, I.,Levesque, R.C.,Bergstrom, C.A.S.,Halliday, N.,Kellam, B.,Emsley, J.,Heeb, S.,Williams, P.,Stocks, M.J.,Camara, M.
Design, Synthesis, and Evaluation of New 1 H -Benzo[ d ]imidazole Based PqsR Inhibitors as Adjuvant Therapy for Pseudomonas aeruginosa Infections.
J.Med.Chem., 67:1008-1023, 2024
Cited by
PubMed: 38170170
DOI: 10.1021/acs.jmedchem.3c00973
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.9 Å)
Structure validation

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