4N95

E. coli sliding clamp in complex with 5-chloroindoline-2,3-dione

Summary for 4N95

• Entry DOI: 10.2210/pdb4n95/pdb
• Related: 4N94 4N96 4N97 4N98 4N99 4N9A
• Descriptor: DNA polymerase III subunit beta, TETRAETHYLENE GLYCOL, DI(HYDROXYETHYL)ETHER, ... (8 entities in total)
• Functional Keywords: sliding clamp, dnan, transferase
• Biological source: Escherichia coli
• Cellular location: Cytoplasm: P0A988
• Total number of polymer chains: 2
• Total formula weight: 82707.58

Authors

Yin, Z.,Oakley, A.J. (deposition date: 2013-10-19, release date: 2013-11-06, Last modification date: 2023-09-20)

Primary citation

Yin, Z.,Whittell, L.R.,Wang, Y.,Jergic, S.,Liu, M.,Harry, E.J.,Dixon, N.E.,Beck, J.L.,Kelso, M.J.,Oakley, A.J.
Discovery of lead compounds targeting the bacterial sliding clamp using a fragment-based approach.
J.Med.Chem., 57:2799-2806, 2014

PubMed Abstract: The bacterial sliding clamp (SC), also known as the DNA polymerase III β subunit, is an emerging antibacterial target that plays a central role in DNA replication, serving as a protein-protein interaction hub with a common binding pocket to recognize linear motifs in the partner proteins. Here, fragment-based screening using X-ray crystallography produced four hits bound in the linear-motif-binding pocket of the Escherichia coli SC. Compounds structurally related to the hits were identified that inhibited the E. coli SC and SC-mediated DNA replication in vitro. A tetrahydrocarbazole derivative emerged as a promising lead whose methyl and ethyl ester prodrug forms showed minimum inhibitory concentrations in the range of 21-43 μg/mL against representative Gram-negative and Gram-positive bacteria species. The work demonstrates the utility of a fragment-based approach for identifying bacterial sliding clamp inhibitors as lead compounds with broad-spectrum antibacterial activity.

PubMed: 24592885
DOI: 10.1021/jm500122r

Experimental method

X-RAY DIFFRACTION (1.8 Å)