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4N9A

E. coli sliding clamp in complex with (R)-6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxylic acid

Summary for 4N9A
Entry DOI10.2210/pdb4n9a/pdb
Related4N94 4N95 4N96 4N97 4N98 4N99
DescriptorDNA polymerase III subunit beta, CALCIUM ION, TETRAETHYLENE GLYCOL, ... (7 entities in total)
Functional Keywordspoliii beta, sliding clamp, dnan, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceEscherichia coli
Cellular locationCytoplasm: P0A988
Total number of polymer chains2
Total formula weight82188.47
Authors
Yin, Z.,Oakley, A.J. (deposition date: 2013-10-19, release date: 2013-11-06, Last modification date: 2023-09-20)
Primary citationYin, 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
Cited by
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
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

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数据于2025-07-02公开中

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