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PDBsum entry 4ovh

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Top Page protein ligands metals Protein-protein interface(s) links
Transferase/transferase inhibitor PDB id
4ovh
Contents
Protein chains
362 a.a.
Ligands
PEG ×5
2VE
PG4
Metals
_CA
_CL
Waters ×321

References listed in PDB file
Key reference
Title Bacterial sliding clamp inhibitors that mimic the sequential binding mechanism of endogenous linear motifs.
Authors Z.Yin, L.R.Whittell, Y.Wang, S.Jergic, C.Ma, P.J.Lewis, N.E.Dixon, J.L.Beck, M.J.Kelso, A.J.Oakley.
Ref. J Med Chem, 2015, 58, 4693-4702. [DOI no: 10.1021/acs.jmedchem.5b00232]
PubMed id 25970224
Abstract
The bacterial DNA replication machinery presents new targets for the development of antibiotics acting via novel mechanisms. One such target is the protein-protein interaction between the DNA sliding clamp and the conserved peptide linear motifs in DNA polymerases. We previously established that binding of linear motifs to the Escherichia coli sliding clamp occurs via a sequential mechanism that involves two subsites (I and II). Here, we report the development of small-molecule inhibitors that mimic this mechanism. The compounds contain tetrahydrocarbazole moieties as "anchors" to occupy subsite I. Functional groups appended at the tetrahydrocarbazole nitrogen bind to a channel gated by the side chain of M362 and lie at the edge of subsite II. One derivative induced the formation of a new binding pocket, termed subsite III, by rearrangement of a loop adjacent to subsite I. Discovery of the extended binding area will guide further inhibitor development.
PROCHECK
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 Headers

 

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