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6TRI

CI-MOR repressor-antirepressor complex of the temperate bacteriophage TP901-1 from Lactococcus lactis

Summary for 6TRI
Entry DOI10.2210/pdb6tri/pdb
DescriptorCI, MOR, SULFATE ION, ... (4 entities in total)
Functional Keywordscomplex, regulation, dna-binding, temperate virus, viral protein
Biological sourceLactococcus phage TP901-1
More
Total number of polymer chains2
Total formula weight19562.27
Authors
Rasmussen, K.K.,Blackledge, M.,Herrmann, T.,Jensen, M.R.,Lo Leggio, L. (deposition date: 2019-12-18, release date: 2020-08-19, Last modification date: 2024-01-24)
Primary citationRasmussen, K.K.,Palencia, A.,Varming, A.K.,El-Wali, H.,Boeri Erba, E.,Blackledge, M.,Hammer, K.,Herrmann, T.,Kilstrup, M.,Lo Leggio, L.,Jensen, M.R.
Revealing the mechanism of repressor inactivation during switching of a temperate bacteriophage.
Proc.Natl.Acad.Sci.USA, 117:20576-20585, 2020
Cited by
PubMed Abstract: Temperate bacteriophages can enter one of two life cycles following infection of a sensitive host: the lysogenic or the lytic life cycle. The choice between the two alternative life cycles is dependent upon a tight regulation of promoters and their cognate regulatory proteins within the phage genome. We investigated the genetic switch of TP901-1, a bacteriophage of , controlled by the CI repressor and the modulator of repression (MOR) antirepressor and their interactions with DNA. We determined the solution structure of MOR, and we solved the crystal structure of MOR in complex with the N-terminal domain of CI, revealing the structural basis of MOR inhibition of CI binding to the DNA operator sites. N NMR Carr-Purcell-Meiboom-Gill (CPMG) relaxation dispersion and rotating frame measurements demonstrate that MOR displays molecular recognition dynamics on two different time scales involving a repacking of aromatic residues at the interface with CI. Mutations in the CI:MOR binding interface impair complex formation in vitro, and when introduced in vivo, the bacteriophage switch is unable to choose the lytic life cycle showing that the CI:MOR complex is essential for proper functioning of the genetic switch. On the basis of sequence alignments, we show that the structural features of the MOR:CI complex are likely conserved among a larger family of bacteriophages from human pathogens implicated in transfer of antibiotic resistance.
PubMed: 32788352
DOI: 10.1073/pnas.2005218117
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.277 Å)
Structure validation

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