B
Barrett S. Perchuk
Researcher at Massachusetts Institute of Technology
Publications - 17
Citations - 1933
Barrett S. Perchuk is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Caulobacter crescentus & Cell cycle. The author has an hindex of 15, co-authored 17 publications receiving 1765 citations. Previous affiliations of Barrett S. Perchuk include Harvard University.
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Two-component signal transduction pathways regulating growth and cell cycle progression in a bacterium: a system-level analysis
TL;DR: A system-level investigation of two-component pathways in the model organism Caulobacter crescentus is reported and a new, highly conserved essential signaling pathway from the histidine kinase CenK to the response regulator CenR is identified, which plays a critical role in controlling cell envelope biogenesis and structure.
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Regulation of the bacterial cell cycle by an integrated genetic circuit
Emanuele G. Biondi,Emanuele G. Biondi,Sarah J. Reisinger,Jeffrey M. Skerker,Jeffrey M. Skerker,Muhammad Arif,Barrett S. Perchuk,Barrett S. Perchuk,Kathleen R. Ryan,Michael T. Laub,Michael T. Laub +10 more
TL;DR: A single integrated circuit whose components and connectivity can account for the cell cycle oscillations of CtrA in Caulobacter is defined.
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Evolving New Protein-Protein Interaction Specificity through Promiscuous Intermediates.
Christopher D. Aakre,Julien Herrou,Tanya N. Phung,Barrett S. Perchuk,Sean Crosson,Michael T. Laub +5 more
TL;DR: It is proposed that the abundance of promiscuous variants promotes the expansion and diversification of toxin-antitoxin systems and other paralogous protein families during evolution.
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Systematic dissection and trajectory-scanning mutagenesis of the molecular interface that ensures specificity of two-component signaling pathways.
Emily J. Capra,Barrett S. Perchuk,Emma A. Lubin,Orr Ashenberg,Jeffrey M. Skerker,Jeffrey M. Skerker,Michael T. Laub +6 more
TL;DR: The results begin to reveal the molecular mechanism by which a small set of amino acids enables an individual kinase to discriminate amongst a large set of highly-related response regulators and vice versa.
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Adaptive Mutations that Prevent Crosstalk Enable the Expansion of Paralogous Signaling Protein Families
TL;DR: The divergent evolution of a model bacterial signaling pathway comprising the kinase PhoR and its cognate substrate PhoB is examined, showing that the specificity-determining residues of these proteins are typically under purifying selection but have, in α-proteobacteria, undergone a burst of diversification followed by extended stasis.