Literature DB >> 28910721

An amino acid domino effect orchestrates ClpP's conformational states.

Matthias Stahl1, Stephan A Sieber2.   

Abstract

Maintaining the cellular protein homeostasis means managing life on the brink of death. This balance is largely based on precise fine-tuning of enzyme activities. For instance, the ClpP protease possesses several conformational switches which are fundamental to regulating its activity. Efforts have focused on revealing the structural basis of ClpP's conformational control. In the last decade, several amino acid clusters have been identified and functionally linked to specific activation states. Researchers have now begun to couple these hotspots to one another, uncovering a global network of residues that switch in response to internal and external stimuli. For these studies, they used small molecules to mimic intermolecular interactions and point-mutational studies to shortcut regulating amino acid circuits.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2017        PMID: 28910721     DOI: 10.1016/j.cbpa.2017.08.007

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  8 in total

1.  Clostridium difficile ClpP Homologues are Capable of Uncoupled Activity and Exhibit Different Levels of Susceptibility to Acyldepsipeptide Modulation.

Authors:  Nathan P Lavey; Tyler Shadid; Jimmy D Ballard; Adam S Duerfeldt
Journal:  ACS Infect Dis       Date:  2018-11-26       Impact factor: 5.084

2.  An allosteric switch regulates Mycobacterium tuberculosis ClpP1P2 protease function as established by cryo-EM and methyl-TROSY NMR.

Authors:  Siavash Vahidi; Zev A Ripstein; Jordan B Juravsky; Enrico Rennella; Alfred L Goldberg; Anthony K Mittermaier; John L Rubinstein; Lewis E Kay
Journal:  Proc Natl Acad Sci U S A       Date:  2020-03-02       Impact factor: 11.205

Review 3.  Reprogramming of the Caseinolytic Protease by ADEP Antibiotics: Molecular Mechanism, Cellular Consequences, Therapeutic Potential.

Authors:  Heike Brötz-Oesterhelt; Andreas Vorbach
Journal:  Front Mol Biosci       Date:  2021-05-13

Review 4.  Mitochondrial ATP-Dependent Proteases-Biological Function and Potential Anti-Cancer Targets.

Authors:  Yue Feng; Kazem Nouri; Aaron D Schimmer
Journal:  Cancers (Basel)       Date:  2021-04-22       Impact factor: 6.639

5.  Acyldepsipeptide Probes Facilitate Specific Detection of Caseinolytic Protease P Independent of Its Oligomeric and Activity State.

Authors:  Barbara Eyermann; Maximilian Meixner; Heike Brötz-Oesterhelt; Iris Antes; Stephan A Sieber
Journal:  Chembiochem       Date:  2020-01-07       Impact factor: 3.164

Review 6.  Mitochondrial ClpP serine protease-biological function and emerging target for cancer therapy.

Authors:  Kazem Nouri; Yue Feng; Aaron D Schimmer
Journal:  Cell Death Dis       Date:  2020-10-09       Impact factor: 8.469

7.  Substrate Profiling of Mitochondrial Caseinolytic Protease P via a Site-Specific Photocrosslinking Approach.

Authors:  Tuan-Anh Nguyen; Thomas F Gronauer; Timon Nast-Kolb; Stephan A Sieber; Kathrin Lang
Journal:  Angew Chem Int Ed Engl       Date:  2022-01-14       Impact factor: 16.823

8.  Cryo-EM structure of the ClpXP protein degradation machinery.

Authors:  Christos Gatsogiannis; Dora Balogh; Felipe Merino; Stephan A Sieber; Stefan Raunser
Journal:  Nat Struct Mol Biol       Date:  2019-10-03       Impact factor: 15.369

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.