Interactome Analysis Identifies MSMEI_3879 as a Substrate of Mycolicibacterium smegmatis ClpC1-Reference-Cited by-同舟云学术

Interactome Analysis Identifies MSMEI_3879 as a Substrate of Mycolicibacterium smegmatis ClpC1

Published:2023-08-17 Issue:4 Volume:11 Page:
ISSN:2165-0497
Container-title:Microbiology Spectrum
language:en
Short-container-title:Microbiol Spectr

Author:

Ogbonna Emmanuel C.¹^ORCID,Anderson Henry R.²,Beardslee Patrick C.²,Bheemreddy Priyanka¹,Schmitz Karl R.¹²^ORCID

Affiliation:

1. Department of Biological Sciences, University of Delaware, Newark, Delaware, USA

2. Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware, USA

Abstract

Drug-resistant tuberculosis infections are a major challenge to global public health. Much effort has been invested in identifying new drug targets in the causative pathogen, Mycobacterium tuberculosis .

Funder

National Institute of General Medical Sciences

HHS | NIH | National Institute of General Medical Sciences

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Cell Biology,Microbiology (medical),Genetics,General Immunology and Microbiology,Ecology,Physiology

Link

https://journals.asm.org/doi/pdf/10.1128/spectrum.04548-22

Reference91 articles.

1. WHO. 2021. Global tuberculosis report 2021. World Health Organization, Geneva, Switzerland.

2. Antibacterial Activity of and Resistance to Small Molecule Inhibitors of the ClpP Peptidase

3. Lassomycin, a Ribosomally Synthesized Cyclic Peptide, Kills Mycobacterium tuberculosis by Targeting the ATP-Dependent Protease ClpC1P1P2

4. The Cyclic Peptide Ecumicin Targeting ClpC1 Is Active against Mycobacterium tuberculosis In Vivo

5. Target Mechanism-Based Whole-Cell Screening Identifies Bortezomib as an Inhibitor of Caseinolytic Protease in Mycobacteria

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