Search Results - "Schmitz, Karl R"
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Bioinformatic identification of ClpI, a distinct class of Clp unfoldases in Actinomycetota
Published in Frontiers in microbiology (17-04-2023)“…All clades of bacteria possess Hsp100/Clp family unfoldase enzymes that contribute to aspects of protein quality control. In Actinomycetota, these include…”
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Structural Evaluation of EGFR Inhibition Mechanisms for Nanobodies/VHH Domains
Published in Structure (London) (02-07-2013)“…The epidermal growth factor receptor (EGFR) is implicated in human cancers and is the target of several classes of therapeutic agents, including antibody-based…”
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3
Nucleotide Binding and Conformational Switching in the Hexameric Ring of a AAA+ Machine
Published in Cell (25-04-2013)“…ClpX, a AAA+ ring homohexamer, uses the energy of ATP binding and hydrolysis to power conformational changes that unfold and translocate target proteins into…”
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Stochastic but Highly Coordinated Protein Unfolding and Translocation by the ClpXP Proteolytic Machine
Published in Cell (31-07-2014)“…ClpXP and other AAA+ proteases recognize, mechanically unfold, and translocate target proteins into a chamber for proteolysis. It is not known whether these…”
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5
Roles of the ClpX IGF loops in ClpP association, dissociation, and protein degradation
Published in Protein science (01-04-2019)“…IGF‐motif loops project from the hexameric ring of ClpX and are required for docking with the self‐compartmentalized ClpP peptidase, which consists of…”
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Crystal structure of Mycobacterium tuberculosis ClpP1P2 suggests a model for peptidase activation by AAA+ partner binding and substrate delivery
Published in Proceedings of the National Academy of Sciences - PNAS (28-10-2014)“…Significance Caseinolytic peptidase P (ClpP) normally collaborates with ATPases associated with diverse activities (AAA+) partner proteins, such as ClpX and…”
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Structural basis for inhibition of the epidermal growth factor receptor by cetuximab
Published in Cancer cell (01-04-2005)“…Recent structural studies of epidermal growth factor receptor (EGFR) family extracellular regions have identified an unexpected mechanism for ligand-induced…”
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Kinase Associated-1 Domains Drive MARK/PAR1 Kinases to Membrane Targets by Binding Acidic Phospholipids
Published in Cell (10-12-2010)“…Phospholipid-binding modules such as PH, C1, and C2 domains play crucial roles in location-dependent regulation of many protein kinases. Here, we identify the…”
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Comparison of Saccharomyces cerevisiae F-BAR Domain Structures Reveals a Conserved Inositol Phosphate Binding Site
Published in Structure (London) (03-02-2015)“…F-BAR domains control membrane interactions in endocytosis, cytokinesis, and cell signaling. Although they are generally thought to bind curved membranes…”
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Identification of Arginine Phosphorylation in Mycolicibacterium smegmatis
Published in Microbiology spectrum (26-10-2022)“…Tuberculosis is a leading cause of worldwide infectious mortality. The prevalence of multidrug-resistant Mycobacterium tuberculosis infections drives an urgent…”
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PtdIns4P recognition by Vps74/GOLPH3 links PtdIns 4-kinase signaling to retrograde Golgi trafficking
Published in The Journal of cell biology (28-12-2009)“…Targeting and retention of resident integral membrane proteins of the Golgi apparatus underly the function of the Golgi in glycoprotein and glycolipid…”
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12
Golgi Localization of Glycosyltransferases Requires a Vps74p Oligomer
Published in Developmental cell (01-04-2008)“…The mechanism of glycosyltransferase localization to the Golgi apparatus is a long-standing question in secretory cell biology. All Golgi glycosyltransferases…”
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Interactome Analysis Identifies MSMEI_3879 as a Substrate of Mycolicibacterium smegmatis ClpC1
Published in Microbiology spectrum (17-08-2023)“…The prevalence of drug-resistant Mycobacterium tuberculosis infections has prompted extensive efforts to exploit new drug targets in this globally important…”
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14
Substrate delivery by the AAA+ ClpX and ClpC1 unfoldases activates the mycobacterial ClpP1P2 peptidase
Published in Molecular microbiology (01-08-2014)“…Summary Mycobacterial Clp‐family proteases function via collaboration of the heteromeric ClpP1P2 peptidase with a AAA+ partner, ClpX or ClpC1. These enzymes…”
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Acyldepsipeptide Antibiotics and a Bioactive Fragment Thereof Differentially Perturb Mycobacterium tuberculosis ClpXP1P2 Activity in Vitro
Published in ACS chemical biology (21-04-2023)“…Proteolytic complexes in Mycobacterium tuberculosis (Mtb), the deadliest bacterial pathogen, are major foci in tuberculosis drug development programs. The Clp…”
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Restriction of the Conformational Dynamics of the Cyclic Acyldepsipeptide Antibiotics Improves Their Antibacterial Activity
Published in Journal of the American Chemical Society (05-02-2014)“…The cyclic acyldepsipeptide (ADEP) antibiotics are a new class of antibacterial agents that kill bacteria via a mechanism that is distinct from all clinically…”
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Subunit asymmetry and roles of conformational switching in the hexameric AAA+ ring of ClpX
Published in Nature structural & molecular biology (01-05-2015)“…The hexameric ClpX AAA+ ATPase requires subunit asymmetry and switching between nucleotide-loadable and nucleotide-unloadable conformations for cooperative ATP…”
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18
Interaction of antibodies with ErbB receptor extracellular regions
Published in Experimental cell research (15-02-2009)“…Antibodies to the extracellular region of the ErbB receptors have played key roles in the development of a mechanistic understanding of this family of receptor…”
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Antibacterial Activity of and Resistance to Small Molecule Inhibitors of the ClpP Peptidase
Published in ACS chemical biology (20-12-2013)“…There is rapidly mounting evidence that intracellular proteases in bacteria are compelling targets for antibacterial drugs. Multiple reports suggest that the…”
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A Simple Fragment of Cyclic Acyldepsipeptides Is Necessary and Sufficient for ClpP Activation and Antibacterial Activity
Published in Chembiochem : a European journal of chemical biology (13-10-2014)“…The development of new antibacterial agents, particularly those with unique biological targets, is essential to keep pace with the inevitable emergence of drug…”
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