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Author Details

Dustin C Ernst
University of California
2009
25
13
PMIDPaper TitleJournal TitlePublished Year
35864165Coupling of distant ATPase domains in the circadian clock protein KaiC.Nat Struct Mol Biol2022
35475644Comparative Genomics of Synechococcus elongatus Explains the Phenotypic Diversity of the Strains.mBio2022
34559917Absence of MMF1 disrupts heme biosynthesis by targeting Hem1pin Saccharomyces cerevisiae.Yeast2021
34618577Reconstitution of an intact clock reveals mechanisms of circadian timekeeping.Science2021
31103411Reactive Enamines and Imines In Vivo: Lessons from the RidA Paradigm.Trends Biochem Sci2019
31878179Integrated Metabolomics and Transcriptomics Suggest the Global Metabolic Response to 2-Aminoacrylate Stress in <i>Salmonella enterica</i>.Metabolites2019
29487232Mmf1p Couples Amino Acid Metabolism to Mitochondrial DNA Maintenance in <i>Saccharomyces cerevisiae</i>.mBio2018
29440255Increased Activity of Cystathionine β-Lyase Suppresses 2-Aminoacrylate Stress in Salmonella enterica.J Bacteriol2018
29791499Perturbation of the metabolic network in Salmonella enterica reveals cross-talk between coenzyme A and thiamine pathways.PLoS One2018
27010356L-2,3-diaminopropionate generates diverse metabolic stresses in Salmonella enterica.Mol Microbiol2016
25645561The STM4195 gene product (PanS) transports coenzyme A precursors in Salmonella enterica.J Bacteriol2015
265745112-Aminoacrylate Stress Induces a Context-Dependent Glycine Requirement in ridA Strains of Salmonella enterica.J Bacteriol2015
25620221From microbiology to cancer biology: the Rid protein family prevents cellular damage caused by endogenously generated reactive nitrogen species.Mol Microbiol2015
25002544Endogenous synthesis of 2-aminoacrylate contributes to cysteine sensitivity in Salmonella enterica.J Bacteriol2014
19913036Bacterial pleckstrin homology domains: a prokaryotic origin for the PH domain.J Mol Biol2010
20944221The structure of BVU2987 from Bacteroides vulgatus reveals a superfamily of bacterial periplasmic proteins with possible inhibitory function.Acta Crystallogr Sect F Struct Biol Cryst Commun2010
20944219The structure of KPN03535 (gi|152972051), a novel putative lipoprotein from Klebsiella pneumoniae, reveals an OB-fold.Acta Crystallogr Sect F Struct Biol Cryst Commun2010
20944217Structure of a putative NTP pyrophosphohydrolase: YP_001813558.1 from Exiguobacterium sibiricum 255-15.Acta Crystallogr Sect F Struct Biol Cryst Commun2010
20944214Structures of the first representatives of Pfam family PF06938 (DUF1285) reveal a new fold with repeated structural motifs and possible involvement in signal transduction.Acta Crystallogr Sect F Struct Biol Cryst Commun2010
20944209Structures of the first representatives of Pfam family PF06684 (DUF1185) reveal a novel variant of the Bacillus chorismate mutase fold and suggest a role in amino-acid metabolism.Acta Crystallogr Sect F Struct Biol Cryst Commun2010
20944208The structure of the first representative of Pfam family PF09836 reveals a two-domain organization and suggests involvement in transcriptional regulation.Acta Crystallogr Sect F Struct Biol Cryst Commun2010
20122942Crystal structure of the first eubacterial Mre11 nuclease reveals novel features that may discriminate substrates during DNA repair.J Mol Biol2010
19127588Crystal structure of the Fic (Filamentation induced by cAMP) family protein SO4266 (gi|24375750) from Shewanella oneidensis MR-1 at 1.6 A resolution.Proteins2009
19173316Crystal structure of a novel Sm-like protein of putative cyanophage origin at 2.60 A resolution.Proteins2009
19567872Structural and functional characterizations of SsgB, a conserved activator of developmental cell division in morphologically complex actinomycetes.J Biol Chem2009
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Collaborators

Genomics Institute of the Novartis Research Foundation
Co-authored papers 11
The Joint Center for Structural Genomics, Stanford University
Co-authored papers 11
Merck & Co., Inc.
Co-authored papers 11
Bridge Institute, University of Southern California
Co-authored papers 11
University of Lucknow
Co-authored papers 11
Co-authored papers 11
Co-authored papers 11
Cardiovascular Institute, Stanford University School of Medicine
Co-authored papers 11
Accelero Biostructures Inc., USA XPose Therapeutics Inc.
Co-authored papers 11
Brown University
Co-authored papers 11
Co-authored papers 11
Joint Center for Structural Genomics
Co-authored papers 11
Joint Center for Structural Genomics ( http:/www.jcsg.org )
Co-authored papers 11
Co-authored papers 11
University of California San Francisco
Co-authored papers 11
Joint Center for Structural Genomics
Co-authored papers 11
Co-authored papers 11
Institute of Science, Banaras Hindu University
Co-authored papers 11
Accelero Biostructures Inc., USA XPose Therapeutics Inc.
Co-authored papers 11
The Scripps Research Institute, USA The Skaggs Institute for Chemical Biology
Co-authored papers 11
Celgene/Bristol-Myers Squibb Corporation
Co-authored papers 11
Co-authored papers 11
Incyte Corporation
Co-authored papers 11
Joint Center for Structural Genomics, Sanford-Burnham Medical Research Institute
Co-authored papers 11
Genomics Institute of the Novartis Research Foundation
Co-authored papers 11
Merck & Co., Inc.
Co-authored papers 11
Regeneron Pharmaceuticals, Inc.
Co-authored papers 11
Joint Center for Structural Genomics
Co-authored papers 11
University of California Riverside School of Medicine
Co-authored papers 11
Rice University
Co-authored papers 11