About: Joseph D. Mougous

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

American professor of microbiology and biochemistry

Attributes	Values
rdf:type	Item
description	ikertzailea (eu) 연구원 (ko) araştırmacı (tr) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) American professor of microbiology and biochemistry (en)
rdfs:label	J.D. Mougous (es) J.D. Mougous (nl) J.D. Mougous (ast) Joseph D. Mougous (en)
skos:prefLabel	J.D. Mougous (es) J.D. Mougous (nl) J.D. Mougous (ast) Joseph D. Mougous (en)
name	J.D. Mougous (es) J.D. Mougous (nl) J.D. Mougous (ast) Joseph D. Mougous (en)
given name	wds:Q67475380-2A7F00A1-3836-4EF5-A83D-90954F0501BF
given name	Joseph
instance of	wds:Q67475380-5D18FC25-CA2C-46BD-AE2B-C05BB4B242AB
instance of	Homo sapiens
award received	wds:Q67475380-000cc725-4300-ed8f-2f9e-332eeefd723f
award received	NAS Award in Molecular Biology
Semantic Scholar author ID	wds:Q67475380-9FDFACFF-8147-4655-AB6A-4820F50383B6
Semantic Scholar author ID	4196311
skos:altLabel	J. D. Mougous (en) Joseph D Mougous (nl) Joseph David Mougous (en) Joseph Mougous (en) Mougous JD (en) Mougous JD (es) Mougous JD (nl) Mougous JD (ast)
occupation	wds:Q67475380-3D1436DA-6130-486B-AFCC-B75561284549
sex or gender	wds:Q67475380-48B23990-F8BF-423B-9927-FEE4E912B714
VIAF ID	wds:Q67475380-4CE88418-0A8C-49C6-8F49-F2DC9F13CCA9
Library of Congress authority ID	wds:Q67475380-6CA2E9EC-E852-4E65-B467-F3EB6D414009
country of citizenship	wds:Q67475380-DD46BDC5-04BD-497C-B7EB-0CE24B384171
VIAF ID	http://viaf.org/viaf/315191251
Library of Congress authority ID	http://id.loc.gov/authorities/names/no2015041919
occupation	researcher
sex or gender	male
VIAF ID	315191251
Library of Congress authority ID	no2015041919
country of citizenship	United States of America
ORCID iD	wds:Q67475380-8A912A30-5158-4A30-8DD9-5A4F21981271
ORCID iD	https://orcid.org/0000-0002-5417-4861
ORCID iD	0000-0002-5417-4861
is owl:sameAs of	Joseph D. Mougous
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q67475380 Joseph Mougous
is author of	A virulence locus of Pseudomonas aeruginosa encodes a protein secretion apparatus Structure of a Peptidoglycan Amidase Effector Targeted to Gram-Negative Bacteria by the Type VI Secretion System Structural Basis for Type VI Secretion Effector Recognition by a Cognate Immunity Protein A type VI secretion system of Pseudomonas aeruginosa targets a toxin to bacteria An interbacterial NAD(P)(+) glycohydrolase toxin requires elongation factor Tu for delivery to target cells Genetically distinct pathways guide effector export through the type VI secretion system Type VI secretion delivers bacteriolytic effectors to target cells A type VI secretion-related pathway in Bacteroidetes mediates interbacterial antagonism Haemolysin coregulated protein is an exported receptor and chaperone of type VI secretion substrates Type VI secretion system effectors: poisons with a purpose Diverse type VI secretion phospholipases are functionally plastic antibacterial effectors Burkholderia type VI secretion systems have distinct roles in eukaryotic and bacterial cell interactions The complete genome of Teredinibacter turnerae T7901: an intracellular endosymbiont of marine wood-boring bivalves (shipworms) A self-lysis pathway that enhances the virulence of a pathogenic bacterium Human symbionts inject and neutralize antibacterial toxins to persist in the gut What is type VI secretion doing in all those bugs? Structure and regulation of the type VI secretion system Identification, function and structure of the mycobacterial sulfotransferase that initiates sulfolipid-1 biosynthesis Kinetic measurements and mechanism determination of Stf0 sulfotransferase using mass spectrometry TagR promotes PpkA-catalysed type VI secretion activation in Pseudomonas aeruginosa In vitro self-assembly of tailorable nanotubes from a simple protein building block Observation of a hybrid random ping-pong mechanism of catalysis for NodST: a mass spectrometry approach Lipidomics reveals control of Mycobacterium tuberculosis virulence lipids via metabolic coupling. A minimalist substrate for enzymatic peptide and protein conjugation. Trehalose is required for growth of Mycobacterium smegmatis 5'-adenosinephosphosulfate lies at a metabolic branch point in mycobacteria Quantitative single-cell characterization of bacterial interactions reveals type VI secretion is a double-edged sword Transferred interbacterial antagonism genes augment eukaryotic innate immune function Molecular basis for G protein control of the prokaryotic ATP sulfurylase MmpL8 is required for sulfolipid-1 biosynthesis and Mycobacterium tuberculosis virulence Threonine phosphorylation post-translationally regulates protein secretion in Pseudomonas aeruginosa A widespread bacterial type VI secretion effector superfamily identified using a heuristic approach Sulfotransferases and sulfatases in mycobacteria A sulfated metabolite produced by stf3 negatively regulates the virulence of Mycobacterium tuberculosis Discovery of sulfated metabolites in mycobacteria with a genetic and mass spectrometric approach Separate inputs modulate phosphorylation-dependent and -independent type VI secretion activation Kin cell lysis is a danger signal that activates antibacterial pathways of Pseudomonas aeruginosa VgrG-5 is a Burkholderia type VI secretion system-exported protein required for multinucleated giant cell formation and virulence Vaccine efficacy of an attenuated but persistent Mycobacterium tuberculosis cysH mutant. 5'-Adenosinephosphosulphate reductase (CysH) protects Mycobacterium tuberculosis against free radicals during chronic infection phase in mice. An ABC transporter and an outer membrane lipoprotein participate in posttranslational activation of type VI secretion in Pseudomonas aeruginosa. From Striking Out to Striking Gold: Discovering that Type VI Secretion Targets Bacteria Secreted Effectors Encoded within and outside of the Francisella Pathogenicity Island Promote Intramacrophage Growth. Bacterial danger sensing A broadly distributed toxin family mediates contact-dependent antagonism between gram-positive bacteria. Conditional toxicity and synergy drive diversity among antibacterial effectors.

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