A TOR (target of rapamycin) and nutritional phosphoproteome of fission yeast reveals novel targets in networks conserved in humans.
Biomarkers
Cell Cycle
/ genetics
Computational Biology
Energy Metabolism
Gene Ontology
Host Microbial Interactions
Humans
Mechanistic Target of Rapamycin Complex 1
/ metabolism
Mechanistic Target of Rapamycin Complex 2
/ metabolism
Nitrogen
/ metabolism
Phosphoproteins
/ genetics
Proteome
Schizosaccharomyces
/ genetics
Schizosaccharomyces pombe Proteins
/ genetics
Signal Transduction
Stress, Physiological
TOR Serine-Threonine Kinases
/ genetics
Byr1 MAPKK
TORC1
TORC2
fission yeast Schizosaccharomyces pombe
nitrogen stress
phosphoproteome
Journal
Open biology
ISSN: 2046-2441
Titre abrégé: Open Biol
Pays: England
ID NLM: 101580419
Informations de publication
Date de publication:
04 2021
04 2021
Historique:
entrez:
7
4
2021
pubmed:
8
4
2021
medline:
3
2
2022
Statut:
ppublish
Résumé
Fluctuations in TOR, AMPK and MAP-kinase signalling maintain cellular homeostasis and coordinate growth and division with environmental context. We have applied quantitative, SILAC mass spectrometry to map TOR and nutrient-controlled signalling in the fission yeast
Identifiants
pubmed: 33823663
doi: 10.1098/rsob.200405
pmc: PMC8025308
doi:
Substances chimiques
Biomarkers
0
Phosphoproteins
0
Proteome
0
Schizosaccharomyces pombe Proteins
0
Mechanistic Target of Rapamycin Complex 1
EC 2.7.11.1
Mechanistic Target of Rapamycin Complex 2
EC 2.7.11.1
TOR Serine-Threonine Kinases
EC 2.7.11.1
Nitrogen
N762921K75
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
200405Subventions
Organisme : Cancer Research UK
ID : C10888/A11178
Pays : United Kingdom
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