Non-canonical phosphorylation

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Metabolite Name

Pa(Pge1/A-25:0) (1)
2,6-Diaminopyridine (1)
Ethyl Malonate (1)
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2-Amino-9-[(2R,4S,5R)-5-(Hydroperoxymethyl)-4-Hydroxyoxolan-2-Yl]-1H-Purin-6-One (1)
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(Z)-[(4-Hydroxyphenyl)Acetaldehyde Oxime] (1)
3-Hydroxy-6-(2-Methyl-4-Oxochromen-5-Yl)-5-Oxohexanoic Acid (1)
(1X,2X)-Guaiacylglycerol 3-Glucoside (1)
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Netupitant (1)
Indan-1-One 1-(4,5-Dihydro-1H-Imidazol-2-Yl)Hydrazone (1)
Sb 222200 (1)
2-[(3S)-1-(3,4-Difluorobenzyl)-3-Pyrrolidinyl]-1,3-Benzoxazole (1)
Tyr-Tyrme-Oh (1)
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1,2,3,6-Tetrahydromethylphthalic Anhydride (1)
2-Ethylanthraquinone (1)
(2S)-2-Hydroxy-2-(Propan-2-Yl)Butanedioylcarnitine (1)

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bacteria (1)

Modification

2x(15)N labeled L-lysine (2)
4x(15)N labeled L-arginine (2)

Study type

Transcription profiling by array (38)
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Lab affiliation

Moffitt Cancer Center Tampa, FL, USA (6)
Amsterdam UMC, Vrije Universiteit Amsterdam, Medical Oncology, Cancer Center Amsterdam, OncoProteomics Laboratory, Amsterdam, Netherlands (3)
Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain Institució Catalana de Recerca i Estudis Avançats (ICREA), 08010 Barcelona, Spain (3)
Cornell University (2)
Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur 208016, India (2)
Guangdong Provincial People's Hospital (2)
Institute for Clinical Biochemistry and Pathobiochemistry German Diabetes Center (DDZ) Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf Auf´m Hennekamp 65 40225 Düsseldorf Germany (2)
Plateforme protéomique 3P5-Necker, Université Paris Descartes - Structure Fédérative de Recherche Necker, INSERM US24/CNRS UMS3633, Paris 75014, France (2)
Queensland Brain Institute, The University of Queensland, St Lucia Campus (Brisbane), QLD 4072, Australia (2)
1. Bioanalytical Mass Spectrometry Group, Max-Planck Institute for Multidisciplinary Sciencies, Am Fassberg 11, 37077 Goettingen, Germany; 2. Clinical Chemistry, University Medical Center Goettingen, Robert-Koch-Str. 40, 37075 Goettingen, Germany. (1)
ARC Centre of Excellence in Plant Energy Biology, School of Molecular Sciences, The University of Western Australia (1)
Beth Israel Deaconess Medical Center and Harvard Medical School (1)
Biomolecular Mass Spectrometry and Proteomics, Utrecht University (1)
Cell Biology, Harvard Medical School, Boston, MA 02115 (1)
Center for Tumor Biology and Immunology (ZTI), Philipps University, Hans-Meerwein-Strasse 3, 35043 Marburg, Germany (1)
Centre for Proteome Research Institute of Integrative Biology University of Liverpool Biosciences Building Crown Street Liverpool L69 7ZB UK (1)
Children's Medical Research Institute (1)
Computational and Experimental Biology Group NOVA MEDICAL SCHOOL / FACULDADE DE CIÊNCIAS MÉDICAS UNIVERSIDADE NOVA DE LISBOA Rua Câmara Pestana, 6-6A | 1150-082 Lisboa Portugal (1)
Department of Biochemistry and Biophysics, RNA Discovery Center, and Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill (1)
Department of Biochemistry and Pharmacology, Bio21 Molecular Science and Biotechnology Institute, University of Melbourne, Parkville, VIC, Australia. (1)
Department of Biochemistry and Pharmacology, The University of Melbourne, Parkville, Victoria, 3052, Australia (1)
Department of Biology, Technion-Israel Institute of Technology, Haifa, Israel (1)
Department of Biology, University of Konstanz, Universitaetsstrasse 10, 78457 Konstanz (1)
Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA., Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA (1)
Department of Cardiology, Smidt Heart Institute and Proteomics and Metabolomics Core Facility (1)
Department of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai (1)
Department of Chemistry, Korea Advanced Institute of Science and Technology, 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea (1)
Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology (NTNU), PO Box 8905, N-7491, Trondheim, Norway Phone: +47 72573075, Fax: +47 72576400 (1)
Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN47907 (1)
Department of Microbiology Icahn School of Medicine at Mount Sinai (1)

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The Expanding Landscape of Human Protein Phosphorylation C4PR_LIV

Investigation of protein phosphorylation in humans has largely focussed on serine (Ser), threonine (Thr) and tyrosine (Tyr), with proven roles for these modifications in all aspects of life. However, mounting evidence suggests that phosphorylation of non-canonical amino acids, including histidine an...

ORGANISM(S): Homo sapiens (Human)

2020-06-16 | PXD012188 | Pride

WNT7 Promotes Proliferation of Pancreatic Progenitor Cells Differentiated from Human Pluripotent Stem Cells through Non-Canonical Wnt Signaling Pathway

A small molecule, AT7867, promotes proliferation of human pluripotent stem cell-derived pancreatic progenitor cells (PPCs), yet detailed mechanisms of its proliferative effect were not fully understood. Here, we performed cell-based siRNA screening on a subset of genes to reveal that WNT7B is a grow...

ORGANISM(S): Homo Sapiens (human)

2022-03-27 | PXD018222 | JPOST Repository

WNT7 Promotes Proliferation of Pancreatic Progenitor Cells Differentiated from Human Pluripotent Stem Cells through Non-Canonical Wnt Signaling Pathway

ORGANISM(S): Homo Sapiens (human)

2021-07-01 | PXD018221 | JPOST Repository

Non-canonical glutamine transamination sustains efferocytosis by coupling redox buffering to oxidative phosphorylation

PRJNA759562 | ENA

The hereditary spastic paraplegia type 21 (SPG21) protein is a RAB7A effector that promotes non-canonical mTORC1-catalyzed TFEB phosphorylation and cytoplasmic retention

PRJNA1302366 | ENA

Strong anion exchange-mediated phosphoproteomics reveals extensive human non-canonical phosphorylation.

Not available

S-EPMC6826212 | biostudies-literature

Intrinsic bias at non-canonical, β-arrestin-coupled seven transmembrane receptors

G protein-coupled receptors (GPCRs) are typically characterized by their seven transmembrane (7TM) architecture, and interaction with two universal signal-transducers namely, the heterotrimeric G-proteins and β-arrestins (βarrs). Synthetic ligands and receptor mutants have been designed to elicit tr...

ORGANISM(S): Homo sapiens (Human)

2021-11-03 | PXD027887 | Pride

Gpcr kinases Gpcrs Β-arrestins Complement c5a Biased signaling Β-arrestin-coupled receptors Seven transmembrane receptors

Molecular basis of non-canonical stop codon recognition by mtRF1 in human mitochondria

PRJNA895374 | ENA

Gene expression of extranodal NK/T cell lymphoma II

Gene expression profiling of extranodal nasal-type NK/T cell lymphoma and other EBV-associated lymphoid proliferation disease patients was analyzed to elucidate association between JAK-STAT pathway and canonical or non-canonical PRC2/EZH2 target pathways using Illumina HumanRef-8 v3 chips. In total,...

ORGANISM(S): Homo sapiens

2016-07-26 | E-GEOD-80631 | biostudies-arrayexpress

Affinity peptide ligands: New tools for chasing non-canonical N-phosphoproteome

Protein N-phosphorylation enrichment is faced with great difficulties due to the intrinsic instability of the N-P bond, which has seriously hindered its biological function unraveling. Current methods for N-phosphopeptides enrichment are challenging to fulfil high selectivity for all types of N-phos...

ORGANISM(S): Homo Sapiens Escherichia Coli Mus Musculus

2024-12-12 | PXD058797 |

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