Mapks - OmicsDI

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Unknown (1619)
Transcriptomics (113)
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Homo sapiens (49)
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fungal pathogen UWFP-388 (1)
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Homo sapiens (24)
Mus musculus (17)
Arabidopsis thaliana (8)
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Saccharomyces cerevisiae (3)
Nicotiana tabacum (2)
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Arabidopsis (1)
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Disease free (3)
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Not Available (1)
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Mass Spectrometry (32)
Shotgun proteomics (18)
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Affinity purification coupled with mass spectrometry proteomics (3)
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MicrOTOF-Q (1)

Publication Date

2010 (20)
2014 (16)
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UNIPROT ID/AC

B2CT00 (2)
C0LGN2 (2)
H9D0Z7 (2)
O04609 (2)
O22921 (2)
P31152 (2)
P45985 (2)
Q02750 (2)
Q0WV96 (2)
Q13163 (2)
Q13233 (2)
Q39023 (2)
Q39026 (2)
Q39028 (2)
Q8S8P5 (2)
Q8VWJ2 (2)
Q93WY4 (2)
Q9C5H5 (2)
Q9FDW1 (2)
Q9FGX2 (2)
Q9S7U9 (2)
Q9SI37 (2)
Q9SUS1 (2)
Q9SZP1 (2)
O14733 (1)
P06784 (1)
P08018 (1)
P16892 (1)
P23561 (1)
P32485 (1)

CHEBI ID

CHEBI:16240 (1)
CHEBI:18153 (1)
CHEBI:26710 (1)
CHEBI:15356 (1)
CHEBI:15414 (1)
CHEBI:15428 (1)
CHEBI:15741 (1)
CHEBI:15846 (1)
CHEBI:15891 (1)
CHEBI:15978 (1)
CHEBI:16015 (1)
CHEBI:16113 (1)
CHEBI:16199 (1)
CHEBI:16235 (1)
CHEBI:16449 (1)
CHEBI:16467 (1)
CHEBI:16474 (1)
CHEBI:16610 (1)
CHEBI:16680 (1)
CHEBI:16708 (1)
CHEBI:16737 (1)
CHEBI:16750 (1)
CHEBI:167606 (1)
CHEBI:16811 (1)
CHEBI:16857 (1)
CHEBI:16908 (1)
CHEBI:16958 (1)
CHEBI:17050 (1)
CHEBI:17148 (1)
CHEBI:17568 (1)

Metabolite Name

(1S,3R,4R,5R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,5-dihydroxy-4-[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxycyclohexane-1-carboxylic acid (1)
(2E,4E,8E)-7,13-dihydroxy-4,8,12-trimethyltetradeca-2,4,8-trienoic acid (1)
(2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-((3-(benzo[d][1,3]dioxol-5-yl)-6-ethyl-2-methyl-4-oxo-4H-chromen-7-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate (1)
(2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-((3-methoxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)thio)tetrahydro-2H-pyran-3,4,5-triyl triacetate (1)
(2S,3R)-2-(((S)-7-acetamido-1,2,3-trimethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-10-yl)amino)-N-(5-chloropyridin-2-yl)-3-methylpentanamide (1)
(2S,3R,4S,5R)-2-[(2R,3R,4S,5S,6R)-2-[[(3S,6S,8R,10R,12R,13R,14R,17S)-3,12-dihydroxy-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol (1)
(3?,5?,9?,16?,18?,22?)-22-Acetoxy-16-hydroxy-13,28-epoxyoleanan-3-yl 6-deoxy-?-L-mannopyranosyl-(1->2)-?-D-galactopyranosyl-(1->3)-[?-D-glucopyranosyl-(1->2)]-?-D-glucopyran osiduronic acid_major (1)
(3S,4S,6aR,6bS,8R,8aR,12aS,14bR)-8-hydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid (1)
(3aS,3a1S,10bR,13S)-3a-ethyl-5-(methoxycarbonyl)-1,2,3,3a,3a1,4,6,11,12,13-decahydroindolizino[8,1-cd]carbazol-13-ium iodide (1)
(4R)-4-((5S,7R,9S,10S,13R,14S,17R)-7-hydroxy-10,13-dimethyl-3-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid (1)
(4R,E)-4-((3R,5R,6S,7R,9S,10R,13R,14S,17R)-3,6,7-trihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pent-2-enoic acid (1)
(6E)-2,6,10-trimethyldodeca-6,11-diene-2,3,10-triol_major (1)
(7S,9E,11S,12R,13S,14S,15S,16R,17S,18S,19E,21Z)-13-(acetyloxy)-15,17-dihydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-6,23,27,29-tetraoxo-26-(pyrrolidin-1-yl)-8,30-dioxa-24-azatetracyclo[23.3.1.1^{4,7}.0^{5,28}]triaconta-1,3,5(28),9,19,21,25-heptae... (1)
(7S,9E,11S,12R,13S,14S,15S,16R,17S,18S,19E,21Z)-26-{4-[(furan-2-yl)carbonyl]piperazin-1-yl}-2,15,17-trihydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-6,23,27,29-tetraoxo-8,30-dioxa-24-azatetracyclo[23.3.1.1^{4,7}.0^{5,28}]triaconta-1,3,5(28),9,19,2... (1)
(G)(NAM)-AemA;(3s-4)-(G)(NAM)-AemA (1)
(NAG)(NAM)-AeKA[3-NH2-GGGG] (1)
(NAG)(NAM)-AemAG;(3s-4)-(G)(NAM)-AemA (1)
(NAG)(NAM)-AqK;(G-G)-(NAG)(NAM)-None (1)
(NAG)(NAM)-AqKAA[3-NH2-n] (1)
(NAG)(NAM)-AqKAK[3-NH2-AA] (1)
(NAG)(NAM)-AqKA[3-NH2-d];(3br-4)-None-KA[3-NH2-d] (1)
(NAG)(NAM)-AqK[3-NH2-n];(G-G)-(NAG)(NAM)-None (1)
(NAG)(anNAM)-AqKAA[3-NH2-GG] (1)
(R)-4-((3R,5S,7S,8S,9S,10S,13R,14R,17R)-3,7,14-trihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid (1)
(R)-4-((3R,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-7,12-dioxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid (1)
(R)-4-((8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid (1)
(R)-4-((8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-oxo-2,3,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid (1)
(S)-2-(((S)-7-acetamido-1,2,3-trimethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-10-yl)amino)-4-(methylthio)-N-(2-(2-oxopyrrolidin-1-yl)ethyl)butanamide (1)
(S)-2-((R)-2-((S)-2-(2-((3-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-5-hydroxy-4-oxo-4H-chromen-7-yl)oxy)acetamido)-3-phenylpropanamido)-4-methylpentanamido)-5-guanidinopentanoic acid (1)
(S)-4-((7-acetamido-1,2,3-trimethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen-10-yl)amino)-N-(benzo[d][1,3]dioxol-5-ylmethyl)butanamide (1)

First Public Date

2014 (19)
2024 (10)
2017 (8)
2025 (7)
2022 (7)
2026 (5)
2023 (5)
2021 (5)
2020 (5)
2018 (4)
2019 (2)
2015 (2)

Modelling Approach

Ordinary differential equation model (3)
Differential equation model (1)
Other (1)

Lab affiliation

Boston University School of Medicine (1)
Cellular & Molecular Metabolism Laboratory, Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University. (1)
Center for Desert Agriculture, 4700 King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia (1)
Centre de Recherche en Cancérologie de Marseille, CRCM Inserm UMR1068, CNRS UMR7258, Aix Marseille Université U105, Institut Paoli Calmettes 27 Boulevard Leï Roure CS30059 13273 Marseille Cedex 09 France (1)
Departement de Chimie, Biochimie et Physisque, Université du Québec à Trois-Rivières (1)
Department for Biochemistry, Max F. Perutz Laboratories, University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria (1)
Department of Biological Engineering, Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA (1)
Department of Cellular Biochemistry Institute for Biochemistry and Biotechnology Martin-Luther-University Halle-Wittenberg Kurt-Mothes-Str. 3 06120 Halle (Saale) (1)
European Molecular Biology Laboratory, 71 avenue des Martyrs, CS 90181 F-38042 Grenoble, France (1)
Faculty of Biology, Technion Israel institute of technology, Haifa, Israel (1)
IPB Department SEB Weinberg 3 06120 Halle (1)
Institute for Genomics, Biocomputing, and Biotechnology, Mississippi State University (1)
Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, P. R. China (1)
KAUST (1)
Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu 610065, Sichuan, China (1)
Key Laboratory of Plant Resources, Institute of Botany, the Chinese Academy of Sciences, Beijing (1)
Laboratory of Fungal Pathogenesis, Centre for DNA Fingerprinting and Diagnostics (CDFD), Hyderabad, India (1)
Leibniz-Institut für Pflanzenbiochemie Weinberg 3 06120 Halle (Saale) (1)
Microbiology Department, Faculty of Sciences, Pontificia Universidad Javeriana, Bogotá 110231, Colombia Microbiology and Parasitology Department, Faculty of Pharmacy, Universidad Complutense de Madrid, Madrid 28040, Spain (1)
Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen (1)
Proteome Analytics Leibniz Institute of Plant Biochemistry Weinberg 3 Halle 06124, Germany (1)
Proteomics Core Facility and Research Group Proteomics, CEITEC-MU, Masaryk University, Brno, Czech Republic (1)
Proteomics Unit, Department of Biochemistry, Institute of Chemistry, Federal University of Rio de Janeiro, Rio de Janeiro, 21941-909 Rio de Janeiro, RJ, Brazil; Laboratory of Proteomics, LADETEC, Institute of Chemistry, Federal University of Rio de Janeiro, Rio de Janeiro, 21941-598 Rio de Janeiro, RJ, Brazi (1)
Shanghai Center for Plant Stress Biology (1)
State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China (1)
The University of Melbourne (1)
Tufts University Chemistry Department, Principal Investigator, Medford, United States (1)
UMR 1347 Agroécologie Agrosup Dijon / INRA / Université de Bourgogne / Dijon / France (1)
University of Geneva (1)
University of Manchester (1)

IsPrivate

False (6)

Classification

fungi (2)

Study type

Transcription profiling by array (44)
RNA-seq of coding RNA (5)
Unknown experiment type (1)
Plant - One-color microarray (1)
Transcription profiling by RT-PCR (1)
ChIP-seq (1)
Proteomic profiling by array (1)

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2012 (38)
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2026 (10)
2006 (9)
2003 (7)
2002 (3)
2001 (3)
2000 (3)
1999 (3)
1998 (2)

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Shared and specific targets of Arabidopsis immune MAPKs

In Arabidopsis, mitogen-activated protein kinases MPK3, MPK4 and MPK6 constitute essential relays for a variety of functions including cell division, development and innate immunity. While some substrates of MPK3, MPK4 and MPK6 have been identified, the picture is still far from complete. To identif...

ORGANISM(S): Arabidopsis thaliana (Mouse-ear cress)

2017-12-06 | PXD006807 | Pride

Fusarium graminearum

Fusarium graminearum MAPKs triple mutant Raw sequence reads

PRJNA769595 | ENA

Impact of Conventional and Atypical MAPKs on the Development of Metabolic Diseases.

Not available

S-EPMC7563211 | biostudies-literature

Endothelial MAPKs Direct ICAM-1 Signaling to Divergent Inflammatory Functions.

Not available

S-EPMC5421301 | biostudies-literature

Balancing MAPKs and AKT signaling pathway from compensated to decompensated state: a critical mechanism of Lingguizhugan decoction in the treatment of heart failure

PRJNA769110 | ENA

p38 MAPKs - roles in skeletal muscle physiology, disease mechanisms, and as potential therapeutic targets.

Not available

S-EPMC8262482 | biostudies-literature

Balancing MAPKs and AKT signaling pathway from compensated to decompensated state: a critical mechanism of Lingguizhugan decoction in the treatment of heart failure

Heart failure (HF), a major health concern worldwide, with high morbidity and mortality, renders the urgent need for new treatments. Lingguizhugan decoction (LD), a classic Chinese formula, has been clinically used to treat HF. However, the molecular mechanisms involved are not fully elucidated. In ...

ORGANISM(S): Mus musculus

2022-03-06 | GSE185450 | GEO

Chromatin phosphoproteomics unravels a function for AT-hook motif nuclear localized protein AHL13 in PAMP-triggered immunity

Mitogen-activated protein kinases constitute essential signaling mechanisms linking external signal perception to gene expression in all eukaryotes. In Arabidopsis, MAPKs are found in the cytoplasmic and nuclear compartments, but no nuclear phosphoproteomic studies of mapk mutants were performed so ...

ORGANISM(S): Arabidopsis thaliana (Mouse-ear cress)

2021-01-07 | PXD009823 | Pride

Arabidopsis thaliana Immune mapks Phosphoproteomics

Role of the MAPKs/TGF-β1/TRAF6 signaling pathway in postoperative atrial fibrillation.

Not available

S-EPMC5360308 | biostudies-literature

Characterization of mitogen activated protein kinases (MAPKs) in the Curcuma longa expressed sequence tag database.

Not available

S-EPMC3218520 | biostudies-literature

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