C-terminus - OmicsDI

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Homo sapiens (127)
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Instrument Platform

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2013 (33)
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2008 (15)
2007 (11)
2005 (6)
2009 (5)
2006 (4)

UNIPROT ID/AC

P01258 (1)

CHEBI ID

CHEBI:17750 (3)
CHEBI:65302 (2)
CHEBI:141588 (2)
CHEBI:42111 (2)
CHEBI:24266 (2)
CHEBI:27997 (2)
CHEBI:64516 (2)
CHEBI:66848 (2)
CHEBI:16113 (2)
CHEBI:44215 (2)
CHEBI:16856 (2)
CHEBI:18237 (2)
CHEBI:17533 (2)
CHEBI:7676 (2)
CHEBI:28867 (2)
CHEBI:16668 (2)
CHEBI:17311 (2)
CHEBI:17924 (2)
CHEBI:28875 (2)
CHEBI:15741 (2)
CHEBI:37024 (2)
CHEBI:16865 (2)
CHEBI:17929 (2)
CHEBI:7916 (2)
CHEBI:17549 (2)
CHEBI:15891 (2)
CHEBI:18183 (2)
CHEBI:16919 (2)
CHEBI:16347 (2)
CHEBI:28716 (2)

Metabolite Name

Beta-Nicotinamide adenine dinucleotide (2)
D-Sorbitol (2)
PC 40:6|PC 18:1_22:5 (1)
PC 38:4|PC 18:1_20:3 (1)
PC 33:1|PC 17:0_16:1 (1)
PC 31:1|PC 15:0_16:1 (1)
PC 31:0|PC 14:0_17:0 (1)
PC 29:0|PC 14:0_15:0 (1)
S-Hydroxymethylglutathione (1)
PC 32:2|PC 16:1_16:1 (1)
PC36:2_14 (1)
PC36:2 (1)
PC34:1_14 (1)
PC34:1 (1)
PC34:2_25 (1)
PC34:2_23 (1)
PC34:2_16 (1)
PC34:2_14 (1)
PC34:2_9 (1)
PC34:2 (1)
PC32:1_25 (1)
PC32:1_23 (1)
PC32:1_16 (1)
PC32:1_14 (1)
PC32:1_9 (1)
PC32:1 (1)
PC32:2_25 (1)
PC32:2_23 (1)
PC32:2_16 (1)
PC32:2_14 (1)

First Public Date

2023 (50)
2026 (43)
2025 (43)
2024 (39)
2020 (36)
2021 (34)
2014 (34)
2022 (30)
2017 (23)
2016 (22)
2013 (22)
2019 (20)
2018 (17)
2015 (17)

Modelling Approach

Ordinary differential equation model (2)

Lab affiliation

Functional Proteomics, ICR (19)
Proteomics Core Facility and Research Group Proteomics, CEITEC-MU, Masaryk University, Brno, Czech Republic (15)
Professor of Genomic Evolution, School of Medicine, Conway Institute of Biomolecular and Biomedical Research, University College Dublin Belfield Dublin 4 (11)
Whitehead Institute for Biomedical Research and Massachusetts Institute of Technology (11)
Medical University of Vienna (9)
North Carolina State University (9)
TIGEM (8)
The Institute of Cancer Research (8)
Department of Oncology-Pathology, Karolinska Institutet, 171 77 Stockholm, Sweden Institute of Molecular and Cell Biology, A*STAR, Singapore 138673, Singapore (6)
The Institute of Cancer Research, London (6)
Analytics Core Facility Essen (ACE), Chemische Biologie, Universität Duisburg-Essen, ZMB, Germany (5)
Associate Professor, Department of Biology, Massachusetts Institute of Technology and Whitehead Institute of Biomedical Research (5)
Department of Chemistry and Chemical Biology, Harvard University (5)
Laboratory of Experimental Cancer Research, Department of Human Structure and Repair, Ghent University, Ghent, Belgium (5)
The University of Sydney (5)
Biochemistry Center Heidelberg, University of Heidelberg, Germany (4)
Institute of Biochemistry II, Faculty of Medicine, Goethe University, Frankfurt am Main, Germany Frankfurt Cancer Institute, Frankfurt am Main, Germany Cardio-Pulmonary Institute, Frankfurt am Main, Germany (4)
Internal Diseases Clinic, Faculty of Veterinary Medicine, University of Zagreb, Zagreb, Croatia (4)
LPHI, Univ Montpellier, CNRS, INSERM, Montpellier, France (4)
Max Planck Institute of Immunobiology and Epigenetics Proteomics Unit Stuebeweg 51 79108 Freiburg Germany (4)
Molecular Cell and Developmental Biology, School of Life Sciences, University of Dundee (4)
Protein Biogenesis Lab, The Francis Crick Institute, 1 Midland Road, London, NW1 1AT (4)
State Key Laboratory of Genetic Engineering, Department of Biochemistry, School of Life Sciences, Fudan University, Shanghai 200438, China (4)
Tokyo Metropolitan Institute of Medical Science (4)
Biochemistry (3)
Biozentrum, University of Basel, Switzerland (3)
Cambridge Institute for Medical Research, University of Cambridge, Cambridge Biomedical Campus, CB2 0XY, UK (3)
Department of Biochemistry and Molecular Biology, University of Calgary, Alberta, Canada; Department of Physiology and Pharmacology, University of Calgary, Alberta, Canada; The Hotchkiss Brain Institute, University of Calgary, Alberta, Canada; McCaig Institute for Bone and Joint Health, University of Calgary, Alberta, Canada (3)
Department of Cardiovascular Medicine, Center for Circadian Metabolism and Cardiovascular Disease, Southwest Hospital, Army Medical University; Chongqing, China. (3)
Department of Immunobiology, College of Life Science and Technology, Jinan University, Guangzhou, China. (3)

IsPrivate

False (2)

Classification

bacteria (14)
viruses (12)
fungi (7)
protozoa (5)

Modification

15.994915 (8)
42.010565 (8)
57.021464 (6)
-17.026549 (5)
45.029395 (4)
6.020129 (3)
N6-dimethyl-L-lysine (3)
+3amu) (2)
10.008269 (2)
56.026215 (2)
N6 (2)
-18.010565 (1)
0.984016 (1)
15.99491 (1)
2x(15)N labeled L-lysine (1)
4-tetrahydrothiazine-3-carboxylic acid (1)
4x(2)H labeled dimethylated L-lysine (1)
4x(2)H labeled dimethylated residue (1)
57.02146 (1)
58.005479 (1)
59.036279 (1)
6x(2)H labeled dimethylated L-arginine (1)

Study type

Transcription profiling by array (102)
RNA-seq of coding RNA (45)
ChIP-seq (34)
RNA-seq of non coding RNA (28)
ChIP-chip by tiling array (10)
ChIP-chip by array (8)
Comparative genomic hybridization by array (4)
Other (3)
Unknown experiment type (2)
Transcription profiling by tiling array (2)
CLIP-seq (2)
MicroRNA profiling by array (2)
Proteomic profiling by array (2)
High-throughput sequencing (1)
RNAi profiling by array (1)
Genotyping by array (1)
Antigen profiling (1)
MicroRNA profiling by high throughput sequencing (1)
Methylation profiling by array (1)
RNA-seq of total RNA (1)

Release Date

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2009 (316)
2008 (303)
2007 (236)
2006 (186)
2005 (176)
2004 (130)
2003 (107)
2000 (81)
2001 (78)
1999 (78)
2002 (61)
1998 (51)
2026 (48)
1997 (25)

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DUX4 recruits p300/CBP through its C-terminus and induces global H3K27 acetylation changes

Ectopic expression of the double homeodomain transcription factor DUX4 causes facioscapulohumeral muscular dystrophy (FSHD). Mechanisms of action of DUX4 are currently unknown. Using immortalized human myoblasts with a titratable DUX4 transgene, we identify by mass spectrometry an interaction betwee...

ORGANISM(S): Homo sapiens

2016-03-10 | E-GEOD-78158 | biostudies-arrayexpress

Signaling suppressive determinants of the FGFR2 C-terminus

PRJEB60417 | ENA

Whole brain transcriptome analysis of PTEN C-terminus mutant mice

PRJNA488572 | ENA

Amino terminus of cardiac myosin binding protein-C regulates cardiac contractility

PRJNA716300 | ENA

Whole brain transcriptome analysis of PTEN C-terminus mutant mice

PTEN contains a C-terminal motif that binds to various PDZ domain-containing proteins including PSD-95. The PTEN C-terminus is known to mediate synaptic translocation of PTEN during long-term depression (LTD) and amyloid-b-induced synaptic depression. However, it remains unknown whether it regulates...

ORGANISM(S): Mus musculus

2020-12-17 | GSE119236 | GEO

The C-terminus of p53 Confers Liver-Specific Gene Regulation and Radio-Resistance in vivo [RNA-Seq]

PRJNA843183 | ENA

Heterologous expression of the C-terminus of voltage gated sodium channel Nav1.2 in neuroblastoma N1E115 cells

PRJNA1302765 | ENA

DUX4 recruits p300/CBP through its C-terminus and induces global H3K27 acetylation changes

ORGANISM(S): Homo sapiens

2016-03-10 | GSE78158 | GEO

The C-terminus of p53 Confers Liver-Specific Gene Regulation and Radio-Resistance in vivo [ChIP-seq]

PRJNA841669 | ENA

Mutations of the histone linker H1-4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1.4