Tripartite Motif Proteins

"Tripartite Motif Proteins" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

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A protein family defined by the presence of three ZINC FINGER domains, one of which is a RING FINGER DOMAIN, a coiled-coil region, and a highly variable C-terminal region. They function in many cellular processes including APOPTOSIS and CELL CYCLE regulation.

Descriptor ID	D000070584
MeSH Number(s)	D12.776.934
Concept/Terms	Tripartite Motif Proteins Tripartite Motif Proteins Motif Proteins, Tripartite Proteins, Tripartite Motif RBCC Proteins Proteins, RBCC RBCC Protein Family Family, RBCC Protein Protein Family, RBCC TRIM Protein Family Family, TRIM Protein Protein Family, TRIM TRIM Proteins Proteins, TRIM

Below are MeSH descriptors whose meaning is more general than "Tripartite Motif Proteins".

Chemicals and Drugs [D]
Amino Acids, Peptides, and Proteins [D12]
Proteins [D12.776]
Tripartite Motif Proteins [D12.776.934]

Below are MeSH descriptors whose meaning is related to "Tripartite Motif Proteins".

Below are MeSH descriptors whose meaning is more specific than "Tripartite Motif Proteins".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Tripartite Motif Proteins" by people in this website by year, and whether "Tripartite Motif Proteins" was a major or minor topic of these publications.

Bar chart showing 7 publications over 6 distinct years, with a maximum of 2 publications in 2011

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2008	0	1	1
2009	0	1	1
2011	0	2	2
2013	0	1	1
2015	0	1	1
2020	1	0	1

Below are the most recent publications written about "Tripartite Motif Proteins" by people in Profiles.

Huang X, Li Y, Li X, Fan D, Xin HB, Fu M. TRIM14 promotes endothelial activation via activating NF-?B signaling pathway. J Mol Cell Biol. 2020 04 24; 12(3):176-189.

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Tseng YC, Kulp SK, Lai IL, Hsu EC, He WA, Frankhouser DE, Yan PS, Mo X, Bloomston M, Lesinski GB, Marcucci G, Guttridge DC, Bekaii-Saab T, Chen CS. Preclinical Investigation of the Novel Histone Deacetylase Inhibitor AR-42 in the Treatment of Cancer-Induced Cachexia. J Natl Cancer Inst. 2015 Dec; 107(12):djv274.

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Rubel CE, Schisler JC, Hamlett ED, DeKroon RM, Gautel M, Alzate O, Patterson C. Diggin' on u(biquitin): a novel method for the identification of physiological E3 ubiquitin ligase substrates. Cell Biochem Biophys. 2013 Sep; 67(1):127-38.

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Powers SK, Hudson MB, Nelson WB, Talbert EE, Min K, Szeto HH, Kavazis AN, Smuder AJ. Mitochondria-targeted antioxidants protect against mechanical ventilation-induced diaphragm weakness. Crit Care Med. 2011 Jul; 39(7):1749-59.

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Shadfar S, Couch ME, McKinney KA, Weinstein LJ, Yin X, Rodríguez JE, Guttridge DC, Willis M. Oral resveratrol therapy inhibits cancer-induced skeletal muscle and cardiac atrophy in vivo. Nutr Cancer. 2011; 63(5):749-62.

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Uchiki T, Kim HT, Zhai B, Gygi SP, Johnston JA, O'Bryan JP, Goldberg AL. The ubiquitin-interacting motif protein, S5a, is ubiquitinated by all types of ubiquitin ligases by a mechanism different from typical substrate recognition. J Biol Chem. 2009 May 08; 284(19):12622-32.

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Cannon T, Shores C, Yin X, Dahlman J, Guttridge D, Lai V, George J, Buzkova P, Couch M. Immunocompetent murine model of cancer cachexia for head and neck squamous cell carcinoma. Head Neck. 2008 Mar; 30(3):320-6.

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