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Estrada-Mondragon, Argel
Publications (2 of 2) Show all publications
Téllez-Arreola, J. L., Martínez-Torres, A., Flores-Moran, A. E., Lazaro-Guevara, J. M. & Estrada-Mondragon, A. (2022). Analysis of the MCTP Amino Acid Sequence Reveals the Conservation of Putative Calcium- and Lipid-Binding Pockets Within the C2 Domains In Silico. Journal of Molecular Evolution, 90, 271-282
Open this publication in new window or tab >>Analysis of the MCTP Amino Acid Sequence Reveals the Conservation of Putative Calcium- and Lipid-Binding Pockets Within the C2 Domains In Silico
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2022 (English)In: Journal of Molecular Evolution, ISSN 0022-2844, E-ISSN 1432-1432, Vol. 90, p. 271-282Article in journal (Refereed) Published
Abstract [en]

MCTPs (Multiple C2 Domains and Transmembrane region Proteins) are evolutionarily and structurally related to other C2 proteins, which are central to exocytosis and membrane trafficking; however, their specific function has been little studied. MCTPs are associated with endosomes and the endoplasmic reticulum and possess three C2 domains (C2A-C2C) and two transmembrane regions (TMRs) well conserved in different species. Here, we generated structural models of the MCTP C2 domains of C. elegans and analyzed their putative function by docking, which revealed that these domains possess Ca2+- and lipid-binding pockets, suggesting that MCTPs play a significant, calcium-dependent role in membrane physiology.

Place, publisher, year, edition, pages
New York, NY, United States: Springer, 2022
Keywords
C2 domain; Calcium signaling; Docking; Membrane traffic
National Category
Biochemistry Molecular Biology
Identifiers
urn:nbn:se:liu:diva-185340 (URN)10.1007/s00239-022-10057-1 (DOI)000800968000001 ()35604448 (PubMedID)2-s2.0-85130527263 (Scopus ID)
Note

Funding: CONACYT [A1-S-7659, 395834]; PAPIIT-UNAM [IN204520]

Available from: 2022-05-26 Created: 2022-05-26 Last updated: 2025-02-20Bibliographically approved
Rosas-Arellano, A., Estrada-Mondragon, A., Pina, R., Mantellero, C. A. & Castro, M. A. (2018). The Tiny Drosophila Melanogaster for the Biggest Answers in Huntingtons Disease. International Journal of Molecular Sciences, 19(8), Article ID 2398.
Open this publication in new window or tab >>The Tiny Drosophila Melanogaster for the Biggest Answers in Huntingtons Disease
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2018 (English)In: International Journal of Molecular Sciences, ISSN 1661-6596, E-ISSN 1422-0067, Vol. 19, no 8, article id 2398Article, review/survey (Refereed) Published
Abstract [en]

The average life expectancy for humans has increased over the last years. However, the quality of the later stages of life is low and is considered a public health issue of global importance. Late adulthood and the transition into the later stage of life occasionally leads to neurodegenerative diseases that selectively affect different types of neurons and brain regions, producing motor dysfunctions, cognitive impairment, and psychiatric disorders that are progressive, irreversible, without remission periods, and incurable. Huntingtons disease (HD) is a common neurodegenerative disorder. In the 25 years since the mutation of the huntingtin (HTT) gene was identified as the molecule responsible for this neural disorder, a variety of animal models, including the fruit fly, have been used to study the disease. Here, we review recent research that used Drosophila as an experimental tool for improving knowledge about the molecular and cellular mechanisms underpinning HD.

Place, publisher, year, edition, pages
MDPI, 2018
Keywords
neurodegenerative diseases; IT15; LOMARS; HTT; HD; huntingtin; mHTT; polyQ; polyglutamine disorders; chorea; neostriatum; fruit fly
National Category
Neurology
Identifiers
urn:nbn:se:liu:diva-151801 (URN)10.3390/ijms19082398 (DOI)000442869800250 ()30110961 (PubMedID)
Note

Funding Agencies|FONDECYT [1151206]; RING-CONICYT [ACT1401]

Available from: 2018-10-04 Created: 2018-10-04 Last updated: 2022-02-10
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