Zobrazeno 1 - 10
of 114
pro vyhledávání: '"Angel L Pey"'
Autor:
Tomas Majtan, Angel L Pey, Roberto Fernández, José A Fernández, Luis A Martínez-Cruz, Jan P Kraus
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e105290 (2014)
Cystathionine beta-synthase (CBS) is a key regulator of sulfur amino acid metabolism diverting homocysteine, a toxic intermediate of the methionine cycle, via the transsulfuration pathway to the biosynthesis of cysteine. Although the pathway itself i
Externí odkaz:
https://doaj.org/article/beefd4db48e5421f9ab4d2d652de855e
Autor:
Noel Mesa-Torres, Israel Fabelo-Rosa, Debora Riverol, Cristina Yunta, Armando Albert, Eduardo Salido, Angel L Pey
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e71963 (2013)
Primary hyperoxaluria type I (PH1) is a conformational disease which result in the loss of alanine:glyoxylate aminotransferase (AGT) function. The study of AGT has important implications for protein folding and trafficking because PH1 mutants may cau
Externí odkaz:
https://doaj.org/article/c2378c142dc74d4a8ba7001559ea2f89
Autor:
Khanh K Dao, Angel L Pey, Anja Underhaug Gjerde, Knut Teigen, In-Ja L Byeon, Stein O Døskeland, Angela M Gronenborn, Aurora Martinez
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e17602 (2011)
BackgroundThe regulatory subunit (R) of cAMP-dependent protein kinase (PKA) is a modular flexible protein that responds with large conformational changes to the binding of the effector cAMP. Considering its highly dynamic nature, the protein is rathe
Externí odkaz:
https://doaj.org/article/31c7d72bd67e4781abe6317a5e2de01e
Autor:
Angel L. Pey
Publikováno v:
Antioxidants, Vol 12, Iss 2, p 379 (2023)
Human NAD(P)H:quinone oxidoreductase 1 (hNQO1) is a multifunctional and antioxidant stress protein whose expression is controlled by the Nrf2 signaling pathway. hNQO1 dysregulation is associated with cancer and neurological disorders. Recent works ha
Externí odkaz:
https://doaj.org/article/d5e27112ffc341cc9961c2f71c48b499
Publikováno v:
Molecules, Vol 27, Iss 24, p 8762 (2022)
The mutations G170R and I244T are the most common disease cause in primary hyperoxaluria type I (PH1). These mutations cause the misfolding of the AGT protein in the minor allele AGT-LM that contains the P11L polymorphism, which may affect the foldin
Externí odkaz:
https://doaj.org/article/70acc055b13a40a58a70307115ca250f
Autor:
Juan Luis Pacheco‐García, Ernesto Anoz‐Carbonell, Dmitry S. Loginov, Daniel Kavan, Eduardo Salido, Petr Man, Milagros Medina, Angel L. Pey
Publikováno v:
The FEBS Journal. 290:1855-1873
Our knowledge on the genetic diversity of the human genome is exponentially growing. However, our capacity to establish genotype–phenotype correlations on a large scale requires a combination of detailed experimental and computational work. This is
Autor:
Juan Luis Pacheco-García, Dmitry S. Loginov, Athi N. Naganathan, Pavla Vankova, Mario Cano-Muñoz, Petr Man, Angel L. Pey
Phosphoglycerate kinase has been a model for the stability, folding cooperativity and catalysis of a two-domain protein. The human isoform 1 (hPGK1) is associated with cancer development and rare genetic diseases that affect several of its features.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::885223ee7bd98a2a21a5e22646fb39b6
https://doi.org/10.21203/rs.3.rs-1945879/v1
https://doi.org/10.21203/rs.3.rs-1945879/v1
Autor:
Juan Luis Pacheco-García, Dmitry S. Loginov, Athi N. Naganathan, Pavla Vankova, Mario Cano-Muñoz, Petr Man, Angel L. Pey
Publikováno v:
Scientific reports. 12(1)
Phosphoglycerate kinase has been a model for the stability, folding cooperativity and catalysis of a two-domain protein. The human isoform 1 (hPGK1) is associated with cancer development and rare genetic diseases that affect several of its features.
Autor:
Juan Luis Pacheco-Garcia, Dmitry S. Loginov, Ernesto Anoz-Carbonell, Pavla Vankova, Rogelio Palomino-Morales, Eduardo Salido, Petr Man, Milagros Medina, Athi N. Naganathan, Angel L. Pey
Publikováno v:
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Zaguán. Repositorio Digital de la Universidad de Zaragoza
Antioxidants; Volume 11; Issue 6; Pages: 1110
instname
Zaguán. Repositorio Digital de la Universidad de Zaragoza
Antioxidants; Volume 11; Issue 6; Pages: 1110
Allosterism is a common phenomenon in protein biochemistry that allows rapid regulation of protein stability; dynamics and function. However, the mechanisms by which allosterism occurs (by mutations or post-translational modifications (PTMs)) may be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::633b41dc901b7e71eff751e94b9e07ac
http://hdl.handle.net/10481/75923
http://hdl.handle.net/10481/75923
Autor:
María Esther Fárez-Vidal, José L. Neira, Angel L. Pey, Bruno Rizzuti, Juan L. Iovanna, Patricia Santofimia-Castaño
Publikováno v:
International Journal of Biological Macromolecules. 170:549-560
Plakophilin 1 (PKP1), a member of the armadillo repeat family of proteins, is a scaffold component of desmosomes, which are key structural components for cell-cell adhesion. However, PKP1 can be also found in the nucleus of several cells. NUPR1 is an