Zobrazeno 1 - 10
of 8 148
pro vyhledávání: '"Membrane Transport Protein"'
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Externí odkaz:
https://doaj.org/article/91faa785b73c46f4aa6371775e73028f
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
The kidney is an important organ that maintains body fluid homeostasis in seawater and freshwater teleost fishes. Seawater teleosts excrete sulfate and magnesium in small amounts of isotonic urine, and freshwater teleosts excrete water in large amoun
Externí odkaz:
https://doaj.org/article/f4f1bd7be77e481e906e23bd121b9fb5
Autor:
Lyubomir Dimitrov Stanchev, Juliana Rizzo, Rebecca Peschel, Lilli A. Pazurek, Lasse Bredegaard, Sarina Veit, Sabine Laerbusch, Marcio L. Rodrigues, Rosa L. López-Marqués, Thomas Günther Pomorski
Publikováno v:
Journal of Fungi, Vol 7, Iss 10, p 843 (2021)
Lipid flippases of the P4-ATPase family are ATP-driven transporters that translocate lipids from the exoplasmic to the cytosolic leaflet of biological membranes. In the encapsulated fungal pathogen Cryptococcus neoformans, the P4-ATPase Apt1p is an i
Externí odkaz:
https://doaj.org/article/5d6bcff620d549f287656bfe50c80614
Autor:
January Weiner 3rd, Taco W.A. Kooij
Publikováno v:
Microbial Cell, Vol 3, Iss 10, Pp 511-521 (2016)
In order to combat the on-going malaria epidemic, discovery of new drug targets remains vital. Proteins that are essential to survival and specific to malaria parasites are key candidates. To survive within host cells, the parasites need to acquire n
Externí odkaz:
https://doaj.org/article/a0ed6842f2854ab6b5545ec73b138f84
Autor:
Irene Lopez-Fabuel, Marina Garcia-Macia, Costantina Buondelmonte, Olga Burmistrova, Nicolo Bonora, Paula Alonso-Batan, Brenda Morant-Ferrando, Carlos Vicente-Gutierrez, Daniel Jimenez-Blasco, Ruben Quintana-Cabrera, Emilio Fernandez, Jordi Llop, Pedro Ramos-Cabrer, Aseel Sharaireh, Marta Guevara-Ferrer, Lorna Fitzpatrick, Christopher D. Thompton, Tristan R. McKay, Stephan Storch, Diego L. Medina, Sara E. Mole, Peter O. Fedichev, Angeles Almeida, Juan P. Bolaños
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-14 (2022)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nature Communications
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nature Communications
CLN7 neuronal ceroid lipofuscinosis is an inherited lysosomal storage neurodegenerative disease highly prevalent in children. CLN7/MFSD8 gene encodes a lysosomal membrane glycoprotein, but the biochemical processes affected by CLN7-loss of function a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c646c3f91c4f2ae3f22b4ced9e7be27
https://doaj.org/article/3a651b3190b84e729467d309cc661713
https://doaj.org/article/3a651b3190b84e729467d309cc661713
Autor:
Apsley, Abner T., Domico, Emma R., Verbiest, Max A., Brogan, Carly A., Buck, Evan R., Burich, Andrew J., Cardone, Kathleen M., Stone, Wesley J., Anisimova, Maria, Vandenbergh, David J.
The dopamine transporter gene, SLC6A3, has received substantial attention in genetic association studies of various phenotypes. Although some variable number tandem repeats (VNTRs) present in SLC6A3 have been tested in genetic association studies, re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5595b553fa59d3c358dcb2b01b5a96a
https://hdl.handle.net/11475/27409
https://hdl.handle.net/11475/27409
Autor:
David R. Thorburn, Yilin Kang, Kenji M Fujihara, Catherine S Palmer, Yau C Low, Ann E. Frazier, Nicholas J. Clemons, Daniella H Hock, David A. Stroud, Thomas Daniel Jackson, Diana Stojanovski, Ching-Seng Ang
Publikováno v:
Molecular Biology of the Cell
Acylglycerol kinase (AGK) is a mitochondrial lipid kinase that contributes to protein biogenesis as a subunit of the TIM22 complex at the inner mitochondrial membrane. Mutations in AGK cause Sengers syndrome, an autosomal recessive condition characte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccccafba6ad7a0d2d6f285b01db97d16
https://doi.org/10.1091/mbc.e20-06-0390
https://doi.org/10.1091/mbc.e20-06-0390
Expression of L-type amino acid transporter 1 is a poor prognostic factor for Non-Hodgkin’s lymphoma
Autor:
Atsushi Kurata, Akihiko Gotoh, Masakatsu Takanashi, Masahiko Kuroda, Keiki Oikawa, Jun Matsubayashi, Kohsuke Kanekura, Toshitaka Nagao, Koji Fujita, Daigo Akahane, Narangerel Jigjidkhorloo, Oyundelger Norov, Hitoshi Endou
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Scientific Reports
Scientific Reports
L-type neutral amino acid transporter 1 (LAT1) is a heterodimeric membrane transport protein involved in neutral amino acid transport. LAT1 is highly expressed in various malignant solid tumors and plays an essential role in cell proliferation. Howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e310310b3994aaafec3f03fff4b4794d
https://doaj.org/article/254f7aaec22f4688a7954b03fd1e965b
https://doaj.org/article/254f7aaec22f4688a7954b03fd1e965b
Publikováno v:
Dyla, M, Kjærgaard, M, Poulsen, H & Nissen, P 2020, ' Structure and Mechanism of P-Type ATPase Ion Pumps ', Annual Review of Biochemistry, vol. 89, pp. 583-603 . https://doi.org/10.1146/annurev-biochem-010611-112801
P-type ATPases are found in all kingdoms of life and constitute a wide range of cation transporters, primarily for H+, Na+, K+, Ca2+, and transition metal ions such as Cu(I), Zn(II), and Cd(II). They have been studied through a wide range of techniqu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::669051c51d2cc4e4d48f49c2e5fc340c
https://doi.org/10.1146/annurev-biochem-010611-112801
https://doi.org/10.1146/annurev-biochem-010611-112801