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ATPase, class VI, type 11B

P-type ATPases, such as ATP11B, are phosphorylated in their intermediate state and drive uphill transport of ions across membranes. Several subfamilies of P-type ATPases have been identified. One subfamily transports heavy metal ions, such as Cu(2+) or Cd(2+). Another subfamily transports non-heavy metal ions, such as H(+), Na(+), K(+), or Ca(+). A third subfamily transports amphipaths, such as phosphatidylserine.[supplied by OMIM, Feb 2005] (from NCBI)
Top mentioned proteins: ATPase, Sox2, Atp10d, POLYMERASE, FGFR2
Papers on ATP11B
Fractal circuit sensors enable rapid quantification of biomarkers for donor lung assessment for transplantation.
Kelley et al., Toronto, Canada. In Sci Adv, Aug 2015
Using fractal circuit sensors (FraCS), three-dimensional metal structures with large surface areas, we were able to rapidly (<20 min) and reproducibly quantify small differences in the expression of interleukin-6 (IL-6), IL-10, and ATP11B mRNA in donor lung biopsies.
ATP11B mediates platinum resistance in ovarian cancer.
Sood et al., Houston, United States. In J Clin Invest, 2013
Here, we report the discovery and characterization of the role of ATP11B, a P-type ATPase membrane protein, in cisplatin resistance.
ATP9B, a P4-ATPase (a putative aminophospholipid translocase), localizes to the trans-Golgi network in a CDC50 protein-independent manner.
Shin et al., Kyoto, Japan. In J Biol Chem, 2011
Here, we show that class 5 (ATP10A, ATP10B, and ATP10D) and class 6 (ATP11A, ATP11B, and ATP11C) P4-ATPases require CDC50 proteins, primarily CDC50A, for their exit from the endoplasmic reticulum (ER) and final subcellular localization.
Impact of human donor lung gene expression profiles on survival after lung transplantation: a case-control study.
Keshavjee et al., Toronto, Canada. In Am J Transplant, 2008
Our microarray analyses of the development set identified four significantly upregulated genes (ATP11B, FGFR2, EGLN1 and MCPH1) in the PGD samples.
Conservation of inter-protein binding sites in RUSH and RFBP, an ATP11B isoform.
Chilton et al., Lubbock, United States. In Mol Cell Endocrinol, 2008
Isoforms of RUSH interact with a RING-finger binding protein (RFBP), which is a splice variant of the Type IV P-type ATPase, ATP11B.
X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase.
Thakker et al., Oxford, United Kingdom. In Genomics, 2004
The colocalization of ATP11C with SOX3 and MCF2/DBL on Xq27 mirrors that of ATP11A with SOX1 and MCF2L on 13q34 and ATP11B with SOX2 on 3q26.
Reanalysis of ATP11B, a type IV P-type ATPase.
Williamson et al., Penn Hills, United States. In J Biol Chem, 2002
the region containing transmembrane domain 4, corresponding to exon 12, is present in the human homolog of the gene, ATP11B
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