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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Vps20-associated 1 homolog

LIP5, Vta1, SBP1, Vta1p
C6ORF55 encodes a protein involved in trafficking of the multivesicular body, an endosomal compartment involved in sorting membrane proteins for degradation in lysosomes (Ward et al., 2005 [PubMed 15644320]).[supplied by OMIM, Mar 2008] (from NCBI)
Top mentioned proteins: Vps4, ATPase, ACID, CAN, SBP2
Papers on LIP5
A Critical Role of Lyst-Interacting Protein5, a Positive Regulator of Multivesicular Body Biogenesis, in Plant Responses to Heat and Salt Stresses.
Chen et al., Hangzhou, China. In Plant Physiol, Sep 2015
We have recently shown that Arabidopsis (Arabidopsis thaliana) Lyst-Interacting Protein5 (LIP5), a positive regulator of the Suppressor of K(+) Transport Growth Defect1 (SKD1) AAA ATPase in MVB biogenesis, is a critical target of the mitogen-activated protein kinases MPK3 and MPK6 and plays an important role in the plant immune system.
Interactions between Plasmodium falciparum skeleton-binding protein 1 and the membrane skeleton of malaria-infected red blood cells.
Cooke et al., Australia. In Biochim Biophys Acta, Jul 2015
We have previously shown that a resident MC protein, skeleton-binding protein 1 (SBP1), is essential for the placement of PfEMP1 onto the RBC surface and hypothesised that the function of SBP1 may be to target MCs to the RBC membrane.
Chromosome VIII disomy influences the nonsense suppression efficiency and transition metal tolerance of the yeast Saccharomyces cerevisiae.
Inge-Vechtomov et al., Saint Petersburg, Russia. In Yeast, Jun 2015
We identified SBP1, a gene that localizes to chromosome VIII, as a dosage-dependent antisuppressor that strongly contributes to the overall antisuppressor effect of chromosome VIII disomy.
The subcellular location of selenoproteins and the impact on their function.
Diamond, Chicago, United States. In Nutrients, May 2015
Each of these proteins have been described to reside in two or more cellular compartments, and in the case of GPx-1 and SBP1, interact with each other.
Distinct mechanisms of recognizing endosomal sorting complex required for transport III (ESCRT-III) protein IST1 by different microtubule interacting and trafficking (MIT) domains.
Xu et al., Ann Arbor, United States. In J Biol Chem, Apr 2015
In mammalian cells, efficient abscission during cytokinesis requires proper function of the ESCRT-III protein IST1, which binds to the microtubule interacting and trafficking (MIT) domains of VPS4, LIP5, and Spartin via its C-terminal MIT-interacting motif (MIM).
A novel mechanism of regulating the ATPase VPS4 by its cofactor LIP5 and the endosomal sorting complex required for transport (ESCRT)-III protein CHMP5.
Xu et al., Ann Arbor, United States. In J Biol Chem, Apr 2015
This reaction is catalyzed by VPS4, an AAA-ATPase whose activity is tightly regulated by a host of proteins, including LIP5 and the ESCRT-III proteins.
Reduction of selenium-binding protein 1 sensitizes cancer cells to selenite via elevating extracellular glutathione: a novel mechanism of cancer-specific cytotoxicity of selenite.
Xiong et al., Wuhan, China. In Free Radic Biol Med, Feb 2015
This study was to investigate the roles of two distinct representatives of selenium-containing proteins, selenium-binding protein 1 (SBP1) and glutathione peroxidase 1 (GPX1), in selenite-mediated cancer-specific cytotoxicity.
Quantitative proteomic analysis reveals that anti-cancer effects of selenium-binding protein 1 in vivo are associated with metabolic pathways.
Bie et al., Nanjing, China. In Plos One, 2014
Previous studies have shown the tumor-suppressive role of selenium-binding protein 1 (SBP1), but the underlying mechanisms are unclear.
Evidence that selenium binding protein 1 is a tumor suppressor in prostate cancer.
Diamond et al., Chicago, United States. In Plos One, 2014
Selenium-Binding Protein 1 (SBP1, SELENBP1, hSP56) is a selenium-associated protein shown to be at lower levels in tumors, and its lower levels are frequently predictive of a poor clinical outcome.
A Critical Role for Cysteine 57 in the Biological Functions of Selenium Binding Protein-1.
Yang et al., Xinxiang, China. In Int J Mol Sci, 2014
The concentration of selenium-binding protein1 (SBP1) is often lower in tumors than in the corresponding tissue and lower levels have been associated with poor clinical outcomes.
Distribution and inhibition effect of Seleno-L-Methionine on 4T1 mouse mammary carcinoma.
Liu et al., Shanghai, China. In Int J Physiol Pathophysiol Pharmacol, 2014
SeMet supplement increased SBP1 expression and decreased GPx1 expression, and greatly inhibited VEGF expression and tumor immune suppression cells accumulation in tumor tissues.
Biochemical and biophysical characterization of the selenium-binding and reducing site in Arabidopsis thaliana homologue to mammals selenium-binding protein 1.
Hugouvieux et al., Grenoble, France. In J Biol Chem, 2014
The function of selenium-binding protein 1 (SBP1), present in almost all organisms, has not yet been established.
Molecular cross-talk between members of distinct families of selenium containing proteins.
Diamond et al., Chicago, United States. In Mol Nutr Food Res, 2014
One of these, selenium-binding protein 1 (SBP1), is a protein of unknown function that has been shown to be reduced in tumors of diverse tissue types as compared to the corresponding normal tissue.
Evaluation of cadmium-induced nephrotoxicity using urinary metabolomic profiles in sprague-dawley male rats.
Kim et al., Pusan, South Korea. In J Toxicol Environ Health A, 2013
High-dose CdCl2 (25 mg/kg) exposure also significantly elevated protein-based urinary biomarkers including osteopontin, monocyte chemoattractant protein-1 (MCP-1), kidney injury molecules-1 (Kim-1), and selenium-binding protein 1 (SBP1) in rat urine.
Functional and physical interaction between the selenium-binding protein 1 (SBP1) and the glutathione peroxidase 1 selenoprotein.
Yang et al., Chicago, United States. In Carcinogenesis, 2010
SP1 is present in reduced levels in several cancer types as compared with normal tissues, and lower levels are associated with poor clinical prognosis.
The lysosomal trafficking regulator interacting protein-5 localizes mainly in epithelial cells.
Deen et al., Nijmegen, Netherlands. In J Mol Histol, 2010
LIP5 protein expression in a mouse tissue panel and various rodent and human tissues were studied.[LIP5]
Cryo-EM structure of dodecameric Vps4p and its 2:1 complex with Vta1p.
Jensen et al., Pasadena, United States. In J Mol Biol, 2008
models in which Vps4p MIT and Vta1p domains engage endosomal sorting complex required for transport-III substrates above the bowl and help transfer them into the bowl to be pumped through the center of the dodecameric assembly
Structural basis of Vta1 function in the multivesicular body sorting pathway.
Xu et al., Ann Arbor, United States. In Dev Cell, 2008
mechanism of regulation by Vta1 in which the C-terminal domain stabilizes the ATP-dependent double ring assembly.
ESCRT-III family members stimulate Vps4 ATPase activity directly or via Vta1.
Katzmann et al., Rochester, United States. In Dev Cell, 2008
impact of Vta1 and ESCRT-III family members on Vps4 ATPase activity
Conservation of plasma regulatory proteins of the complement system in evolution: humans and fish.
Zipfel et al., Hamburg, Germany. In Exp Clin Immunogenet, 1999
The complement regulatory protein of barred sand bass, SBP1, is related to both the human alternative pathway regulator factor H, and to the classical pathway regulator C4bp, and displays regulatory activities in both human pathways.
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