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J Biol Chem
2003 Oct 17;27842:41114-25. doi: 10.1074/jbc.M306150200.
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Structure-function analysis of the bestrophin family of anion channels.
Tsunenari T
,
Sun H
,
Williams J
,
Cahill H
,
Smallwood P
,
Yau KW
,
Nathans J
.
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The bestrophins are a newly described family of anion channels unrelated in primary sequence to any previously characterized channel proteins. The human genome codes for four bestrophins, each of which confers a distinctive plasma membrane conductance on transfected 293 cells. Extracellular treatment with methanethiosulfonate ethyltrimethylammonium (MTSET) of a series of substitution mutants that eliminate one or more cysteines from human bestrophin1 demonstrates that cysteine 69 is the single endogenous cysteine responsible for MTSET inhibition of whole-cell current. Cysteines introduced between positions 78-99 and 223-226 are also accessible to external MTSET, with MTSET modification at positions 79, 80, 83, and 90 producing a 2-6-fold increase in whole-cell current. The latter set of four cysteine-substitution mutants define a region that appears to mediate allosteric control of channel activity. Mapping of transmembrane topography by insertion of N-linked glycosylation sites and tobacco etch virus protease cleavage sites provides evidence for cytosolic N and C termini and an unexpected transmembrane topography with at least three extracellular loops that include positions 60-63, 212-227, and 261-267. These experiments provide the first structural analysis of the bestrophin channel family.
Bakall,
The mutation spectrum of the bestrophin protein--functional implications.
1999, Pubmed
Bakall,
The mutation spectrum of the bestrophin protein--functional implications.
1999,
Pubmed
Betz,
Structure and functions of inhibitory and excitatory glycine receptors.
1999,
Pubmed
Carrington,
A viral cleavage site cassette: identification of amino acid sequences required for tobacco etch virus polyprotein processing.
1988,
Pubmed
Chang,
Mapping of cystic fibrosis transmembrane conductance regulator membrane topology by glycosylation site insertion.
1994,
Pubmed
Cunningham,
Cloning of an epithelial chloride channel from bovine trachea.
1995,
Pubmed
,
Xenbase
Deutman,
Electro-oculography in families with vitelliform dystrophy of the fovea. Detection of the carrier state.
1969,
Pubmed
Dutzler,
X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity.
2002,
Pubmed
Ellgaard,
Quality control in the endoplasmic reticulum.
2003,
Pubmed
Faber,
A novel method to determine the topology of peroxisomal membrane proteins in vivo using the tobacco etch virus protease.
2001,
Pubmed
François,
Electro-oculography in vitelliform degeneration of the macula.
1967,
Pubmed
Frangieh,
A histopathologic study of Best's macular dystrophy.
1982,
Pubmed
Gandhi,
Molecular and functional characterization of a calcium-sensitive chloride channel from mouse lung.
1998,
Pubmed
George,
From stones to bones: the biology of ClC chloride channels.
2001,
Pubmed
Ghosh,
Mannose 6-phosphate receptors: new twists in the tale.
2003,
Pubmed
Günther,
ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells.
1998,
Pubmed
Hirokawa,
SOSUI: classification and secondary structure prediction system for membrane proteins.
1998,
Pubmed
Hofmann,
PROFILEGRAPH: an interactive graphical tool for protein sequence analysis.
1992,
Pubmed
Illing,
The 220-kDa rim protein of retinal rod outer segments is a member of the ABC transporter superfamily.
1997,
Pubmed
Iyer,
A biological role for prokaryotic ClC chloride channels.
2002,
Pubmed
Janz,
Characterization of a brain-specific Sp1-like activity interacting with an unusual binding site within the myelin proteolipid protein promoter.
1993,
Pubmed
Jentsch,
Chloride channels: an emerging molecular picture.
1997,
Pubmed
Karlin,
Substituted-cysteine accessibility method.
1998,
Pubmed
Kyte,
A simple method for displaying the hydropathic character of a protein.
1982,
Pubmed
Leahy,
A mammalian expression vector for expression and purification of secreted proteins for structural studies.
2000,
Pubmed
Lotery,
Allelic variation in the VMD2 gene in best disease and age-related macular degeneration.
2000,
Pubmed
Lucast,
Large-scale purification of a stable form of recombinant tobacco etch virus protease.
2001,
Pubmed
Macke,
Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin.
1993,
Pubmed
Marchant,
Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophy.
2001,
Pubmed
Marmorstein,
Bestrophin interacts physically and functionally with protein phosphatase 2A.
2002,
Pubmed
Marmorstein,
Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium.
2000,
Pubmed
Marquardt,
Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease).
1998,
Pubmed
Mohler,
Long-term evaluation of patients with Best's vitelliform dystrophy.
1981,
Pubmed
Nathans,
Molecular genetics of human color vision: the genes encoding blue, green, and red pigments.
1986,
Pubmed
NULL,
Proceedings of the 6th International Conference on Intelligent Systems for Molecular Biology. Montreal, Quebec, Canada. June 28-July 1, 1998.
1998,
Pubmed
Petrukhin,
Identification of the gene responsible for Best macular dystrophy.
1998,
Pubmed
Popov,
Mapping the ends of transmembrane segments in a polytopic membrane protein. Scanning N-glycosylation mutagenesis of extracytosolic loops in the anion exchanger, band 3.
1997,
Pubmed
Rost,
Topology prediction for helical transmembrane proteins at 86% accuracy.
1996,
Pubmed
Stöhr,
Three novel human VMD2-like genes are members of the evolutionary highly conserved RFP-TM family.
2002,
Pubmed
Sun,
The vitelliform macular dystrophy protein defines a new family of chloride channels.
2002,
Pubmed
Turk,
Membrane topology of the human Na+/glucose cotransporter SGLT1.
1996,
Pubmed
,
Xenbase
Tusnády,
Principles governing amino acid composition of integral membrane proteins: application to topology prediction.
1998,
Pubmed
Tusnády,
The HMMTOP transmembrane topology prediction server.
2001,
Pubmed
Urabe,
A switching system regulating subcellular localization of nuclear proteins using a viral protease.
1999,
Pubmed
Weingeist,
Histopathology of Best's macular dystrophy.
1982,
Pubmed
White,
VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies.
2000,
Pubmed
Wisden,
GABAA receptor channels: from subunits to functional entities.
1992,
Pubmed
Yellen,
The voltage-gated potassium channels and their relatives.
2002,
Pubmed
Zelenski,
Membrane topology of S2P, a protein required for intramembranous cleavage of sterol regulatory element-binding proteins.
1999,
Pubmed
Zielenski,
Cystic fibrosis: genotypic and phenotypic variations.
1995,
Pubmed