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Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth Syndrome
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scholarly article
1 reference
stated in
PubMed
PubMed ID
16135531
retrieved
1 December 2016
title
Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth Syndrome
(English)
1 reference
stated in
PubMed
PubMed ID
16135531
retrieved
1 December 2016
main subject
cell biology
0 references
Lysophosphatidylcholine acyltransferase YPR140W
1 reference
stated in
GOA release 2020-03-11
mitochondrion
1 reference
based on heuristic
inferred from title
membrane protein
1 reference
based on heuristic
inferred from title
Barth syndrome
1 reference
based on heuristic
inferred from title
author
Chris Meisinger
series ordinal
5
0 references
Peter Rehling
series ordinal
6
0 references
David U Mick
object named as
David U Mick
series ordinal
2
0 references
author name string
Katrin Brandner
series ordinal
1
0 references
Ann E Frazier
series ordinal
3
0 references
Rebecca D Taylor
series ordinal
4
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language of work or name
English
0 references
publication date
November 2005
0 references
published in
Molecular Biology of the Cell
1 reference
stated in
PubMed
PubMed ID
16135531
retrieved
1 December 2016
volume
16
0 references
page(s)
5202-14
0 references
issue
11
0 references
cites work
Ypr140wp, 'the yeast tafazzin', displays a mitochondrial lysophosphatidylcholine (lyso-PC) acyltransferase activity related to triacylglycerol and mitochondrial lipid synthesis
1 reference
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PubMed Central
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The human TAZ gene complements mitochondrial dysfunction in the yeast taz1Delta mutant. Implications for Barth syndrome
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PubMed Central
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Pam16 has an essential role in the mitochondrial protein import motor
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PubMed Central
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Evolutionary conservation of biogenesis of beta-barrel membrane proteins
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20 March 2017
Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndrome.
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PubMed Central
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A J-protein is an essential subunit of the presequence translocase-associated protein import motor of mitochondria
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The proteome of Saccharomyces cerevisiae mitochondria
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An essential role of Sam50 in the protein sorting and assembly machinery of the mitochondrial outer membrane
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Only one splice variant of the human TAZ gene encodes a functional protein with a role in cardiolipin metabolism
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PubMed Central
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Machinery for protein sorting and assembly in the mitochondrial outer membrane
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Protein insertion into the mitochondrial inner membrane by a twin-pore translocase
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Crystal structure of the yeast cytochrome bc1 complex with its bound substrate cytochrome c
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Multistep assembly of the protein import channel of the mitochondrial outer membrane.
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Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome
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Absence of cardiolipin in the crd1 null mutant results in decreased mitochondrial membrane potential and reduced mitochondrial function
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20 March 2017
Supercomplexes in the respiratory chains of yeast and mammalian mitochondria
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20 March 2017
Biogenesis of Tim proteins of the mitochondrial carrier import pathway: differential targeting mechanisms and crossing over with the main import pathway
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Yeast mitochondrial F1F0-ATP synthase exists as a dimer: identification of three dimer-specific subunits
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20 March 2017
The Tim core complex defines the number of mitochondrial translocation contact sites and can hold arrested preproteins in the absence of matrix Hsp70-Tim44.
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20 March 2017
Barth syndrome may be due to an acyltransferase deficiency
1 reference
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PubMed Central
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20 March 2017
Tom5 functionally links mitochondrial preprotein receptors to the general import pore.
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20 March 2017
Subunit VIa of yeast cytochrome c oxidase is not necessary for assembly of the enzyme complex but modulates the enzyme activity. Isolation and characterization of the nuclear-coded gene
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A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae
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20 March 2017
Epitope tagging of yeast genes using a PCR-based strategy: more tags and improved practical routines
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X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update
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A novel X-linked gene, G4.5. is responsible for Barth syndrome
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PubMed Central
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20 March 2017
Cardiolipins and biomembrane function
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20 March 2017
Cardiolipin stabilizes respiratory chain supercomplexes
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Mitochondrial respiratory-chain diseases
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7 April 2017
The biosynthesis and functional role of cardiolipin
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7 April 2017
Protein import into mitochondria
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7 April 2017
Cardiolipin is essential for organization of complexes III and IV into a supercomplex in intact yeast mitochondria
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29 September 2017
Biogenesis of cytochrome oxidase-sophisticated assembly lines in the mitochondrial inner membrane
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29 September 2017
Assembling the mitochondrial outer membrane
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New developments in mitochondrial assembly
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Mitochondrial import and the twin-pore translocase
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29 September 2017
Cell biology of cardiac mitochondrial phospholipids
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29 September 2017
Biogenesis of the protein import channel Tom40 of the mitochondrial outer membrane: intermembrane space components are involved in an early stage of the assembly pathway
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29 September 2017
The Tim8-Tim13 complex of Neurospora crassa functions in the assembly of proteins into both mitochondrial membranes
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Mitochondrial import of the ADP/ATP carrier: the essential TIM complex of the intermembrane space is required for precursor release from the TOM complex
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29 September 2017
Gluing the respiratory chain together. Cardiolipin is required for supercomplex formation in the inner mitochondrial membrane
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29 September 2017
Protein import into and across the mitochondrial inner membrane: role of the TIM23 and TIM22 translocons
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29 September 2017
Assembly of cytochrome c oxidase: what can we learn from patients with cytochrome c oxidase deficiency?
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Membrane potential-driven protein import into mitochondria. The sorting sequence of cytochrome b(2) modulates the deltapsi-dependence of translocation of the matrix-targeting sequence
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29 September 2017
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29 September 2017
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.
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29 September 2017
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29 September 2017
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29 September 2017
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2 June 2018
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27 November 2018
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27 November 2018
Assaying protein import into mitochondria
1 reference
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PubMed
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retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Transport into mitochondria and intramitochondrial sorting of the Fe/S protein of ubiquinol-cytochrome c reductase
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16135531
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16135531
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)-MIM 302060
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16135531
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1091/MBC.E05-03-0256
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4744170
OpenCitations bibliographic resource ID
4744170
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4744170
PMCID
1266419
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4744170
PubMed ID
16135531
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4744170
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