(Q28211318)

2

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N Mühlenbein

3

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S A Paschen

4

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K D Gerbitz

5

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W Neupert

6

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M Brunner

7

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M F Bauer

Journal of Biological Chemistry

8

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language of work or name

English

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publication date

5 October 2001

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published in

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volume

276

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page(s)

37327-34

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issue

40

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cites work

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Protein transport into mitochondria

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Protein translocation into mitochondria: the role of TIM complexes

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The MIM complex mediates preprotein translocation across the mitochondrial inner membrane and couples it to the mt-Hsp70/ATP driving system

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Import of carrier proteins into the mitochondrial inner membrane mediated by Tim22.

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Carrier protein import into mitochondria mediated by the intermembrane proteins Tim10/Mrs11 and Tim12/Mrs5.

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The Tim54p-Tim22p complex mediates insertion of proteins into the mitochondrial inner membrane

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Tim9p, an essential partner subunit of Tim10p for the import of mitochondrial carrier proteins

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Import of mitochondrial carriers mediated by essential proteins of the intermembrane space

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Role of Tim23 as voltage sensor and presequence receptor in protein import into mitochondria

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Tim23 links the inner and outer mitochondrial membranes.

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The TIM17.23 preprotein translocase of mitochondria: composition and function in protein transport into the matrix

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Tim9, a new component of the TIM22.54 translocase in mitochondria

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Transport of the ADP/ATP carrier of mitochondria from the TOM complex to the TIM22.54 complex

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Different import pathways through the mitochondrial intermembrane space for inner membrane proteins

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The mitochondrial TIM22 preprotein translocase is highly conserved throughout the eukaryotic kingdom

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Human deafness dystonia syndrome is a mitochondrial disease

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The human family of Deafness/Dystonia peptide (DDP) related mitochondrial import proteins

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The role of the TIM8-13 complex in the import of Tim23 into mitochondria

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Two intermembrane space TIM complexes interact with different domains of Tim23p during its import into mitochondria

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A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.

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A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndrome

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Analysis of molecular masses and oligomeric states of protein complexes by blue native electrophoresis and isolation of membrane protein complexes by two-dimensional native electrophoresis

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Blue native electrophoresis for isolation of membrane protein complexes in enzymatically active form

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An efficient mRNA-dependent translation system from reticulocyte lysates

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Translocation arrest of an intramitochondrial sorting signal next to Tim11 at the inner-membrane import site

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Mitochondrial import: crossing the aqueous intermembrane space

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