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Pam16 has an essential role in the mitochondrial protein import motor
- Source :
- Nature Structural & Molecular Biology. 11:226-233
- Publication Year :
- 2004
- Publisher :
- Springer Science and Business Media LLC, 2004.
-
Abstract
- Mitochondrial preproteins destined for the matrix are translocated by two channel-forming transport machineries, the translocase of the outer membrane and the presequence translocase of the inner membrane. The presequence translocase-associated protein import motor (PAM) contains four essential subunits: the matrix heat shock protein 70 (mtHsp70) and its three cochaperones Mge1, Tim44 and Pam18. Here we report that the PAM contains a fifth essential subunit, Pam16 (encoded by Saccharomyces cerevisiae YJL104W), which is selectively required for preprotein translocation into the matrix, but not for protein insertion into the inner membrane. Pam16 interacts with Pam18 and is needed for the association of Pam18 with the presequence translocase and for formation of a mtHsp70-Tim44 complex. Thus, Pam16 is a newly identified type of motor subunit and is required to promote a functional PAM reaction cycle, thereby driving preprotein import into the matrix.
- Subjects :
- Saccharomyces cerevisiae Proteins
Translocase of the outer membrane
Protein subunit
Mitochondrial Membrane Transport Proteins
Mitochondrial Proteins
Mitochondrial membrane transport protein
Structural Biology
Yeasts
Mitochondrial Precursor Protein Import Complex Proteins
Translocase
Inner membrane
HSP70 Heat-Shock Proteins
Protein Precursors
Molecular Biology
biology
Membrane transport protein
Molecular Motor Proteins
Membrane Proteins
Membrane Transport Proteins
Intracellular Membranes
Mitochondria
Cell biology
Transport protein
Protein Transport
Translocase of the inner membrane
biology.protein
Carrier Proteins
Protein Binding
Subjects
Details
- ISSN :
- 15459985 and 15459993
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- Nature Structural & Molecular Biology
- Accession number :
- edsair.doi.dedup.....f9083239ad7a2759ff53278ba67107e0
- Full Text :
- https://doi.org/10.1038/nsmb735