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PMID: 12191769 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Mitochondrial processing peptidases.

Biochimica et biophysica acta ·Vol. 1592 ·No. 1 ·2002-09-02 ·Pages 63-77

Gakh O, Cavadini P, Isaya G

Abstract

Three peptidases are responsible for the proteolytic processing of both nuclearly and mitochondrially encoded precursor polypeptides targeted to the various subcompartments of the mitochondria. Mitochondrial processing peptidase (MPP) cleaves the vast majority of mitochondrial proteins, while inner membrane peptidase (IMP) and mitochondrial intermediate peptidase (MIP) process specific subsets of precursor polypeptides. All three enzymes are structurally and functionally conserved across species, and their human homologues begin to be recognized as potential players in mitochondrial disease.

MeSH Terms
Amino Acid Sequence Animals Binding Sites Escherichia coli Humans Intracellular Membranes/enzymology Metalloendopeptidases/chemistry,genetics,metabolism Mitochondria/enzymology Mitochondrial Proteins/chemistry,metabolism Molecular Sequence Data Phylogeny Protein Precursors/metabolism Saccharomyces cerevisiae Sequence Alignment Structure-Activity Relationship Substrate Specificity
Chemicals
Mitochondrial Proteins Protein Precursors Metalloendopeptidases mitochondrial intermediate peptidase mitochondrial processing peptidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Gakh Oleksandr
Departments of Pediatric & Adolescent Medicine and Biochemistry & Molecular Biology, Mayo Clinic and Foundation, 200 First Street SW, Stabile 7-48, Rochester, MN 55905, USA.
Cavadini Patrizia
Isaya Grazia
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
2002-09-02
Pages
63-77
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
Grants
NIA NIH HHS · AG15709 · United States
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