Sequence anatomy of mitochondrial anion carriers

FEBS Lett. 2003 Jan 16;534(1-3):15-25. doi: 10.1016/s0014-5793(02)03779-1.

Abstract

Two hundred and eighty-four genes of eight eukaryotic genomes for mitochondrial anion carriers were sorted into 43 (+18 single protein) subfamilies. Subfamilies differ by the number, nature, and locations of charges and polar residues in the transmembrane alpha-helices. Consequently, these residues and the rarely unique residues of the matrix and cytosolic segments most likely determine the different molecular phenotypes (functions). 'Common ancestral hydrophilic segments' were found in matrix and cytosolic segments, with interchangeable polar residues. Thus the hydrophobic microstructures of hydrophilic carrier parts are supposed to predetermine structure/conformation, whereas polar and charged microstructures should predetermine function, namely in the transmembrane spanning alpha-helices.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Anion Transport Proteins / chemistry*
  • Anion Transport Proteins / genetics
  • Anion Transport Proteins / metabolism*
  • Conserved Sequence
  • Cytosol / metabolism
  • Humans
  • Mitochondria / metabolism*
  • Protein Conformation
  • Protein Structure, Tertiary
  • Sequence Analysis, Protein

Substances

  • Anion Transport Proteins