A large family of endosome-localized proteins related to sorting nexin 1

Biochem J. 2001 Aug 15;358(Pt 1):7-16. doi: 10.1042/0264-6021:3580007.


Sorting nexin 1 (SNX1), a peripheral membrane protein, has previously been shown to regulate the cell-surface expression of the human epidermal growth factor receptor [Kurten, Cadena and Gill (1996) Science 272, 1008-1010]. Searches of human expressed sequence tag databases with SNX1 revealed eleven related human cDNA sequences, termed SNX2 to SNX12, eight of them novel. Analysis of SNX1-related sequences in the Saccharomyces cerevisiae genome clearly shows a greatly expanded SNX family in humans in comparison with yeast. On the basis of the predicted protein sequences, all members of this family of hydrophilic molecules contain a conserved 70-110-residue Phox homology (PX) domain, referred to as the SNX-PX domain. Within the SNX family, subgroups were identified on the basis of the sequence similarities of the SNX-PX domain and the overall domain structure of each protein. The members of one subgroup, which includes human SNX1, SNX2, SNX4, SNX5 and SNX6 and the yeast Vps5p and YJL036W, all contain coiled-coil regions within their large C-terminal domains and are found distributed in both membrane and cytosolic fractions, typical of hydrophilic peripheral membrane proteins. Localization of the human SNX1 subgroup members in HeLa cells transfected with the full-length cDNA species revealed a similar intracellular distribution that in all cases overlapped substantially with the early endosome marker, early endosome autoantigen 1. The intracellular localization of deletion mutants and fusions with green fluorescent protein showed that the C-terminal regions of SNX1 and SNX5 are responsible for their endosomal localization. On the basis of these results, the functions of these SNX molecules are likely to be unique to endosomes, mediated in part by interactions with SNX-specific C-terminal sequences and membrane-associated determinants.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Anticoagulants / pharmacology
  • Autoantigens / chemistry
  • Blotting, Northern
  • Carrier Proteins / chemistry*
  • Carrier Proteins / metabolism*
  • Cell Line
  • Cell Membrane / metabolism
  • Cytosol / metabolism
  • DNA / metabolism
  • DNA, Complementary / metabolism
  • Databases, Factual
  • Dextrans / pharmacology
  • Endosomes / metabolism*
  • Expressed Sequence Tags
  • Gene Deletion
  • Gene Library
  • Genome, Fungal
  • Green Fluorescent Proteins
  • HeLa Cells
  • Humans
  • Luminescent Proteins / chemistry
  • Luminescent Proteins / metabolism
  • Microscopy, Fluorescence
  • Molecular Sequence Data
  • Multigene Family
  • Mutation
  • Phenotype
  • Phylogeny
  • Protein Structure, Tertiary
  • Protein Transport
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / metabolism
  • Saccharomyces cerevisiae / chemistry
  • Saccharomyces cerevisiae / metabolism
  • Sequence Homology, Amino Acid
  • Sorting Nexins
  • Subcellular Fractions / metabolism
  • Tissue Distribution
  • Transfection
  • Vesicular Transport Proteins*


  • Anticoagulants
  • Autoantigens
  • Carrier Proteins
  • DNA, Complementary
  • Dextrans
  • Luminescent Proteins
  • Recombinant Fusion Proteins
  • SNX4 protein, human
  • SNX5 protein, human
  • SNX6 protein, human
  • Sorting Nexins
  • Vesicular Transport Proteins
  • Green Fluorescent Proteins
  • DNA