-
Peroxins (or peroxisomal/peroxisome
biogenesis factors)
represent several protein families found in peroxisomes.
Deficiencies are ****ociated with several...
-
Peroxin-7 is a
receptor ****ociated with Refsum's
disease and
rhizomelic chondrodysplasia punctata type 1.
Peroxin GeneReviews/NCBI/NIH/UW
entry on Refsum...
-
called peroxins,
which parti****te in the
process of
peroxisome ****embly in
different organisms. In
mammalian cells,
there are 13
characterized peroxins. In...
- due to
defects in
single enzymes important for
peroxisome function or in
peroxins,
proteins encoded by PEX
genes that are
critical for
normal peroxisome...
-
autosomal recessive disorder caused by
mutations in
genes that
encode peroxins,
proteins required for the
normal ****embly of peroxisomes. Most commonly...
- tissues. This may be due to
deficiencies of phytanoyl-CoA
hydroxylase or
peroxin-7 activity,
encoded by the
genes PHYH and PEX7, respectively. In general...
- PMID 11865044.
Okumoto K, Abe I,
Fujiki Y (Aug 2000). "Molecular
anatomy of the
peroxin Pex12p: ring
finger domain is
essential for Pex12p
function and interacts...
- Heat
shock proteins Heat
shock factor Ion
channels Membrane-spanning 4A
Peroxin Protocadherin gene
family Roundabout family SNARE family Protein family...
- to
pathogenic mutations in at
least 13
different PEX
genes that
encode peroxins. It
affects the peroxisomes,
which are
organelles in the body that are...
-
matrix is
dependent upon
binding to
another cytosolic protein called pex5 (
peroxin 5). Once bound, pex5
interacts with a
peroxisomal membrane protein pex14...
