about
P527
P688
Targeting of the tail-anchored peroxisomal membrane proteins PEX26 and PEX15 occurs through C-terminal PEX19-binding sitesMutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complexAnalysis of human Pex19p's domain structure by pentapeptide scanning mutagenesisAlternative splicing suggests extended function of PEX26 in peroxisome biogenesis.
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in Peroxisomal biogenesis factor 26
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Peroxisomal biogenesis factor 26
@en
type
label
Peroxisomal biogenesis factor 26
@en
altLabel
PEX26
@en
peroxin-26
@en
peroxisome assembly protein 26
@en
peroxisome biogenesis disorder, complementation group 8
@en
peroxisome biogenesis disorder, complementation group A
@en
peroxisome biogenesis factor 26
@en
prefLabel
Peroxisomal biogenesis factor 26
@en
P637
P680
P681
P682
P705
P352
P31
P352
P637
NP_001121121
NP_001186248
P681
P682
P702
P703
P705
ENSP00000331106
ENSP00000382648
ENSP00000412441
ENSP00000434235
ENSP00000482091
P7260
3.A.20.1.1