Peroxisomal biogenesis factor 16

Peroxisomal biogenesis factor 16

Item
http://www.wikidata.org/entity/Q21122505
PEX16
P688
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.Peroxisome synthesis in the absence of preexisting peroxisomesAnalysis of human Pex19p's domain structure by pentapeptide scanning mutagenesisRequirement for microtubules and dynein motors in the earliest stages of peroxisome biogenesisThe membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assemblyThe peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathwayPex3p-dependent peroxisomal biogenesis initiates in the endoplasmic reticulum of human fibroblastsSec16B is involved in the endoplasmic reticulum export of the peroxisomal membrane biogenesis factor peroxin 16 (Pex16) in mammalian cellsThe origin and maintenance of mammalian peroxisomes involves a de novo PEX16-dependent pathway from the ER
P921

Peroxisomal biogenesis factor 16

Item
http://www.wikidata.org/entity/Q21122505
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in Peroxisomal biogenesis factor 16
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Peroxisomal biogenesis factor 16
@en
type
label
Peroxisomal biogenesis factor 16
@en
altLabel
PEX16
@en
Peroxin-16
@en
peroxin 16
@en
peroxisomal biogenesis factor 16
@en
peroxisomal membrane protein PEX16
@en
peroxisome biogenesis factor 16
@en
prefLabel
Peroxisomal biogenesis factor 16
@en
P31
P352
P361
P637
P680
P681
P682
P702
P703
P705
P7260
P352
P637
P31
P352
P361
P637
P680
P681
P682
P702
P703
P705
P7260