Details for: PEX16
Associated with
Other Information
Genular Protein ID: 1670156209
Symbol: PEX16_HUMAN
Name: Peroxisomal membrane protein PEX16
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 9837814
Title: Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
PubMed ID: 9837814
DOI: 10.1086/302161
PubMed ID: 9922452
Title: Peroxisome synthesis in the absence of preexisting peroxisomes.
PubMed ID: 9922452
PubMed ID: 16554811
Title: Human chromosome 11 DNA sequence and analysis including novel gene identification.
PubMed ID: 16554811
DOI: 10.1038/nature04632
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 10704444
Title: PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis.
PubMed ID: 10704444
PubMed ID: 11390669
Title: Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences.
PubMed ID: 11390669
PubMed ID: 12223482
Title: The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly.
PubMed ID: 12223482
PubMed ID: 14709540
Title: PEX19 is a predominantly cytosolic chaperone and import receptor for class 1 peroxisomal membrane proteins.
PubMed ID: 14709540
PubMed ID: 16717127
Title: The origin and maintenance of mammalian peroxisomes involves a de novo PEX16-dependent pathway from the ER.
PubMed ID: 16717127
PubMed ID: 21768384
Title: Sec16B is involved in the endoplasmic reticulum export of the peroxisomal membrane biogenesis factor peroxin 16 (Pex16) in mammalian cells.
PubMed ID: 21768384
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
DOI: 10.1021/pr300630k
PubMed ID: 25944712
Title: N-terminome analysis of the human mitochondrial proteome.
PubMed ID: 25944712
PubMed ID: 20647552
Title: Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene.
PubMed ID: 20647552
Sequence Information:
- Length: 336
- Mass: 38629
- Checksum: 57243AEE0B165C59
- Sequence:
MEKLRLLGLR YQEYVTRHPA ATAQLETAVR GFSYLLAGRF ADSHELSELV YSASNLLVLL NDGILRKELR KKLPVSLSQQ KLLTWLSVLE CVEVFMEMGA AKVWGEVGRW LVIALVQLAK AVLRMLLLLW FKAGLQTSPP IVPLDRETQA QPPDGDHSPG NHEQSYVGKR SNRVVRTLQN TPSLHSRHWG APQQREGRQQ QHHEELSATP TPLGLQETIA EFLYIARPLL HLLSLGLWGQ RSWKPWLLAG VVDVTSLSLL SDRKGLTRRE RRELRRRTIL LLYYLLRSPF YDRFSEARIL FLLQLLADHV PGVGLVTRPL MDYLPTWQKI YFYSWG
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.