Details for: PEX26
Associated with
Other Information
Genular Protein ID: 1076650530
Symbol: PEX26_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 12717447
Title: The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes.
PubMed ID: 12717447
DOI: 10.1038/ncb982
PubMed ID: 12851857
Title: Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.
PubMed ID: 12851857
DOI: 10.1086/377004
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 15461802
Title: A genome annotation-driven approach to cloning the human ORFeome.
PubMed ID: 15461802
PubMed ID: 10591208
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: 10737800
Title: Shotgun sequencing of the human transcriptome with ORF expressed sequence tags.
PubMed ID: 10737800
PubMed ID: 16854980
Title: Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p.
PubMed ID: 16854980
PubMed ID: 16763195
Title: Targeting of the tail-anchored peroxisomal membrane proteins PEX26 and PEX15 occurs through C-terminal PEX19-binding sites.
PubMed ID: 16763195
DOI: 10.1242/jcs.02979
PubMed ID: 21362118
Title: Recruiting mechanism of the AAA peroxins, Pex1p and Pex6p, to Pex26p on the peroxisomal membrane.
PubMed ID: 21362118
PubMed ID: 16257970
Title: Mutations 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 complex.
PubMed ID: 16257970
PubMed ID: 19105186
Title: Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.
PubMed ID: 19105186
DOI: 10.1002/humu.20932
PubMed ID: 22814378
Title: N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.
PubMed ID: 22814378
PubMed ID: 25944712
Title: N-terminome analysis of the human mitochondrial proteome.
PubMed ID: 25944712
PubMed ID: 33912394
Title: A novel mutation in the PEX26 gene in a family from Dagestan with members affected by Zellweger spectrum disorder.
PubMed ID: 33912394
Sequence Information:
- Length: 305
- Mass: 33898
- Checksum: 0B9FCF8E2B3178E1
- Sequence:
MKSDSSTSAA PLRGLGGPLR SSEPVRAVPA RAPAVDLLEE AADLLVVHLD FRAALETCER AWQSLANHAV AEEPAGTSLE VKCSLCVVGI QALAEMDRWQ EVLSWVLQYY QVPEKLPPKV LELCILLYSK MQEPGAVLDV VGAWLQDPAN QNLPEYGALA EFHVQRVLLP LGCLSEAEEL VVGSAAFGEE RRLDVLQAIH TARQQQKQEH SGSEEAQKPN LEGSVSHKFL SLPMLVRQLW DSAVSHFFSL PFKKSLLAAL ILCLLVVRFD PASPSSLHFL YKLAQLFRWI RKAAFSRLYQ LRIRD
Genular Protein ID: 2661961931
Symbol: Q7Z2D7_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 12851857
Title: Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.
PubMed ID: 12851857
DOI: 10.1086/377004
Sequence Information:
- Length: 113
- Mass: 10597
- Checksum: EBA20628ADAFC1E8
- Sequence:
MKSDSSTSAA PPQGARGTPA QQRAGARGPG PGAGRGPSGG GGRPPGGAPG LPGGAGDLRA GLAESGQPRR GRGTRGHLIG GEVLPVCCGD PGPGRNGSVA RSPLLGPSVL PGP
Genular Protein ID: 2481355530
Symbol: A0A0S2Z5M7_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 26871637
Title: Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.
PubMed ID: 26871637
Sequence Information:
- Length: 256
- Mass: 28388
- Checksum: D53D85F08A6DA5BB
- Sequence:
MKSDSSTSAA PLRGLGGPLR SSEPVRAVPA RAPAVDLLEE AADLLVVHLD FRAALETCER AWQSLANHAV AEEPAGTSLE VKCSLCVVGI QALAEMDRWQ EVLSWVLQYY QVPEKLPPKV LELCILLYSK MQEPGAVLDV VGAWLQDPAN QNLPEYGALA EFHVQRVLLP LGCLSEAEEL VVGSAAFGEE RRLDVLQAIH TARQQQKQEH SGSEEAQKPN LEASPSSLHF LYKLAQLFRW IRKAAFSRLY QLRIRD
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.