Entity Details

Primary name PEX19_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP40855
EntryNamePEX19_HUMAN
FullNamePeroxisomal biogenesis factor 19
TaxID9606
Evidenceevidence at protein level
Length299
SequenceStatuscomplete
DateCreated1995-02-01
DateModified2021-06-02

Ontological Relatives

GenesPEX19

GO terms

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GOName
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005777 peroxisome
GO:0005778 peroxisomal membrane
GO:0005829 cytosol
GO:0006625 protein targeting to peroxisome
GO:0006869 lipid transport
GO:0007031 peroxisome organization
GO:0016021 integral component of membrane
GO:0016557 peroxisome membrane biogenesis
GO:0016559 peroxisome fission
GO:0031526 brush border membrane
GO:0032991 protein-containing complex
GO:0033328 peroxisome membrane targeting sequence binding
GO:0036105 peroxisome membrane class-1 targeting sequence binding
GO:0045046 protein import into peroxisome membrane
GO:0047485 protein N-terminus binding
GO:0050821 protein stabilization
GO:0051117 ATPase binding
GO:0061077 chaperone-mediated protein folding
GO:0072321 obsolete chaperone-mediated protein transport
GO:0072663 establishment of protein localization to peroxisome
GO:0140597 protein carrier activity
GO:1900131 negative regulation of lipid binding

Subcellular Location

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Subcellular Location
Cytoplasm
Peroxisome membrane

Domains

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DomainNameCategoryType
IPR006708 Pex19 proteinFamilyFamily
IPR038322 Pex19, C-terminal domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
614886 OMIMPeroxisome biogenesis disorder complementation group 14 (PBD-CG14)A peroxisomal disorder arising from a failure of protein import into the peroxisomal membrane or matrix. The peroxisome biogenesis disorders (PBD group) are genetically heterogeneous with at least 14 distinct genetic groups as concluded from complementation studies. Include disorders are: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). ZWS, NALD and IRD are distinct from RCDP and constitute a clinical continuum of overlapping phenotypes known as the Zellweger spectrum (PBD-ZSS). The disease is caused by variants affecting the gene represented in this entry.
614886 OMIMPeroxisome biogenesis disorder complementation group 14 (PBD-CG14)A peroxisomal disorder arising from a failure of protein import into the peroxisomal membrane or matrix. The peroxisome biogenesis disorders (PBD group) are genetically heterogeneous with at least 14 distinct genetic groups as concluded from complementation studies. Include disorders are: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). ZWS, NALD and IRD are distinct from RCDP and constitute a clinical continuum of overlapping phenotypes known as the Zellweger spectrum (PBD-ZSS). The disease is caused by variants affecting the gene represented in this entry.

Interactions

46 interactions

InteractorPartnerSourcesPublicationsLink
PEX19_HUMANPX11B_HUMANBioGRID, HPRD, IntAct, MINT, UniProt10704444 11390669 12096124 14709540 20531392 25416956 26264872 29997244 31467278 32814053 details
PEX19_HUMANPEX3_HUMANBioGRID, HPRD, IntAct, MINT10704444 11390669 11883941 12096124 16189514 16280322 21102411 25007327 25416956 25502805 26186194 26264872 27107012 28514442 29997244 31467278 31515488 32296183 32814053 34079125 details
PEX19_HUMANPEX16_HUMANBioGRID, HPRD, IntAct, MINT, UniProt10704444 11390669 12096124 14709540 20531392 25416956 26186194 26264872 28514442 29997244 31467278 32814053 details
PEX19_HUMANPEX14_HUMANBioGRID, HPRD, IntAct, MINT10704444 12096124 19197237 21525035 26264872 29997244 31467278 34079125 details
PEX19_HUMANPEX10_HUMANBioGRID, HPRD, IntAct10704444 11390669 12096124 details
PEX19_HUMANPEX12_HUMANBioGRID, HPRD, IntAct10704444 11390669 12096124 details
PEX19_HUMANPEX13_HUMANBioGRID, HPRD, IntAct, MINT10704444 11390669 12096124 20531392 details
PEX19_HUMANPM34_HUMANBioGRID, HPRD, IntAct, UniProt10704444 11402059 14709540 details
PEX19_HUMANABCD3_HUMANBioGRID, HPRD, IntAct, MINT, UniProt10704444 10777694 11453642 11883941 14709540 21102411 details
PEX19_HUMANABCD2_HUMANBioGRID, HPRD, IntAct10704444 10777694 11883941 details
PEX19_HUMANSMAD2_HUMANBioGRID, HPRD, MINT15231748 details
PEX19_HUMANPEX2_HUMANMINT20531392 details
PEX19_HUMANPEX26_HUMANBioGRID, IntAct, MINT20531392 30366024 32296183 details
PEX19_HUMANPEX19_HUMANMINT20531392 details
PEX19_HUMANABCD1_HUMANBioGRID, HPRD, MINT10777694 11883941 20531392 details
PEX19_HUMANPXMP2_HUMANBioGRID, IntAct, MINT, UniProt11590176 14709540 21102411 26186194 28514442 34079125 details
PEX19_HUMANMPIP1_HUMANBioGRID, IntAct21988832 details
PEX19_HUMANIRF3_HUMANBioGRID, IntAct21988832 details
PEX19_HUMANSRPK1_HUMANBioGRID, IntAct21988832 details
PEX19_HUMANSTK3_HUMANBioGRID, IntAct21988832 details
PEX19_HUMANEIF1B_HUMANBioGRID, IntAct21988832 details
PEX19_HUMANMS18B_HUMANBioGRID, IntAct21988832 details
PEX19_HUMANKIFA3_HUMANBioGRID, IntAct21988832 details
PEX19_HUMANJAM1_HUMANBioGRID, IntAct21988832 details
PEX19_HUMANGSKIP_HUMANBioGRID, IntAct21988832 details
PEX19_HUMANMFSD5_HUMANBioGRID, IntAct21988832 details
PEX19_HUMANTMM54_HUMANBioGRID, IntAct21988832 details
PEX19_HUMANPPIB_HUMANBioGRID, IntAct25416956 32296183 details
PEX19_HUMANIL23A_HUMANBioGRID, IntAct25416956 32296183 details
PEX19_HUMANFKBP7_HUMANBioGRID, IntAct25416956 details
PEX19_HUMANIFNB_HUMANBioGRID, IntAct32296183 details
PEX19_HUMANNAT8L_HUMANBioGRID, IntAct32296183 details
PEX19_HUMANPS1C2_HUMANBioGRID, IntAct32296183 details
PEX19_HUMANB2L11_HUMANBioGRID, IntAct32296183 details
PEX19_HUMANTHIOM_HUMANBioGRID, IntAct32296183 details
PEX19_HUMANSUOX_HUMANBioGRID, IntAct32296183 details
PEX19_HUMANPX11A_HUMANBioGRID, HPRD10704444 20531392 details
PEX19_HUMANARF_HUMANHPRD16582619 details
PEX19_HUMANNPT2A_HUMANHPRD14558883 details
PEX19_HUMANEGFR_HUMANBioGRID, IntAct15657067 23956138 details
PEX19_HUMANPXMP4_HUMANBioGRID, HPRD, UniProt10704444 14709540 details
PEX19_HUMANDLG4_HUMANMINT21653829 details
PEX19_HUMANPMP22_HUMANBioGRID, HPRD10704444 14709540 details
PEX19_HUMANTERA_HUMANBioGRID23457492 details
PEX19_HUMANHACD3_HUMANBioGRID25036637 details
PEX19_HUMANGLE1_HUMANBioGRID29395067 details