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The role of conserved PEX3 regions in PEX19-binding and peroxisome biogenesis.

Schmidt F, Dietrich D, Eylenstein R, Groemping Y, Stehle T, Dodt G.

Traffic. 2012 Sep;13(9):1244-60. doi: 10.1111/j.1600-0854.2012.01380.x. Epub 2012 Jun 19.


The interaction between human PEX3 and PEX19 characterized by fluorescence resonance energy transfer (FRET) analysis.

Muntau AC, Roscher AA, Kunau WH, Dodt G.

Eur J Cell Biol. 2003 Jul;82(7):333-42.


Insights into peroxisome function from the structure of PEX3 in complex with a soluble fragment of PEX19.

Schmidt F, Treiber N, Zocher G, Bjelic S, Steinmetz MO, Kalbacher H, Stehle T, Dodt G.

J Biol Chem. 2010 Aug 13;285(33):25410-7. doi: 10.1074/jbc.M110.138503. Epub 2010 Jun 16.


PEX3 functions as a PEX19 docking factor in the import of class I peroxisomal membrane proteins.

Fang Y, Morrell JC, Jones JM, Gould SJ.

J Cell Biol. 2004 Mar 15;164(6):863-75. Epub 2004 Mar 8.


Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G.

Muntau AC, Mayerhofer PU, Paton BC, Kammerer S, Roscher AA.

Am J Hum Genet. 2000 Oct;67(4):967-75. Epub 2000 Aug 24.


Functional regions of the peroxin Pex19 necessary for peroxisome biogenesis.

Agrawal G, Shang HH, Xia ZJ, Subramani S.

J Biol Chem. 2017 Jul 7;292(27):11547-11560. doi: 10.1074/jbc.M116.774067. Epub 2017 May 19.


New insights into the distribution, protein abundance and subcellular localisation of the endogenous peroxisomal biogenesis proteins PEX3 and PEX19 in different organs and cell types of the adult mouse.

Colasante C, Chen J, Ahlemeyer B, Bonilla-Martinez R, Karnati S, Baumgart-Vogt E.

PLoS One. 2017 Aug 17;12(8):e0183150. doi: 10.1371/journal.pone.0183150. eCollection 2017.


Association between the intrinsically disordered protein PEX19 and PEX3.

Hattula K, Hirschberg D, Kalkkinen N, Butcher SJ, Ora A.

PLoS One. 2014 Jul 25;9(7):e103101. doi: 10.1371/journal.pone.0103101. eCollection 2014.


Peroxisome biogenesis disorders: molecular basis for impaired peroxisomal membrane assembly: in metabolic functions and biogenesis of peroxisomes in health and disease.

Fujiki Y, Yagita Y, Matsuzaki T.

Biochim Biophys Acta. 2012 Sep;1822(9):1337-42. doi: 10.1016/j.bbadis.2012.06.004. Epub 2012 Jun 13. Review.


PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.

Ghaedi K, Honsho M, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y.

Am J Hum Genet. 2000 Oct;67(4):976-81. Epub 2000 Aug 31.


Identification and characterization of the human peroxin PEX3.

Soukupova M, Sprenger C, Gorgas K, Kunau WH, Dodt G.

Eur J Cell Biol. 1999 Jun;78(6):357-74.


Two splice variants of human PEX19 exhibit distinct functions in peroxisomal assembly.

Mayerhofer PU, Kattenfeld T, Roscher AA, Muntau AC.

Biochem Biophys Res Commun. 2002 Mar 15;291(5):1180-6.


Hydrophobic handoff for direct delivery of peroxisome tail-anchored proteins.

Chen Y, Pieuchot L, Loh RA, Yang J, Kari TM, Wong JY, Jedd G.

Nat Commun. 2014 Dec 17;5:5790. doi: 10.1038/ncomms6790.


Targeting of the tail-anchored peroxisomal membrane proteins PEX26 and PEX15 occurs through C-terminal PEX19-binding sites.

Halbach A, Landgraf C, Lorenzen S, Rosenkranz K, Volkmer-Engert R, Erdmann R, Rottensteiner H.

J Cell Sci. 2006 Jun 15;119(Pt 12):2508-17.


The cytosolic domain of PEX3, a protein involved in the biogenesis of peroxisomes, binds membrane lipids.

Pinto MP, Grou CP, Fransen M, Sá-Miranda C, Azevedo JE.

Biochim Biophys Acta. 2009 Nov;1793(11):1669-75. doi: 10.1016/j.bbamcr.2009.08.007. Epub 2009 Aug 26.


Tail-anchored PEX26 targets peroxisomes via a PEX19-dependent and TRC40-independent class I pathway.

Yagita Y, Hiromasa T, Fujiki Y.

J Cell Biol. 2013 Mar 4;200(5):651-66. doi: 10.1083/jcb.201211077.


Functional domain mapping of peroxin Pex19p: interaction with Pex3p is essential for function and translocation.

Matsuzono Y, Matsuzaki T, Fujiki Y.

J Cell Sci. 2006 Sep 1;119(Pt 17):3539-50. Epub 2006 Aug 8.


PEX16 contributes to peroxisome maintenance by constantly trafficking PEX3 via the ER.

Aranovich A, Hua R, Rutenberg AD, Kim PK.

J Cell Sci. 2014 Sep 1;127(Pt 17):3675-86. doi: 10.1242/jcs.146282. Epub 2014 Jul 7.


Contribution of the endoplasmic reticulum to peroxisome formation.

Hoepfner D, Schildknegt D, Braakman I, Philippsen P, Tabak HF.

Cell. 2005 Jul 15;122(1):85-95.


Characterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of TRP-104 IN Pex3p as a critical residue for the interaction.

Sato Y, Shibata H, Nakano H, Matsuzono Y, Kashiwayama Y, Kobayashi Y, Fujiki Y, Imanaka T, Kato H.

J Biol Chem. 2008 Mar 7;283(10):6136-44. doi: 10.1074/jbc.M706139200. Epub 2008 Jan 3.

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