Literature DB >> 6432918

Dopachrome oxidoreductase: a new enzyme in the pigment pathway.

J I Barber, D Townsend, D P Olds, R A King.   

Abstract

We report our preliminary characterization of a new enzyme in the pigment pathway which we propose to call dopachrome oxidoreductase (DCOR). This enzyme, prepared from mouse melanoma, catalyzed the conversion of dopachrome to 5,6-dihydroxyindole and also appeared to block the pigment pathway at this latter compound in the absence of tyrosinase. DCOR was protease-sensitive, heat-labile, and showed maximum stability in the range of pH 6-8. The molecular weight of DCOR was estimated to be 34,000 by gel filtration. DCOR had a subcellular distribution within the melanocyte which was similar to that of tyrosinase, but DCOR activity was found in melanocytes devoid of tyrosinase activity and was not inhibited by tyrosinase inhibitors. DCOR may prove to be an active regulatory enzyme in melanogenesis.

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Year:  1984        PMID: 6432918     DOI: 10.1111/1523-1747.ep12263381

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  22 in total

1.  Genetic controls over activities of tyrosinase and dopachrome conversion factor in murine melanocytes.

Authors:  M L Lamoreux; C Woolley; P Pendergast
Journal:  Genetics       Date:  1986-08       Impact factor: 4.562

2.  The action of glycosylases on dopachrome (2-carboxy-2,3-dihydroindole-5,6-quinone) tautomerase.

Authors:  P Aroca; J H Martinez-Liarte; F Solano; J C García-Borrón; J A Lozano
Journal:  Biochem J       Date:  1992-05-15       Impact factor: 3.857

Review 3.  Melanization in living organisms: a perspective of species evolution.

Authors:  Christopher J Vavricka; Bruce M Christensen; Jianyong Li
Journal:  Protein Cell       Date:  2010-10-07       Impact factor: 14.870

4.  A cDNA encoding tyrosinase-related protein maps to the brown locus in mouse.

Authors:  I J Jackson
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

5.  2,4,5-trihydroxyphenylalanine in solution forms a non-N-methyl-D-aspartate glutamatergic agonist and neurotoxin.

Authors:  P A Rosenberg; R Loring; Y Xie; V Zaleskas; E Aizenman
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-01       Impact factor: 11.205

6.  Identification of Drosophila melanogaster yellow-f and yellow-f2 proteins as dopachrome-conversion enzymes.

Authors:  Qian Han; Jianmin Fang; Haizhen Ding; Jody K Johnson; Bruce M Christensen; Jianyong Li
Journal:  Biochem J       Date:  2002-11-15       Impact factor: 3.857

7.  A new dopachrome-rearranging enzyme from the ejected ink of the cuttlefish Sepia officinalis.

Authors:  A Palumbo; M d'Ischia; G Misuraca; L De Martino; G Prota
Journal:  Biochem J       Date:  1994-05-01       Impact factor: 3.857

8.  5,6-Dihydroxyindole-2-carboxylic acid is incorporated in mammalian melanin.

Authors:  K Tsukamoto; A Palumbo; M D'Ischia; V J Hearing; G Prota
Journal:  Biochem J       Date:  1992-09-01       Impact factor: 3.857

9.  Mammalian tyrosinase: biosynthesis, processing, and modulation by melanocyte-stimulating hormone.

Authors:  M Jiménez; K Kameyama; W L Maloy; Y Tomita; V J Hearing
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

10.  Activation of tyrosinase in mouse melanoma cell cultures.

Authors:  B B Fuller
Journal:  In Vitro Cell Dev Biol       Date:  1987-09
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