Alkyl-dihydroxyacetonephosphate synthase: Fate in peroxisome biogenesis disorders and identification of the point mutation underlying a single enzyme deficiency

Journal of Biological Chemistry

Volumn 273, Issue 17, 1998, Pages 10296-10301

  De Vet, Edwin C J M ^a   Ijlst, Lodewijk ^b   Oostheim, Wendy ^b   Wanders, Ronald J A ^b   Van Den Bosch, Henk ^a,c  

^a UTRECHT UNIVERSITY   (Netherlands)

^b ACADEMIC MEDICAL CENTER   (Netherlands)

^c Centre for Biomembranes and Lipid Enzymology   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

BENZYLSULFONYL FLUORIDE; DIHYDROXYACETONE PHOSPHATE; ENZYME PRECURSOR; ETHER PHOSPHOLIPID; PHENYLGLYOXAL;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CHEMICAL REACTION KINETICS; CHONDRODYSPLASIA PUNCTATA; CHROMOSOME 2Q; CHROMOSOME MAP; CONTROLLED STUDY; DISORDERS OF PEROXISOMAL FUNCTIONS; DNA SEQUENCE; ENZYME ACTIVE SITE; ENZYME DEFICIENCY; ENZYME INHIBITION; GUINEA PIG; HUMAN; NONHUMAN; PEROXISOME; PHOSPHOLIPID SYNTHESIS; POINT MUTATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; ZELLWEGER SYNDROME;

ALKYL AND ARYL TRANSFERASES; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; CLONING, MOLECULAR; DNA, COMPLEMENTARY; GUINEA PIGS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PEROXISOMAL DISORDERS; POINT MUTATION;

EID: 0032562566     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.273.17.10296     Document Type: Article

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