Functional Domains in the Carnitine Transporter OCTN2, Defective in Primary Carnitine Deficiency

Journal of Biological Chemistry

Volumn 278, Issue 48, 2003, Pages 47776-47784

  Di San Filippo, Cristina Amat ^a   Wang, Yuhuan ^b   Longo, Nicola ^a,b  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FATTY ACIDS; MUTAGENESIS; OXIDATION; RESTORATION; SUBSTITUTION REACTIONS;

MUTATIONS;

BIOCHEMISTRY;

AMINO ACID; ARGININE; CARNITINE; CARRIER PROTEIN; COMPLEMENTARY DNA; LEUCINE; PROTEIN OCTN1; PROTEIN OCTN2; THREONINE; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CARBOXY TERMINAL SEQUENCE; CARNITINE DEFICIENCY; CHIMERA; FATTY ACID OXIDATION; HEART MUSCLE; HYPOGLYCEMIA; MOLECULAR RECOGNITION; MYOPATHY; NONHUMAN; PRIORITY JOURNAL; PROTEIN DOMAIN; SITE DIRECTED MUTAGENESIS; SKELETAL MUSCLE;

AMINO ACID SEQUENCE; ANIMALS; ARGININE; BINDING SITES; BIOLOGICAL TRANSPORT; CARNITINE; CARRIER PROTEINS; CHO CELLS; CRICETINAE; DNA, COMPLEMENTARY; DOSE-RESPONSE RELATIONSHIP, DRUG; GENETIC VECTORS; HUMANS; KINETICS; LEUCINE; MEMBRANE PROTEINS; MEMBRANE TRANSPORT PROTEINS; MODELS, BIOLOGICAL; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; MUTATION; ORGANIC CATION TRANSPORT PROTEINS; PROTEIN STRUCTURE, TERTIARY; SODIUM; THREONINE; TIME FACTORS;

ANIMALIA;

EID: 0348111470     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M307911200     Document Type: Article

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