Vulnerability of the cysteine-less proton-coupled folate transporter (PCFT-SLC46A1) to mutational stress associated with the substituted cysteine accessibility method

Biochimica et Biophysica Acta - Biomembranes

Volumn 1808, Issue 4, 2011, Pages 1140-1145

  Zhao, Rongbao ^a   Shin, Daniel Sanghoon ^a   Goldman, I David ^a  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

Folate; Hereditary folate malabsorption; Proton coupled folate transporter; Substituted cysteine accessibility method

Indexed keywords

MEMBRANE PROTEIN; PROTON COUPLED FOLATE TRANSPORTER; UNCLASSIFIED DRUG;

ARTICLE; BIOTINYLATION; CONTROLLED STUDY; DISULFIDE BOND; GENE MUTATION; HUMAN; HUMAN CELL; MEMBRANE STRUCTURE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PROCESSING; PROTEIN STABILITY; PROTEIN STRUCTURE; SITE DIRECTED MUTAGENESIS;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; BIOLOGICAL TRANSPORT; BLOTTING, WESTERN; CYSTEINE; HELA CELLS; HUMANS; LYSINE; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; MUTATION; PROTEIN STABILITY; PROTON-COUPLED FOLATE TRANSPORTER;

EID: 79751535507     PISSN: 00052736     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbamem.2011.01.008     Document Type: Article

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