Functional analysis of genetic mutations in nucleotide binding domain 2 of the human retina specific ABC transporter

Biochemistry

Volumn 42, Issue 36, 2003, Pages 10683-10696

  Biswas Fiss, Esther E ^a  

^a THOMAS JEFFERSON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENETIC MUTATIONS;

ADENOSINETRIPHOSPHATE; ATTENUATION; HYDROLYSIS; PROTEINS;

GENETIC ENGINEERING;

ABC TRANSPORTER; ADENOSINE TRIPHOSPHATE; RETINAL;

ARTICLE; BINDING SITE; CONFORMATIONAL TRANSITION; FLUORESCENCE; GENE MUTATION; HYDROLYSIS; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; RETINA MACULA DEGENERATION; RETINA ROD; RETINA ROD OUTER SEGMENT; SEQUENCE ALIGNMENT;

ADENOSINE DIPHOSPHATE; ADENOSINE TRIPHOSPHATASES; ADENOSINE TRIPHOSPHATE; AMINO ACID SEQUENCE; ATP-BINDING CASSETTE TRANSPORTERS; FLUORESCENCE POLARIZATION; HUMANS; HYDROLYSIS; KINETICS; MACULAR DEGENERATION; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; RECOMBINANT PROTEINS; RETINA; SEQUENCE HOMOLOGY, AMINO ACID; SPECTROMETRY, FLUORESCENCE; THERMODYNAMICS;

EID: 0042820053     PISSN: 00062960     EISSN: None     Source Type: Journal    
DOI: 10.1021/bi034481l     Document Type: Article

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