Impaired transport of nucleotides in a mitochondrial carrier explains severe human genetic diseases

ACS Chemical Biology

Volumn 7, Issue 7, 2012, Pages 1164-1169

  Ravaud, Stéphanie ^a,b,c   Bidon Chanal, Axel ^d,e   Blesneac, Iulia ^a,b,c   MacHillot, Paul ^a,b,c   Juillan Binard, Céline ^a,b,c   Dehez, François ^d,e   Chipot, Chris ^d,e   Pebay Peyroula, Eva ^a,b,c  

^a UNIV GRENOBLE ALPES   (France)

^b CEA GRENOBLE   (France)

^c INSTITUT DE BIOLOGIE STRUCTURALE   (France)

^d UNIVERSITÉ DE LORRAINE   (France)

^e NANCY UNIVERSITÉ   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE DIPHOSPHATE; ADENOSINE TRIPHOSPHATE; MEMBRANE PROTEIN; NUCLEOTIDE;

ARTICLE; BINDING AFFINITY; CYTOPLASM; DISEASE SEVERITY; GENE MUTATION; GENETIC DISORDER; HUMAN; MEDICAL DOCUMENTATION; MITOCHONDRION; MOLECULAR DYNAMICS; NUCLEOTIDE TRANSPORT; PLASTICITY; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN MODIFICATION; SIMULATION;

GENETIC DISEASES, INBORN; HUMANS; MITOCHONDRIAL ADP, ATP TRANSLOCASES; NUCLEOTIDES; POINT MUTATION; PROTEIN STRUCTURE, SECONDARY; PROTEIN TRANSPORT; SEVERITY OF ILLNESS INDEX;

EID: 84864142914     PISSN: 15548929     EISSN: 15548937     Source Type: Journal    
DOI: 10.1021/cb300012j     Document Type: Article

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