The N-DRC forms a conserved biochemical complex that maintains outer doublet alignment and limits microtubule sliding in motile axonemes

Molecular Biology of the Cell

Volumn 24, Issue 8, 2013, Pages 1134-1152

  Bower, Raqual ^a   Tritschler, Douglas ^a   VanderWaal, Kristyn ^a   Perrone, Catherine A ^a   Mueller, Joshua ^a   Fox, Laura ^b   Sale, Winfield S ^b   Porter, M E ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

^b EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; DRC4 PROTEIN; DYNEIN ADENOSINE TRIPHOSPHATASE; EPITOPE; NEXIN DYNEIN REGULATORY COMPLEX; PROTEASE NEXIN; UNCLASSIFIED DRUG;

ARTICLE; AXONEME; BIOCHEMICAL COMPOSITION; CALCIUM SIGNALING; CELL ISOLATION; CELL MOTILITY; CHLAMYDOMONAS; ENZYME REACTIVATION; GENE MUTATION; HUMAN; HUMAN CELL; MASS SPECTROMETRY; MICROTUBULE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN MOTIF; TRYPANOSOMA;

AMINO ACID SEQUENCE; AXONEMAL DYNEINS; AXONEME; CHLAMYDOMONAS REINHARDTII; CONSERVED SEQUENCE; DNA TRANSPOSABLE ELEMENTS; FLAGELLA; MICROTUBULES; MOLECULAR SEQUENCE DATA; MUTAGENESIS, INSERTIONAL; PLANT PROTEINS; PROTEIN INTERACTION MAPPING; SEQUENCE HOMOLOGY, AMINO ACID; SORTING NEXINS;

EID: 84876552918     PISSN: 10591524     EISSN: 19394586     Source Type: Journal    
DOI: 10.1091/mbc.E12-11-0801     Document Type: Article

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