Trypanosoma brucei harbours a divergent XPB helicase paralogue that is specialized in nucleotide excision repair and conserved among kinetoplastid organisms

Molecular Microbiology

Volumn 90, Issue 6, 2013, Pages 1293-1308

  Badjatia, Nitika ^a   Nguyen, Tu N ^a   Lee, Ju Huck ^a,b   Günzl, Arthur ^a  

^a UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

^b UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HELICASE; RNA POLYMERASE II; TRANSCRIPTION FACTOR IIH; UNCLASSIFIED DRUG; XPB HELICASE;

ARTICLE; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; EXCISION REPAIR; GENE; GENE SILENCING; GENETIC TRANSCRIPTION; IN VITRO STUDY; IN VIVO STUDY; KINETOPLASTIDA; NONHUMAN; PRIORITY JOURNAL; PROMOTER REGION; SLRNA GENE; TRYPANOSOMA BRUCEI; ULTRAVIOLET RADIATION; XPB R GENE;

KINETOPLASTIDA; PROTISTA; TRYPANOSOMA; TRYPANOSOMA BRUCEI;

DNA HELICASES; DNA REPAIR; EVOLUTION, MOLECULAR; GENE KNOCKOUT TECHNIQUES; GENES, PROTOZOAN; HUMANS; KINETOPLASTIDA; PHYLOGENY; PROTOZOAN PROTEINS; SEQUENCE ANALYSIS, PROTEIN; SEQUENCE HOMOLOGY, AMINO ACID; TRANSCRIPTION FACTOR TFIIH; TRYPANOSOMA BRUCEI BRUCEI;

EID: 84890119069     PISSN: 0950382X     EISSN: 13652958     Source Type: Journal    
DOI: 10.1111/mmi.12435     Document Type: Article

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