Pat1 protects centromere-specific histone H3 variant Cse4 from Psh1-mediated ubiquitination

Molecular Biology of the Cell

Volumn 26, Issue 11, 2015, Pages 2067-2079

  Mishra, Prashant K ^a   Guo, Jiasheng ^b   Dittman, Lauren E ^a   Haase, Julian ^b   Yeh, Elaine ^b   Bloom, Kerry ^b   Basrai, Munira A ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

^b UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HISTONE H3; HISTONE VARIANT CSE4; PROTEIN; PROTEIN PAT1; UBIQUITIN PROTEIN LIGASE E3; UNCLASSIFIED DRUG; CHROMATIN; CSE4 PROTEIN, S CEREVISIAE; DNA BINDING PROTEIN; ELONGATION FACTOR; HISTONE; NONHISTONE PROTEIN; PAT1 PROTEIN, S CEREVISIAE; PSH1 PROTEIN, S CEREVISIAE; RNA BINDING PROTEIN; SACCHAROMYCES CEREVISIAE PROTEIN; UBIQUITIN PROTEIN LIGASE;

ARTICLE; BUDDING; CELL CYCLE; CELL PROTECTION; CENTROMERE; CHROMOSOME SEGREGATION; GENE DELETION; HISTONE UBIQUITINATION; IN VIVO STUDY; NONHUMAN; NUCLEOSOME; PHENOTYPE; PRIORITY JOURNAL; PROTEIN INTERACTION; PROTEIN STRUCTURE; SPATIAL ANALYSIS; UBIQUITINATION; WILD TYPE; YEAST; CHROMATIN; METABOLISM; PHYSIOLOGY; SACCHAROMYCES CEREVISIAE;

SACCHAROMYCETALES;

CENTROMERE; CHROMATIN; CHROMOSOMAL PROTEINS, NON-HISTONE; DNA-BINDING PROTEINS; HISTONES; PEPTIDE ELONGATION FACTORS; RNA-BINDING PROTEINS; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; UBIQUITIN-PROTEIN LIGASES; UBIQUITINATION;

EID: 84930404764     PISSN: 10591524     EISSN: 19394586     Source Type: Journal    
DOI: 10.1091/mbc.E14-08-1335     Document Type: Article

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