Mitochondrial ribonuclease P structure provides insight into the evolution of catalytic strategies for precursor-tRNA 5′ processing

Proceedings of the National Academy of Sciences of the United States of America

Volumn 109, Issue 40, 2012, Pages 16149-16154

  Howard, Michael J ^a   Lim, Wan Hsin ^b   Fierke, Carol A ^a,b   Koutmos, Markos ^c  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

^c UNIFORMED SERVICES UNIVERSITY OF THE HEALTH SCIENCES   (United States)

Author keywords

Catalytic mechanism; Magnesium; Molecular recognition

Indexed keywords

PRORP1 PROTEIN; RIBONUCLEASE P; TRANSFER RNA; UBIQUITIN PROTEIN LIGASE NEDD4; UNCLASSIFIED DRUG;

ARABIDOPSIS; ARTICLE; CATALYST; CRYSTAL STRUCTURE; HUMAN; HUMAN CELL; MITOCHONDRIAL GENOME; MITOCHONDRION; NONHUMAN; PENTATRICOPEPTIDE REPEAT DOMAIN; PRIORITY JOURNAL; PROLINE RICH PROTEIN DOMAIN; PROTEIN DOMAIN; PROTEIN INTERACTION; PROTEIN STRUCTURE;

ARABIDOPSIS; CRYSTALLOGRAPHY, X-RAY; EVOLUTION, MOLECULAR; HUMANS; MITOCHONDRIA; MODELS, MOLECULAR; PROTEIN STRUCTURE, TERTIARY; RIBONUCLEASE P; RNA PRECURSORS; RNA PROCESSING, POST-TRANSCRIPTIONAL;

ARABIDOPSIS THALIANA; EUKARYOTA;

EID: 84867071659     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1209062109     Document Type: Article

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