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Plos One|June 8, 2011
Common peptides study of aminoacyl-tRNA synthetasesAssaf Gottlieb, Milana Frenkel-Morgenstern, Mark Safro, et al.
Structure (London, England : 1993)|December 13, 2005
Structural basis for discrimination of L-phenylalanine from L-tyrosine by phenylalanyl-tRNA synthetaseOlga Kotik-Kogan, Nina Moor, Dmitry Tworowski, et al.
Nucleic Acids Research|October 27, 2009
'RNA walk' a novel approach to study RNA-RNA interactions between a small RNA and its targetYaniv Lustig, Chaim Wachtel, Mark Safro, et al.
Protein Science : a Publication of the Protein Society|December 10, 2015
Chimeric human mitochondrial PheRS exhibits editing activity to discriminate nonprotein amino acidsEkaterine Kartvelishvili, Moshe Peretz, Dmitry Tworowski, et al.
Biochemistry|August 31, 2006
The crystal structure of the ternary complex of phenylalanyl-tRNA synthetase with tRNAPhe and a phenylalanyl-adenylate analogue reveals a conformational switch of the CCA endNina Moor, Olga Kotik-Kogan, Dmitry Tworowski, et al.
Structure (London, England : 1993)|July 10, 2008
The tRNA-induced conformational activation of human mitochondrial phenylalanyl-tRNA synthetaseLiron Klipcan, Inna Levin, Naama Kessler, et al.
The FEBS Journal|March 3, 2020
Breaking a single hydrogen bond in the mitochondrial tRNAPhe -PheRS complex leads to phenotypic pleiotropy of human diseaseMoshe Peretz, Dmitry Tworowski, Ekaterine Kartvelishvili, et al.
FEBS Letters|September 10, 2009
Large-scale movement of functional domains facilitates aminoacylation by human mitochondrial phenylalanyl-tRNA synthetaseSrujana S Yadavalli, Liron Klipcan, Alexey Zozulya, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|September 5, 2007
Purification, crystallization and preliminary X-ray characterization of a human mitochondrial phenylalanyl-tRNA synthetaseInna Levin, Naama Kessler, Nina Moor, et al.
Protein Science : a Publication of the Protein Society|April 19, 2017
Kinetic and structural changes in HsmtPheRS, induced by pathogenic mutations in human FARS2Ekaterine Kartvelishvili, Dmitry Tworowski, Hilary Vernon, et al.
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