Crystal structure of human prolyl-tRNA synthetase (halofuginone bound form)
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Crystal structure of human prolyl-tRNA synthetase (halofuginone bound form) Descriptor: 7-bromo-6-chloro-3-{3-[(2R,3S)-3-hydroxypiperidin-2-yl]-2-oxopropyl}quinazolin-4(3H)-one, Proline--tRNA ligase, ZINC ION Authors: Hwang, K.Y, Son, J.H, Lee, E.H. Deposit date: 2013-04-18 Release date: 2013-10-09 Last modified: 2024-03-20 Method: X-RAY DIFFRACTION (2.619 Å) Cite: Conformational changes in human prolyl-tRNA synthetase upon binding of the substrates proline and ATP and the inhibitor halofuginone. Acta Crystallogr.,Sect.D, 69, 2013
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2013-04-18
