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Publikováno v:
Journal of Applied Crystallography. 30:476-486
A simple and efficient method to prepare isomorphous derivatives of protein crystals with xenon as a heavy atom is described. The method consists of exposing a crystal to xenon gas of pressures above 5 atm (~ 0.5 MPa) for several minutes and subseque
Publikováno v:
Helvetica Chimica Acta. 77:445-452
The optically active urobilin model compound 7 was synthesized, in which Me groups instead of H-atoms are bound to the asymmetric centers, thus preventing loss of chirality by tautomerization. The key intermediate of the eleven-step synthesis of 7 is
Publikováno v:
ChemInform. 22
Publikováno v:
ChemInform. 22
Autor:
M. Widhalm, C. Kratky
Publikováno v:
ChemInform. 24
Publikováno v:
ChemInform. 25
The optically active urobilin model compound 7 was synthesized, in which Me groups instead of H-atoms are bound to the asymmetric centers, thus preventing loss of chirality by tautomerization. The key intermediate of the eleven-step synthesis of 7 is
Publikováno v:
Structure (London, England : 1993). 9(9)
Cyanogenesis is a defense process of several thousand plant species. Hydroxynitrile lyase, a key enzyme of this process, cleaves a cyanohydrin into hydrocyanic acid and the corresponding aldehyde or ketone. The reverse reaction constitutes an importa
Publikováno v:
Biological chemistry. 380(7-8)
The X-ray crystal structure of native hydroxynitrile lyase from Hevea brasiliensis (Hb-HNL) has been determined at 1.1 A resolution. It refined to a final R of 11.5% for all data and an Rfree of 14.4%. The favorable data-to-parameter ratio at atomic
Autor:
C. Kratky
Publikováno v:
Chirality ISBN: 9783642765711
Most biological and many other molecules are chiral, i.e. they cannot be superimposed on their mirror image. The two mirror images of a chiral molecule are called enantiomers. Chiral molecules show the phenomenon of optical activity, i.e. a solution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d104f58c244a76fb7299ebbed752740
https://doi.org/10.1007/978-3-642-76569-8_5
https://doi.org/10.1007/978-3-642-76569-8_5