Voir la notice de l'article provenant de la source Math-Net.Ru
@article{MBB_2008_3_a2, author = {O. V. Sobolev and V. Yu. Lunin}, title = {Unrestrained reciprocal space refinement of macromolecular structures as a~tool to indicate alternative conformations}, journal = {Matemati\v{c}eska\^a biologi\^a i bioinformatika}, pages = {50--59}, publisher = {mathdoc}, volume = {3}, year = {2008}, language = {ru}, url = {http://geodesic.mathdoc.fr/item/MBB_2008_3_a2/} }
TY - JOUR AU - O. V. Sobolev AU - V. Yu. Lunin TI - Unrestrained reciprocal space refinement of macromolecular structures as a~tool to indicate alternative conformations JO - Matematičeskaâ biologiâ i bioinformatika PY - 2008 SP - 50 EP - 59 VL - 3 PB - mathdoc UR - http://geodesic.mathdoc.fr/item/MBB_2008_3_a2/ LA - ru ID - MBB_2008_3_a2 ER -
%0 Journal Article %A O. V. Sobolev %A V. Yu. Lunin %T Unrestrained reciprocal space refinement of macromolecular structures as a~tool to indicate alternative conformations %J Matematičeskaâ biologiâ i bioinformatika %D 2008 %P 50-59 %V 3 %I mathdoc %U http://geodesic.mathdoc.fr/item/MBB_2008_3_a2/ %G ru %F MBB_2008_3_a2
O. V. Sobolev; V. Yu. Lunin. Unrestrained reciprocal space refinement of macromolecular structures as a~tool to indicate alternative conformations. Matematičeskaâ biologiâ i bioinformatika, Tome 3 (2008), pp. 50-59. http://geodesic.mathdoc.fr/item/MBB_2008_3_a2/
[1] Engh R., Huber R., “Accurate bond and angle parameters for X-ray protein-structure refinement”, Acta Crystallogr D Biol Crystallogr., 47 (1991), 392–400
[2] Jaskolski M., Gilski M., Dauter Z., Wlodawer A., “Stereochemical restraints revisited: how accurate are refinement targets and how much should protein structures be allowed to deviate from them?”, Acta Cryst., 63 (2007), 611–620
[3] Sheldrick G. M., “Phase Annealing in SHELX-90: Direct Methods for Larger Structures”, Acta Cryst. A, 46 (1990), 467–473 <ext-link ext-link-type='doi' href='https://doi.org/10.1107/S0108767390000277'>10.1107/S0108767390000277</ext-link>
[4] Morris R. J., Bricogne G., “Sheldrick's 1.2 $\AA$ rule and beyond”, Acta Cryst. D, 59 (2003), 615–617 <ext-link ext-link-type='doi' href='https://doi.org/10.1107/S090744490300163X'>10.1107/S090744490300163X</ext-link>
[5] Bernstein F. C., Koetzle T. F., Williams G. J. B., Meyer E. F. Jr, Brice M. D., Rogers J. R., Kennard O., Shimanouchi T., Tasumi M., “The Protein Data Bank: a computer based archival file for macromolecular structures”, J. Mol Biol., 112 (1977), 535–547 <ext-link ext-link-type='doi' href='https://doi.org/10.1016/S0022-2836(77)80200-3'>10.1016/S0022-2836(77)80200-3</ext-link>
[6] Berman H. M., Westbrook J., Feng Z., Gilliland G., Bhat T. N., Weissig H., Shindyalov I. N., Bourne P. E., “The Protein Data Bank”, Nucleic Acids Res., 28 (2000), 235–242 <ext-link ext-link-type='doi' href='https://doi.org/10.1093/nar/28.1.235'>10.1093/nar/28.1.235</ext-link>
[7] Antson A. A., Smith D. J., Roper D. I., Lewis S., Caves L. S., Verma C. S., Buckley S. L., Lillford P. J., Hubbard R. E., “Understanding the mechanism of ice binding by type III Antifreeze Proteins”, J. Mol. Biol., 305 (2001) <ext-link ext-link-type='doi' href='https://doi.org/10.1006/jmbi.2000.4336'>10.1006/jmbi.2000.4336</ext-link>
[8] Kang B. S., Devedjiev Y., Derewenda U., Derewenda Z. S., “The Pdz2 domain of syntenin at ultra-high resolution: bridging the gap between small molecule and macromolecular crystal chemistry”, J. Mol. Biol., 338 (2004) <ext-link ext-link-type='doi' href='https://doi.org/10.1016/j.jmb.2004.02.057'>10.1016/j.jmb.2004.02.057</ext-link>
[9] Afonine P. V., Grosse-Kunstleve R. W., Adams P. S., “The Phenix refinement framework”, CCP4 Newsletters, 42 (2005), contribution 8