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doi:10.1016/j.bpc.2007.03.011
www-jackson.ch.cam.ac.uk/publications/2007/2007_biophys_chem_UBQ.pdf8 Feb 2008: caused by aggregation of the native state, WT⁎ at 2 μM, pH 7.4and 37 C was equilibrated for 24 h in 300 g/L glucose. ... Side-. chain transfer is not, however, sufficient to overcome theunfavourable transfer of the backbone, as observed with -
doi:10.1016/j.str.2008.04.004
www-jackson.ch.cam.ac.uk/publications/2008/2008_Structure_Jackson_commentary.pdf1 Aug 2008: 2008). Biol. Cell, in press. Pub-lished online January 24, 2008. 10.1042/BC20070149. -
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www-jackson.ch.cam.ac.uk/publications/2002/2002_JACS.pdf15 Sep 2003: L.; Rose, G. D.Trends Biochem. Sci. 1999, 24, 77-83.(60) Baldwin, R. ... L.; Rose, G. D.Trends Biochem. Sci. 1999, 24, 26-33.(61) Fersht, A. -
doi:10.1098/rsif.2004.0025
www-jackson.ch.cam.ac.uk/publications/2005/2005_Interface_Marianayagam_ubiquitin.pdf17 Jul 2005: J. Mol. Biol. 307, 17–24. Ceruso, M. A., Amadei, A. & Di Nola, A. -
doi:10.1016/j.jmb.2007.04.039
www-jackson.ch.cam.ac.uk/publications/2007/2007_J_mol_biol_GFP_unfolding.pdf8 Feb 2008: 19–24 as well as on cooperatively unfoldingregions of proteins.11,14 Although H/D exchangeresults have been reported for GFP, the conditionsused did not allow a quantitative analysis of theresults ... Thesymbols are the same as for (a) except the first -
Mapping the Interactions Present in the Transition State for…
www-jackson.ch.cam.ac.uk/publications/1999/1999_JMB1.pdf15 Sep 2003: Ala75 2.6 0.11 ÿ5.51 0.12 1.01 0.02 ÿ1.55 0.04 0.34 0.03 0.24 0.01Thr! ... Val76 0.76 0.12 ÿ7.90 0.12 0.94 0.02 ÿ4.24 0.05 0.56 0.2 0.43 0.09Ile! -
doi:10.1016/j.jmb.2004.12.055
www-jackson.ch.cam.ac.uk/publications/2005/2005_Mallam_JMB_KnottedPortein.pdf17 Jul 2005: This observation is notexpected for a simple two-state denaturation mech-anism, and indicates that a more complex scheme isnecessary to describe the system fully.24,25 In particu-lar, the ... transition is biphasic33–37 and each transition can -
Protein folding: Defining a “standard” set ofexperimental conditions…
www-jackson.ch.cam.ac.uk/publications/2005/2005_Maxwell_ProSci_proteinfolding.pdf19 Apr 2005: Forexample, 13 of the proteins characterized here were in-cluded in an earlier 24-protein data set that was used toillustrate the relationship between an empirical measure oftopology termed relative contact ... 07 2.04 0.03 13.0 1.9 4.2 0.5 -
doi:10.1016/j.str.2006.11.007
www-jackson.ch.cam.ac.uk/publications/2007/2007_structure_YibK.pdf8 Feb 2008: Sextuple 2.6 ( 0.4) 3 102 2.0 ( 0.6) 3 103 0.24 0.07 0.33 0.03 0.6 0.1 1.5 0.3. -
doi:10.1016/j.jmb.2007.06.065
www-jackson.ch.cam.ac.uk/publications/2007/2007_J_mol_biol_Hsp90_inhibition.pdf8 Feb 2008: with a Kd of 29(3) nM, following incubationfor 24 h (Figure 2(d)). ... Kd (nM)4 h. Kd (nM)8 h. Kd (nM)24 h. kon(μM1 s1) koff.
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