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1 Aug 2008: 2008). Biol. Cell, in press. Pub-lished online January 24, 2008. 10.1042/BC20070149.

8 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.

8 Dec 2008: J Mol Biol346:1409 –1421. 24. Tanford C (1968) Protein denaturation. Part A. ... Theoretical models for the mechanismof denaturation. Adv Protein Chem 24:1–95. 26.

8 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

11 Feb 2008: W.; Fesinmeyer, R. M.; Andersen, N. H.Nature Struct. Biol. 2002, 9, 425-430.(24) Frisch, M. ... 2 ) 1.26 1020, HFC2 ) 6.24 1018, andXG,HFC) -4.26 1018.

4 Jun 2008: 5b), confirming that Cyp40 insolution exists in this state23,24, suggesting that theobserved structure of the tetragonal crystal form islikely to be a crystallographic artifact. ... Structure, 9, 431–438. 24. Ward, B. K., Allan, R. K., Mok, D., Temple,

8 Feb 2008: Structuresfor the isolated, individual domains have beenreported either for human or yeast Hsp90, the ERhomologue Grp94 or the Escherichia coli homologue,HtpG.18–24 In addition, a number of structures oflarger ... Trends Biochem. Sci. 24, 136–141. 4.

8 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

8 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.

1 Aug 2008: AM. CHEM. SOC. 2008, 130, 7898–7907. identified as a continuum-of-substates,19 expansion or collapseof the unfolded state,18,23,24 or just assigned to changes in thedye’s ... Proc. Natl. Acad. Sci. U.S.A. 2006, 103, 11539–11543. (24) Hoffmann, A.;