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21 Apr 2006: p23appears to stabilise the interaction between Hsp90and a client protein in vitro,23,24 correlating with itsability to increase the activation of heterologouslyexpressed estrogen receptor in vivo.25 In contrast,another

23 Aug 2004: Wild-type and mutant proteins wereexpressed and purified as described elsewhere (24-25). ... Struct. Biol. 8, 331-333. 24. Finucane, M. D., Tuna, M., Lees, J.

11 Sep 2003: given here is twice that of the monomer [23]. mInitial reports suggested that wild-type ubiquitin folded with two-state kinetics [24]. ... 4]), activation domain procarboxypeptidase (ADAh2; [22]), ubiquitin[24,25], histidine-containing phosphocarrier

16 Sep 2003: Received 19 November 2002; accepted 19 December 2002. The first international meeting on the Hsp90 (heat-shock protein 90)chaperone machine was held in Arolla, Switzerland, from 24 to 28 August

16 Nov 2006: In contrast to the above mechanisms, one computational DFTstudy suggested that oxidation could precede cyclization [24]. ... 14 hours 24 hours 48 hours 1 week2 weeks3 weeks 4 weeks 5 weeks 6 weeks 7 weeks 8 weeks.

17 Jul 2005: first 24 h, then the number of scans wasdoubled, and data were collected over the next 5– 40 days. ... 1 T kin† T eq.‡. CTPR2 19,860 6,692 50 2.24 0.19 0.35 0.21 2.06 0.18 0.5 0.4CTPR3 35,032 7,601

16 Sep 2003: In addition, we have shown that TFE does not significantly change the fold-ing pathway of FKBP12 [24]. ... However, although TFE affects the folding andunfolding rate of FKBP12, we have established that this effect is not caused bythe stabilisation of a

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.

6 Jan 2005: Mol. Biol. Cell 12, 3307–3316. (2001).24. Hossain, M.M. & Nakamoto, H.

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,