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Protein denaturation and protein:drugs interactions from intrinsic…
www-jackson.ch.cam.ac.uk/publications/2010/2010_Prot_Sci%20_Gaudet.pdf26 Jul 2010: AttoOxa11 dyes,24,25 or the use of highly fluorescent. proteins such as yellow fluorescent protein (YFP).26. ... Biotechnol Prog23:1506–1512. 24. Hoffmann A, Kane A, Nettels D, Hertzog DE, Baum-gartel P, Lengefeld J, Reichardt G, Horsley DA, SecklerR, -
doi:10.1016/j.jmb.2007.04.059
www-jackson.ch.cam.ac.uk/publications/2007/2007_J_mol_biol_Hsp90+co.pdf8 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. -
doi:10.1098/rsif.2004.0025
www-jackson.ch.cam.ac.uk/publications/2006/2006_Marianayagam_Interface_UBQ.pdf13 Sep 2006: J. Mol. Biol. 307, 17–24. Ceruso, M. A., Amadei, A. & Di Nola, A. -
doi:10.1016/j.bpc.2004.05.009
www-jackson.ch.cam.ac.uk/publications/2004/2004_Biophys_Chem_UBQ_Mariana.pdf23 Aug 2004: Received 24 March 2004; received in revised form 14 May 2004; accepted 17 May 2004. ... 24] within the GROMACS software package. This. method divides the conformational space of the protein. -
Untangling the folding mechanism of the 52-knottedprotein…
www-jackson.ch.cam.ac.uk/publications/2009/2009_FEBS_J_UCH-L3.pdf3 Apr 2009: disease [22–24]. No stability or folding studies on any of the 52-knot-. ... 24 Setsuie R & Wada K (2007) The functions of UCH-L1. -
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 -
201106261 17939..17944
www-jackson.ch.cam.ac.uk/publications/2011/2011_PNAS_Hsp90_complexes.pdf14 Nov 2011: There is a general view that Hop/FKBP52 may competefor available binding sites in the Hsp90 dimer (13, 16, 23, 24).The lack of reliable dissociation constants means that it is ... J Biol Chem 273:18007–18010. 24. Radanyi C, Chambraud B, Baulieu EE (1994 -
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! -
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www-jackson.ch.cam.ac.uk/publications/2006/2006_Khan_JACS_19FGFP.pdf25 Aug 2006: W.Prog. Nucl. Magn. Reson. Spectrosc.1993,. 25, 345-402.(24) Kaptein, R.Bio. Magn. Reson.1982, 4, 145-91.(25) Kaptein, R.; Dijkstra, K.; Nicolay, K.Nature 1978, 274, -
Structures and folding pathways of topologically knotted proteins
www-jackson.ch.cam.ac.uk/publications/2010/2010_J_Phys_Conds_Matt_Knotted_review.pdf21 Feb 2011: The folding of YibKis complex due to its dimeric nature and the existence ofheterogeneous species in the unfolded state that give rise tomultiple folding pathways [24]. ... c) and (d) The folding mechanism proposed for wild-type dimeric YibK (c) and YbeA
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