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b600829c.dvi
www-jackson.ch.cam.ac.uk/publications/2006/2006_Jackson_Ubiquitin_OBC.pdf5 Jun 2006: groups have also studied the effect of mutation of hydrophobiccore groups on the stability.22–24 In these cases, mutation of buriedhydrophobic core residues destabilises the native state of ubiquitinwith the ... Acad. Sci. U. S. A., 2004, 101, -
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. -
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.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. -
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 -
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 -
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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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