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21 - 30 of 52 search results for TALK:Vb20 24 / |u:www-jackson.ch.cam.ac.uk where 0 match all words and 52 match some words.
  1. Results that match 1 of 2 words

  2. Untangling the folding mechanism of the 52-knottedprotein…

    www-jackson.ch.cam.ac.uk/publications/2009/2009_FEBS_J_UCH-L3.pdf
    3 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.
  3. 201106261 17939..17944

    www-jackson.ch.cam.ac.uk/publications/2011/2011_PNAS_Hsp90_complexes.pdf
    14 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
  4. doi:10.1016/j.jmb.2007.04.059

    www-jackson.ch.cam.ac.uk/publications/2007/2007_J_mol_biol_Hsp90+co.pdf
    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.
  5. Folding and stability of the ligand-bindingdomain of the…

    www-jackson.ch.cam.ac.uk/publications/2002/2002_prot_sci.pdf
    17 Sep 2003: Sci.24: 136–141. Chen, S., Prapapanich, V., Rimerman, R.A., Honore, B., and Smith, D.F.
  6. Evidence of an Intermediate and Parallel Pathways in ProteinUnfolding …

    www-jackson.ch.cam.ac.uk/publications/2008/2008_JACS_SM_GFP.pdf
    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.;
  7. doi:10.1016/j.jmb.2004.12.055

    www-jackson.ch.cam.ac.uk/publications/2005/2005_Mallam_JMB_KnottedPortein.pdf
    17 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
  8. doi:10.1016/j.bpc.2004.05.009

    www-jackson.ch.cam.ac.uk/publications/2004/2004_Biophys_Chem_UBQ_Mariana.pdf
    23 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.
  9. Mapping the Interactions Present in the Transition State for…

    www-jackson.ch.cam.ac.uk/publications/1999/1999_JMB1.pdf
    15 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!
  10. doi:10.1016/j.str.2006.11.007

    www-jackson.ch.cam.ac.uk/publications/2007/2007_structure_YibK.pdf
    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.
  11. The extremely slow-exchanging core andacid-denatured state of green…

    www-jackson.ch.cam.ac.uk/publications/2008/2008_HFSP_J_GFP.pdf
    19 Dec 2008: Neuberger, A (ed.), pp 23–24,Methuen, London. Mayo, SL, and Baldwin, RL (1993).

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