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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. 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).
  11. 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.

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