169 related articles for article (PubMed ID: 12826672)
1. Influence of pH on NMR structure and stability of the human prion protein globular domain.
Calzolai L; Zahn R
J Biol Chem; 2003 Sep; 278(37):35592-6. PubMed ID: 12826672
[TBL] [Abstract][Full Text] [Related]
2. NMR solution structure of the human prion protein.
Zahn R; Liu A; Lührs T; Riek R; von Schroetter C; López García F; Billeter M; Calzolai L; Wider G; Wüthrich K
Proc Natl Acad Sci U S A; 2000 Jan; 97(1):145-50. PubMed ID: 10618385
[TBL] [Abstract][Full Text] [Related]
3. NMR structure of the human doppel protein.
Lührs T; Riek R; Güntert P; Wüthrich K
J Mol Biol; 2003 Mar; 326(5):1549-57. PubMed ID: 12595265
[TBL] [Abstract][Full Text] [Related]
4. A scrapie-like unfolding intermediate of the prion protein domain PrP(121-231) induced by acidic pH.
Hornemann S; Glockshuber R
Proc Natl Acad Sci U S A; 1998 May; 95(11):6010-4. PubMed ID: 9600908
[TBL] [Abstract][Full Text] [Related]
5. Prion protein fragments spanning helix 1 and both strands of beta sheet (residues 125-170) show evidence for predominantly helical propensity by CD and NMR.
Sharman GJ; Kenward N; Williams HE; Landon M; Mayer RJ; Searle MS
Fold Des; 1998; 3(5):313-20. PubMed ID: 9806936
[TBL] [Abstract][Full Text] [Related]
6. Peptides and proteins in neurodegenerative disease: helix propensity of a polypeptide containing helix 1 of the mouse prion protein studied by NMR and CD spectroscopy.
Liu A; Riek R; Zahn R; Hornemann S; Glockshuber R; Wüthrich K
Biopolymers; 1999; 51(2):145-52. PubMed ID: 10397798
[TBL] [Abstract][Full Text] [Related]
7. Conformational polymorphism of the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein.
De Gioia L; Selvaggini C; Ghibaudi E; Diomede L; Bugiani O; Forloni G; Tagliavini F; Salmona M
J Biol Chem; 1994 Mar; 269(11):7859-62. PubMed ID: 7907586
[TBL] [Abstract][Full Text] [Related]
8. Molecular dynamics simulations of human prion protein: importance of correct treatment of electrostatic interactions.
Zuegg J; Gready JE
Biochemistry; 1999 Oct; 38(42):13862-76. PubMed ID: 10529232
[TBL] [Abstract][Full Text] [Related]
9. Molecular mechanism for low pH triggered misfolding of the human prion protein.
DeMarco ML; Daggett V
Biochemistry; 2007 Mar; 46(11):3045-54. PubMed ID: 17315950
[TBL] [Abstract][Full Text] [Related]
10. NMR structure of the mouse prion protein domain PrP(121-231).
Riek R; Hornemann S; Wider G; Billeter M; Glockshuber R; Wüthrich K
Nature; 1996 Jul; 382(6587):180-2. PubMed ID: 8700211
[TBL] [Abstract][Full Text] [Related]
11. Assessing the acid-base and conformational properties of histidine residues in human prion protein (125-228) by means of pK(a) calculations and molecular dynamics simulations.
Langella E; Improta R; Crescenzi O; Barone V
Proteins; 2006 Jul; 64(1):167-77. PubMed ID: 16639746
[TBL] [Abstract][Full Text] [Related]
12. NMR structure of the J-domain and the Gly/Phe-rich region of the Escherichia coli DnaJ chaperone.
Pellecchia M; Szyperski T; Wall D; Georgopoulos C; Wüthrich K
J Mol Biol; 1996 Jul; 260(2):236-50. PubMed ID: 8764403
[TBL] [Abstract][Full Text] [Related]
13. Multiple folding pathways for heterologously expressed human prion protein.
Jackson GS; Hill AF; Joseph C; Hosszu L; Power A; Waltho JP; Clarke AR; Collinge J
Biochim Biophys Acta; 1999 Apr; 1431(1):1-13. PubMed ID: 10209273
[TBL] [Abstract][Full Text] [Related]
14. Exploring the propensities of helices in PrP(C) to form beta sheet using NMR structures and sequence alignments.
Dima RI; Thirumalai D
Biophys J; 2002 Sep; 83(3):1268-80. PubMed ID: 12202354
[TBL] [Abstract][Full Text] [Related]
15. Prion protein peptides induce alpha-helix to beta-sheet conformational transitions.
Nguyen J; Baldwin MA; Cohen FE; Prusiner SB
Biochemistry; 1995 Apr; 34(13):4186-92. PubMed ID: 7703230
[TBL] [Abstract][Full Text] [Related]
16. NMR structure of the bovine prion protein.
López Garcia F; Zahn R; Riek R; Wüthrich K
Proc Natl Acad Sci U S A; 2000 Jul; 97(15):8334-9. PubMed ID: 10899999
[TBL] [Abstract][Full Text] [Related]
17. pH-dependent stability and conformation of the recombinant human prion protein PrP(90-231).
Swietnicki W; Petersen R; Gambetti P; Surewicz WK
J Biol Chem; 1997 Oct; 272(44):27517-20. PubMed ID: 9346881
[TBL] [Abstract][Full Text] [Related]
18. Folding and intrinsic stability of deletion variants of PrP(121-231), the folded C-terminal domain of the prion protein.
Eberl H; Glockshuber R
Biophys Chem; 2002 May; 96(2-3):293-303. PubMed ID: 12034448
[TBL] [Abstract][Full Text] [Related]
19. Solution structure of Syrian hamster prion protein rPrP(90-231).
Liu H; Farr-Jones S; Ulyanov NB; Llinas M; Marqusee S; Groth D; Cohen FE; Prusiner SB; James TL
Biochemistry; 1999 Apr; 38(17):5362-77. PubMed ID: 10220323
[TBL] [Abstract][Full Text] [Related]
20. Aggregation and fibrillization of the recombinant human prion protein huPrP90-231.
Swietnicki W; Morillas M; Chen SG; Gambetti P; Surewicz WK
Biochemistry; 2000 Jan; 39(2):424-31. PubMed ID: 10631004
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
