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Volumn 11, Issue 5, 2002, Pages 1004-1016

Distance dependence and salt sensitivity of pairwise, coulombic interactions in a protein

Author keywords

Coulombic interactions; Determinants of pKa values; Electrostatics; Ionic strength; Poisson Boltzmann; Salt effects; Staphylococcal nuclease

Indexed keywords

HISTIDINE; NUCLEASE; PROTEIN; SODIUM CHLORIDE;

EID: 0036228118     PISSN: 09618368     EISSN: None     Source Type: Journal    
DOI: 10.1110/ps.4700102     Document Type: Article
Times cited : (106)

References (53)
  • 3
    • 0025327584 scopus 로고
    • Protein stability and electrostatic interactions between solvent exposed charged side chains
    • (1990) Proteins , vol.8 , pp. 23-29
    • Akke, M.1    Forsen, S.2
  • 6
    • 0029665693 scopus 로고    scopus 로고
    • as in proteins
    • (1996) Biochemistry , vol.35 , pp. 7819-7833
  • 20
    • 0027477251 scopus 로고
    • Multiple-site titration and molecular modeling: Two rapid methods for computing energies and forces for ionizable groups in proteins
    • (1993) Proteins , vol.15 , pp. 266-282
    • Gilson, M.K.1
  • 23
    • 0025877987 scopus 로고
    • The crystal structure of staphylococcal nuclease refined at 1.7 Å resolution
    • (1991) Proteins , vol.10 , pp. 92-105
    • Hynes, T.T.1    Fox, R.O.2
  • 27
    • 0033551039 scopus 로고    scopus 로고
    • a values and the pH dependent stability of the N-terminal domain of L9 as probes of electrostatic interactions in the denatured state. Differentiation between local and nonlocal interactions
    • (1999) Biochemistry , vol.38 , pp. 4896-4903
    • Kuhlman, B.1    Luisi, D.2    Young, P.3    Raleigh, D.4
  • 31
    • 0002870406 scopus 로고
    • Observation of histidine residues in proteins by means of nuclear magnetic resonance spectroscopy
    • (1975) Acc. Chem. Res. , vol.8 , pp. 70-80
    • Markley, J.1
  • 34
    • 0027980588 scopus 로고
    • Thermodynamic study of the acid denaturation of bamase and its dependence on ionic strength: Evidence for residual electrostatic interactions in the acid/thermally denatured state
    • (1994) Biochemistry , vol.33 , pp. 8826-8832
    • Oliveberg, M.1    Vuilleumier, S.2    Fersht, A.3
  • 41
    • 0035451052 scopus 로고    scopus 로고
    • What are the dielectric "constants" of proteins and how to validate electrostatic models?
    • (2001) Proteins , vol.44 , pp. 400-417
    • Schutz, C.N.1    Warshel, A.2
  • 53
    • 0028859420 scopus 로고
    • Conformation and hydrogen ion titration of proteins: A continuum electrostatic model with conformational flexibility
    • (1995) Biophys. J. , vol.69 , pp. 1721-1733
    • You, T.1    Bashford, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.