Literature DB >> 6947264

Electron nuclear double resonance spectroscopy of a hen egg-white lysozyme--Cu2+ complex in tetragonal single crystals.

C A Hutchison, D J Singel.   

Abstract

We have used the electron paramagnetic resonance of Cu2+ bound in a tetragonal single crystal of hen egg-white lysozyme to obtain the electron nuclear double resonance spectra of protons in the vicinity of the Cu2+ at the site designated as B by Teichberg et al. [Teichberg, V. I., Sharon, N., Moult, J., Smilansky, A. & Yonath, A. (1974) J. Mol. Biol. 87, 357-368]. The values of the hyperfine interaction parameters and the coordinates of eight protons are reported. The configuration of the H2O molecules coordinated to the Cu2+ and their relationships to the protein molecule structure are discussed.

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Year:  1981        PMID: 6947264      PMCID: PMC349156          DOI: 10.1073/pnas.78.11.6883

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  3 in total

1.  Binding of divalent copper ions to aspartic acid residue 52 in hen egg-white lysozyme.

Authors:  V I Teichberg; N Sharon; J Moult; A Smilansky; A Yonath
Journal:  J Mol Biol       Date:  1974-08-05       Impact factor: 5.469

2.  Real-space refinement of the structure of hen egg-white lysozyme.

Authors:  R Diamond
Journal:  J Mol Biol       Date:  1974-01-25       Impact factor: 5.469

3.  Electron paramagnetic resonance spectroscopy of Cu2+ in hen egg-white lysozyme.

Authors:  C A Hutchison; D J Singel; M N Hadad; M D Kemple
Journal:  Proc Natl Acad Sci U S A       Date:  1980-09       Impact factor: 11.205

  3 in total

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