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PMID: 3691523 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

1H-NMR sequential assignments and cation-binding studies of spinach plastocyanin.

European journal of biochemistry ·Vol. 170 ·No. 1-2 ·1987-12-30 ·Pages 279-92

Driscoll PC, Hill HA, Redfield C

Abstract

The essentially complete assignment of the 1H-NMR spectrum of the Cu(i) form of spinach plastocyanin has been achieved using two-dimensional NMR techniques and sequence-specific resonance assignment procedures. A variety of pH and temperature conditions was utilised to overcome the problems of resonance overlap in the spectrum, degeneracy of C alpha H and solvent H2O chemical shifts, and cross-saturation of labile NH resonances. A qualitative analysis of the long-range nuclear Overhauser effects observed indicates that the backbone fold of spinach plastocyanin is very similar to that of poplar plastocyanin, whose structure has been solved by X-ray crystallography and differs in 22 of its 99 amino acid residues. The assignments provide a basis for further investigations into the structural and ion- and protein-binding properties of plastocyanin in solution.

MeSH Terms
Binding Sites Cations Hydrogen Kinetics Magnetic Resonance Spectroscopy/methods Plant Proteins/metabolism Plants/metabolism Plastocyanin/metabolism Protein Binding Protein Conformation Species Specificity
Chemicals
Cations Plant Proteins Hydrogen Plastocyanin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Driscoll P C
Inorganic Chemistry Laboratory, University of Oxford, England.
Hill H A
Redfield C
Article Info
Journal
European journal of biochemistry
Abbr.
Eur J Biochem
ISSN
0014-2956
Published
1987-12-30
Pages
279-92
Language
English
Region
England
NLM ID
0107600
Subset
IM
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