Literature DB >> 9566312

Chemical shift homology in proteins.

B C Potts1, W J Chazin.   

Abstract

The degree of chemical shift similarity for homologous proteins has been determined from a chemical shift database of over 50 proteins representing a variety of families and folds, and spanning a wide range of sequence homologies. After sequence alignment, the similarity of the secondary chemical shifts of C alpha protons was examined as a function of amino acid sequence identity for 37 pairs of structurally homologous proteins. A correlation between sequence identity and secondary chemical shift rmsd was observed. Important insights are provided by examining the sequence identity of homologous proteins versus percentage of secondary chemical shifts that fall within 0.1 and 0.3 ppm thresholds. These results begin to establish practical guidelines for the extent of chemical shift similarity to expect among structurally homologous proteins.

Mesh:

Substances:

Year:  1998        PMID: 9566312     DOI: 10.1023/a:1008245501057

Source DB:  PubMed          Journal:  J Biomol NMR        ISSN: 0925-2738            Impact factor:   2.835


  21 in total

1.  1H NMR studies of human lysozyme: spectral assignment and comparison with hen lysozyme.

Authors:  C Redfield; C M Dobson
Journal:  Biochemistry       Date:  1990-08-07       Impact factor: 3.162

2.  1H NMR assignments of apo calcyclin and comparative structural analysis with calbindin D9k and S100 beta.

Authors:  B C Potts; G Carlström; K Okazaki; H Hidaka; W J Chazin
Journal:  Protein Sci       Date:  1996-11       Impact factor: 6.725

3.  Application of 1H NMR chemical shifts to measure the quality of protein structures.

Authors:  M P Williamson; J Kikuchi; T Asakura
Journal:  J Mol Biol       Date:  1995-04-07       Impact factor: 5.469

4.  Identification of N-terminal helix capping boxes by means of 13C chemical shifts.

Authors:  A M Gronenborn; G M Clore
Journal:  J Biomol NMR       Date:  1994-05       Impact factor: 2.835

5.  Common structural changes accompany the functional inactivation of HPr by seryl phosphorylation or by serine to aspartate substitution.

Authors:  M Wittekind; J Reizer; J Deutscher; M H Saier; R E Klevit
Journal:  Biochemistry       Date:  1989-12-26       Impact factor: 3.162

Review 6.  Copper protein structures.

Authors:  E T Adman
Journal:  Adv Protein Chem       Date:  1991

7.  1H, 13C and 15N chemical shift referencing in biomolecular NMR.

Authors:  D S Wishart; C G Bigam; J Yao; F Abildgaard; H J Dyson; E Oldfield; J L Markley; B D Sykes
Journal:  J Biomol NMR       Date:  1995-09       Impact factor: 2.835

8.  The 13C chemical-shift index: a simple method for the identification of protein secondary structure using 13C chemical-shift data.

Authors:  D S Wishart; B D Sykes
Journal:  J Biomol NMR       Date:  1994-03       Impact factor: 2.835

Review 9.  Chemical shifts and three-dimensional protein structures.

Authors:  E Oldfield
Journal:  J Biomol NMR       Date:  1995-04       Impact factor: 2.835

10.  Structural and functional relations among thioredoxins of different species.

Authors:  H Eklund; F K Gleason; A Holmgren
Journal:  Proteins       Date:  1991
View more
  2 in total

1.  RefDB: a database of uniformly referenced protein chemical shifts.

Authors:  Haiyan Zhang; Stephen Neal; David S Wishart
Journal:  J Biomol NMR       Date:  2003-03       Impact factor: 2.835

2.  SHIFTX2: significantly improved protein chemical shift prediction.

Authors:  Beomsoo Han; Yifeng Liu; Simon W Ginzinger; David S Wishart
Journal:  J Biomol NMR       Date:  2011-03-30       Impact factor: 2.835

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.