Literature DB >> 11023921

Cation-binding sites of subtilisin Carlsberg probed with Eu(III) luminescence.

S Lee1, D J Jang.   

Abstract

Two Ca(2+)-binding sites of subtilisin Carlsberg are studied by monitoring static and time-resolved luminescence of selectively substituted Eu(3+) at each site, and they are found to be characteristically quite different from each other. Compared with the coordination sphere of free Eu(3+), two sites are very similar to each other, so that both have a well-defined binding structure with low coordination symmetry. However, compared with the weak site, the strong site is relatively more polar, more symmetrical, and more easily accessible. Furthermore, despite the absence of water reported in the x-ray crystal structure (, Eur. J. Biochem. 166:673-692), one water molecule is found to exist in the coordination sphere of the strong site in aqueous solution. Thus it is suggested that in solution the Ca(2+) bound in the strong site forms an additional coordination bond to a solvent or substrate molecule.

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Year:  2000        PMID: 11023921      PMCID: PMC1301107          DOI: 10.1016/S0006-3495(00)76465-4

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  15 in total

1.  Large increases in general stability for subtilisin BPN' through incremental changes in the free energy of unfolding.

Authors:  M W Pantoliano; M Whitlow; J F Wood; S W Dodd; K D Hardman; M L Rollence; P N Bryan
Journal:  Biochemistry       Date:  1989-09-05       Impact factor: 3.162

Review 2.  Homology modelling and protein engineering strategy of subtilases, the family of subtilisin-like serine proteinases.

Authors:  R J Siezen; W M de Vos; J A Leunissen; B W Dijkstra
Journal:  Protein Eng       Date:  1991-10

3.  The refined crystal structure of subtilisin Carlsberg at 2.5 A resolution.

Authors:  D J Neidhart; G A Petsko
Journal:  Protein Eng       Date:  1988-10

4.  Subtilisin Carlsberg. V. The complete sequence; comparison with subtilisin BPN'; evolutionary relationships.

Authors:  E L Smith; R J DeLange; W H Evans; M Landon; F S Markland
Journal:  J Biol Chem       Date:  1968-05-10       Impact factor: 5.157

5.  An engineered disulfide cross-link accelerates the refolding rate of calcium-free subtilisin by 850-fold.

Authors:  S Strausberg; P Alexander; L Wang; T Gallagher; G Gilliland; P Bryan
Journal:  Biochemistry       Date:  1993-10-05       Impact factor: 3.162

6.  Absorption and emission spectroscopy of Eu3+ in metaphosphate glasses.

Authors: 
Journal:  Phys Rev B Condens Matter       Date:  1990-10-01

7.  The high-resolution X-ray crystal structure of the complex formed between subtilisin Carlsberg and eglin c, an elastase inhibitor from the leech Hirudo medicinalis. Structural analysis, subtilisin structure and interface geometry.

Authors:  W Bode; E Papamokos; D Musil
Journal:  Eur J Biochem       Date:  1987-08-03

8.  Dissecting the catalytic triad of a serine protease.

Authors:  P Carter; J A Wells
Journal:  Nature       Date:  1988-04-07       Impact factor: 49.962

9.  Stability of subtilisins and related proteinases (subtilases).

Authors:  N Genov; B Filippi; P Dolashka; K S Wilson; C Betzel
Journal:  Int J Pept Protein Res       Date:  1995-04

10.  Directed evolution of a subtilisin with calcium-independent stability.

Authors:  S L Strausberg; P A Alexander; D T Gallagher; G L Gilliland; B L Barnett; P N Bryan
Journal:  Biotechnology (N Y)       Date:  1995-07
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  2 in total

1.  Progressive rearrangement of subtilisin Carlsberg into orderly and inflexible conformation with Ca(2+) binding.

Authors:  S Lee; D J Jang
Journal:  Biophys J       Date:  2001-11       Impact factor: 4.033

2.  "Fluctuograms" reveal the intermittent intra-protein communication in subtilisin Carlsberg and correlate mechanical coupling with co-evolution.

Authors:  Jordi Silvestre-Ryan; Yuchun Lin; Jhih-Wei Chu
Journal:  PLoS Comput Biol       Date:  2011-03-24       Impact factor: 4.475

  2 in total

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