Literature DB >> 10449376

Protein redesign.

L Regan1.   

Abstract

It has been demonstrated that, for a number of proteins, it is possible to dramatically alter the connectivities between elements of secondary structure. Remarkably large loop insertions are tolerated and many redesigns have generated proteins that successfully fold to stable, active structures. Some redesigns have been entirely the choice of the investigators, whereas others have incorporated a randomization and selection step to identify optimal sequences. These studies have provided basic guidelines for the rational manipulation of protein structure and stability, they have allowed the dissection of folding pathways and they have generated proteins with the potential for practical therapeutic applications.

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Year:  1999        PMID: 10449376     DOI: 10.1016/S0959-440X(99)80070-0

Source DB:  PubMed          Journal:  Curr Opin Struct Biol        ISSN: 0959-440X            Impact factor:   6.809


  6 in total

1.  Altering dimerization specificity by changes in surface electrostatics.

Authors:  M J Nohaile; Z S Hendsch; B Tidor; R T Sauer
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-27       Impact factor: 11.205

2.  A rewired green fluorescent protein: folding and function in a nonsequential, noncircular GFP permutant.

Authors:  Philippa J Reeder; Yao-Ming Huang; Jonathan S Dordick; Christopher Bystroff
Journal:  Biochemistry       Date:  2010-12-03       Impact factor: 3.162

3.  Design of protein struts for self-assembling nanoconstructs.

Authors:  Paul Hyman; Regina Valluzzi; Edward Goldberg
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-17       Impact factor: 11.205

4.  Chimeric glutathione S-transferases containing inserts of kininogen peptides: potential novel protein therapeutics.

Authors:  Amber A Bentley; Sergei M Merkulov; Yi Peng; Rita Rozmarynowycz; Xiaoping Qi; Marianne Pusztai-Carey; William C Merrick; Vivien C Yee; Keith R McCrae; Anton A Komar
Journal:  J Biol Chem       Date:  2012-05-10       Impact factor: 5.157

5.  Dead-end elimination with perturbations (DEEPer): a provable protein design algorithm with continuous sidechain and backbone flexibility.

Authors:  Mark A Hallen; Daniel A Keedy; Bruce R Donald
Journal:  Proteins       Date:  2012-09-18

6.  CATS (Coordinates of Atoms by Taylor Series): protein design with backbone flexibility in all locally feasible directions.

Authors:  Mark A Hallen; Bruce R Donald
Journal:  Bioinformatics       Date:  2017-07-15       Impact factor: 6.937

  6 in total

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