SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:uu-81328"
 

Search: onr:"swepub:oai:DiVA.org:uu-81328" > A new enzyme by rat...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

A new enzyme by rational design - the incorporation of a single His residue enables efficient thioester hydrolysis by human glutathione transferase A1-1

Hederos, Sofia (author)
Broo, Kerstin (author)
Jakobsson, Emma (author)
Uppsala universitet,Institutionen för cell- och molekylärbiologi,Organisk kemi II,Biokemi,Strukturell molekylärbiologi
show more...
Kleywegt, Gerard J (author)
Uppsala universitet,Institutionen för cell- och molekylärbiologi,Organisk kemi II,Biokemi,Strukturell molekylärbiologi
Mannervik, Bengt (author)
Uppsala universitet,Organisk kemi II,Biokemi,Strukturell molekylärbiologi
Baltzer, Lars (author)
Uppsala universitet,Organisk kemi II,Biokemi,Strukturell molekylärbiologi
show less...
 (creator_code:org_t)
2004
2004
English.
In: Proc. Nat. Acad. Sci.. ; 101, s. 13163-13167
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • A strategy for rational enzyme design is reported and illustrated by the engineering of a protein catalyst for thiol-ester hydrolysis. Five mutants of human glutathione (GSH; gamma-Glu-Cys-Gly) transferase A1-1 were designed in the search for a catalyst and to provide a set of proteins from which the reaction mechanism could be elucidated. The single mutant A216H catalyzed the hydrolysis of the S-benzoyl ester of GSH under turnover conditions with a k(cat)/K(M) of 156 M(-1) x min(-1), and a catalytic proficiency of >10(7) M(-1) when compared with the first-order rate constant of the uncatalyzed reaction. The wild-type enzyme did not hydrolyze the substrate, and thus, the introduction of a single histidine residue transformed the wild-type enzyme into a turnover system for thiol-ester hydrolysis. By kinetic analysis of single, double, and triple mutants, as well as from studies of reaction products, it was established that the enzyme A216H catalyzes the hydrolysis of the thiol-ester substrate by a mechanism that includes an acyl intermediate at the side chain of Y9. Kinetic measurements and the crystal structure of the A216H GSH complex provided compelling evidence that H216 acts as a general-base catalyst. The introduction of a single His residue into human GSH transferase A1-1 created an unprecedented enzymatic function, suggesting a strategy that may be of broad applicability in the design of new enzymes. The protein catalyst has the hallmarks of a native enzyme and is expected to catalyze various hydrolytic, as well as transesterification, reactions.

Subject headings

NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Strukturbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Structural Biology (hsv//eng)

Keyword

Organic chemistry
Organisk kemi
Biochemistry
Biokemi
Structural biology
Strukturbiologi

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Find more in SwePub

By the author/editor
Hederos, Sofia
Broo, Kerstin
Jakobsson, Emma
Kleywegt, Gerard ...
Mannervik, Bengt
Baltzer, Lars
About the subject
NATURAL SCIENCES
NATURAL SCIENCES
and Chemical Science ...
and Organic Chemistr ...
NATURAL SCIENCES
NATURAL SCIENCES
and Biological Scien ...
and Biochemistry and ...
NATURAL SCIENCES
NATURAL SCIENCES
and Biological Scien ...
and Structural Biolo ...
Articles in the publication
By the university
Uppsala University

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view