SwePub
Sök i LIBRIS databas

  Utökad sökning

L773:1097 0134 OR L773:0887 3585
 

Sökning: L773:1097 0134 OR L773:0887 3585 > Computational asses...

Computational assessment of folding energy landscapes in heterodimeric coiled coils

Andre, Ingemar (författare)
Lund University, Sweden
Bjelic, Sinisa (författare)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB)
 (creator_code:org_t)
2018-05-06
2018
Engelska.
Ingår i: Proteins. - : Wiley-Blackwell. - 0887-3585 .- 1097-0134. ; 86:7, s. 790-801
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The coiled coil structural motif consists of alpha helices supercoiling around each other to form staggered knobs-into-holes packing. Such structures are deceptively simple, especially as they often can be described with parametric equations, but are known to exist in various conformations. Even the simplest systems, consisting of 2 monomers, can assemble into a wide range of states. They can form canonical as well as noncanonical coiled coils, be parallel or antiparallel, where helices associate with different degrees of shift, tilt, and rotation. Here, we investigate the energy landscape of heterodimeric coiled coils by carrying out de novo folding simulations starting from amino acid sequence. We folded a diverse set of 22 heterodimers and demonstrate that the approach is capable of identifying the atomic details in the experimental structure in the majority of cases. Our methodology also enables exploration of alternative states that can be accessible in solution beyond the experimentally determined structure. For many systems, we observe folding energy landscapes with multiple energy minima and several isoenergetic states. By comparing coiled coils from single domains and those extracted from larger proteins, we find that standalone coiled coils have deeper energy wells at the experimentally determined conformation. By folding the competing homodimeric states in addition to the heterodimers, we observe that the structural specificity towards the heteromeric state is often small. Taken together, our results demonstrate that de novo folding simulations can be a powerful tool to characterize structural specificity of coiled coils when coupled to assessment of energy landscapes.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

coiled coil
de novo folding
energy landscapes
Rosetta
structural specificity
Biokemi
Biochemistry

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

  • Proteins (Sök värdpublikationen i LIBRIS)

Till lärosätets databas

Hitta mer i SwePub

Av författaren/redakt...
Andre, Ingemar
Bjelic, Sinisa
Om ämnet
NATURVETENSKAP
NATURVETENSKAP
och Biologi
och Biokemi och mole ...
Artiklar i publikationen
Proteins
Av lärosätet
Linnéuniversitetet

Sök utanför 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 Stäng

Kopiera och spara länken för att återkomma till aktuell vy