Endre søk
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
Galactoside-binding site in LacY
University of California at Irvine, United States.ORCID-id: 0000-0002-3364-6647
Vise andre og tillknytning
2014 (engelsk)Inngår i: Biochemistry, ISSN 0006-2960, E-ISSN 1520-4995, Vol. 53, nr 9, s. 1536-1543Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Although an X-ray crystal structure of lactose permease (LacY) has been presented with bound galactopyranoside, neither the sugar nor the residues ligating the sugar can be identified with precision at ∼3.5 Å. Therefore, additional evidence is important for identifying side chains likely to be involved in binding. On the basis of a clue from site-directed alkylation suggesting that Asn272, Gly268, and Val264 on one face of helix VIII might participate in galactoside binding, molecular dynamics simulations were conducted initially. The simulations indicate that Asn272 (helix VIII) is sufficiently close to the galactopyranosyl ring of a docked lactose analogue to play an important role in binding, the backbone at Gly268 may be involved, and Val264 does not interact with the bound sugar. When the three side chains are subjected to site-directed mutagenesis, with the sole exception of mutant Asn272 → Gln, various other replacements for Asn272 either markedly decrease affinity for the substrate (i.e., high KD) or abolish binding altogether. However, mutant Gly268 → Ala exhibits a moderate 8-fold decrease in affinity, and binding by mutant Val264 → Ala is affected only minimally. Thus, Asn272 and possibly Gly268 may comprise additional components of the galactoside-binding site in LacY.

sted, utgiver, år, opplag, sider
2014. Vol. 53, nr 9, s. 1536-1543
Emneord [en]
Galactopyranoside, High- k, Lactose permease, Molecular dynamics simulations, Side-chains, Site directed mutagenesis, X ray crystal structures
HSV kategori
Identifikatorer
URN: urn:nbn:se:kth:diva-161775DOI: 10.1021/bi401716zISI: 000332913600016PubMedID: 24520888Scopus ID: 2-s2.0-84896088314OAI: oai:DiVA.org:kth-161775DiVA, id: diva2:800009
Forskningsfinansiär
EU, FP7, Seventh Framework Programme, FP7-MC-CIG-618558
Merknad

QC 20150401

Tilgjengelig fra: 2015-04-01 Laget: 2015-03-17 Sist oppdatert: 2017-12-04bibliografisk kontrollert

Open Access i DiVA

Fulltekst mangler i DiVA

Andre lenker

Forlagets fulltekstPubMedScopus

Personposter BETA

Andersson, Magnus

Søk i DiVA

Av forfatter/redaktør
Andersson, Magnus
I samme tidsskrift
Biochemistry

Søk utenfor DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric

doi
pubmed
urn-nbn
Totalt: 23 treff
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf