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Structure paper

TitleMolecular basis for inhibiting human glucose transporters by exofacial inhibitors.
Journal, issue, pagesNat Commun, Vol. 13, Page 2632-2632, Year 2022
Publish dateNov 3, 2021 (structure data deposition date)
AuthorsWang, N. / Zhang, S. / Yuan, Y. / Xu, H. / Defossa, E. / Matter, H. / Besenius, M. / Derdau, V. / Dreyer, M. / Halland, N. ...Wang, N. / Zhang, S. / Yuan, Y. / Xu, H. / Defossa, E. / Matter, H. / Besenius, M. / Derdau, V. / Dreyer, M. / Halland, N. / He, K.H. / Petry, S. / Podeschwa, M. / Tennagels, N. / Jiang, X. / Yan, N.
External linksNat Commun / PubMed:35552392
MethodsX-ray diffraction
Resolution2.1 - 2.3 Å
Structure data

PDB-7sps:
Crystal structure of human glucose transporter GLUT3 bound with exofacial inhibitor SA47
Method: X-RAY DIFFRACTION / Resolution: 2.3 Å

PDB-7spt:
Crystal structure of exofacial state human glucose transporter GLUT3
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

Chemicals

ChemComp-A0E:
methyl N-[(2-{4-[4-(5-fluoro-2-methoxyphenyl)piperazin-1-yl]-1H-pyrazolo[3,4-d]pyrimidin-1-yl}phenyl)methyl]-beta-alaninate

ChemComp-OLC:
(2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate

ChemComp-HOH:
WATER

ChemComp-GLC:
alpha-D-glucopyranose

Source
  • homo sapiens (human)
KeywordsTRANSPORT PROTEIN/INHIBITOR / MFS / hexose transporter / inhibitor / TRANSPORT PROTEIN-INHIBITOR complex / TRANSPORT PROTEIN

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