7CRZ
Crystal structure of human glucose transporter GLUT3 bound with C3361
Summary for 7CRZ
Entry DOI | 10.2210/pdb7crz/pdb |
Related | 6M2L |
Descriptor | Solute carrier family 2, facilitated glucose transporter member 3, (2S,3R,4S,5R,6R)-6-(hydroxymethyl)-4-undec-10-enoxy-oxane-2,3,5-triol, (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate, ... (4 entities in total) |
Functional Keywords | mfs, hexose transporter, inhibitor, plasmodium falciparum, transport protein |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 1 |
Total formula weight | 58946.16 |
Authors | Yuan, Y.Y.,Zhang, S.,Wang, N.,Jiang, X.,Yan, N. (deposition date: 2020-08-14, release date: 2021-01-13, Last modification date: 2023-11-29) |
Primary citation | Huang, J.,Yuan, Y.,Zhao, N.,Pu, D.,Tang, Q.,Zhang, S.,Luo, S.,Yang, X.,Wang, N.,Xiao, Y.,Zhang, T.,Liu, Z.,Sakata-Kato, T.,Jiang, X.,Kato, N.,Yan, N.,Yin, H. Orthosteric-allosteric dual inhibitors of PfHT1 as selective antimalarial agents. Proc.Natl.Acad.Sci.USA, 118:-, 2021 Cited by PubMed: 33402433DOI: 10.1073/pnas.2017749118 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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