7sps | pdb_00007sps

Crystal structure of human glucose transporter GLUT3 bound with exofacial inhibitor SA47

spinqualitylabelsall models 7sps, resolution 2.30Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 7sps is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 2.3Å Ligands: A0E, OLC Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease GTR3_HUMAN Huntington disease. Function GTR3_HUMAN Facilitative glucose transporter. Probably a neuronal glucose transporter. Publication Abstract from PubMed Human glucose transporters (GLUTs) are responsible for cellular uptake of hexoses. Elevated expression of GLUTs, particularly GLUT1 and GLUT3, is required to fuel the hyperproliferation of cancer cells, making GLUT inhibitors potential anticancer therapeutics. Meanwhile, GLUT inhibitor-conjugated insulin is being explored to mitigate the hypoglycemia side effect of insulin therapy in type 1 diabetes. Reasoning that exofacial inhibitors of GLUT1/3 may be favored for therapeutic applications, we report here the engineering of a GLUT3 variant, designated GLUT3exo, that can be probed for screening and validating exofacial inhibitors. We identify an exofacial GLUT3 inhibitor SA47 and elucidate its mode of action by a 2.3 A resolution crystal structure of SA47-bound GLUT3. Our studies serve as a framework for the discovery of GLUTs exofacial inhibitors for therapeutic development. Molecular basis for inhibiting human glucose transporters by exofacial inhibitors.,Wang N, Zhang S, Yuan Y, Xu H, Defossa E, Matter H, Besenius M, Derdau V, Dreyer M, Halland N, He KH, Petry S, Podeschwa M, Tennagels N, Jiang X, Yan N Nat Commun. 2022 May 12;13(1):2632. doi: 10.1038/s41467-022-30326-3. PMID:35552392 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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