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7U6E

Head region of insulin receptor ectodomain (A-isoform) bound to the non-insulin agonist IM462

Summary for 7U6E
Entry DOI10.2210/pdb7u6e/pdb
EMDB information26363 26364
DescriptorInsulin A chain, Insulin B chain, Isoform Short of Insulin receptor, ... (6 entities in total)
Functional Keywordsinsulin receptor, insulin-mimic peptide, insulin receptor agonist, hormone-signaling protein-agonist complex, hormone/signaling protein/agonist
Biological sourceHomo sapiens (human)
More
Total number of polymer chains6
Total formula weight226315.45
Authors
Kirk, N.S.,Lawrence, M.C. (deposition date: 2022-03-03, release date: 2022-10-05)
Primary citationKirk, N.S.,Chen, Q.,Wu, Y.G.,Asante, A.L.,Hu, H.,Espinosa, J.F.,Martinez-Olid, F.,Margetts, M.B.,Mohammed, F.A.,Kiselyov, V.V.,Barrett, D.G.,Lawrence, M.C.
Activation of the human insulin receptor by non-insulin-related peptides
Nat Commun, 13:5695-, 2022
Cited by
PubMed Abstract: The human insulin receptor signalling system plays a critical role in glucose homeostasis. Insulin binding brings about extensive conformational change in the receptor extracellular region that in turn effects trans-activation of the intracellular tyrosine kinase domains and downstream signalling. Of particular therapeutic interest is whether insulin receptor signalling can be replicated by molecules other than insulin. Here, we present single-particle cryoEM structures that show how a 33-mer polypeptide unrelated to insulin can cross-link two sites on the receptor surface and direct the receptor into a signalling-active conformation. The 33-mer polypeptide engages the receptor by two helical binding motifs that are each potentially mimicable by small molecules. The resultant conformation of the receptor is distinct from-but related to-those in extant three-dimensional structures of the insulin-complexed receptor. Our findings thus illuminate unexplored pathways for controlling the signalling of the insulin receptor as well as opportunities for development of insulin mimetics.
PubMed: 36171189
DOI: 10.1038/s41467-022-33315-8
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3 Å)
Structure validation

227344

數據於2024-11-13公開中

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