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7F9F

Thrombocorticin

Summary for 7F9F
Entry DOI10.2210/pdb7f9f/pdb
Related7F91
DescriptorThrombocorticin, MAGNESIUM ION (3 entities in total)
Functional Keywordsbioactive protein, thrombocorticin, sugar binding protein
Biological sourceCorticium sp. (in: Fungi)
Total number of polymer chains4
Total formula weight54744.10
Authors
Kageyama, H.,Onodera, K.,Sakai, R.,Tanaka, Y.,Freymann, D.M. (deposition date: 2021-07-04, release date: 2022-07-06, Last modification date: 2024-10-16)
Primary citationWatari, H.,Kageyama, H.,Masubuchi, N.,Nakajima, H.,Onodera, K.,Focia, P.J.,Oshiro, T.,Matsui, T.,Kodera, Y.,Ogawa, T.,Yokoyama, T.,Hirayama, M.,Hori, K.,Freymann, D.M.,Imai, M.,Komatsu, N.,Araki, M.,Tanaka, Y.,Sakai, R.
A marine sponge-derived lectin reveals hidden pathway for thrombopoietin receptor activation.
Nat Commun, 13:7262-7262, 2022
Cited by
PubMed Abstract: N-glycan-mediated activation of the thrombopoietin receptor (MPL) under pathological conditions has been implicated in myeloproliferative neoplasms induced by mutant calreticulin, which forms an endogenous receptor-agonist complex that traffics to the cell surface and constitutively activates the receptor. However, the molecular basis for this mechanism is elusive because oncogenic activation occurs only in the cell-intrinsic complex and is thus cannot be replicated with external agonists. Here, we describe the structure and function of a marine sponge-derived MPL agonist, thrombocorticin (ThC), a homodimerized lectin with calcium-dependent fucose-binding properties. In-depth characterization of lectin-induced activation showed that, similar to oncogenic activation, sugar chain-mediated activation persists due to limited receptor internalization. The strong synergy between ThC and thrombopoietin suggests that ThC catalyzes the formation of receptor dimers on the cell surface. Overall, the existence of sugar-mediated MPL activation, in which the mode of activation is different from the original ligand, suggests that receptor activation is unpredictably diverse in living organisms.
PubMed: 36433967
DOI: 10.1038/s41467-022-34921-2
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.411 Å)
Structure validation

237735

数据于2025-06-18公开中

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