8C18
Solution structure of carotenoid-binding protein AstaPo1 in complex with astaxanthin
Summary for 8C18
| Entry DOI | 10.2210/pdb8c18/pdb |
| NMR Information | BMRB: 34781 |
| Descriptor | Astaxanthin binding fasciclin family protein, ASTAXANTHIN (2 entities in total) |
| Functional Keywords | protein, transport protein, astaxanthin, carotenoid |
| Biological source | Coelastrella astaxanthina |
| Total number of polymer chains | 1 |
| Total formula weight | 22230.98 |
| Authors | Kornilov, F.D.,Savitskaya, A.G.,Slonimskiy, Y.B.,Goncharuk, S.A.,Sluchanko, N.N.,Mineev, K.S. (deposition date: 2022-12-20, release date: 2023-04-05, Last modification date: 2024-06-19) |
| Primary citation | Kornilov, F.D.,Slonimskiy, Y.B.,Lunegova, D.A.,Egorkin, N.A.,Savitskaya, A.G.,Kleymenov, S.Y.,Maksimov, E.G.,Goncharuk, S.A.,Mineev, K.S.,Sluchanko, N.N. Structural basis for the ligand promiscuity of the neofunctionalized, carotenoid-binding fasciclin domain protein AstaP. Commun Biol, 6:471-471, 2023 Cited by PubMed Abstract: Fasciclins (FAS1) are ancient adhesion protein domains with no common small ligand binding reported. A unique microalgal FAS1-containing astaxanthin (AXT)-binding protein (AstaP) binds a broad repertoire of carotenoids by a largely unknown mechanism. Here, we explain the ligand promiscuity of AstaP-orange1 (AstaPo1) by determining its NMR structure in complex with AXT and validating this structure by SAXS, calorimetry, optical spectroscopy and mutagenesis. α1-α2 helices of the AstaPo1 FAS1 domain embrace the carotenoid polyene like a jaw, forming a hydrophobic tunnel, too short to cap the AXT β-ionone rings and dictate specificity. AXT-contacting AstaPo1 residues exhibit different conservation in AstaPs with the tentative carotenoid-binding function and in FAS1 proteins generally, which supports the idea of AstaP neofunctionalization within green algae. Intriguingly, a cyanobacterial homolog with a similar domain structure cannot bind carotenoids under identical conditions. These structure-activity relationships provide the first step towards the sequence-based prediction of the carotenoid-binding FAS1 members. PubMed: 37117801DOI: 10.1038/s42003-023-04832-z PDB entries with the same primary citation |
| Experimental method | SOLUTION NMR |
Structure validation
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