STRUCTURAL STUDIES OF THE DYNAMICS OF BINDING OF MIF TO PHENYLISOTHIOCYANATE
- Authors: Nemchinova A.R1, Ivanova A.G1, Sokolov A.V2, Samygina V.R1
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Affiliations:
- Shubnikov Institute of Crystallography of the Kurchatov Complex Crystallography and Photonics of the NRC "Kurchatov Institute"
- Smorodentsev Influenza Research Institute of the Russian Ministry of Health
- Issue: Vol 70, No 6 (2025)
- Pages: 969-975
- Section: STRUCTURE OF MACROMOLECULAR COMPOUNDS
- URL: https://bakhtiniada.ru/0023-4761/article/view/356306
- DOI: https://doi.org/10.7868/S3034551025060115
- ID: 356306
Cite item
Abstract
About the authors
A. R Nemchinova
Shubnikov Institute of Crystallography of the Kurchatov Complex Crystallography and Photonics of the NRC "Kurchatov Institute"Moscow, Russia
A. G Ivanova
Shubnikov Institute of Crystallography of the Kurchatov Complex Crystallography and Photonics of the NRC "Kurchatov Institute"Moscow, Russia
A. V Sokolov
Smorodentsev Influenza Research Institute of the Russian Ministry of HealthSt. Petersburg, Russia
V. R Samygina
Shubnikov Institute of Crystallography of the Kurchatov Complex Crystallography and Photonics of the NRC "Kurchatov Institute"
Email: lera@crys.ras.ru
Moscow, Russia
References
- Bloom B.R., Bennett B.M. // Science. 1966. V. 153. № 3731. P. 80. https://doi.org/10.1126/science.153.3731.80
- Sumaiya K., Langford D., Natarajaseenivasan K. et al. // Pharmacol. Ther. 2022. V. 233. P. 108024. https://doi.org/10.1016/j.pharmthera.2021.108024
- Aryuzina M.A., Vetrova E.S. // Food Systems. 2021. V. 4. № 3S. P. 8. https://doi.org/10.21323/2618–9771-2021-4-3S-8-11
- Liang J., Lei K., Liang R. et al. // Cell. Signalling. 2024. V. 117. P. 111093. https://doi.org/10.1016/j.cellsig.2024.111093
- Huang G., Ma L., Shen L. et al. // J. Cell. Mol. Med. 2022. V. 26. № 12. P. 3410. https://doi.org/10.1111/jcmm.17352
- Gaynitdinova V.V., Avdeev S.N. // Kardiologiia. 2019. V. 59. № 7. P. 84. https://doi.org/10.18087/cardio.2019.7.10259
- Emonts M., Sweep F.C., Grebenchtchikov N. et al. // Clin. Infect. Dis. 2007. V. 44. № 10. P. 1321. https://doi.org/10.1086/514344
- Sain N., Hooda V., Singh A. et al. // Cytokine. 2024. V. 176. P. 156516. https://doi.org/10.1016/j.cyto.2024.156516
- Noels H., Bernhagen J., Weber C. // Trends Cardiovasc. Med. 2009. V. 19. № 3. P. 76. https://doi.org/10.1016/j.tcm.2009.05.002
- Meyer-Siegier K., Iczkowski K., Vera P. // J. Urol. 2006. V. 175. № 4. P. 1523. https://doi.org/10.1016/S0022-5347(05)00650-6
- Petoukhov M.V., Sokolov A.V., Dadinova L.A. et al. // Crystallography Reports. 2018. V. 63. P. 589. https://doi.org/10.1134/S106377451804020X
- Lue H., Kapurniotu A., Fingerle-Rowson G. et al. // Cell. Signalling. 2006. V. 18. № 5. P. 688. https://doi.org/10.1016/j.cellsig.2005.06.013
- Yoo S.A., Leng L., Kim B.J. et al. // PNAS. 2016. V. 113. № 49. P. E7917. https://doi.org/10.1073/pnas.1612717113
- Sokolov A.V., Dadinova L.A., Petoukhov M.V. et al. // Biochemistry (Moscow). 2018. V. 83. P. 701. https://doi.org/10.1134/S000629791806007X
- Timofeev V., Samygina V. // Crystals. 2023. V. 13. № 1. P. 71. https://doi.org/10.3390/cryst13010071
- Bijak V., Szczygiel M., Lenkiewicz J. et al. // Expert Opin. Drug Discovery. 2023. V. 18. № 11. P. 1221. https://doi.org/10.1080/17460441.2023.2246881
- Wei H., McCammon J.A. // npj Drug Discovery. 2024. V. 1. № 1. P. 1. https://doi.org/10.1038/s44386-024-00001-2
- Samygina V.R. // Russ. Chem. Rev. 2016. V. 85. № 5. P. 464. https://doi.org/10.1070/RCR4529
- Zhu S., Yang S., Chen Y. et al. // J. Enzyme Inhib. Med. Chem. 2025. V. 40. № 1. P. 2501378. https://doi.org/10.1080/14756366.2025.2501378
- Lubetsky J., Dios A., Han J. et al. // J. Biol. Chem. 2002. V. 277. № 28. P. 24976. https://doi.org/10.1074/jbc.M203220200
- Dziedzic P., Cisneros J., Robertson M. et al. // JACS. 2015. V. 137. № 8. P. 2996. https://doi.org/10.1021/ja512112j
- McLean L., Zhang Y., Li H. et al. // Bioorg. Med. Chem. Lett. 2010. V. 20. № 6. P. 1821. https://doi.org/10.1016/j.bmcl.2010.02.009
- Crichlow G., Cheng K., Dabideen D. et al. // J. Biol. Chem. 2007. V. 282. № 32. P. 23089. https://doi.org/10.1074/jbc.M701825200
- McLean L., Zhang Y., Li H. et al. // Bioorg. Med. Chem. Lett. 2009. V. 19. № 23. P. 6717. https://doi.org/10.1016/j.bmcl.2009.09.106
- Crichlow G., Fan C., Keeler C. et al. // Biochem. 2012. V. 51. № 38. P. 7506. https://doi.org/10.1021/bi3005494
- Spencer E.S., Dale E.G., Gommans A.L. et al. // Eur. J. Med. Chem. 2015. V. 93. P. 501. https://doi.org/10.1016/j.ejmech.2015.02.012
- Dubova K., Sokolov A., Gorbunov N. et al. // Crystallography Reports. 2018. V. 63. P. 951. https://doi.org/10.1134/S1063774518060111
- Boyko K.M., Timofeev V.I., Samygina V.R. et al. // Crystallography Reports. 2016. V. 61. № 5. P. 691. https://doi.org/10.7868/S0023476116050052
- Rigaku Oxford Diffraction. CrysAlis PRO; Oxford Diffraction Ltd.: Oxfordshire, UK, 2017. https://rigaku.com/products/crystallography/x-ray-diffraction/crysalispro
- Kabsch W. // Acta Cryst. D. 2010. V. 66. P. 133. https://doi.org/10.1107/S0907444909047374
- Vagin A., Teplyakov A. // J. Appl. Cryst. 1997. V. 30. № 6. P. 1022. https://doi.org/10.1107/S0021889897006766
- Kovalevskiy O., Nicholls R.A., Long F. et al. // Acta Cryst. D. 2018. V. 74. № 3. P. 215. https://doi.org/10.1107/S2059798318000979
- Agirre J., Atanasova M., Bagdonas H. et al. // Acta Cryst. D. 2023. V. 79. № 6. P. 449. https://doi.org/10.1107/ S2059798323003595
- Emsley P., Cowtan K. // Acta Cryst. D. 2004. V. 60. № 12. P. 2126. https://doi.org/10.1107/S0907444904019158
- Schrödinger L., DeLano W. 2020. PyMOL. http://www.pymol.org/pymol
- Dubovskii P.V., Dubova K.M., Bourenkov G. et al. // Toxins. 2022. V. 14. № 2. P. 149. https://doi.org/10.3390/toxins14020149
- Shabalin I.G., Serov A.E., Skirgello O.E. et al. // Crystallography Reports. 2010. V. 55. № 5. P. 806. https://doi.org/10.1134/S1063774510050159
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