5VB9
IL-17A in complex with peptide
Summary for 5VB9
| Entry DOI | 10.2210/pdb5vb9/pdb |
| Descriptor | Interleukin-17A, Peptide inhibitor, 1,2-ETHANEDIOL, ... (5 entities in total) |
| Functional Keywords | il17, inhibitor, immune system - inhibitor complex, immune system / inhibitor |
| Biological source | Homo sapiens (Human) More |
| Cellular location | Secreted: Q16552 |
| Total number of polymer chains | 4 |
| Total formula weight | 31412.98 |
| Authors | Antonysamy, S.,Russell, M.,Zhang, A.,Groshong, C.,Manglicmot, D.,Lu, F.,Benach, J.,Wasserman, S.R.,Zhang, F.,Afshar, S.,Bina, H.,Broughton, H.,Chalmers, M.,Dodge, J.,Espada, A.,Jones, S.,Ting, J.P.,Woodman, M. (deposition date: 2017-03-28, release date: 2018-02-14, Last modification date: 2024-10-30) |
| Primary citation | Ting, J.P.,Tung, F.,Antonysamy, S.,Wasserman, S.,Jones, S.B.,Zhang, F.F.,Espada, A.,Broughton, H.,Chalmers, M.J.,Woodman, M.E.,Bina, H.A.,Dodge, J.A.,Benach, J.,Zhang, A.,Groshong, C.,Manglicmot, D.,Russell, M.,Afshar, S. Utilization of peptide phage display to investigate hotspots on IL-17A and what it means for drug discovery. PLoS ONE, 13:e0190850-e0190850, 2018 Cited by PubMed Abstract: To date, IL-17A antibodies remain the only therapeutic approach to correct the abnormal activation of the IL-17A/IL-17R signaling complex. Why is it that despite the remarkable success of IL-17 antibodies, there is no small molecule antagonist of IL-17A in the clinic? Here we offer a unique approach to address this question. In order to understand the interaction of IL-17A with its receptor, we combined peptide discovery using phage display with HDX, crystallography, and functional assays to map and characterize hot regions that contribute to most of the energetics of the IL-17A/IL-17R interaction. These functional maps are proposed to serve as a guide to aid in the development of small molecules that bind to IL-17A and block its interaction with IL-17RA. PubMed: 29329326DOI: 10.1371/journal.pone.0190850 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.7 Å) |
Structure validation
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