7MSG
The crystal structure of LIGHT in complex with HVEM and CD160
Summary for 7MSG
Entry DOI | 10.2210/pdb7msg/pdb |
Descriptor | Tumor necrosis factor ligand superfamily member 14, membrane form, CD160 antigen, soluble form,Tumor necrosis factor receptor superfamily member 14, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total) |
Functional Keywords | immunity, n-glycosylation, membrane, secreted protein, cytokine, jelly-roll fold, cysteine rich domain, signaling, cell membrane, secreted, immune system, immunoglobulin superfamily, tnf |
Biological source | Homo sapiens (Human) More |
Total number of polymer chains | 6 |
Total formula weight | 136542.53 |
Authors | Liu, W.,Ramagopal, U.,Garrett-Thompson, S.C.,Fedorov, E.,Bonanno, J.B.,Almo, S.C. (deposition date: 2021-05-11, release date: 2021-10-27, Last modification date: 2024-10-30) |
Primary citation | Liu, W.,Chou, T.F.,Garrett-Thomson, S.C.,Seo, G.Y.,Fedorov, E.,Ramagopal, U.A.,Bonanno, J.B.,Wang, Q.,Kim, K.,Garforth, S.J.,Kakugawa, K.,Cheroutre, H.,Kronenberg, M.,Almo, S.C. HVEM structures and mutants reveal distinct functions of binding to LIGHT and BTLA/CD160. J.Exp.Med., 218:-, 2021 Cited by PubMed Abstract: HVEM is a TNF (tumor necrosis factor) receptor contributing to a broad range of immune functions involving diverse cell types. It interacts with a TNF ligand, LIGHT, and immunoglobulin (Ig) superfamily members BTLA and CD160. Assessing the functional impact of HVEM binding to specific ligands in different settings has been complicated by the multiple interactions of HVEM and HVEM binding partners. To dissect the molecular basis for multiple functions, we determined crystal structures that reveal the distinct HVEM surfaces that engage LIGHT or BTLA/CD160, including the human HVEM-LIGHT-CD160 ternary complex, with HVEM interacting simultaneously with both binding partners. Based on these structures, we generated mouse HVEM mutants that selectively recognized either the TNF or Ig ligands in vitro. Knockin mice expressing these muteins maintain expression of all the proteins in the HVEM network, yet they demonstrate selective functions for LIGHT in the clearance of bacteria in the intestine and for the Ig ligands in the amelioration of liver inflammation. PubMed: 34709351DOI: 10.1084/jem.20211112 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.5 Å) |
Structure validation
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