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| Title | Mechanistic basis for functional promiscuity in the TNF and TNF receptor superfamilies: structure of the LIGHT:DcR3 assembly. |
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| Journal, issue, pages | Structure, Vol. 22, Page 1252-1262, Year 2014 |
| Publish date | Apr 12, 2012 (structure data deposition date) |
Authors | Liu, W. / Zhan, C. / Cheng, H. / Kumar, P.R. / Bonanno, J.B. / Nathenson, S.G. / Almo, S.C. |
External links | Structure / PubMed:25087510 |
| Methods | X-ray diffraction |
| Resolution | 2.25 - 2.78 Å |
| Structure data | ![]() PDB-4en0: ![]() PDB-4j6g: ![]() PDB-4kg8: ![]() PDB-4kgg: ![]() PDB-4kgq: |
| Chemicals | ![]() ChemComp-PO4: ![]() ChemComp-GOL: ![]() ChemComp-NAG: ![]() ChemComp-HOH: ![]() ChemComp-CL: ![]() ChemComp-MG: |
| Source |
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Keywords | CYTOKINE / STRUCTURAL GENOMICS / PSI-BIOLOGY / NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM / NYSGRC / IMMUNITY / TNF SUPERFAMILY / HVEM / DCR3 / N-GLYCOSYLATION / MEMBRANE / SECRETED PROTEIN / ATOMS-TO-ANIMALS: THE IMMUNE FUNCTION NETWORK / IFN / Jelly-roll Fold / Bind TNF receptor HVEM and LTbR / LTbR / IMMUNE SYSTEM / LIGHT / TNF / TNFR / TNF14 / NEW HVEM / Protein Structure Initiative / Cytokine/Signaling Protein / Cytokine-Signaling Protein complex |
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