8CZD
Cryo-EM structure of BCL10 R58Q filament
Summary for 8CZD
| Entry DOI | 10.2210/pdb8czd/pdb |
| EMDB information | 27095 |
| Descriptor | B-cell lymphoma/leukemia 10 (1 entity in total) |
| Functional Keywords | filament, cbm complex, immune system |
| Biological source | Homo sapiens (human) |
| Total number of polymer chains | 20 |
| Total formula weight | 251710.04 |
| Authors | |
| Primary citation | Xia, M.,David, L.,Teater, M.,Gutierrez, J.,Wang, X.,Meydan, C.,Lytle, A.,Slack, G.W.,Scott, D.W.,Morin, R.D.,Onder, O.,Elenitoba-Johnson, K.S.J.,Zamponi, N.,Cerchietti, L.,Lu, T.,Philippar, U.,Fontan, L.,Wu, H.,Melnick, A.M. BCL10 Mutations Define Distinct Dependencies Guiding Precision Therapy for DLBCL. Cancer Discov, 12:1922-1941, 2022 Cited by PubMed Abstract: Activated B cell-like diffuse large B-cell lymphomas (ABC-DLBCL) have unfavorable outcomes and chronic activation of CARD11-BCL10-MALT1 (CBM) signal amplification complexes that form due to polymerization of BCL10 subunits, which is affected by recurrent somatic mutations in ABC-DLBCLs. Herein, we show that BCL10 mutants fall into at least two functionally distinct classes: missense mutations of the BCL10 CARD domain and truncation of its C-terminal tail. Truncating mutations abrogated a motif through which MALT1 inhibits BCL10 polymerization, trapping MALT1 in its activated filament-bound state. CARD missense mutations enhanced BCL10 filament formation, forming glutamine network structures that stabilize BCL10 filaments. Mutant forms of BCL10 were less dependent on upstream CARD11 activation and thus manifested resistance to BTK inhibitors, whereas BCL10 truncating but not CARD mutants were hypersensitive to MALT1 inhibitors. Therefore, BCL10 mutations are potential biomarkers for BTK inhibitor resistance in ABC-DLBCL, and further precision can be achieved by selecting therapy based on specific biochemical effects of distinct mutation classes. PubMed: 35658124DOI: 10.1158/2159-8290.CD-21-1566 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (4.6 Å) |
Structure validation
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