+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-27100 | |||||||||
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Title | Cryo-EM structure of BCL10 CARD - MALT1 DD filament | |||||||||
Map data | CryoEM structure BCL10 CARD-MALT1 | |||||||||
Sample |
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Keywords | filament / CBM complex / IMMUNE SYSTEM | |||||||||
Function / homology | Function and homology information positive regulation of lymphotoxin A production / polkadots / B-1 B cell differentiation / positive regulation of T-helper 17 cell differentiation / CBM complex / regulation of T cell receptor signaling pathway / protein kinase B binding / response to fungus / antifungal innate immune response / CARD domain binding ...positive regulation of lymphotoxin A production / polkadots / B-1 B cell differentiation / positive regulation of T-helper 17 cell differentiation / CBM complex / regulation of T cell receptor signaling pathway / protein kinase B binding / response to fungus / antifungal innate immune response / CARD domain binding / positive regulation of mast cell cytokine production / T cell apoptotic process / B cell apoptotic process / negative regulation of mature B cell apoptotic process / programmed cell death / CLEC7A/inflammasome pathway / nuclear export / positive regulation of extrinsic apoptotic signaling pathway / non-canonical NF-kappaB signal transduction / response to food / toll-like receptor signaling pathway / small molecule binding / : / positive regulation of T cell receptor signaling pathway / cytoplasmic microtubule / B cell activation / general transcription initiation factor binding / immunological synapse / NF-kappaB binding / immunoglobulin mediated immune response / cellular defense response / lipopolysaccharide-mediated signaling pathway / positive regulation of phosphorylation / T cell proliferation / positive regulation of interleukin-2 production / positive regulation of interleukin-1 beta production / positive regulation of protein ubiquitination / proteolysis involved in protein catabolic process / neural tube closure / positive regulation of interleukin-8 production / Activation of NF-kappaB in B cells / protein homooligomerization / positive regulation of T cell cytokine production / CLEC7A (Dectin-1) signaling / fibrillar center / defense response / cellular response to mechanical stimulus / FCERI mediated NF-kB activation / positive regulation of interleukin-6 production / ubiquitin-protein transferase activity / positive regulation of T cell activation / Downstream TCR signaling / E3 ubiquitin ligases ubiquitinate target proteins / peptidase activity / positive regulation of NF-kappaB transcription factor activity / T cell receptor signaling pathway / protein-macromolecule adaptor activity / cellular response to lipopolysaccharide / protease binding / regulation of apoptotic process / positive regulation of canonical NF-kappaB signal transduction / endopeptidase activity / adaptive immune response / Hydrolases; Acting on peptide bonds (peptidases); Cysteine endopeptidases / transcription coactivator activity / lysosome / positive regulation of apoptotic process / membrane raft / cysteine-type endopeptidase activity / innate immune response / ubiquitin protein ligase binding / protein-containing complex binding / negative regulation of apoptotic process / positive regulation of DNA-templated transcription / perinuclear region of cytoplasm / protein-containing complex / proteolysis / identical protein binding / nucleus / cytosol / cytoplasm Similarity search - Function | |||||||||
Biological species | Homo sapiens (human) | |||||||||
Method | helical reconstruction / cryo EM / Resolution: 4.3 Å | |||||||||
Authors | David L / Wu H | |||||||||
Funding support | 1 items
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Citation | Journal: Cancer Discov / Year: 2022 Title: BCL10 Mutations Define Distinct Dependencies Guiding Precision Therapy for DLBCL. Authors: Min Xia / Liron David / Matt Teater / Johana Gutierrez / Xiang Wang / Cem Meydan / Andrew Lytle / Graham W Slack / David W Scott / Ryan D Morin / Ozlem Onder / Kojo S J Elenitoba-Johnson / ...Authors: Min Xia / Liron David / Matt Teater / Johana Gutierrez / Xiang Wang / Cem Meydan / Andrew Lytle / Graham W Slack / David W Scott / Ryan D Morin / Ozlem Onder / Kojo S J Elenitoba-Johnson / Nahuel Zamponi / Leandro Cerchietti / Tianbao Lu / Ulrike Philippar / Lorena Fontan / Hao Wu / Ari M Melnick / 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 ...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. SIGNIFICANCE: ABC-DLBCLs feature frequent mutations of signaling mediators that converge on the CBM complex. We use structure-function approaches to reveal that BCL10 mutations fall into two distinct ...SIGNIFICANCE: ABC-DLBCLs feature frequent mutations of signaling mediators that converge on the CBM complex. We use structure-function approaches to reveal that BCL10 mutations fall into two distinct biochemical classes. Both classes confer resistance to BTK inhibitors, whereas BCL10 truncations confer hyperresponsiveness to MALT1 inhibitors, providing a road map for precision therapies in ABC-DLBCLs. See related commentary by Phelan and Oellerich, p. 1844. This article is highlighted in the In This Issue feature, p. 1825. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_27100.map.gz | 118.9 MB | EMDB map data format | |
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Header (meta data) | emd-27100-v30.xml emd-27100.xml | 16.2 KB 16.2 KB | Display Display | EMDB header |
Images | emd_27100.png | 173.3 KB | ||
Filedesc metadata | emd-27100.cif.gz | 5.4 KB | ||
Others | emd_27100_half_map_1.map.gz emd_27100_half_map_2.map.gz | 108.1 MB 108.1 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-27100 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-27100 | HTTPS FTP |
-Validation report
Summary document | emd_27100_validation.pdf.gz | 940.8 KB | Display | EMDB validaton report |
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Full document | emd_27100_full_validation.pdf.gz | 940.4 KB | Display | |
Data in XML | emd_27100_validation.xml.gz | 14.3 KB | Display | |
Data in CIF | emd_27100_validation.cif.gz | 16.9 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-27100 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-27100 | HTTPS FTP |
-Related structure data
Related structure data | 8czoMC 8czdC M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_27100.map.gz / Format: CCP4 / Size: 137.1 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | CryoEM structure BCL10 CARD-MALT1 | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.1019 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: half2 map
File | emd_27100_half_map_1.map | ||||||||||||
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Annotation | half2 map | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: half1 map
File | emd_27100_half_map_2.map | ||||||||||||
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Annotation | half1 map | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
-Entire : filament
Entire | Name: filament |
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Components |
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-Supramolecule #1: filament
Supramolecule | Name: filament / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: Homo sapiens (human) |
-Macromolecule #1: Mucosa-associated lymphoid tissue lymphoma translocation protein 1
Macromolecule | Name: Mucosa-associated lymphoid tissue lymphoma translocation protein 1 type: protein_or_peptide / ID: 1 / Number of copies: 22 / Enantiomer: LEVO EC number: Hydrolases; Acting on peptide bonds (peptidases); Cysteine endopeptidases |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 10.615389 KDa |
Recombinant expression | Organism: Escherichia phage EcSzw-2 (virus) |
Sequence | String: TLNRLREPLL RRLSELLDQA PEGRGWRRLA ELAGSRGRLR LSCLDLEQCS LKVLEPEGSP SLCLLKLMGE KGCTVTELSD FLQAMEHTE VLQLL UniProtKB: Mucosa-associated lymphoid tissue lymphoma translocation protein 1 |
-Macromolecule #2: B-cell lymphoma/leukemia 10
Macromolecule | Name: B-cell lymphoma/leukemia 10 / type: protein_or_peptide / ID: 2 / Number of copies: 22 / Enantiomer: LEVO |
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Source (natural) | Organism: Homo sapiens (human) |
Molecular weight | Theoretical: 12.614566 KDa |
Recombinant expression | Organism: Escherichia phage EcSzw-2 (virus) |
Sequence | String: EEDLTEVKKD ALENLRVYLC EKIIAERHFD HLRAKKILSR EDTEEISCRT SSRKRAGKLL DYLQENPKGL DTLVESIRRE KTQNFLIQK ITDEVLKLRN IKLEHLK UniProtKB: B-cell lymphoma/leukemia 10 |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | helical reconstruction |
Aggregation state | filament |
-Sample preparation
Buffer | pH: 7.5 Component:
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Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Instrument: FEI VITROBOT MARK III |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: FEI FALCON II (4k x 4k) / Number grids imaged: 1 / Number real images: 700 / Average electron dose: 55.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 2.7 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.5 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 47000 |
Sample stage | Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Final reconstruction | Applied symmetry - Helical parameters - Δz: 5.0 Å Applied symmetry - Helical parameters - Δ&Phi: -100.8 ° Applied symmetry - Helical parameters - Axial symmetry: C1 (asymmetric) Resolution.type: BY AUTHOR / Resolution: 4.3 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: RELION (ver. 3.1) / Number images used: 23000 |
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Startup model | Type of model: EMDB MAP EMDB ID: |
Final angle assignment | Type: NOT APPLICABLE |