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5ONB

Drosophila Bag-of-marbles CBM peptide bound to human CAF40

Summary for 5ONB
Entry DOI10.2210/pdb5onb/pdb
Related5onb
DescriptorCCR4-NOT transcription complex subunit 9, Protein bag-of-marbles, GLYCEROL (3 entities in total)
Functional Keywordsdeadenylation, ccr4-not, translational repression, translation, gene regulation
Biological sourceHomo sapiens (Human)
More
Cellular locationNucleus : Q92600
Total number of polymer chains8
Total formula weight135877.24
Authors
Raisch, T.,Sgromo, A.,Backhaus, C.,Izaurralde, E.,Weichenrieder, O. (deposition date: 2017-08-03, release date: 2017-12-27, Last modification date: 2024-01-17)
Primary citationSgromo, A.,Raisch, T.,Backhaus, C.,Keskeny, C.,Alva, V.,Weichenrieder, O.,Izaurralde, E.
DrosophilaBag-of-marbles directly interacts with the CAF40 subunit of the CCR4-NOT complex to elicit repression of mRNA targets.
RNA, 24:381-395, 2018
Cited by
PubMed Abstract: Bag-of-marbles (Bam) promotes germline stem cell (GSC) differentiation by repressing the expression of mRNAs encoding stem cell maintenance factors. Bam interacts with Benign gonial cell neoplasm (Bgcn) and the CCR4 deadenylase, a catalytic subunit of the CCR4-NOT complex. Bam has been proposed to bind CCR4 and displace it from the CCR4-NOT complex. Here, we investigated the interaction of Bam with the CCR4-NOT complex by using purified recombinant proteins. Unexpectedly, we found that Bam does not interact with CCR4 directly but instead binds to the CAF40 subunit of the complex in a manner mediated by a conserved N-terminal CAF40-binding motif (CBM). The crystal structure of the Bam CBM bound to CAF40 reveals that the CBM peptide adopts an α-helical conformation after binding to the concave surface of the crescent-shaped CAF40 protein. We further show that Bam-mediated mRNA decay and translational repression depend entirely on Bam's interaction with CAF40. Thus, Bam regulates the expression of its mRNA targets by recruiting the CCR4-NOT complex through interaction with CAF40.
PubMed: 29255063
DOI: 10.1261/rna.064584.117
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3 Å)
Structure validation

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數據於2025-06-11公開中

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