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7W6L

The crystal structure of MLL3-RBBP5-ASH2L in complex with H3K4me0 peptide

Summary for 7W6L
Entry DOI10.2210/pdb7w6l/pdb
DescriptorSet1/Ash2 histone methyltransferase complex subunit ASH2, Histone-lysine N-methyltransferase 2C, Retinoblastoma-binding protein 5, ... (7 entities in total)
Functional Keywordsmll family methyltransferases, product specificity, f/y switch, protein binding, protein binding-transferase complex, protein binding/transferase
Biological sourceHomo sapiens (human)
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Total number of polymer chains7
Total formula weight86552.41
Authors
Zhao, L.,Li, Y.,Chen, Y. (deposition date: 2021-12-01, release date: 2022-09-07, Last modification date: 2023-11-29)
Primary citationLi, Y.,Zhao, L.,Zhang, Y.,Wu, P.,Xu, Y.,Mencius, J.,Zheng, Y.,Wang, X.,Xu, W.,Huang, N.,Ye, X.,Lei, M.,Shi, P.,Tian, C.,Peng, C.,Li, G.,Liu, Z.,Quan, S.,Chen, Y.
Structural basis for product specificities of MLL family methyltransferases.
Mol.Cell, 82:3810-3825.e8, 2022
Cited by
PubMed Abstract: Human mixed-lineage leukemia (MLL) family methyltransferases methylate histone H3 lysine 4 to different methylation states (me1/me2/me3) with distinct functional outputs, but the mechanism underlying the different product specificities of MLL proteins remains unclear. Here, we develop methodologies to quantitatively measure the methylation rate difference between mono-, di-, and tri-methylation steps and demonstrate that MLL proteins possess distinct product specificities in the context of the minimum MLL-RBBP5-ASH2L complex. Comparative structural analyses of MLL complexes by X-ray crystal structures, fluorine-19 nuclear magnetic resonance, and molecular dynamics simulations reveal that the dynamics of two conserved tyrosine residues at the "F/Y (phenylalanine/tyrosine) switch" positions fine-tune the product specificity. The variation in the intramolecular interaction between SET-N and SET-C affects the F/Y switch dynamics, thus determining the product specificities of MLL proteins. These results indicate a modified F/Y switch rule applicable for most SET domain methyltransferases and implicate the functional divergence of MLL proteins.
PubMed: 36108631
DOI: 10.1016/j.molcel.2022.08.022
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.26 Å)
Structure validation

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數據於2024-11-06公開中

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