7W6L
The crystal structure of MLL3-RBBP5-ASH2L in complex with H3K4me0 peptide
Summary for 7W6L
Entry DOI | 10.2210/pdb7w6l/pdb |
Descriptor | Set1/Ash2 histone methyltransferase complex subunit ASH2, Histone-lysine N-methyltransferase 2C, Retinoblastoma-binding protein 5, ... (7 entities in total) |
Functional Keywords | mll family methyltransferases, product specificity, f/y switch, protein binding, protein binding-transferase complex, protein binding/transferase |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 7 |
Total formula weight | 86552.41 |
Authors | |
Primary citation | Li, 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: 36108631DOI: 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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