inactive histone-lysine N-methyltransferase 2E isoform X3 [Rattus norv - Protein

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The Human Mixed Lineage Leukemia 5 (MLL5), a Sequentially and Structurally Divergent SET Domain-Containing Protein with No Intrinsic Catalytic Activity. [PLoS One. 2016]
The Human Mixed Lineage Leukemia 5 (MLL5), a Sequentially and Structurally Divergent SET Domain-Containing Protein with No Intrinsic Catalytic Activity.
Mas-Y-Mas S, Barbon M, Teyssier C, Déméné H, Carvalho JE, Bird LE, Lebedev A, Fattori J, Schubert M, Dumas C, et al. PLoS One. 2016; 11(11):e0165139. Epub 2016 Nov 3.
De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder. [Cell Rep. 2014]
De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder.
Dong S, Walker MF, Carriero NJ, DiCola M, Willsey AJ, Ye AY, Waqar Z, Gonzalez LE, Overton JD, Frahm S, et al. Cell Rep. 2014 Oct 9; 9(1):16-23. Epub 2014 Oct 2.
Mixed Lineage Leukemia 5 (MLL5) Protein Stability Is Cooperatively Regulated by O-GlcNac Transferase (OGT) and Ubiquitin Specific Protease 7 (USP7). [PLoS One. 2015]
Mixed Lineage Leukemia 5 (MLL5) Protein Stability Is Cooperatively Regulated by O-GlcNac Transferase (OGT) and Ubiquitin Specific Protease 7 (USP7).
Ding X, Jiang W, Zhou P, Liu L, Wan X, Yuan X, Wang X, Chen M, Chen J, Yang J, et al. PLoS One. 2015; 10(12):e0145023. Epub 2015 Dec 17.

inactive histone-lysine N-methyltransferase 2E isoform X3 [Rattus norvegicus]
inactive histone-lysine N-methyltransferase 2E isoform X3 [Rattus norvegicus]
gi|2678937386|ref|XP_063142023.1|

Protein
similar to KALIG-1 [Homo sapiens]; similar to S17982 (PID:g106846) [Homo sapiens...
similar to KALIG-1 [Homo sapiens]; similar to S17982 (PID:g106846) [Homo sapiens]
gi|5870308|gb|AAD54510.1|AC006371_2 WUGSC|H_NH0304C24.2

Protein

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Protein