2igq
From Proteopedia
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Human euchromatic histone methyltransferase 1
Disease
Known diseases associated with this structure: Chromosome 9q subtelomeric deletion syndrome OMIM:[607001]
About this Structure
2IGQ is a Single protein structure of sequence from Homo sapiens with and as ligands. Active as Histone-lysine N-methyltransferase, with EC number 2.1.1.43 Full crystallographic information is available from OCA.
Page seeded by OCA on Fri Feb 15 17:36:16 2008
Categories: Histone-lysine N-methyltransferase | Homo sapiens | Single protein | Antoshenko, T. | Arrowsmith, C.H. | Bochkarev, A. | Edwards, A.M. | Loppnau, P. | Min, J. | Plotnikov, A.N. | SGC, Structural.Genomics.Consortium. | Sundstrom, M. | Weigelt, J. | Wu, H. | SAH | ZN | Euchromatic histone methyltransferase 1 | Sgc | Structural genomics | Structural genomics consortium
