2igq | pdb_00002igq
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 ZN and SAH 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 Mon Nov 12 22:44:32 2007
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- 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
