2jm1 | pdb_00002jm1
Structures and chemical shift assignments for the ADD domain of the ATRX protein
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Disease
Known diseases associated with this structure: Alpha-thalassemia myelodysplasia syndrome, somatic OMIM:[300032], Alpha-thalassemia/mental retardation syndrome OMIM:[300032], Breast cancer, invasive intraductal OMIM:[603615], Chudley-Lowry syndrome OMIM:[300032], Colon adenocarcinoma OMIM:[603615], Juberg-Marsidi syndrome OMIM:[300032], Lymphoma, non-Hodgkin OMIM:[603615], Mental retardation-hypotonic facies syndrome, X-linked OMIM:[300032], Smith-Fineman-Myers syndrome OMIM:[300032], Sutherland-Haan syndrome-like OMIM:[300032]
About this Structure
2JM1 is a Single protein structure of sequence from Homo sapiens with ZN as ligand. Full crystallographic information is available from OCA.
Page seeded by OCA on Mon Nov 12 22:56:20 2007
