This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
2cue
From Proteopedia
Solution structure of the homeobox domain of the human paired box protein Pax-6
Disease
Known disease associated with this structure: Aniridia, type II OMIM:[607108], Cataract, congenital, with late-onset corneal dystrophy OMIM:[607108], Coloboma, ocular OMIM:[607108], Ectopia pupillae OMIM:[607108], Eye anomalies, multiplex OMIM:[607108], Foveal hypoplasia, isolated OMIM:[607108], Keratitis OMIM:[607108], Morning glory disc anomaly OMIM:[607108], Optic nerve hypoplasia/aplasia OMIM:[607108], Peters anomaly OMIM:[607108]
About this Structure
2CUE is a 1 chain structure of sequence from Homo sapiens. Full experimental information is available from OCA.
Page seeded by OCA on Sun Nov 16 15:40:22 2008
Categories: Homo sapiens | Inoue, M. | Kigawa, T. | Koshiba, S. | Ohnishi, S. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Tochio, N. | Tomizawa, T. | Yokoyama, S. | Homeobox domain | National project on protein structural and functional analyse | Nppsfa | Paired box protein | Pax6 | Riken structural genomics/proteomics initiative | Rsgi | Structural genomic | Transcription factor
