2cue
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(New page: 200px<br /> <applet load="2cue" size="450" color="white" frame="true" align="right" spinBox="true" caption="2cue" /> '''Solution structure of the homeobox domain o...)
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Revision as of 19:17, 12 November 2007
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Solution structure of the homeobox domain of the human paired box protein Pax-6
Disease
Known diseases 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 Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Mon Nov 12 21:23:59 2007
Categories: Homo sapiens | Single protein | 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 analyses | Nppsfa | Paired box protein | Pax6 | Riken structural genomics/proteomics initiative | Rsgi | Structural genomics | Transcription factor
