2k27
From Proteopedia
Solution structure of Human Pax8 Paired Box Domain
Disease
Known disease associated with this structure: Hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia OMIM:[167415]
About this Structure
2K27 is a Single protein structure of sequence from Homo sapiens. Full experimental information is available from OCA.
Page seeded by OCA on Wed Oct 1 21:33:05 2008
Categories: Homo sapiens | Single protein | Boelens, R. | Codutti, L. | Corazza, A. | Esposito, G. | Fogolari, F. | Ingen, H van. | Quadrifoglio, F. | Tell, G. | Vascotto, C. | Viglino, P. | 3d nmr | Alternative splicing | Developmental protein | Differentiation | Disease mutation | Dna-binding | Induced fit | Nmr | Nucleus | Paired box | Paired domain | Pax8 | Phosphoprotein | Polymorphism | Solution structure | Transcription | Transcription regulation | Transcription regulator | Triple frequency
