3k1r
From Proteopedia
Structure of harmonin NPDZ1 in complex with the SAM-PBM of Sans
Disease
Known disease associated with this structure: Deafness, autosomal recessive 18 OMIM:[605242], Usher syndrome, type 1C OMIM:[605242], Usher syndrome, type 1G OMIM:[607696]
About this Structure
3K1R is a 2 chains structure with sequences from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Wed Jan 27 20:02:05 2010
Categories: Homo sapiens | Pan, L. | Yan, J. | Zhang, M. | Alternative splicing | Ank repeat | Coiled coil | Deafness | Disease mutation | Hearing | Non-syndromic deafness | Polymorphism | Protein-protein complex | Retinitis pigmentosa | Sensory transduction | Structural protein | Usher syndrome | Vision
