5IU9
Crystal Structure of Zebrafish Protocadherin-19 EC1-4
Summary for 5IU9
| Entry DOI | 10.2210/pdb5iu9/pdb |
| Descriptor | Protocadherin-19 isoform 1, CALCIUM ION, SODIUM ION, ... (4 entities in total) |
| Functional Keywords | adhesion, epilepsy, cell adhesion |
| Biological source | Danio rerio (Zebrafish) |
| Total number of polymer chains | 2 |
| Total formula weight | 96163.96 |
| Authors | Cooper, S.R.,Jontes, J.D.,Sotomayor, M. (deposition date: 2016-03-17, release date: 2016-11-02, Last modification date: 2024-11-06) |
| Primary citation | Cooper, S.R.,Jontes, J.D.,Sotomayor, M. Structural determinants of adhesion by Protocadherin-19 and implications for its role in epilepsy. Elife, 5:-, 2016 Cited by PubMed Abstract: Non-clustered δ-protocadherins are homophilic cell adhesion molecules essential for the development of the vertebrate nervous system, as several are closely linked to neurodevelopmental disorders. Mutations in () result in a female-limited, infant-onset form of epilepsy (PCDH19-FE). Over 100 mutations in have been identified in patients with PCDH19-FE, about half of which are missense mutations in the adhesive extracellular domain. Neither the mechanism of homophilic adhesion by PCDH19, nor the biochemical effects of missense mutations are understood. Here we present a crystallographic structure of the minimal adhesive fragment of the zebrafish Pcdh19 extracellular domain. This structure reveals the adhesive interface for Pcdh19, which is broadly relevant to both non-clustered δ and clustered protocadherin subfamilies. In addition, we show that several PCDH19-FE missense mutations localize to the adhesive interface and abolish Pcdh19 adhesion in assays, thus revealing the biochemical basis of their pathogenic effects during brain development. PubMed: 27787195DOI: 10.7554/eLife.18529 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (3.59 Å) |
Structure validation
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