6UWM
Single particle cryo-EM structure of KvAP
Summary for 6UWM
| Entry DOI | 10.2210/pdb6uwm/pdb |
| EMDB information | 20924 |
| Descriptor | Voltage-gated potassium channel (1 entity in total) |
| Functional Keywords | voltage-gated potassium channel, non-domain-swapped, transport protein |
| Biological source | Aeropyrum pernix |
| Total number of polymer chains | 4 |
| Total formula weight | 126596.83 |
| Authors | Tao, X.,MacKinnon, R. (deposition date: 2019-11-05, release date: 2019-12-04, Last modification date: 2024-03-06) |
| Primary citation | Tao, X.,MacKinnon, R. Cryo-EM structure of the KvAP channel reveals a non-domain-swapped voltage sensor topology. Elife, 8:-, 2019 Cited by PubMed Abstract: Conductance in voltage-gated ion channels is regulated by membrane voltage through structural domains known as voltage sensors. A single structural class of voltage sensor domain exists, but two different modes of voltage sensor attachment to the pore occur in nature: domain-swapped and non-domain-swapped. Since the more thoroughly studied Kv1-7, Nav and Cav channels have domain-swapped voltage sensors, much less is known about non-domain-swapped voltage-gated ion channels. In this paper, using cryo-EM, we show that KvAP from has non-domain-swapped voltage sensors as well as other unusual features. The new structure, together with previous functional data, suggests that KvAP and the Shaker channel, to which KvAP is most often compared, probably undergo rather different voltage-dependent conformational changes when they open. PubMed: 31755864DOI: 10.7554/eLife.52164 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (5.9 Å) |
Structure validation
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