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7T65

Rabbit RyR1 disease mutant Y523S in complex with FKBP12.6 embedded in lipidic nanodisc in the open state

This is a non-PDB format compatible entry.
Summary for 7T65
Entry DOI10.2210/pdb7t65/pdb
EMDB information25710
DescriptorRyanodine receptor 1, Peptidyl-prolyl cis-trans isomerase FKBP1B, ADENOSINE-5'-TRIPHOSPHATE, ... (5 entities in total)
Functional Keywordsryanodine receptor, ryr, ryr1, calcium channel, mutation, ntdc mutation, malignant hyperthermia, central core disease, membrane protein, excitation-contraction coupling
Biological sourceOryctolagus cuniculus (rabbit)
More
Total number of polymer chains8
Total formula weight2312450.14
Authors
Iyer, K.A.,Hu, Y.,Murayama, T.,Samso, M. (deposition date: 2021-12-13, release date: 2022-07-20, Last modification date: 2022-08-03)
Primary citationIyer, K.A.,Hu, Y.,Klose, T.,Murayama, T.,Samso, M.
Molecular mechanism of the severe MH/CCD mutation Y522S in skeletal ryanodine receptor (RyR1) by cryo-EM.
Proc.Natl.Acad.Sci.USA, 119:e2122140119-e2122140119, 2022
Cited by
PubMed: 35867837
DOI: 10.1073/pnas.2122140119
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (4.05 Å)
Structure validation

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