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5JSI

Structure of membrane protein

Summary for 5JSI
Entry DOI10.2210/pdb5jsi/pdb
DescriptorBacteriorhodopsin, EICOSANE, IODIDE ION, ... (6 entities in total)
Functional Keywordsmembrane protein, iodide, unknown function, transferase
Biological sourceCandidatus Actinomarina minuta
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Total number of polymer chains2
Total formula weight58487.49
Authors
Melnikov, I.,Polovinkin, V.,Kovalev, K.,Shevchenko, V.,Gushchin, I.,Popov, A.,Gordeliy, V. (deposition date: 2016-05-08, release date: 2017-05-31, Last modification date: 2025-04-09)
Primary citationMelnikov, I.,Polovinkin, V.,Kovalev, K.,Gushchin, I.,Shevtsov, M.,Shevchenko, V.,Mishin, A.,Alekseev, A.,Rodriguez-Valera, F.,Borshchevskiy, V.,Cherezov, V.,Leonard, G.A.,Gordeliy, V.,Popov, A.
Fast iodide-SAD phasing for high-throughput membrane protein structure determination.
Sci Adv, 3:e1602952-e1602952, 2017
Cited by
PubMed Abstract: We describe a fast, easy, and potentially universal method for the de novo solution of the crystal structures of membrane proteins via iodide-single-wavelength anomalous diffraction (I-SAD). The potential universality of the method is based on a common feature of membrane proteins-the availability at the hydrophobic-hydrophilic interface of positively charged amino acid residues with which iodide strongly interacts. We demonstrate the solution using I-SAD of four crystal structures representing different classes of membrane proteins, including a human G protein-coupled receptor (GPCR), and we show that I-SAD can be applied using data collection strategies based on either standard or serial x-ray crystallography techniques.
PubMed: 28508075
DOI: 10.1126/sciadv.1602952
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

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数据于2025-07-23公开中

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