| Structural highlights
4a7d is a 1 chain structure with sequence from Gallus gallus. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
| | Ligands: | ,
| | Related: | 1w6z, 1kxx, 2ybi, 2ybn, 4lyo, 3lyo, 1t6v, 1kip, 1ic7, 1vds, 1lzt, 2xbr, 1kir, 1lys, 132l, 1e8l, 1bwj, 1yil, 1heo, 1sfg, 1kxw, 2c8o, 2x0a, 1yl1, 1sf4, 1g7l, 1ior, 1h87, 1ljg, 3lyt, 1dpx, 1iot, 1v7s, 1ja6, 1jis, 1ir8, 2w1m, 1uic, 1ykz, 1xgq, 1uie, 2war, 1lji, 1lj3, 1dpw, 8lyz, 2iff, 2lyo, 1bwi, 1g7h, 1jj0, 1lks, 1rfp, 5lyt, 1jiy, 1sfb, 1ir7, 1iee, 1xei, 1hel, 1xek, 1at6, 1ljf, 2ydg, 1mlc, 2b5z, 1f10, 1lsz, 193l, 2ybm, 1ljk, 6lyt, 1sq2, 1zmy, 2ybh, 1vdq, 2d91, 2xth, 1lje, 1b2k, 1lze, 9lyz, 2ybj, 1aki, 1hen, 1uia, 1yik, 1xfp, 2d6b, 1lpi, 1ndg, 1lsd, 1flw, 2blx, 6lyz, 1lsg, 1nbz, 4lyt, 3hfm, 1ved, 1jit, 1lzn, 1uuz, 1lyz, 1ja2, 1wtn, 2d4i, 2xbs, 2fbb, 1fdl, 2lym, 1lz9, 1lse, 1lzh, 1gxx, 1lsm, 3lym, 7lyz, 1jj3, 1yky, 1t3p, 1heq, 1kiq, 1kxy, 2lzh, 1uih, 2w1l, 2bly, 1b0d, 1g7j, 1her, 1bhz, 1wtm, 1hep, 1ioq, 1nby, 1jtt, 1qio, 1lza, 1xgp, 1ps5, 1gwd, 3zvq, 1v7t, 1jpo, 1h6m, 1dqj, 2a7d, 1j1p, 1ljj, 1z55, 2c8p, 1lsb, 1f0w, 2w1x, 1lzg, 1flq, 1lzc, 1jj1, 1rcm, 2ybl, 1uid, 1yqv, 1hsx, 1bgi, 1lcn, 1lzd, 1hew, 2cds, 2vb1, 2aub, 1hf4, 1uib, 1ir9, 2cgi, 1ios, 1j1x, 1rjc, 1uc0, 1azf, 1ic4, 1ljh, 4lyz, 1gpq, 2a6u, 2d4k, 1xej, 1ja7, 1mel, 1ri8, 1uig, 1bvx, 1qtk, 1c10, 1lkr, 1lyo, 2xjw, 1hsw, 1n4f, 2w1y, 1jto, 1g7m, 1sf7, 1lsf, 1fn5, 2d4j, 5lyz, 1c08, 3lzt, 1ndm, 1sf6, 3lyz, 1bvk, 1uif, 1vau, 2lyz, 1fly, 1lma, 1hc0, 1j1o, 1yl0, 2lzt, 1a2y, 4lzt, 1uco, 1lsy, 1lsa, 5lym, 1gxv, 1p2c, 1ic5, 1ua6, 1at5, 1vfb, 1f3j, 1vat, 1hem, 1lj4, 1ja4, 2a7f, 4lym, 1flu, 194l, 1lz8, 1ykx, 1bwh, 1vdt, 2hfm, 1io5, 1lsn, 1g7i, 2bpu, 1lzb, 1lsc, 1vdp, 4a7e |
| Activity: | Lysozyme, with EC number 3.2.1.17 |
| Resources: | FirstGlance, OCA, RCSB, PDBsum |
Publication Abstract from PubMed
High-pressure freezing (HPF) is a method which allows sample vitrification without cryoprotectants. In the present work, protein crystals were cooled to cryogenic temperatures at a pressure of 210 MPa. In contrast to other HPF methods published to date in the field of cryocrystallography, this protocol involves rapid sample cooling using a standard HPF device. The fast cooling rates allow HPF of protein crystals directly in their mother liquor without the need for cryoprotectants or external reagents. HPF was first attempted with hen egg-white lysozyme and cubic insulin crystals, yielding good to excellent diffraction quality. Non-cryoprotected crystals of the membrane protein photosystem II have been successfully cryocooled for the first time. This indicates that the presented HPF method is well suited to the vitrification of challenging systems with large unit cells and weak crystal contacts.
Fast high-pressure freezing of protein crystals in their mother liquor.,Burkhardt A, Warmer M, Panneerselvam S, Wagner A, Zouni A, Glockner C, Reimer R, Hohenberg H, Meents A Acta Crystallogr Sect F Struct Biol Cryst Commun. 2012 Apr 1;68(Pt 4):495-500., Epub 2012 Mar 31. PMID:22505429[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Burkhardt A, Warmer M, Panneerselvam S, Wagner A, Zouni A, Glockner C, Reimer R, Hohenberg H, Meents A. Fast high-pressure freezing of protein crystals in their mother liquor. Acta Crystallogr Sect F Struct Biol Cryst Commun. 2012 Apr 1;68(Pt 4):495-500., Epub 2012 Mar 31. PMID:22505429 doi:10.1107/S1744309112009670
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