2OQU
High Pressure Cryocooling of Capillary Sample Cryoprotection and Diffraction Phasing at Long Wavelengths
Summary for 2OQU
Entry DOI | 10.2210/pdb2oqu/pdb |
Related | 2OQN |
Descriptor | Elastase-1, CALCIUM ION, SULFATE ION, ... (5 entities in total) |
Functional Keywords | high pressure cryocooling, xenon, sad phasing, hydrolase |
Biological source | Sus scrofa (pig) |
Cellular location | Secreted: P00772 |
Total number of polymer chains | 1 |
Total formula weight | 26196.45 |
Authors | Kim, C.U.,Hao, Q.,Gruner, S.M. (deposition date: 2007-02-01, release date: 2007-05-01, Last modification date: 2023-08-30) |
Primary citation | Kim, C.U.,Hao, Q.,Gruner, S.M. High-pressure cryocooling for capillary sample cryoprotection and diffraction phasing at long wavelengths. Acta Crystallogr.,Sect.D, 63:653-659, 2007 Cited by PubMed Abstract: Crystal cryocooling is usually employed to reduce radiation damage during X-ray crystallography. Recently, a high-pressure cryocooling method has been developed which results in excellent diffraction-quality crystals without the use of penetrative cryoprotectants. Three new developments of the method are presented here: (i) Xe-He high-pressure cryocooling for Xe SAD phasing, (ii) native sulfur SAD phasing and (iii) successful cryopreservation of crystals in thick-walled capillaries without additional cryoprotectants other than the native mother liquor. These developments may be useful for structural solution of proteins without the need for selenomethionine incorporation and for high-throughput protein crystallography. PubMed: 17452791DOI: 10.1107/S0907444907011924 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.8 Å) |
Structure validation
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