1ex3: Difference between revisions
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New page: left|200px<br /><applet load="1ex3" size="450" color="white" frame="true" align="right" spinBox="true" caption="1ex3, resolution 3.0Å" /> '''CRYSTAL STRUCTURE OF ... |
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[[Image:1ex3.gif|left|200px]]<br /><applet load="1ex3" size=" | [[Image:1ex3.gif|left|200px]]<br /><applet load="1ex3" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="1ex3, resolution 3.0Å" /> | caption="1ex3, resolution 3.0Å" /> | ||
'''CRYSTAL STRUCTURE OF BOVINE CHYMOTRYPSINOGEN A (TETRAGONAL)'''<br /> | '''CRYSTAL STRUCTURE OF BOVINE CHYMOTRYPSINOGEN A (TETRAGONAL)'''<br /> | ||
==Overview== | ==Overview== | ||
Protein crystals are usually obtained by an empirical approach based on | Protein crystals are usually obtained by an empirical approach based on extensive screening to identify suitable crystallization conditions. In contrast, we have used a systematic predictive procedure to produce data-quality crystals of bovine chymotrypsinogen A and used them to obtain a refined X-ray structure to 3 A resolution. Measurements of the osmotic second virial coefficient of chymotrypsinogen solutions were used to identify suitable solvent conditions, following which crystals were grown for approximately 30 hours by ultracentrifugal crystallization, without the use of any precipitants. Existing structures of chymotrypsinogen were obtained in solutions including 10-30 % ethanol, whereas simple buffered NaCl solutions were used here. The protein crystallized in the tetragonal space group P4(1)2(1)2, with one molecule per asymmetric unit. The quality of the refined map was very high throughout, with the main-chain atoms of all but four residues clearly defined and with nearly all side-chains also defined. Although only minor differences are seen compared to the structures previously reported, they indicate the possibility of structural changes due to the crystallization conditions used in those studies. Our results show that more systematic crystallization of proteins is possible, and that the procedure can expand the range of conditions under which crystals can be grown successfully and can make new crystal forms available. | ||
==About this Structure== | ==About this Structure== | ||
1EX3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus]. Active as [http://en.wikipedia.org/wiki/Chymotrypsin Chymotrypsin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.1 3.4.21.1] Full crystallographic information is available from [http:// | 1EX3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus]. Active as [http://en.wikipedia.org/wiki/Chymotrypsin Chymotrypsin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.1 3.4.21.1] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1EX3 OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Chymotrypsin]] | [[Category: Chymotrypsin]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Gittis, A | [[Category: Gittis, A G.]] | ||
[[Category: Lenhoff, A | [[Category: Lenhoff, A M.]] | ||
[[Category: Leonard, S | [[Category: Leonard, S A.]] | ||
[[Category: Pjura, P | [[Category: Pjura, P E.]] | ||
[[Category: hydrolase]] | [[Category: hydrolase]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:32:24 2008'' | ||