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| | <StructureSection load='4x3b' size='340' side='right'caption='[[4x3b]], [[Resolution|resolution]] 2.10Å' scene=''> | | <StructureSection load='4x3b' size='340' side='right'caption='[[4x3b]], [[Resolution|resolution]] 2.10Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[4x3b]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Gallus_gallus Gallus gallus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4X3B OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4X3B FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[4x3b]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Gallus_gallus Gallus gallus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4X3B OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4X3B FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1Å</td></tr> |
| - | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Lysozyme Lysozyme], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.17 3.2.1.17] </span></td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene></td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4x3b FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4x3b OCA], [http://pdbe.org/4x3b PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4x3b RCSB], [http://www.ebi.ac.uk/pdbsum/4x3b PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4x3b ProSAT]</span></td></tr> | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4x3b FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4x3b OCA], [https://pdbe.org/4x3b PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4x3b RCSB], [https://www.ebi.ac.uk/pdbsum/4x3b PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4x3b ProSAT]</span></td></tr> |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/LYSC_CHICK LYSC_CHICK]] Lysozymes have primarily a bacteriolytic function; those in tissues and body fluids are associated with the monocyte-macrophage system and enhance the activity of immunoagents. Has bacteriolytic activity against M.luteus.<ref>PMID:22044478</ref> | + | [https://www.uniprot.org/uniprot/LYSC_CHICK LYSC_CHICK] Lysozymes have primarily a bacteriolytic function; those in tissues and body fluids are associated with the monocyte-macrophage system and enhance the activity of immunoagents. Has bacteriolytic activity against M.luteus.<ref>PMID:22044478</ref> |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | [[Category: Gallus gallus]] | | [[Category: Gallus gallus]] |
| | [[Category: Large Structures]] | | [[Category: Large Structures]] |
| - | [[Category: Lysozyme]]
| + | [[Category: David C]] |
| - | [[Category: David, C]] | + | [[Category: Duman R]] |
| - | [[Category: Duman, R]] | + | [[Category: Lorbeer O]] |
| - | [[Category: Lorbeer, O]] | + | [[Category: Meents A]] |
| - | [[Category: Meents, A]] | + | [[Category: Panneerselvam S]] |
| - | [[Category: Panneerselvam, S]] | + | [[Category: Roedig P]] |
| - | [[Category: Roedig, P]] | + | [[Category: Stuart DI]] |
| - | [[Category: Stuart, D I]] | + | [[Category: Stuebe N]] |
| - | [[Category: Stuebe, N]] | + | [[Category: Sutton G]] |
| - | [[Category: Sutton, G]] | + | [[Category: Vartiainen I]] |
| - | [[Category: Vartiainen, I]] | + | [[Category: Wagner A]] |
| - | [[Category: Wagner, A]] | + | [[Category: Warmer M]] |
| - | [[Category: Warmer, M]] | + | [[Category: Weckert E]] |
| - | [[Category: Weckert, E]] | + | |
| - | [[Category: Hydrolase]]
| + | |
| - | [[Category: Lysozyme microcrystal]]
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| Structural highlights
Function
LYSC_CHICK Lysozymes have primarily a bacteriolytic function; those in tissues and body fluids are associated with the monocyte-macrophage system and enhance the activity of immunoagents. Has bacteriolytic activity against M.luteus.[1]
Publication Abstract from PubMed
At low emittance synchrotron sources it has become possible to perform structure determinations from the measurement of multiple microcrystals which were previously considered too small for diffraction experiments. Conventional mounting techniques do not fulfill the requirements of these new experiments. They significantly contribute to background scattering and it is difficult to locate the crystals, making them incompatible with automated serial crystallography. We have developed a micro-fabricated sample holder from single crystalline silicon with micropores, which carries up to thousands of crystals and significantly reduces the background scattering level. For loading, the suspended microcrystals are pipetted onto the chip and excess mother liquor is subsequently soaked off through the micropores. Crystals larger than the pore size are retained and arrange themselves according to the micropore pattern. Using our chip we were able to collect 1.5 A high resolution diffraction data from protein microcrystals with sizes of 4 micrometers and smaller.
A micro-patterned silicon chip as sample holder for macromolecular crystallography experiments with minimal background scattering.,Roedig P, Vartiainen I, Duman R, Panneerselvam S, Stube N, Lorbeer O, Warmer M, Sutton G, Stuart DI, Weckert E, David C, Wagner A, Meents A Sci Rep. 2015 May 29;5:10451. doi: 10.1038/srep10451. PMID:26022615[2]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Maehashi K, Matano M, Irisawa T, Uchino M, Kashiwagi Y, Watanabe T. Molecular characterization of goose- and chicken-type lysozymes in emu (Dromaius novaehollandiae): evidence for extremely low lysozyme levels in emu egg white. Gene. 2012 Jan 15;492(1):244-9. doi: 10.1016/j.gene.2011.10.021. Epub 2011 Oct, 25. PMID:22044478 doi:10.1016/j.gene.2011.10.021
- ↑ Roedig P, Vartiainen I, Duman R, Panneerselvam S, Stube N, Lorbeer O, Warmer M, Sutton G, Stuart DI, Weckert E, David C, Wagner A, Meents A. A micro-patterned silicon chip as sample holder for macromolecular crystallography experiments with minimal background scattering. Sci Rep. 2015 May 29;5:10451. doi: 10.1038/srep10451. PMID:26022615 doi:http://dx.doi.org/10.1038/srep10451
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