tag:blogger.com,1999:blog-72894019927731321942024-03-13T15:00:07.222-07:00Beautiful ProteinsProteins are stunning molecules. In this blog i collect renderings of protein folds that i find aesthetically pleasing.
Follow me on twitter <a href="http://www.twitter.com/mtyka">@mtyka</a>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.comBlogger18125tag:blogger.com,1999:blog-7289401992773132194.post-41018739964197146252012-03-16T10:12:00.002-07:002012-05-17T21:26:35.351-07:00Copper Protein SculptureI haven't posted for a while since I've been busy exploring beautiful proteins in a different way. I started to make sculptures out of them out of metal :) I have a thrid one in the works so watch this space.<br />
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<strong style="margin-bottom: 0px; margin-left: 0px; margin-right: 0px; margin-top: 0px; padding-bottom: 0px; padding-left: 0px; padding-right: 0px; padding-top: 0px;"><a href="http://www.miketyka.com/ubiquitin.html">Ubiquitin</a></strong></div>
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Ubiquitin is a small regulatory protein found in almost all tissues of eukaryotic organisms. The cell attaches short chains of Ubiquitin molecules to proteins, which labels them for destruction and subsequent recycling. The Ubiquitin tag directs proteins to the proteasome, which is a large protein complex in the cell that degrades unneeded proteins back into their amino acid constituents. These are then reused to synthesize new proteins. The constant recycling of proteins not only ensures damaged proteins are removed quickly but also allows rapid regulation of enzyme levels in the cell.</div>
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Structurally, Ubiquitin features all of the major structural features of typical proteins including two a-helices a curved b-sheet. Its small size (76 amino acids) makes it one of the most studied proteins for protein folding and dynamics.</div>
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<strong style="margin-bottom: 0px; margin-left: 0px; margin-right: 0px; margin-top: 0px; padding-bottom: 0px; padding-left: 0px; padding-right: 0px; padding-top: 0px;"><a href="http://www.miketyka.com/potassium.html">KcsA Potassium Channel</a></strong></div>
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<em style="margin-bottom: 0px; margin-left: 0px; margin-right: 0px; margin-top: 0px; padding-bottom: 0px; padding-left: 0px; padding-right: 0px; padding-top: 0px;">Copper, Steel</em></div>
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Potassium channels form potassium-selective pores that span cell membranes. They are the most widely distributed type of ion channel found in virtually all living organisms. The four identical subunits are situated in a four-fold symmetrical manner around a central pore, which allows potassium ions to pass freely. At the top of the structure, formed by four loops lining the pore, a selectivity filter is situated which prevents other ions (such as sodium ions) from passing. The correct ions are detected by their size and charge. Note that that no active pumping of ions occurs; it merely allows passive conductance of ions down the con-centration gradient between the two sides of the membrane.</div>
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The KcsA is an archetypal membrane protein with eight tightly packed membrane-spanning a-helices. The four short helices in the center where the chain crosses half the membrane and then returns to the top are a more unusual feature.</div>
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<a href="http://www.miketyka.com/wp-content/uploads/2011/10/side1-678x1024.jpg"><img alt="" border="0" src="http://www.miketyka.com/wp-content/uploads/2011/10/side1-678x1024.jpg" style="cursor: hand; cursor: pointer; display: block; height: 624px; margin: 0px auto 10px; text-align: center; width: 408px;" /></a></div>
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More pics on: <a href="http://www.miketyka.com/art/">http://www.miketyka.com/art/</a>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com24tag:blogger.com,1999:blog-7289401992773132194.post-28715325740136922482011-02-17T13:51:00.000-08:002011-06-22T14:30:42.183-07:00Traptavidin 2Y3E<div><br /></div><a href="http://3.bp.blogspot.com/-cDZPoP31C0g/TV2Y3kbBksI/AAAAAAAABnQ/55D9o51O4E0/s1600/2y3e_beautiful.png" onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}"><img style="display:block; margin:0px auto 10px; text-align:center;cursor:pointer; cursor:hand;width: 400px; height: 368px;" src="http://3.bp.blogspot.com/-cDZPoP31C0g/TV2Y3kbBksI/AAAAAAAABnQ/55D9o51O4E0/s400/2y3e_beautiful.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5574779994191794882" /></a><br /><div>Streptavidin is a tetrameric protein purified from the bacterium <i>Streptomyces avidinii</i>. It has an extraordinarily high affinity for a molecule called biotin (also known as vitamin B7); </div><div>Streptavidin is used extensively in molecular biology and bionanotechnology due to the streptavidin-biotin complex's resistance to organic solvents, denaturants (e.g. guanidinium chloride), detergents (e.g. SDS, Triton), proteolytic enzymes, and extremes of temperature and pH. Essentially you can use it to attach different molecules to each other in a specific way like attaching pieces of velcro to things.</div><div><br>Traptavidin (Shown above) is a human engineered mutant of Streptavidin with an even higher binding affinity (10x better) showing that we're now able to improve and modify natures machines for our purposes.</div><div><br /></div>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com5tag:blogger.com,1999:blog-7289401992773132194.post-51426853482010295922011-01-30T23:26:00.000-08:002011-01-30T23:31:31.982-08:00Cystatin C<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://2.bp.blogspot.com/_HK1LuizCXdI/TUZk1SIQ8RI/AAAAAAAABmY/gWBJeytGlZg/s1600/1r4c_cystatin.png"><img style="display:block; margin:0px auto 10px; text-align:center;cursor:pointer; cursor:hand;width: 400px; height: 282px;" src="http://2.bp.blogspot.com/_HK1LuizCXdI/TUZk1SIQ8RI/AAAAAAAABmY/gWBJeytGlZg/s400/1r4c_cystatin.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5568248855852544274" /></a><br /><div>Cystatin C or cystatin 3 (formerly gamma trace, post-gamma-globulin or neuroendocrine basic polypeptide),[1] a protein encoded by the CST3 gene, is mainly used as a biomarker of kidney function. Recently, it has been studied for its role in predicting new-onset or deteriorating cardiovascular disease. It also seems to play a role in brain disorders involving amyloid (a specific type of protein deposition), such as Alzheimer's disease. [wikipedia]</div><div><br /></div><div>The image above shows part of the cystatin C crystal obtained for crystallography and actually shows 8 cystatin C molecules in a complex arrangement of symmetries. </div><div><br /></div><div>In humans, all cells with a nucleus (cell core containing the DNA) produce cystatin C as a chain of 120 amino acids. It is found in virtually all tissues and bodily fluids. It is a potent inhibitor of lysosomal proteinases (enzymes from a special subunit of the cell that break down proteins) and probably one of the most important extracellular inhibitors of cysteine proteases (it prevents the breakdown of proteins outside the cell by a specific type of protein degrading enzymes). Cystatin C belongs to the type 2 cystatin gene family. [wikipedia]</div><div><br /></div>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com5tag:blogger.com,1999:blog-7289401992773132194.post-42497795655678839312011-01-30T23:21:00.000-08:002011-01-30T23:26:12.408-08:00Molybdenum cofactor biosynthesis protein MoaC.<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://3.bp.blogspot.com/_HK1LuizCXdI/TUZj9oJUIvI/AAAAAAAABmQ/hAKRFT98Q6U/s1600/1ekr.png"><img style="display:block; margin:0px auto 10px; text-align:center;cursor:pointer; cursor:hand;width: 400px; height: 376px;" src="http://3.bp.blogspot.com/_HK1LuizCXdI/TUZj9oJUIvI/AAAAAAAABmQ/hAKRFT98Q6U/s400/1ekr.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5568247899689853682" /></a><br /><br />The molybdenum cofactor (Moco) is an essential component of a large family of enzymes involved in important transformations in carbon, nitrogen and sulfur metabolism. The Moco biosynthetic pathway is evolutionarily conserved and found in archaea, eubacteria and eukaryotes. In humans, genetic deficiencies of enzymes involved in thispathway trigger an autosomal recessive and usually deadly disease with severe neurological symptoms. The MoaC protein,together with the MoaA protein, is involved in the first step of Moco biosynthesis. (from paper abstract)<div><span class="Apple-style-span"><span class="Apple-style-span" style="font-size: 12px; line-height: 18px;"><i>Wuebbens et al. Structure Fold.Des. 8: 709-717</i></span></span></div>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com12tag:blogger.com,1999:blog-7289401992773132194.post-56770195447012160222010-12-08T15:27:00.002-08:002010-12-08T15:40:24.539-08:00Möbius fold ? Human apolipoprotein A-I<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://2.bp.blogspot.com/_HK1LuizCXdI/TQAUihXFM-I/AAAAAAAABlU/T79U1H1WvCY/s1600/1av1.png"><img style="text-align: left;display: block; margin-top: 0px; margin-right: auto; margin-bottom: 10px; margin-left: auto; cursor: pointer; width: 220px; height: 400px; " src="http://2.bp.blogspot.com/_HK1LuizCXdI/TQAUihXFM-I/AAAAAAAABlU/T79U1H1WvCY/s400/1av1.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5548457324223738850" /></a><div style="text-align: left;"><span class="Apple-style-span"><span class="Apple-style-span" style="line-height: 18px;"><br /></span></span></div><div style="text-align: left;"><br /></div>The structure of truncated human apolipoprotein A-I (PDB code 1AV1) is the major protein component of high density lipoprotein. High-density lipoprotein (HDL) is one of the five major groups of lipoproteins which, in order of sizes, largest to smallest, are chylomicrons, VLDL, IDL, LDL and HDL, which enable lipids like cholesterol and triglycerides to be transported within the blood stream.<br />The molecule consists almost entirely of a pseudo-continuous, amphipathic alpha-helix that is punctuated by kinks at regularly spaced proline residues; it adopts a shape similar to a horseshoe of dimensions 12.5 x 8.0 x 4.0 nanometers. Four molecules in the asymmetric unitassociate via their hydrophobic faces to form an antiparallel four-helix bundle with an elliptical ring shape.Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com13tag:blogger.com,1999:blog-7289401992773132194.post-62717415722333173292010-10-15T14:56:00.000-07:002010-10-15T14:59:06.314-07:00Platelet activating factor - T0297<div><br /></div><div><br /></div><a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://1.bp.blogspot.com/_HK1LuizCXdI/TLjOGYnZYGI/AAAAAAAABkY/q7seYnPxWsk/s1600/BeautifulProteins_t297_2hsj.png"><img style="display:block; margin:0px auto 10px; text-align:center;cursor:pointer; cursor:hand;width: 302px; height: 384px;" src="http://1.bp.blogspot.com/_HK1LuizCXdI/TLjOGYnZYGI/AAAAAAAABkY/q7seYnPxWsk/s320/BeautifulProteins_t297_2hsj.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5528395151679512674" /></a>This is 2HSJ, a putative platelet activating factor from Streptococcus pneumonia (The causative agent of pneumonia). To me this is T0297, a target from the CASP7 protein structure prediction contest and has since been on eof my pet proteins for studying folding and prediction.Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com2tag:blogger.com,1999:blog-7289401992773132194.post-25597164835527512552010-10-01T18:07:00.000-07:002010-10-01T18:10:19.195-07:00Proteinase Inhibitor CI-2 from Barley Seeds<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://2.bp.blogspot.com/_HK1LuizCXdI/TKaGbpy7DQI/AAAAAAAABkQ/k-veMgMop4o/s1600/2ci2.png"><img style="cursor:pointer; cursor:hand;width: 384px; height: 378px;" src="http://2.bp.blogspot.com/_HK1LuizCXdI/TKaGbpy7DQI/AAAAAAAABkQ/k-veMgMop4o/s320/2ci2.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5523249802650520834" /></a>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com4tag:blogger.com,1999:blog-7289401992773132194.post-77458440395028726802010-06-29T18:42:00.000-07:002010-06-29T18:59:43.333-07:00Tudor domain<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://4.bp.blogspot.com/_HK1LuizCXdI/TCqib4XYueI/AAAAAAAABjM/bBqEGwKm5Kg/s1600/2gfa.png"><span class="Apple-style-span" style="font-size: small;"><img style="cursor:pointer; cursor:hand;width: 400px; height: 260px;" src="http://4.bp.blogspot.com/_HK1LuizCXdI/TCqib4XYueI/AAAAAAAABjM/bBqEGwKm5Kg/s400/2gfa.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5488377695775013346" /></span></a><div><span class="Apple-style-span" style="font-family:sans-serif;"><span class="Apple-style-span" style=" line-height: 28px; -webkit-border-horizontal-spacing: 8px; -webkit-border-vertical-spacing: 8px;"><b><span class="Apple-style-span" style="font-size: small;"><br /></span></b></span></span></div><div><span class="Apple-style-span" style=" font-weight: bold; line-height: 24px; -webkit-border-horizontal-spacing: 7px; -webkit-border-vertical-spacing: 7px; font-family:sans-serif;"><span class="Apple-style-span" style="font-size: small;"><br /></span></span></div><div><span class="Apple-style-span" style="font-size: small;"><a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://4.bp.blogspot.com/_HK1LuizCXdI/TCqib4XYueI/AAAAAAAABjM/bBqEGwKm5Kg/s1600/2gfa.png"></a>The double tudor domain is part of the human </span><span class="Apple-style-span"><span class="Apple-style-span" style="font-size: small;">Lysine-specific demethylase 4A </span></span><span class="Apple-style-span" style="font-size: small;"> and recognizes the methylation state of histones. Histones are proteins found in the nucleus of cells where they organize the DNA by wrapping it around them selves. They are intimately involved in the regulation of gene expression through their methylation state. This proteins allows the cells to "sense" the methylation and is part of Lysine-specific demethylase 4A which is able to remove the methylation from histones allowing them to bind to DNA again. This would switch of any genes in the affected stretch of DNA.<br /></span><br /></div>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com0tag:blogger.com,1999:blog-7289401992773132194.post-83298671716218784712010-06-21T23:06:00.000-07:002010-06-23T11:57:43.451-07:007-bladed propeller fold<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://4.bp.blogspot.com/_HK1LuizCXdI/TCBTE9N2w9I/AAAAAAAABi8/Z_0yq-H5biU/s1600/1erj_propeller.png"><span class="Apple-style-span" style="font-size: small;"><img style="cursor:pointer; cursor:hand;width: 400px; height: 386px;" src="http://4.bp.blogspot.com/_HK1LuizCXdI/TCBTE9N2w9I/AAAAAAAABi8/Z_0yq-H5biU/s400/1erj_propeller.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5485475690754524114" /></span></a><span class="Apple-style-span" style="font-size: small;"><br /></span><div><span class="Apple-style-span" style="font-size: small;"><br /></span></div><div><span class="Apple-style-span" style="font-size: small;">Amongst the most intruiging protein folds, the propeller fold comes in a number of varieties. Shown here is a 7 bladed version, but they occur in 3 to 8 bladed varieties. Note that this fold is constructed from a single chain, rather than from 7 identical units, although this fold almost certainly arose from internal duplications of gene segments. </span><span class="Apple-style-span"><span class="Apple-style-span" style="font-size: small;">Many hundreds of protein structures with this fold have been determined. In the case of enzymes the enzyme's active site is often found in the cleft formed in the center of the propeller by loops connecting the successive four-sheet motifs. Examples include the the influenza virus protein neuraminidase - one of two proteins present in the viral envelope. It catalyzes the cleavage of sialic acid moieties from cell-membrane proteins to aid in the targeting of newly produced virions to previously uninfected cells. </span></span></div><div><br /></div>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com1tag:blogger.com,1999:blog-7289401992773132194.post-12590501226850393202010-06-21T22:17:00.000-07:002010-06-21T22:22:01.987-07:00"peptide self-assembly mimic" (PSAM) scaffold<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://3.bp.blogspot.com/_HK1LuizCXdI/TCBHten3LgI/AAAAAAAABi0/cLs6C77NNTg/s1600/3ec5.png"><img style="cursor:pointer; cursor:hand;width: 400px; height: 170px;" src="http://3.bp.blogspot.com/_HK1LuizCXdI/TCBHten3LgI/AAAAAAAABi0/cLs6C77NNTg/s400/3ec5.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5485463192777207298" /></a><br /><div><br /></div><div><br /></div><div> PSAMs are engineered water-soluble proteins that mimic a segment of beta-rich peptide self-assembly, and they are amenable to standard biophysical techniques and systematic mutagenesis. The PSAM beta-sheet contains rows of repetitive amino acid patterns running perpendicular to the strands (cross-strand ladders) that represent a ubiquitous structural feature of fibril-like surfaces. These engineered proteins are study systems for understanding degenerative amyloid diseases such as Alzheimer's or Creuzfeld-Jacob disease.</div>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com2tag:blogger.com,1999:blog-7289401992773132194.post-35914301523189956252010-06-15T23:25:00.000-07:002010-06-15T23:27:35.504-07:00Synthetic DNA Binding Construct<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://1.bp.blogspot.com/_HK1LuizCXdI/TBhukNzKrSI/AAAAAAAABiU/yEVPM9FoKNs/s1600/1wvl.png"><img style="cursor:pointer; cursor:hand;width: 379px; height: 400px;" src="http://1.bp.blogspot.com/_HK1LuizCXdI/TBhukNzKrSI/AAAAAAAABiU/yEVPM9FoKNs/s400/1wvl.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5483254114782194978" /></a>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com0tag:blogger.com,1999:blog-7289401992773132194.post-7476693148913889932010-06-13T20:44:00.001-07:002010-06-13T20:46:08.984-07:00Bactericidal permeability-increasing protein<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://4.bp.blogspot.com/_HK1LuizCXdI/TBWl2oNO9RI/AAAAAAAABiM/skJt1-pJk-0/s1600/Bacterial+Permeability+protein.png"><img style="cursor:pointer; cursor:hand;width: 174px; height: 400px;" src="http://4.bp.blogspot.com/_HK1LuizCXdI/TBWl2oNO9RI/AAAAAAAABiM/skJt1-pJk-0/s400/Bacterial+Permeability+protein.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5482470479317890322" /></a>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com0tag:blogger.com,1999:blog-7289401992773132194.post-87012774814343716472010-06-10T12:22:00.000-07:002010-06-16T12:30:20.634-07:00DNA Gyrase<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://2.bp.blogspot.com/_HK1LuizCXdI/TBE7jcWh2EI/AAAAAAAABiE/7gL4HvEhBHM/s1600/DNA_gyrase.png"><img style="cursor:pointer; cursor:hand;width: 400px; height: 394px;" src="http://2.bp.blogspot.com/_HK1LuizCXdI/TBE7jcWh2EI/AAAAAAAABiE/7gL4HvEhBHM/s400/DNA_gyrase.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5481227701578750018" /></a><div><br /></div><div>DNA Gyrase from E.Coli is an enzyme belonging to the class of Topoisomerases, which allows the organism to modify the topology of its DNA. In other words it helps untangle, un-knot and relax supercoils in its DNA genome. It does so by binding to a strand of DNA, cutting both strands and then, while keeping hold of both cut ends, passing another piece of double stranded DNA through the gap. It then reseals the double stranded break. Essentially it allows portions of the large circular bacterial genome to pass through itself, such as to prevent knotting and entanglement. A number of antibiotics (e.g. Simocyclinone D8) target this enzyme, since it is essential to the organism's survival. Humans also have a form of this enzyme but it's construction is different and we are thus not affected by the antibiotics.</div>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com1tag:blogger.com,1999:blog-7289401992773132194.post-2037454947199146712010-06-08T19:11:00.000-07:002010-06-16T11:23:31.948-07:00Insulin hexamer<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://4.bp.blogspot.com/_HK1LuizCXdI/TA74cBfPqiI/AAAAAAAABh8/MDszGy5_3eQ/s1600/insulin.png"><img style="cursor:pointer; cursor:hand;width: 398px; height: 400px;" src="http://4.bp.blogspot.com/_HK1LuizCXdI/TA74cBfPqiI/AAAAAAAABh8/MDszGy5_3eQ/s400/insulin.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5480590956875983394" /></a><div><br /></div><div>Insulin is produced by the Islets of Langerhans in the Pancreas of mammals and induces liver and muscle cells to take up glucos (typically after a meal) from the blood. Shown here is a hexameric form, coordinated by two zinc ions, believed to be the form in which it is stored in the beta-cells of the islets of Langerhans prior to release. Inability to produce insulin (forvarious reasons) leads to the common disease of diabetes.</div>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com4tag:blogger.com,1999:blog-7289401992773132194.post-85571444457053163492010-06-08T15:07:00.000-07:002010-06-08T15:09:38.089-07:00Hydroperoxide resistance protein OsmC (1vla)<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://4.bp.blogspot.com/_HK1LuizCXdI/TA6_LG2XgMI/AAAAAAAABh0/sjlzNC_5LiU/s1600/1vla_Hydroperoxide_reistance_protein_osmc.png"><img style="cursor:pointer; cursor:hand;width: 393px; height: 400px;" src="http://4.bp.blogspot.com/_HK1LuizCXdI/TA6_LG2XgMI/AAAAAAAABh0/sjlzNC_5LiU/s400/1vla_Hydroperoxide_reistance_protein_osmc.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5480527994094584002" /></a>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com5tag:blogger.com,1999:blog-7289401992773132194.post-57131154486110295382010-06-08T13:27:00.000-07:002010-06-08T13:38:07.901-07:00Apoptosome-Procaspase-9 - CARD Complex<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://3.bp.blogspot.com/_HK1LuizCXdI/TA6qIt9ERqI/AAAAAAAABhs/tJNaagLxHOo/s1600/Apoptosis+factor.png"><img style="cursor:pointer; cursor:hand;width: 400px; height: 352px;" src="http://3.bp.blogspot.com/_HK1LuizCXdI/TA6qIt9ERqI/AAAAAAAABhs/tJNaagLxHOo/s400/Apoptosis+factor.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5480504863307876002" /></a><br /><br /><div><br /></div><div><br /></div>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com8tag:blogger.com,1999:blog-7289401992773132194.post-82861943788417891042010-06-08T12:52:00.001-07:002010-06-16T22:53:46.599-07:00Neurotrophin (Nerve growth factor (NGF))<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://2.bp.blogspot.com/_HK1LuizCXdI/TA6fnDL5CoI/AAAAAAAABhc/WfHRaW-v3FY/s1600/1bet.png"><img style="cursor:pointer; cursor:hand;width: 400px; height: 326px;" src="http://2.bp.blogspot.com/_HK1LuizCXdI/TA6fnDL5CoI/AAAAAAAABhc/WfHRaW-v3FY/s400/1bet.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5480493289775368834" /></a><div><br /></div><div><a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://2.bp.blogspot.com/_HK1LuizCXdI/TA6fnDL5CoI/AAAAAAAABhc/WfHRaW-v3FY/s1600/1bet.png"></a>NGF is a signaling molecule that binds to sympathetic and sensory neuron surfaces and prevents them from going into apoptosis (cell death). It is part of a larger family of signaling proteins collectively knows as neurotrophins. NGF has been shown to play a role in disorders as varied as coronary atherosclerosis, obesity, type 2 diabetes, and metabolic syndrome.</div>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com2tag:blogger.com,1999:blog-7289401992773132194.post-9826237057764996252010-06-08T12:38:00.000-07:002010-06-16T22:54:37.147-07:00Human liver alcohol dehydrogenase.<a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://4.bp.blogspot.com/_HK1LuizCXdI/TA6caYkyGFI/AAAAAAAABhU/d6xhVhlWPnc/s1600/Human_alcohol_dehydrogenase.png"><img style="cursor:pointer; cursor:hand;width: 400px; height: 256px;" src="http://4.bp.blogspot.com/_HK1LuizCXdI/TA6caYkyGFI/AAAAAAAABhU/d6xhVhlWPnc/s400/Human_alcohol_dehydrogenase.png" border="0" alt="" id="BLOGGER_PHOTO_ID_5480489773643733074" /></a><div><br /></div><div><a onblur="try {parent.deselectBloggerImageGracefully();} catch(e) {}" href="http://4.bp.blogspot.com/_HK1LuizCXdI/TA6caYkyGFI/AAAAAAAABhU/d6xhVhlWPnc/s1600/Human_alcohol_dehydrogenase.png"></a>Alcohol dehydrogenase (ADH) is found in the human liver and is part of a group of seven dehydrogenase enzymes that occur in many organisms and facilitate the interconversion between alcohols and aldehydes or ketones with the reduction of NAD+ to NADH. In humans and many other animals, they serve to break down alcohols which could otherwise be toxic, including ethanol.</div>Mike Tykahttp://www.blogger.com/profile/02832785814779269321noreply@blogger.com22