{"id":498248,"date":"2022-10-04T21:36:48","date_gmt":"2022-10-04T18:36:48","guid":{"rendered":"https:\/\/en.buradabiliyorum.com\/protein-family-shows-how-life-adapted-to-oxygen\/"},"modified":"2022-10-04T21:36:48","modified_gmt":"2022-10-04T18:36:48","slug":"protein-family-shows-how-life-adapted-to-oxygen","status":"publish","type":"post","link":"https:\/\/buradabiliyorum.com\/en\/protein-family-shows-how-life-adapted-to-oxygen\/","title":{"rendered":"#Protein family shows how life adapted to oxygen"},"content":{"rendered":"<div id=\"ez-toc-container\" class=\"ez-toc-v2_0_85 counter-hierarchy ez-toc-counter ez-toc-custom ez-toc-container-direction\">\n<p class=\"ez-toc-title\" style=\"cursor:inherit\">Table of Contents<\/p>\n<label for=\"ez-toc-cssicon-toggle-item-6a3be3c8d0b73\" class=\"ez-toc-cssicon-toggle-label\"><span class=\"\"><span class=\"eztoc-hide\" style=\"display:none;\">Toggle<\/span><span class=\"ez-toc-icon-toggle-span\"><svg style=\"fill: #dd3333;color:#dd3333\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" class=\"list-377408\" width=\"20px\" height=\"20px\" viewBox=\"0 0 24 24\" fill=\"none\"><path d=\"M6 6H4v2h2V6zm14 0H8v2h12V6zM4 11h2v2H4v-2zm16 0H8v2h12v-2zM4 16h2v2H4v-2zm16 0H8v2h12v-2z\" fill=\"currentColor\"><\/path><\/svg><svg style=\"fill: #dd3333;color:#dd3333\" class=\"arrow-unsorted-368013\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"10px\" height=\"10px\" viewBox=\"0 0 24 24\" version=\"1.2\" baseProfile=\"tiny\"><path d=\"M18.2 9.3l-6.2-6.3-6.2 6.3c-.2.2-.3.4-.3.7s.1.5.3.7c.2.2.4.3.7.3h11c.3 0 .5-.1.7-.3.2-.2.3-.5.3-.7s-.1-.5-.3-.7zM5.8 14.7l6.2 6.3 6.2-6.3c.2-.2.3-.5.3-.7s-.1-.5-.3-.7c-.2-.2-.4-.3-.7-.3h-11c-.3 0-.5.1-.7.3-.2.2-.3.5-.3.7s.1.5.3.7z\"\/><\/svg><\/span><\/span><\/label><input type=\"checkbox\"  id=\"ez-toc-cssicon-toggle-item-6a3be3c8d0b73\" checked aria-label=\"Toggle\" \/><nav><ul class='ez-toc-list ez-toc-list-level-1 ' ><li class='ez-toc-page-1 ez-toc-heading-level-1'><a class=\"ez-toc-link ez-toc-heading-1\" href=\"https:\/\/buradabiliyorum.com\/en\/protein-family-shows-how-life-adapted-to-oxygen\/#%E2%80%9CProtein_family_shows_how_life_adapted_to_oxygen%E2%80%9D\" >&#8220;Protein family shows how life adapted to oxygen&#8221;<\/a><\/li><\/ul><\/nav><\/div>\n<h1><span class=\"ez-toc-section\" id=\"%E2%80%9CProtein_family_shows_how_life_adapted_to_oxygen%E2%80%9D\"><\/span>&#8220;Protein family shows how life adapted to oxygen&#8221;<span class=\"ez-toc-section-end\"><\/span><\/h1>\n<div>\n<div class=\"article-gallery lightGallery\">\n<div data-thumb=\"https:\/\/scx1.b-cdn.net\/csz\/news\/tmb\/2022\/protein-family-shows-h.jpg\" data-src=\"https:\/\/scx2.b-cdn.net\/gfx\/news\/hires\/2022\/protein-family-shows-h.jpg\" data-sub-html=\"The catalytic fold of the ribonucleotide reductase (RNR) family is a unique 10-stranded \u0251\/\u03b2 barrel, consisting of 10 \u03b2-strands (light green) and 8 \u0251-helices (light blue). (&lt;b&gt;A&lt;\/b&gt;) Each half of the barrel contains a five-stranded parallel \u03b2-sheet (\u03b2A-\u03b2E and \u03b2F-\u03b2J) that is arranged in anti-parallel orientation with respect to each other. The two halves are connected by the so-called 'finger loop' (yellow) which typically begins with a short \u0251-helix and contains a conserved cysteine that has been shown to be the site of the catalytically essential thiyl radical in all biochemically characterized RNRs. Diversity among the RNRs is generated by N- and C-terminal extensions as well as the insertions (dashed curves) between the secondary structure elements in the \u0251\/\u03b2 barrel. Loops 1\u20133 (dark green, red, blue) have special names in the RNR literature for their involvement in specificity regulation. The gray secondary structure elements (starred) are partially integrated in the \u0251\/\u03b2 barrel and are involved in substrate binding. (&lt;b&gt;B&lt;\/b&gt;) The barrel portion (top) of the &lt;i&gt;Escherichia coli&lt;\/i&gt; class Ia catalytic subunit (bottom dimer). The ATP-cone domain is colored in orange. (&lt;b&gt;C&lt;\/b&gt;) The barrel portion (top) of the &lt;i&gt;Thermotoga maritima&lt;\/i&gt; class II catalytic subunit (bottom dimer). (&lt;b&gt;D&lt;\/b&gt;) The barrel portion (top) of the T4 phage class III catalytic subunit (bottom dimer). In class III RNRs, the loop 1 region (dark green) is a long helix that is involved in dimerization. Credit: &lt;i&gt;eLife&lt;\/i&gt; (2022). DOI: 10.7554\/eLife.79790\">\n<figure class=\"article-img\">\n            <img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/scx1.b-cdn.net\/csz\/news\/800a\/2022\/protein-family-shows-h.jpg\" alt=\"Protein family shows how life adapted to oxygen\" title=\"The catalytic fold of the ribonucleotide reductase (RNR) family is a unique 10-stranded \u0251\/\u03b2 barrel, consisting of 10 \u03b2-strands (light green) and 8 \u0251-helices (light blue). (&lt;b&gt;A&lt;\/b&gt;) Each half of the barrel contains a five-stranded parallel \u03b2-sheet (\u03b2A-\u03b2E and \u03b2F-\u03b2J) that is arranged in anti-parallel orientation with respect to each other. The two halves are connected by the so-called 'finger loop' (yellow) which typically begins with a short \u0251-helix and contains a conserved cysteine that has been shown to be the site of the catalytically essential thiyl radical in all biochemically characterized RNRs. Diversity among the RNRs is generated by N- and C-terminal extensions as well as the insertions (dashed curves) between the secondary structure elements in the \u0251\/\u03b2 barrel. Loops 1\u20133 (dark green, red, blue) have special names in the RNR literature for their involvement in specificity regulation. The gray secondary structure elements (starred) are partially integrated in the \u0251\/\u03b2 barrel and are involved in substrate binding. (&lt;b&gt;B&lt;\/b&gt;) The barrel portion (top) of the &lt;i&gt;Escherichia coli&lt;\/i&gt; class Ia catalytic subunit (bottom dimer). The ATP-cone domain is colored in orange. (&lt;b&gt;C&lt;\/b&gt;) The barrel portion (top) of the &lt;i&gt;Thermotoga maritima&lt;\/i&gt; class II catalytic subunit (bottom dimer). (&lt;b&gt;D&lt;\/b&gt;) The barrel portion (top) of the T4 phage class III catalytic subunit (bottom dimer). In class III RNRs, the loop 1 region (dark green) is a long helix that is involved in dimerization. Credit: &lt;i&gt;eLife&lt;\/i&gt; (2022). DOI: 10.7554\/eLife.79790\" width=\"800\" height=\"530\"\/><figcaption class=\"text-darken text-low-up text-truncate-js text-truncate mt-3\">\n                The catalytic fold of the ribonucleotide reductase (RNR) family is a unique 10-stranded \u0251\/\u03b2 barrel, consisting of 10 \u03b2-strands (light green) and 8 \u0251-helices (light blue). (<b>A<\/b>) Each half of the barrel contains a five-stranded parallel \u03b2-sheet (\u03b2A-\u03b2E and \u03b2F-\u03b2J) that is arranged in anti-parallel orientation with respect to each other. The two halves are connected by the so-called &#8216;finger loop&#8217; (yellow) which typically begins with a short \u0251-helix and contains a conserved cysteine that has been shown to be the site of the catalytically essential thiyl radical in all biochemically characterized RNRs. Diversity among the RNRs is generated by N- and C-terminal extensions as well as the insertions (dashed curves) between the secondary structure elements in the \u0251\/\u03b2 barrel. Loops 1\u20133 (dark green, red, blue) have special names in the RNR literature for their involvement in specificity regulation. The gray secondary structure elements (starred) are partially integrated in the \u0251\/\u03b2 barrel and are involved in substrate binding. (<b>B<\/b>) The barrel portion (top) of the <i>Escherichia coli<\/i> class Ia catalytic subunit (bottom dimer). The ATP-cone domain is colored in orange. (<b>C<\/b>) The barrel portion (top) of the <i>Thermotoga maritima<\/i> class II catalytic subunit (bottom dimer). (<b>D<\/b>) The barrel portion (top) of the T4 phage class III catalytic subunit (bottom dimer). In class III RNRs, the loop 1 region (dark green) is a long helix that is involved in dimerization. Credit: <i>eLife<\/i> (2022). DOI: 10.7554\/eLife.79790<br \/>\n            <\/figcaption><\/figure>\n<\/p><\/div>\n<\/div>\n<p>Cornell scientists have created an evolutionary model that connects organisms living in today&#8217;s oxygen-rich atmosphere to a time, billions of years ago, when Earth&#8217;s atmosphere had little oxygen\u2014by analyzing ribonucleotide reductases (RNRs), a family of proteins used by all free-living organisms and many viruses to repair and replicate DNA.<\/p>\n<section class=\"article-banner first-banner ads-336x280\">\n         <!-- \/4988204\/Phys_Story_InText_Box --><\/p>\n<\/section>\n<p>&#8220;By understanding the evolution of these proteins, we can understand how nature adapts to environmental changes at the molecular level. In turn, we also learn about our planet&#8217;s past,&#8221; said Nozomi Ando, associate professor of chemistry and chemical biology in the College of Arts and <a href=\"https:\/\/buradabiliyorum.com\/en\/category\/sciencee\/\" data-internallinksmanager029f6b8e52c=\"5\" title=\"Science\" target=\"_blank\" rel=\"noopener\">Science<\/a>s and corresponding author of the study. &#8220;Comprehensive phylogenetic analysis of the ribonucleotide reductase family reveals an ancestral clade&#8221; published in <i>eLife<\/i> on Oct. 4.<\/p>\n<p>Co-first authors of the study are Audrey Burnim and Da Xu, doctoral students in chemistry and chemical biology, and Matthew Spence, Research School of Chemistry, Australian National University, Canberra. Colin J. Jackson, professor of chemistry, Australian National University, Canberra, is a corresponding author.<\/p>\n<p>This undertaking involved a large dataset of 6,779 RNR sequences; the phylogeny took several high-performance computers a combined seven months (1.4 million CPU hours) to calculate. Made possible by computing advances, the <a href=\"https:\/\/buradabiliyorum.com\/en\/category\/download-scripts-themes-apps\/\" data-internallinksmanager029f6b8e52c=\"9\" title=\"Download Scripts &amp; Themes &amp; Apps\" target=\"_blank\" rel=\"noopener\">app<\/a>roach opens up a new way to study other diverse protein families that have evolutionary or medical significance.<\/p>\n<p>RNRs have adapted to changes in the environment over billions of years to conserve their catalytic mechanism because of their essential role for all DNA-based life, Ando said. Her lab studies protein allostery\u2014how proteins are able to change activity in response to the environment. The evolutionary information in a phylogeny gives us a way to study the relationship between the primary sequence of a protein and its three-dimensional structure, dynamics and function.<\/p>\n<p>RNRs are thought to have ancient origins because they catalyze the reaction of converting RNA building blocks into DNA building blocks, Ando said, making them ideal for finding a molecular record.<\/p>\n<p>&#8220;This chemistry would have been needed to transition from the hypothesized RNA world to the DNA\/protein world that we currently live in,&#8221; Ando said. &#8220;Based on the co-factors that RNRs use, it also is clear that this enzyme family has adapted to oxygen increasing in the Earth&#8217;s atmosphere. Both of these transitions took place billions of years ago.&#8221;<\/p>\n<p>When scientists build a phylogeny of a protein family, they calculate how the currently existing sequences came to be, Ando said. In that process, they have to estimate what happened in the past to get the sequences that exist now.<\/p>\n<p>The researchers calculated the RNR phylogeny by gathering a dataset of more than 100,000 sequences and curating down to a computationally tractable dataset of 6,779 sequences while maintaining the diversity of the entire family, Burnim said. The sequences range in length from about 400 to 1,100 amino acids. Using models of how amino acids mutate, they compared the sequences with each other to determine when they diverged.<\/p>\n<p>From this work, the researchers discovered a new distinct group of RNRs that would explain how two different adaptations to oxygen on Earth emerged within this protein family.<\/p>\n<p>They used small-angle X-ray scattering at the Cornell High Energy Synchrotron Source, cryogenic-electron microscopy at the Cornell Center for Materials Research and the artificial intelligence program AlphaFold2 to study the RNR from Synechococcus phage S-CBP4, a virus that infects a cyanobacterium, Xu said.<\/p>\n<p>&#8220;When we calculated the RNR family tree, it turned out that there was a branch of RNRs that we didn&#8217;t know was a distinct lineage,&#8221; Ando said. &#8220;This branch included sequences from marine organisms including cyanophages. Our characterization of one of the sequences suggests that there was an early adaptation to oxygen. The cyanophage connection was interesting because it suggests that their hosts (cyanobacteria) were around at the same time, and cyanobacteria are credited for oxygenating the Earth.&#8221;<\/p>\n<p>The findings support the idea that molecular adaptations to oxygen occurred much earlier than the large-scale environmental changes to the planet, as dated by geochemical records, Ando said.<\/p>\n<p>This first-ever unified evolutionary model for all classes of RNRs could offer many future directions for the field, Xu said.<\/p>\n<p>Ando plans to use the same approach to study how enzymes with the same overall structure evolved to catalyze totally different chemical reactions.<\/p>\n<hr\/>\n<div class=\"article-main__explore my-4 d-print-none\">\n<p>                                            RNR &#8216;switch&#8217; offers hope in battling antibiotic resistant bacteria\n                                        <\/p><\/div>\n<hr class=\"mb-4\"\/>\n<div class=\"article-main__more p-4\">\n                                                                                                <strong>More information:<\/strong><br \/>\n                                                Audrey A Burnim et al, Comprehensive phylogenetic analysis of the ribonucleotide reductase family reveals an ancestral clade, <i>eLife<\/i> (2022).  <a rel=\"nofollow noopener\" target=\"_blank\" data-doi=\"1\" href=\"https:\/\/dx.doi.org\/10.7554\/eLife.79790\">DOI: 10.7554\/eLife.79790<\/a><\/p>\n<div class=\"mt-3\">\n                                                    <strong>Journal information:<\/strong><br \/>\n                                                                                                            <cite>eLife<\/cite><br \/>\n                                                        <a rel=\"nofollow noopener\" target=\"_blank\" class=\"icon_open\" href=\"http:\/\/www.elifesciences.org\/\"><br \/>\n                                                            <svg>\n                                                                <use href=\"https:\/\/phys.b-cdn.net\/tmpl\/v6\/img\/svg\/sprite.svg#icon_open\" x=\"0\" y=\"0\"\/>\n                                                            <\/svg><br \/>\n                                                        <\/a> <\/p><\/div>\n<\/p><\/div>\n<div class=\"d-inline-block text-medium my-4\">\n                                                Provided by<br \/>\n                                                                                                    Cornell University<br \/>\n                                                                                                        <a rel=\"nofollow noopener\" target=\"_blank\" class=\"icon_open\" href=\"http:\/\/www.cornell.edu\/\"><br \/>\n                                                        <svg>\n                                                            <use href=\"https:\/\/phys.b-cdn.net\/tmpl\/v6\/img\/svg\/sprite.svg#icon_open\" x=\"0\" y=\"0\"\/>\n                                                        <\/svg><br \/>\n                                                    <\/a><\/p><\/div>\n<p>                                        <!-- print only --><\/p>\n<div class=\"d-none d-print-block\">\n<p>                                                 <strong>Citation<\/strong>:<br \/>\n                                                 Protein family shows how life adapted to oxygen (2022, October  4)<br \/>\n                                                 retrieved  4 October 2022<br \/>\n                                                 from https:\/\/phys.org\/<a href=\"https:\/\/buradabiliyorum.com\/en\/category\/news\/\" data-internallinksmanager029f6b8e52c=\"2\" title=\"News\" target=\"_blank\" rel=\"noopener\">news<\/a>\/2022-10-protein-family-life-oxygen.html<\/p>\n<p>                                            This document is subject to copyright. 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Follow us on\u00a0<span style=\"color: #ff0000;\"><a style=\"color: #ff0000;\" href=\"https:\/\/news.google.com\/publications\/CAAqBwgKMLG0nwswvr63Aw\" target=\"_blank\" rel=\"nofollow noopener noreferrer\">Google News<\/a><\/span>\u00a0too, click on the star and choose us from your favorites.<\/span><\/strong><\/p><\/blockquote>\n<blockquote>\n<p style=\"text-align: center;\">For forums sites go to <span style=\"color: #ff9900;\"><a style=\"color: #ff9900;\" href=\"https:\/\/forum.buradabiliyorum.com\/\" target=\"_blank\" rel=\"noopener\">Forum.BuradaBiliyorum.Com<\/a><\/span><\/strong>\n<\/p><\/blockquote>\n<blockquote>\n<p style=\"text-align: center;\"><strong>If you want to read more Like this articles, you can visit our <span style=\"color: #ff9900;\"><a style=\"color: #ff9900;\" href=\"https:\/\/en.buradabiliyorum.com\/science\/\" target=\"_blank\" rel=\"noopener\">Science category.<\/a><\/span><\/strong><\/p>\n<\/blockquote>\n<p><span style=\"color: black;\"><a style=\"color: #ff9900;\" href=\"https:\/\/phys.org\/news\/2022-10-protein-family-life-oxygen.html\" target=\"_blank\" rel=\"noopener\">Source<\/a><\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>&#8220;Protein family shows how life adapted to oxygen&#8221; The catalytic fold of the ribonucleotide reductase (RNR) family is a unique 10-stranded \u0251\/\u03b2 barrel, consisting of 10 \u03b2-strands (light green) and 8 \u0251-helices (light blue). (A) Each half of the barrel contains a five-stranded parallel \u03b2-sheet (\u03b2A-\u03b2E and \u03b2F-\u03b2J) that is arranged in anti-parallel orientation with&#8230;<\/p>\n","protected":false},"author":1,"featured_media":498249,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"fifu_image_url":"https:\/\/scx2.b-cdn.net\/gfx\/news\/hires\/2022\/protein-family-shows-h.jpg","fifu_image_alt":"","footnotes":""},"categories":[16],"tags":[],"class_list":["post-498248","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-sciencee"],"_links":{"self":[{"href":"https:\/\/buradabiliyorum.com\/en\/wp-json\/wp\/v2\/posts\/498248","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/buradabiliyorum.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/buradabiliyorum.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/buradabiliyorum.com\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/buradabiliyorum.com\/en\/wp-json\/wp\/v2\/comments?post=498248"}],"version-history":[{"count":0,"href":"https:\/\/buradabiliyorum.com\/en\/wp-json\/wp\/v2\/posts\/498248\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/buradabiliyorum.com\/en\/wp-json\/wp\/v2\/media\/498249"}],"wp:attachment":[{"href":"https:\/\/buradabiliyorum.com\/en\/wp-json\/wp\/v2\/media?parent=498248"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/buradabiliyorum.com\/en\/wp-json\/wp\/v2\/categories?post=498248"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/buradabiliyorum.com\/en\/wp-json\/wp\/v2\/tags?post=498248"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}