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   <subfield code="u">Department of Biological Sciences, Dartmouth College, 03755, Hanover, NH, USA</subfield>
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   <subfield code="a">A Model of Proto-Anti-Codon RNA Enzymes Requiring l -Amino Acid Homochirality</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Albert Erives]</subfield>
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   <subfield code="a">All living organisms encode the 20 natural amino acid units of polypeptides using a universal scheme of triplet nucleotide &quot;codons”. Disparate features of this codon scheme are potentially informative of early molecular evolution: (i) the absence of any codons for d-amino acids; (ii) the odd combination of alternate codon patterns for some amino acids; (iii) the confinement of synonymous positions to a codon's third nucleotide; (iv) the use of 20 specific amino acids rather than a number closer to the full coding potential of 64; and (v) the evolutionary relationship of patterns in stop codons to amino acid codons. Here I propose a model for an ancestral proto-anti-codon RNA (pacRNA) auto-aminoacylation system and show that pacRNAs would naturally manifest features of the codon table. I show that pacRNAs could implement all the steps for auto-aminoacylation: amino acid coordination, intermediate activation of the amino acid by the 5′-end of the pacRNA, and 3′-aminoacylation of the pacRNA. The anti-codon cradles of pacRNAs would have been able to recognize and coordinate only a small number of l-amino acids via hydrogen bonding. A need for proper spatial coordination would have limited the number of chargeable amino acids for all anti-codon sequences, in addition to making some anti-codon sequences unsuitable. Thus, the pacRNA model implies that the idiosyncrasies of the anti-codon table and l-amino acid homochirality co-evolved during a single evolutionary period. These results further imply that early life consisted of an aminoacylated RNA world with a richer enzymatic potential than ribonucleotides alone.</subfield>
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   <subfield code="a">The Author(s), 2011</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">RNA world</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Proto-anti-codons</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Homochirality</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Molecular evolution</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Ribozymes</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="773" ind1="0" ind2=" ">
   <subfield code="t">Journal of Molecular Evolution</subfield>
   <subfield code="d">Springer-Verlag</subfield>
   <subfield code="g">73/1-2(2011-08-01), 10-22</subfield>
   <subfield code="x">0022-2844</subfield>
   <subfield code="q">73:1-2&lt;10</subfield>
   <subfield code="1">2011</subfield>
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   <subfield code="D">Albert</subfield>
   <subfield code="u">Department of Biological Sciences, Dartmouth College, 03755, Hanover, NH, USA</subfield>
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   <subfield code="B">NATIONALLICENCE</subfield>
   <subfield code="P">773</subfield>
   <subfield code="E">0-</subfield>
   <subfield code="t">Journal of Molecular Evolution</subfield>
   <subfield code="d">Springer-Verlag</subfield>
   <subfield code="g">73/1-2(2011-08-01), 10-22</subfield>
   <subfield code="x">0022-2844</subfield>
   <subfield code="q">73:1-2&lt;10</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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