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New page: left|200px<br /><applet load="1goa" size="450" color="white" frame="true" align="right" spinBox="true" caption="1goa, resolution 1.9Å" /> '''COOPERATIVE STABILIZA...
 
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[[Image:1goa.gif|left|200px]]<br /><applet load="1goa" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1goa.gif|left|200px]]<br /><applet load="1goa" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1goa, resolution 1.9&Aring;" />
caption="1goa, resolution 1.9&Aring;" />
'''COOPERATIVE STABILIZATION OF ESCHERICHIA COLI RIBONUCLEASE HI BY INSERTION OF GLY-80B AND GLY-77-> ALA SUBSTITUTION'''<br />
'''COOPERATIVE STABILIZATION OF ESCHERICHIA COLI RIBONUCLEASE HI BY INSERTION OF GLY-80B AND GLY-77-> ALA SUBSTITUTION'''<br />


==Overview==
==Overview==
The insertion of a Gly residue (designated as Gly-80b) between the C-cap, of the alpha II-helix (Gln-80) and the N-cap of the alpha III-helix, (Trp-81) in Escherichia coli ribonuclease HI enhances the protein, stability by 0.4 kcal/mol in delta G (Kimura, S., Nakamura, H., Hashimoto, T., Oobatake, M., &amp; Kanaya, S. (1992) J. Biol. Chem. 267, 21535-21542)., Another mutation within the alpha II-helix, Gly-77--&gt;Ala, reduces the, stability by 0.9 kcal/mol. Simultaneous introduction of these mutations, enhances the stability by 0.8 kcal/mol, indicating that the effects of, these mutations are cooperative and not simply independent. We determined, the crystal structures of these three mutant proteins (G80b-, A77-, and, A77/G80b-RNase H) to investigate this cooperative mechanism of the protein, stabilization. The structures revealed that the inserted Gly-80b assumes a, left-handed helical conformation in both the G80b- and the A77/G80b-RNase, H. This inserted glycine residue allows the formation of a "paperclip", which is a common motif at the C-termini of alpha-helices. Accompanying, the formation of the paperclip motif, two intrahelical hydrogen bonds are, formed between the backbone atoms (O78-N80b and O80b-N84). The, stabilization caused by the insertion of Gly-80b can be ascribed to the, formation of these hydrogen bonds. The Gly-77--&gt;Ala substitution, destabilizes the protein due to the deformed packing interactions in the, hydrophobic core around Ala-77 and the stress in the wedged indole ring of, Trp-81. These effects are alleviated by the insertion of Gly-80b, which, relaxes the backbone structure.(ABSTRACT TRUNCATED AT 250 WORDS)
The insertion of a Gly residue (designated as Gly-80b) between the C-cap of the alpha II-helix (Gln-80) and the N-cap of the alpha III-helix (Trp-81) in Escherichia coli ribonuclease HI enhances the protein stability by 0.4 kcal/mol in delta G (Kimura, S., Nakamura, H., Hashimoto, T., Oobatake, M., &amp; Kanaya, S. (1992) J. Biol. Chem. 267, 21535-21542). Another mutation within the alpha II-helix, Gly-77--&gt;Ala, reduces the stability by 0.9 kcal/mol. Simultaneous introduction of these mutations enhances the stability by 0.8 kcal/mol, indicating that the effects of these mutations are cooperative and not simply independent. We determined the crystal structures of these three mutant proteins (G80b-, A77-, and A77/G80b-RNase H) to investigate this cooperative mechanism of the protein stabilization. The structures revealed that the inserted Gly-80b assumes a left-handed helical conformation in both the G80b- and the A77/G80b-RNase H. This inserted glycine residue allows the formation of a "paperclip", which is a common motif at the C-termini of alpha-helices. Accompanying the formation of the paperclip motif, two intrahelical hydrogen bonds are formed between the backbone atoms (O78-N80b and O80b-N84). The stabilization caused by the insertion of Gly-80b can be ascribed to the formation of these hydrogen bonds. The Gly-77--&gt;Ala substitution destabilizes the protein due to the deformed packing interactions in the hydrophobic core around Ala-77 and the stress in the wedged indole ring of Trp-81. These effects are alleviated by the insertion of Gly-80b, which relaxes the backbone structure.(ABSTRACT TRUNCATED AT 250 WORDS)


==About this Structure==
==About this Structure==
1GOA is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Active as [http://en.wikipedia.org/wiki/Ribonuclease_H Ribonuclease H], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.26.4 3.1.26.4] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1GOA OCA].  
1GOA is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Active as [http://en.wikipedia.org/wiki/Ribonuclease_H Ribonuclease H], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.26.4 3.1.26.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1GOA OCA].  


==Reference==
==Reference==
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[[Category: hydrolase(endoribonuclease)]]
[[Category: hydrolase(endoribonuclease)]]


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