1loy

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(New page: 200px<br /><applet load="1loy" size="450" color="white" frame="true" align="right" spinBox="true" caption="1loy, resolution 1.55&Aring;" /> '''X-ray structure of t...)
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[[Image:1loy.gif|left|200px]]<br /><applet load="1loy" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:1loy.gif|left|200px]]<br /><applet load="1loy" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1loy, resolution 1.55&Aring;" />
caption="1loy, resolution 1.55&Aring;" />
'''X-ray structure of the H40A/E58A mutant of Ribonuclease T1 complexed with 3'-guanosine monophosphate'''<br />
'''X-ray structure of the H40A/E58A mutant of Ribonuclease T1 complexed with 3'-guanosine monophosphate'''<br />
==Overview==
==Overview==
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Ribonucleases (RNases) catalyze the cleavage of the phosphodiester bond in, RNA up to 10(15)-fold, as compared with the uncatalyzed reaction. High, resolution crystal structures of these enzymes in complex with, 3'-mononucleotide substrates demonstrate the accommodation of the, nucleophilic 2'-OH group in a binding pocket comprising the catalytic base, (glutamate or histidine) and a charged hydrogen bond donor (lysine or, histidine). Ab initio quantum chemical calculations performed on such, Michaelis complexes of the mammalian RNase A (EC ) and the microbial RNase, T(1) (EC ) show negative charge build up on the 2'-oxygen upon substrate, binding. The increased nucleophilicity results from stronger hydrogen, bonding to the catalytic base, which is mediated by a hydrogen bond from, the charged donor. This hitherto unrecognized catalytic dyad in, ribonucleases constitutes a general mechanism for nucleophile activation, in both enzymic and RNA-catalyzed phosphoryl transfer reactions.
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Ribonucleases (RNases) catalyze the cleavage of the phosphodiester bond in RNA up to 10(15)-fold, as compared with the uncatalyzed reaction. High resolution crystal structures of these enzymes in complex with 3'-mononucleotide substrates demonstrate the accommodation of the nucleophilic 2'-OH group in a binding pocket comprising the catalytic base (glutamate or histidine) and a charged hydrogen bond donor (lysine or histidine). Ab initio quantum chemical calculations performed on such Michaelis complexes of the mammalian RNase A (EC ) and the microbial RNase T(1) (EC ) show negative charge build up on the 2'-oxygen upon substrate binding. The increased nucleophilicity results from stronger hydrogen bonding to the catalytic base, which is mediated by a hydrogen bond from the charged donor. This hitherto unrecognized catalytic dyad in ribonucleases constitutes a general mechanism for nucleophile activation in both enzymic and RNA-catalyzed phosphoryl transfer reactions.
==About this Structure==
==About this Structure==
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1LOY is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Aspergillus_oryzae Aspergillus oryzae] with CA and 3GP as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Ribonuclease_T(1) Ribonuclease T(1)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.27.3 3.1.27.3] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1LOY OCA].
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1LOY is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Aspergillus_oryzae Aspergillus oryzae] with <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=3GP:'>3GP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Ribonuclease_T(1) Ribonuclease T(1)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.27.3 3.1.27.3] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1LOY OCA].
==Reference==
==Reference==
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[[Category: rnase]]
[[Category: rnase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 20:44:25 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:47:00 2008''

Revision as of 11:47, 21 February 2008


1loy, resolution 1.55Å

Drag the structure with the mouse to rotate

X-ray structure of the H40A/E58A mutant of Ribonuclease T1 complexed with 3'-guanosine monophosphate

Overview

Ribonucleases (RNases) catalyze the cleavage of the phosphodiester bond in RNA up to 10(15)-fold, as compared with the uncatalyzed reaction. High resolution crystal structures of these enzymes in complex with 3'-mononucleotide substrates demonstrate the accommodation of the nucleophilic 2'-OH group in a binding pocket comprising the catalytic base (glutamate or histidine) and a charged hydrogen bond donor (lysine or histidine). Ab initio quantum chemical calculations performed on such Michaelis complexes of the mammalian RNase A (EC ) and the microbial RNase T(1) (EC ) show negative charge build up on the 2'-oxygen upon substrate binding. The increased nucleophilicity results from stronger hydrogen bonding to the catalytic base, which is mediated by a hydrogen bond from the charged donor. This hitherto unrecognized catalytic dyad in ribonucleases constitutes a general mechanism for nucleophile activation in both enzymic and RNA-catalyzed phosphoryl transfer reactions.

About this Structure

1LOY is a Single protein structure of sequence from Aspergillus oryzae with and as ligands. Active as Ribonuclease T(1), with EC number 3.1.27.3 Full crystallographic information is available from OCA.

Reference

A nucleophile activation dyad in ribonucleases. A combined X-ray crystallographic/ab initio quantum chemical study., Mignon P, Steyaert J, Loris R, Geerlings P, Loverix S, J Biol Chem. 2002 Sep 27;277(39):36770-4. Epub 2002 Jul 16. PMID:12122018

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