1s2d: Difference between revisions

Revision as of 07:12, 28 July 2008

This article has been automatically seeded. Changes to this page should pertain to the PDB entry only and not to the protein or biomolecule in general.

File:1s2d.png

Template:STRUCTURE 1s2d

Purine 2'-Deoxyribosyl complex with arabinoside: Ribosylated Intermediate (AraA)Purine 2'-Deoxyribosyl complex with arabinoside: Ribosylated Intermediate (AraA)

Template:ABSTRACT PUBMED 14992575

About this StructureAbout this Structure

1S2D is a Single protein structure of sequence from Lactobacillus helveticus. Full crystallographic information is available from OCA.

ReferenceReference

Structures of purine 2'-deoxyribosyltransferase, substrate complexes, and the ribosylated enzyme intermediate at 2.0 A resolution., Anand R, Kaminski PA, Ealick SE, Biochemistry. 2004 Mar 9;43(9):2384-93. PMID:14992575

Page seeded by OCA on Mon Jul 28 07:12:47 2008

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

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-'''Purine 2'-Deoxyribosyl complex with arabinoside: Ribosylated Intermediate (AraA)'''
+===Purine 2'-Deoxyribosyl complex with arabinoside: Ribosylated Intermediate (AraA)===
-==Overview==
+<!--
-The structure of class I N-deoxyribosyltransferase from Lactobacillus helveticus was determined by X-ray crystallography. Unlike class II N-deoxyribosyltransferases, which accept either purine or pyrimidine deoxynucleosides, class I enzymes are specific for purines as both the donor and acceptor base. Both class I and class II enzymes are highly specific for deoxynucleosides. The class I structure reveals similarities with the previously determined class II enzyme from Lactobacillus leichmanni [Armstrong, S. A., Cook, W. J., Short, S. A., and Ealick, S. E. (1996) Structure 4, 97-107]. The specificity of the class I enzyme for purine deoxynucleosides can be traced to a loop (residues 48-62), which shields the active site in the class II enzyme. In the class I enzyme, the purine base itself shields the active site from the solvent, while the smaller pyrimidine base cannot. The structure of the enzyme with a bound ribonucleoside shows that the nucleophilic oxygen atom of Glu101 hydrogen bonds to the O2' atom, rendering it unreactive and thus explaining the specificity for 2'-deoxynucleosides. The structure of a ribosylated enzyme intermediate reveals movements that occur during cleavage of the N-glycosidic bond. The structures of complexes with substrates and substrate analogues show that the purine base can bind in several different orientations, thus explaining the ability of the enzyme to catalyze alternate deoxyribosylation at the N3 or N7 position.
+The line below this paragraph, {{ABSTRACT_PUBMED_14992575}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 14992575 is the PubMed ID number.
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+{{ABSTRACT_PUBMED_14992575}}
 ==About this Structure==
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 [[Category: Ptd]]
 [[Category: Ribosylate intermediate]]
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