'''CRYSTAL STRUCTURE OF ADENINE PHOSPHORIBOSYLTRANSFERASE'''
===CRYSTAL STRUCTURE OF ADENINE PHOSPHORIBOSYLTRANSFERASE===
==Overview==
<!--
Adenine phosphoribosyltransferase (APRTase) is a widely distributed enzyme, and its deficiency in humans causes the accumulation of 2,8-dihydroxyadenine. It is the sole catalyst for adenine recycling in most eukaryotes. The most commonly expressed APRTase has subunits of approximately 187 amino acids, but the only crystal structure is from Leishmania donovani, which expresses a long form of the enzyme with 237 residues. Saccharomyces cerevisiae APRTase was selected as a representative of the short APRTases, and the structure of the apo-enzyme and sulfate bound forms were solved to 1.5 and 1.75 A, respectively. Yeast APRTase is a dimeric molecule, and each subunit is composed of a central five-stranded beta-sheet surrounded by five alpha-helices, a structural theme found in all known purine phosphoribosyltransferases. The structures reveal several important features of APRTase function: (i) sulfate ions bound at the 5'-phosphate and pyrophosphate binding sites; (ii) a nonproline cis peptide bond (Glu67-Ser68) at the pyrophosphate binding site in both apo-enzyme and sulfate-bound forms; and (iii) a catalytic loop that is open and ordered in the apo-enzyme but open and disordered in the sulfate-bound form. Alignment of conserved amino acids in short-APRTases from 33 species reveals 13 invariant and 15 highly conserved residues present in hinges, catalytic site loops, and the catalytic pocket. Mutagenesis of conserved residues in the catalytic loop, subunit interface, and phosphoribosylpyrophosphate binding site indicates critical roles for the tip of the catalytic loop (Glu106) and a catalytic site residue Arg69, respectively. Mutation of one loop residue (Tyr103Phe) increases k(cat) by 4-fold, implicating altered dynamics for the catalytic site loop.
The line below this paragraph, {{ABSTRACT_PUBMED_11535055}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 11535055 is the PubMed ID number.
-->
{{ABSTRACT_PUBMED_11535055}}
==About this Structure==
==About this Structure==
Line 30:
Line 34:
[[Category: Dimer]]
[[Category: Dimer]]
[[Category: Single domain]]
[[Category: Single domain]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 17:03:53 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 1 04:19:27 2008''
Revision as of 04:19, 1 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.
