1xv5

From Proteopedia
Revision as of 07:14, 21 November 2007 by OCA (talk | contribs) (New page: left|200px<br /><applet load="1xv5" size="450" color="white" frame="true" align="right" spinBox="true" caption="1xv5, resolution 1.73Å" /> '''alpha-glucosyltransf...)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search
File:1xv5.gif


1xv5, resolution 1.73Å

Drag the structure with the mouse to rotate

alpha-glucosyltransferase (AGT) in complex with UDP

OverviewOverview

The Escherichia coli T4 bacteriophage uses two glycosyltransferases to, glucosylate and thus protect its DNA: the retaining, alpha-glucosyltransferase (AGT) and the inverting beta-glucosyltransferase, (BGT). They glucosylate 5-hydroxymethyl cytosine (5-HMC) bases of duplex, DNA using UDP-glucose as the sugar donor to form an alpha-glucosidic, linkage and a beta-glucosidic linkage, respectively. Five structures of, AGT have been determined: a binary complex with the UDP product and four, ternary complexes with UDP or UDP-glucose and oligonucleotides containing, an A:G, HMU:G (hydroxymethyl uracyl) or AP:G (apurinic/apyrimidinic), mismatch at the target base-pair. AGT adopts the GT-B fold, one of the two, folds known for GTs. However, while the sugar donor binding mode is, classical for a GT-B enzyme, the sugar acceptor binding mode is unexpected, and breaks the established consensus: AGT is the first GT-B enzyme that, predominantly binds both the sugar donor and acceptor to the C-terminal, domain. Its active site pocket is highly similar to four retaining GT-B, glycosyltransferases (trehalose-6-phosphate synthase, glycogen synthase, glycogen and maltodextrin phosphorylases) strongly suggesting a common, evolutionary origin and catalytic mechanism for these enzymes., Structure-guided mutagenesis and kinetic analysis do not permit, identification of a nucleophile residue responsible for a glycosyl-enzyme, intermediate for the classical double displacement mechanism., Interestingly, the DNA structures reveal partially flipped-out bases. They, provide evidence for a passive role of AGT in the base-flipping mechanism, and for its specific recognition of the acceptor base.

About this StructureAbout this Structure

1XV5 is a Single protein structure of sequence from Bacteriophage t4 with CL, UDP, EDO and GOL as ligands. Active as DNA alpha-glucosyltransferase, with EC number 2.4.1.26 Full crystallographic information is available from OCA.

ReferenceReference

Structural evidence of a passive base-flipping mechanism for AGT, an unusual GT-B glycosyltransferase., Lariviere L, Sommer N, Morera S, J Mol Biol. 2005 Sep 9;352(1):139-50. PMID:16081100

Page seeded by OCA on Wed Nov 21 06:21:50 2007

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

OCA