2o1h: Difference between revisions

caption="2o1h, resolution 1.67Å" />

'''Naturally occurring mutation of Humna ABO(H) Galactosyltransferase in complex with UDP: GTB/M214T_UDP'''<br />

==Overview==

Human blood group A and B antigens are produced by two closely related, glycosyltransferase enzymes. An N-acetylgalactosaminyltransferase (GTA), utilizes UDP-GalNAc to extend H antigen acceptors (Fuc alpha(1-2)Gal, beta-OR) producing A antigens, whereas a galactosyltransferase (GTB), utilizes UDP-Gal as a donor to extend H structures producing B antigens., GTA and GTB have a characteristic (211)DVD(213) motif that coordinates to, a Mn(2+) ion shown to be critical in donor binding and catalysis. Three, GTB mutants, M214V, M214T, and M214R, with alterations adjacent to the, (211)DVD(213) motif have been identified in blood banking laboratories., From serological phenotyping, individuals with the M214R mutation show the, B(el) variant expressing very low levels of B antigens, whereas those with, M214T and M214V mutations give rise to A(weak)B phenotypes. Kinetic, analysis of recombinant mutant GTB enzymes revealed that M214R has a, 1200-fold decrease in k(cat) compared with wild type GTB. The crystal, structure of M214R showed that DVD motif coordination to Mn(2+) was, disrupted by Arg-214 causing displacement of the metal by a water, molecule. Kinetic characterizations of the M214T and M214V mutants, revealed they both had GTA and GTB activity consistent with the serology., The crystal structure of the M214T mutant showed no change in DVD, coordination to Mn(2+). Instead a critical residue, Met-266, which is, responsible for determining donor specificity, had adopted alternate, conformations. The conformation with the highest occupancy opens up the, active site to accommodate the larger A-specific donor, UDP-GalNAc, accounting for the dual specificity.

==About this Structure==

==Reference==

[[Category: gtb]]