Search Results - "Mulichak, A.M"

The Structure of the MUR1 GDP-mannose 4,67-deydratase from A. thaliana: Implications for Ligand Binding Specificity by Mulichak, A.M., Bonin, C.P., Reiter, W.-D., Garavito, R.M.

“…GDP-D-mannose 4,6-dehydratase catalyzes the first step in the de novo synthesis of GDP-L-fucose, the activated form of L-fucose, which is a component of…”
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Crystal Structure of Vancosaminyltransferase GtfD from the Vancomycin Biosynthetic Pathway: Interactions with Acceptor and Nucleotide Ligands by Mulichak, A.M., Lu, W., Losey, H.C., Walsh, C.T., Garavito, R.M.

“…The TDP-vancosaminyltransferase GtfD catalyzes the attachment of L-vancosamine to a monoglucosylated heptapeptide intermediate during the final stage of…”
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Crystal structure of SQD1, an enzyme involved in the biosynthesis of the plant sulfolipid headgroup donor UDP-sulfoquinovose by Mulichak, A.M, Theisen, M.J, Essigmann, B, Benning, C, Garavito, R.M

“…The SQD1 enzyme is believed to be involved in the biosynthesis of the sulfoquinovosyl headgroup of plant sulfolipids, catalyzing the transfer of SO(3)- to…”
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Crystal Structure of Human α-Thrombin Complexed with Hirugen and p-Amidinophenylpyruvate at 1.6 Å Resolution by Chen, Z.G., Li, Y., Mulichak, A.M., Lewis, S.D., Shafer, J.A.

“…Crystals of human α-thrombin complexed with hirugen and the α-keto acid thrombin inhibitor APPA ( p-amidinophenylpyruvate) that diffract to 1.6 Å resolution…”
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The crystallographic structure of the protease from human immunodeficiency virus type 2 with two synthetic peptidic transition state analog inhibitors by MULICHAK, A. M, HUI, J. O, TOMASSELLI, A. G, HEINRIKSON, R. L, CURRY, K. A, CHE-SHEN TOMICH, SUVIT THAISRIVONGS, SAWYER, T. K, WATENPAUGH, K. D

“…The crystal structure of human immunodeficiency virus (HIV) type 2 protease has been determined in complexes with peptidic inhibitors Noa-His-Cha psi…”
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