The crystal structure of guinea pig 11beta-hydroxysteroid dehydrogenase type 1 provides a model for enzyme-lipid bilayer interactions. Read more about The crystal structure of guinea pig 11beta-hydroxysteroid dehydrogenase type 1 provides a model for enzyme-lipid bilayer interactions.
Structure of human phytanoyl-CoA 2-hydroxylase identifies molecular mechanisms of Refsum disease. Read more about Structure of human phytanoyl-CoA 2-hydroxylase identifies molecular mechanisms of Refsum disease.
Structure and substrate specificity of the Pim-1 kinase. Read more about Structure and substrate specificity of the Pim-1 kinase.
Regulation of the wild-type and Y1235D mutant Met kinase activation. Read more about Regulation of the wild-type and Y1235D mutant Met kinase activation.
Structural basis of inhibitor specificity of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM-1) kinase. Read more about Structural basis of inhibitor specificity of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM-1) kinase.
Characterization of human DHRS6, an orphan short chain dehydrogenase/reductase enzyme: a novel, cytosolic type 2 R-beta-hydroxybutyrate dehydrogenase. Read more about Characterization of human DHRS6, an orphan short chain dehydrogenase/reductase enzyme: a novel, cytosolic type 2 R-beta-hydroxybutyrate dehydrogenase.
Ruthenium half-sandwich complexes bound to protein kinase Pim-1. Read more about Ruthenium half-sandwich complexes bound to protein kinase Pim-1.
Disseminating structural genomics data to the public: from a data dump to an animated story. Read more about Disseminating structural genomics data to the public: from a data dump to an animated story.
Structure and function of human 17beta-hydroxysteroid dehydrogenases. Read more about Structure and function of human 17beta-hydroxysteroid dehydrogenases.
Active site variability of type 1 11beta-hydroxysteroid dehydrogenase revealed by selective inhibitors and cross-species comparisons. Read more about Active site variability of type 1 11beta-hydroxysteroid dehydrogenase revealed by selective inhibitors and cross-species comparisons.