Extremely tight binding of a ruthenium complex to glycogen synthase kinase 3. Read more about Extremely tight binding of a ruthenium complex to glycogen synthase kinase 3.
The human short-chain dehydrogenase/reductase (SDR) superfamily: a bioinformatics summary. Read more about The human short-chain dehydrogenase/reductase (SDR) superfamily: a bioinformatics summary.
Analysis of the substrate-binding site of human carbonyl reductases CBR1 and CBR3 by site-directed mutagenesis. Read more about Analysis of the substrate-binding site of human carbonyl reductases CBR1 and CBR3 by site-directed mutagenesis.
An intact SAM-dependent methyltransferase fold is encoded by the human endothelin-converting enzyme-2 gene. Read more about An intact SAM-dependent methyltransferase fold is encoded by the human endothelin-converting enzyme-2 gene.
Discovery of a potent and selective inhibitor for human carbonyl reductase 1 from propionate scanning applied to the macrolide zearalenone. Read more about Discovery of a potent and selective inhibitor for human carbonyl reductase 1 from propionate scanning applied to the macrolide zearalenone.
Targeting a uniquely nonspecific prenyl synthase with bisphosphonates to combat cryptosporidiosis. Read more about Targeting a uniquely nonspecific prenyl synthase with bisphosphonates to combat cryptosporidiosis.
Structure of the pseudokinase VRK3 reveals a degraded catalytic site, a highly conserved kinase fold, and a putative regulatory binding site. Read more about Structure of the pseudokinase VRK3 reveals a degraded catalytic site, a highly conserved kinase fold, and a putative regulatory binding site.
Discovery of indoline-based, natural-product-like compounds as probes of focal adhesion kinase signaling pathways. Read more about Discovery of indoline-based, natural-product-like compounds as probes of focal adhesion kinase signaling pathways.
Structure of the human RECQ1 helicase reveals a putative strand-separation pin. Read more about Structure of the human RECQ1 helicase reveals a putative strand-separation pin.
Targeting group II PAKs in cancer and metastasis. Read more about Targeting group II PAKs in cancer and metastasis.
