Evaluation of thieno[3,2-b]pyrrole[3,2-d]pyridazinones as activators of the tumor cell specific M2 isoform of pyruvate kinase. Read more about Evaluation of thieno[3,2-b]pyrrole[3,2-d]pyridazinones as activators of the tumor cell specific M2 isoform of pyruvate kinase.
Biodegradation of bisphenol A and its halogenated analogues by Cunninghamella elegans ATCC36112. Read more about Biodegradation of bisphenol A and its halogenated analogues by Cunninghamella elegans ATCC36112.
Biophysical characterization of recombinant proteins: a key to higher structural genomics success. Read more about Biophysical characterization of recombinant proteins: a key to higher structural genomics success.
Calcium-dependent protein kinase 1 is an essential regulator of exocytosis in Toxoplasma. Read more about Calcium-dependent protein kinase 1 is an essential regulator of exocytosis in Toxoplasma.
Superfamilies SDR and MDR: from early ancestry to present forms. Emergence of three lines, a Zn-metalloenzyme, and distinct variabilities. Read more about Superfamilies SDR and MDR: from early ancestry to present forms. Emergence of three lines, a Zn-metalloenzyme, and distinct variabilities.
Crystal structure of human RNA helicase A (DHX9): structural basis for unselective nucleotide base binding in a DEAD-box variant protein. Read more about Crystal structure of human RNA helicase A (DHX9): structural basis for unselective nucleotide base binding in a DEAD-box variant protein.
High-throughput production of human proteins for crystallization: the SGC experience. Read more about High-throughput production of human proteins for crystallization: the SGC experience.
Structural basis for Par-4 recognition by the SPRY domain- and SOCS box-containing proteins SPSB1, SPSB2, and SPSB4. Read more about Structural basis for Par-4 recognition by the SPRY domain- and SOCS box-containing proteins SPSB1, SPSB2, and SPSB4.
Structural basis for the interaction between tankyrase-2 and a potent Wnt-signaling inhibitor. Read more about Structural basis for the interaction between tankyrase-2 and a potent Wnt-signaling inhibitor.
