Exploitation of binding energy for catalysis and design. Submitted by Anonymous on Sun, 2015-03-15 06:45 Read more about Exploitation of binding energy for catalysis and design.
Kinetics of the transfer of ubiquitin from UbcH7 to E6AP. Submitted by Anonymous on Sun, 2015-03-15 06:45 Read more about Kinetics of the transfer of ubiquitin from UbcH7 to E6AP.
Metal templated design of protein interfaces. Submitted by Anonymous on Sun, 2015-03-15 06:45 Read more about Metal templated design of protein interfaces.
Computational design of second-site suppressor mutations at protein-protein interfaces. Submitted by Anonymous on Sun, 2015-03-15 06:45 Read more about Computational design of second-site suppressor mutations at protein-protein interfaces.
Computational predictions of the mutant behavior of AraC. Submitted by Anonymous on Sun, 2015-03-15 06:45 Read more about Computational predictions of the mutant behavior of AraC.
Ubiquitination and degradation of the inhibitors of NF-kappaB. Submitted by Anonymous on Sun, 2015-03-15 06:45 Read more about Ubiquitination and degradation of the inhibitors of NF-kappaB.
The structural basis of peptide-protein binding strategies. Submitted by Anonymous on Sun, 2015-03-15 06:45 Read more about The structural basis of peptide-protein binding strategies.
On the use of structural templates for high-resolution docking. Submitted by Anonymous on Sun, 2015-03-15 06:45 Read more about On the use of structural templates for high-resolution docking.
Exploitation of binding energy for catalysis and design. Submitted by Anonymous on Sun, 2015-03-15 06:45 Read more about Exploitation of binding energy for catalysis and design.
Unique gating properties of C. elegans ClC anion channel splice variants are determined by altered CBS domain conformation and the R-helix linker. Submitted by Anonymous on Sun, 2015-03-15 06:45 Read more about Unique gating properties of C. elegans ClC anion channel splice variants are determined by altered CBS domain conformation and the R-helix linker.