Crystal structure of human diphosphoinositol phosphatase 1. Read more about Crystal structure of human diphosphoinositol phosphatase 1.
Propionate analogues of zearalenone bind to Hsp90. Read more about Propionate analogues of zearalenone bind to Hsp90.
Structural recognition of an optimized substrate for the ephrin family of receptor tyrosine kinases. Read more about Structural recognition of an optimized substrate for the ephrin family of receptor tyrosine kinases.
Out of the box binding determines specificity of SH2 domain interaction. Read more about Out of the box binding determines specificity of SH2 domain interaction.
Vital role for the Plasmodium actin capping protein (CP) beta-subunit in motility of malaria sporozoites. Read more about Vital role for the Plasmodium actin capping protein (CP) beta-subunit in motility of malaria sporozoites.
Dissection of PIM serine/threonine kinases in FLT3-ITD-induced leukemogenesis reveals PIM1 as regulator of CXCL12-CXCR4-mediated homing and migration. Read more about Dissection of PIM serine/threonine kinases in FLT3-ITD-induced leukemogenesis reveals PIM1 as regulator of CXCL12-CXCR4-mediated homing and migration.
Crystallographic structure of the tetratricopeptide repeat domain of Plasmodium falciparum FKBP35 and its molecular interaction with Hsp90 C-terminal pentapeptide. Read more about Crystallographic structure of the tetratricopeptide repeat domain of Plasmodium falciparum FKBP35 and its molecular interaction with Hsp90 C-terminal pentapeptide.
Investigating the genetic association between ERAP1 and ankylosing spondylitis. Read more about Investigating the genetic association between ERAP1 and ankylosing spondylitis.
Evaluation of virtual screening as a tool for chemical genetic applications. Read more about Evaluation of virtual screening as a tool for chemical genetic applications.
A survey of proteins encoded by non-synonymous single nucleotide polymorphisms reveals a significant fraction with altered stability and activity. Read more about A survey of proteins encoded by non-synonymous single nucleotide polymorphisms reveals a significant fraction with altered stability and activity.
