Structural insights into molecular chaperone activity

Insights into the function and structural flexibility of the periplasmic molecular chaperone SurA.

SurA is the primary periplasmic molecular chaperone that facilitates the folding and assembling of outer membrane proteins (OMPs) in Gram-negative bacteria. Deletion of the surA gene in Escherichia coli leads to a decrease in outer membrane density and an increase in bacterial drug susceptibility. Here, we conducted mutational studies on SurA to identify residues that are critical for function....

Structural insights into sGC

The membrane and soluble guanylyl cyclases (sGCs) are key families of enzymes that produce the second messenger cGMP. Although both families recognize different ligands and have therefore different N-terminal input domains, they do have similar C-terminal output domains containing a coiled-coil domain and a guanylyl cyclase catalytic domain. We present here our latest structure-function studies...

Structural Insights into the Molecular Design of HER2 Inhibitors

Methods: An energy optimized pharmacophore (E-pharmacophore) model was developed and used to screen the molecular databases (such as ASINEX and NCI databases) against a six site (ADHRRR) hypothesis. The shape similarity of the retrieved hits was calculated and then filtered applying ADME and Lipinski’s filters. Further, these hits were docked into the crystal structure of HER2 protein (3W32) us...

RIBONUCLEASES: STRUCTURAL AND BIOCHEMICAL INSIGHTS INTO CYTOTOXIC ACTIVITY by

Structural insights into yeast histone chaperone Hif1: a scaffold protein recruiting protein complexes to core histones.

Yeast Hif1 [Hat1 (histone acetyltransferase 1)-interacting factor], a homologue of human NASP (nuclear autoantigenic sperm protein), is a histone chaperone that is involved in various protein complexes which modify histones during telomeric silencing and chromatin reassembly. For elucidating the structural basis of Hif1, in the present paper we demonstrate the crystal structure of Hif1 consisti...