Mapping Soluble Guanylyl Cyclase and Protein Disulfide Isomerase Regions of Interaction.

In the current study, the construction and computational analysis of protein interaction networks (PINs) based on expression data of proteins involved in 10 major cancer

Biotechnol- ogy Information indicated that the UL136 protein could possibly interact with the C-terminal of the ATP1B1 protein in vitroA. To confirm the interaction

In order to extend the analysis of lectin binding to protein fractions, the kinetic interaction of immobilized CFL and soluble proteins from albumin, globulin,

In an attempt to determine if the results are compatible with the distribution of NO receptor protein, immunoperoxidase staining for the common b 1 guanylyl cyclase subunit was

Strikingly, both of the regions of marked conformational restriction in MSP2, the conserved N-terminal region and the region around the disulfide in the conserved C-terminal region,

These results indicate that the two tyrosines in the amino-terminal part of the GIT1 polypeptide are needed for the interaction with the carboxy-terminal portion of the protein to

Human-Mtb Protein Interaction Functional Analysis To understand the functional features of the predicted human- Mtb interactions, we are interested in the biological processes in

In this work, we report the expression of the N-terminal domain of TPL in Pichia pastoris to study the effect of the C-terminal domain deletion on the enzyme activity, and to verify