Ontology highlight
ABSTRACT:
SUBMITTER: Hoerschinger VJ
PROVIDER: S-EPMC10685443 | biostudies-literature | 2023 Nov
REPOSITORIES: biostudies-literature
Hoerschinger Valentin J VJ Waibl Franz F Pomarici Nancy D ND Loeffler Johannes R JR Deane Charlotte M CM Georges Guy G Kettenberger Hubert H Fernández-Quintero Monica L ML Liedl Klaus R KR
Journal of chemical information and modeling 20231107 22
The electrostatic properties of proteins arise from the number and distribution of polar and charged residues. Electrostatic interactions in proteins play a critical role in numerous processes such as molecular recognition, protein solubility, viscosity, and antibody developability. Thus, characterizing and quantifying electrostatic properties of a protein are prerequisites for understanding these processes. Here, we present PEP-Patch, a tool to visualize and quantify the electrostatic potential ...[more]