patcHwork: a user-friendly pH sensitivity analysis web server for protein sequences and structures

Abstract: pH regulates protein function and interactions by altering the charge of individual residues causing loss or gain of intramolecular noncovalent bonds, which may lead to structural rearrangements. While tools to analyze residue-specific charge distribution of proteins at a given pH exist, currently no tool is available to investigate noncovalent bond changes at two different pH values. To make protein pH sensitivity analysis more accessible, we developed patcHwork, a web server that combines the identification of amino acids undergoing a charge shift with the determination of affected noncovalent bonds at two user-defined pH values. At the sequence-only level, patcHwork applies the Henderson–Hasselbalch equation to determine pH-sensitive residues. When the 3D protein structure is available, patcHwork can be employed to gain mechanistic understanding of the effect of pH. This is achieved using the PDB2PQR and PROPKA tools and noncovalent bond determination algorithms. A user-friendly interface allows visualizing pH-sensitive residues, affected salt bridges, hydrogen bonds and aromatic (pi–pi and cation–pi) interactions. patcHwork can be used to identify patches, a new concept we propose of pH-sensitive residues in close proximity on the protein, which may have a major impact on function. We demonstrate the attractiveness of patcHwork studying experimentally investigated pH-sensitive proteins (https://patchwork.biologie.uni-freiburg.de/)

Objekt anzeigen

• Standort: Deutsche Nationalbibliothek Frankfurt am Main
• Umfang: Online-Ressource
• Sprache: Englisch
• Anmerkungen: Nucleic acids research. - 50, W1 (2022) , W560-W567, ISSN: 1362-4962

Beteiligte, Orts- und Zeitangaben

• Ereignis: Veröffentlichung
• (wo): Freiburg
• (wer): Universität
• (wann): 2022
• Urheber: Schmitz, Mirko ; Schultze, Anne ; Vanags, Raimonds ; Voigt, Karsten ; Di Ventura, Barbara ; Öztürk, Mehmet Ali
• Beteiligte Personen und Organisationen: Arbeitsgruppe: Biologische Signalforschung

Weitere Informationen

• DOI: 10.1093/nar/gkac252
• URN: urn:nbn:de:bsz:25-freidok-2278496
• Rechteinformation: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.