Next Article in Journal
Identification and Characterization of Process-Related Impurities of Trans-Resveratrol
Previous Article in Journal
Synthesis of 1,2,3-Triazole Derivatives and Evaluation of their Anticancer Activity
 
 
Scientia Pharmaceutica is published by MDPI from Volume 84 Issue 3 (2016). Previous articles were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence, and they are hosted by MDPI on mdpi.com as a courtesy and upon agreement with Austrian Pharmaceutical Society (Österreichische Pharmazeutische Gesellschaft, ÖPhG).
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Short Communication

How to Solve the Problems of Docking into a Symmetric Binding Site: The Example of the hERG Channel

by
Andrea SCHIESARO
,
Lars RICHTER
and
Gerhard F. ECKER
*
University of Vienna, Department of Medicinal Chemistry, Althanstraße 14, 1090, Vienna, Austria
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2013, 81(3), 677-682; https://doi.org/10.3797/scipharm.1307-01
Submission received: 1 July 2013 / Accepted: 31 July 2013 / Published: 31 July 2013

Abstract

Many proteins, such as the hERG K+ channel or the HIV-1 protease, have a high degree of rotational symmetry. If the binding site of a ligand is composed of symmetrical subunits, the analysis of the docking poses of ligands is quite challenging. In the case of hERG, the four-fold symmetry of the entire channel is fully reflected in the binding site, which allows up to four poses with different coordinates of the ligand, but an identical interaction pattern. In light of our docking studies into the hERG potassium channel, we developed an algorithm (ROTALI) to detect the poses that are duplicates due to the symmetry of the channel. This led to a reduction in the number of poses to be considered in the subsequent steps by up to 52%.
Keywords: Symmetric Binding site; Docking; Duplicate poses; hERG Symmetric Binding site; Docking; Duplicate poses; hERG

Share and Cite

MDPI and ACS Style

SCHIESARO, A.; RICHTER, L.; ECKER, G.F. How to Solve the Problems of Docking into a Symmetric Binding Site: The Example of the hERG Channel. Sci. Pharm. 2013, 81, 677-682. https://doi.org/10.3797/scipharm.1307-01

AMA Style

SCHIESARO A, RICHTER L, ECKER GF. How to Solve the Problems of Docking into a Symmetric Binding Site: The Example of the hERG Channel. Scientia Pharmaceutica. 2013; 81(3):677-682. https://doi.org/10.3797/scipharm.1307-01

Chicago/Turabian Style

SCHIESARO, Andrea, Lars RICHTER, and Gerhard F. ECKER. 2013. "How to Solve the Problems of Docking into a Symmetric Binding Site: The Example of the hERG Channel" Scientia Pharmaceutica 81, no. 3: 677-682. https://doi.org/10.3797/scipharm.1307-01

APA Style

SCHIESARO, A., RICHTER, L., & ECKER, G. F. (2013). How to Solve the Problems of Docking into a Symmetric Binding Site: The Example of the hERG Channel. Scientia Pharmaceutica, 81(3), 677-682. https://doi.org/10.3797/scipharm.1307-01

Article Metrics

Back to TopTop