% IMPORTANT: The following is UTF-8 encoded. This means that in the presence % of non-ASCII characters, it will not work with BibTeX 0.99 or older. % Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or % “biber”. @ARTICLE{Ribeiro:1024531, author = {Ribeiro, Rui P and Giorgetti, A.}, title = {py{GOM}o{D}o: {GPCR}s modeling and docking with python}, journal = {Bioinformatics}, volume = {39}, number = {5}, issn = {0266-7061}, address = {Oxford}, publisher = {Oxford Univ. Press}, reportid = {FZJ-2024-02218}, pages = {btad294}, year = {2023}, abstract = {Motivation: We present pyGOMoDo, a Python library to perform homology modeling and docking, specifically designed for human GPCRs.pyGOMoDo is a python wrap-up of the updated functionalities of GOMoDo web server (https://molsim.sci.univr.it/gomodo). It was developedhaving in mind its usage through Jupyter notebooks, where users can create their own protocols of modeling and docking of GPCRs. In this article, we focus on the internal structure and general capabilities of pyGOMoDO and on how it can be useful for carrying out structural biology studies of GPCRs.Results: The source code is freely available at https://github.com/rribeiro-sci/pygomodo under the Apache 2.0 license. Tutorial notebooks containing minimal working examples can be found at https://github.com/rribeiro-sci/pygomodo/tree/main/examples.}, cin = {IAS-5 / INM-9}, ddc = {570}, cid = {I:(DE-Juel1)IAS-5-20120330 / I:(DE-Juel1)INM-9-20140121}, pnm = {5241 - Molecular Information Processing in Cellular Systems (POF4-524)}, pid = {G:(DE-HGF)POF4-5241}, typ = {PUB:(DE-HGF)16}, pubmed = {37137232}, UT = {WOS:000988604300005}, doi = {10.1093/bioinformatics/btad294}, url = {https://juser.fz-juelich.de/record/1024531}, }