Molecular recognition features (MoRFs) in three domains of life.
By Jing Yan, A. Keith Dunker, Vladimir N Uversky, Lukasz Kurgan. 2016
147 citations recorded by the source corpus.
Subfields: Materials Chemistry, Molecular Biology
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Materials Chemistry
- Lukasz Kurgan
- Zsuzsanna Dosztányi
- Vladimir N Uversky
- Fanchi Meng
- Yaoqi Zhou
- Kuldip K. Paliwal
- Bálint Mészáros
- Jack Hanson
In Molecular Biology
- Lukasz Kurgan
- Vladimir N Uversky
- Zsuzsanna Dosztányi
- Fanchi Meng
- Gábor Erdös
- Yaoqi Zhou
- Bálint Mészáros
- Kuldip K. Paliwal
Citations in the corpus
- SPOT-Disorder2: Improved Protein Intrinsic Disorder Prediction by Ensembled Deep Learning (2019, methodology): “For comparison with other models, besides the web servers of MoRFpred, fMoRFpred, and Dis-oRDPbind [58,59] (http://biomine.cs.vcu.edu/#webservers), we also used ANCHOR2 [60] (https://iupred2a.elte.hu/), (https://gsponerlab.msl.ubc.ca/software/morf_chibi/), and the local version of MoRFPred-plus…”
- IUPred2A: context-dependent prediction of protein disorder as a function of redox state and protein binding (2018, methodology): “MoRFpred and fMoRFpred utilize SVM models in their predictions incorporating sequence conservation data and amino-acid physicochemical properties, in addition to predictions of intrinsic disorder, relative solvent accessibility and residue flexibility (30,31).”
- MoRFchibi SYSTEM: software tools for the identification of MoRFs in protein sequences (2016, methodology): “MoRFs are found in proteins that are involved in diverse cellular processes in all three domains of life (8).”
- Comprehensive review of methods for prediction of intrinsic disorder and its molecular functions (2017, methodology): “fMoRFpred 2015 [130] Protein binding WS Yes Yes http://biomine.”