Prediction of metal ion ligand binding residues by adding disorder value and propensity factors based on deep learning algorithm
Proteins need to interact with different ligands to perform their functions. Among the ligands, the metal ion is a major ligand. At present, the prediction of protein metal ion ligand binding residues is a challenge. In this study, we selected Zn 2+ , Cu 2+ , Fe 2+ , Fe 3+ , Co 2+ , Mn 2+ , Ca 2+ an...
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| Veröffentlicht in: | Frontiers in genetics Jg. 13; S. 969412 |
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| Hauptverfasser: | , , , , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
Frontiers Media S.A
11.08.2022
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| Schlagworte: | |
| ISSN: | 1664-8021, 1664-8021 |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | Proteins need to interact with different ligands to perform their functions. Among the ligands, the metal ion is a major ligand. At present, the prediction of protein metal ion ligand binding residues is a challenge. In this study, we selected Zn
2+
, Cu
2+
, Fe
2+
, Fe
3+
, Co
2+
, Mn
2+
, Ca
2+
and Mg
2+
metal ion ligands from the BioLip database as the research objects. Based on the amino acids, the physicochemical properties and predicted structural information, we introduced the disorder value as the feature parameter. In addition, based on the component information, position weight matrix and information entropy, we introduced the propensity factor as prediction parameters. Then, we used the deep neural network algorithm for the prediction. Furtherly, we made an optimization for the hyper-parameters of the deep learning algorithm and obtained improved results than the previous IonSeq method. |
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| Bibliographie: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Pu-Feng Du, Tianjin University, China This article was submitted to Computational Genomics, a section of the journal Frontiers in Genetics Chunhua Li, Beijing University of Technology, China Reviewed by: Yongchun Zuo, Inner Mongolia University, China |
| ISSN: | 1664-8021 1664-8021 |
| DOI: | 10.3389/fgene.2022.969412 |