Table 2.
A comprehensive summary of the implemented architectures for AMP prediction
| Type | Architecture | Year | Feature space size | Feature extraction | Feature selection | Algorithm | Reference |
|---|---|---|---|---|---|---|---|
| Deep learning-based architectures | AMPScanner V2 | 2018 | 128 | Embedding | none | DNN with convolutional, maximal pooling and LSTM layers | [46] |
| Deep-AmPEP30 | 2020 | 86 | PseKRAAC | none | CNN with two convolutional layers, two maximum pooling layers, and one fully connected hidden layer | [49] | |
| Non-deep learning-based architectures | CS-AMPpred | 2012 | 9 |
-helix, -helix propensity, -sheet, loop formation, charge, hydrophobicity, flexibility, amphipathicity, hydrophobic moment |
PCA | SVM | [42] |
| iAMP-2L | 2013 | 40 | PseAAC | none | FKNN | [43] | |
| SVM-LZ | 2015 | 1000 | LZ complexity pairwise similarity scores | none | sequence alignment (blastp), SVM | [50] | |
| MLAMP | 2016 | 30 | PseAAC with grey model coefficients | none | RF | [51] | |
| AmPEP | 2018 | 23 | Selected distribution descriptors | none | RF | [52] | |
| AMAP | 2019 | 20 | AAC | none | SVM | [44] | |
| AmPEPpy | 2020 | 105 | CTD | none | RF | [53] | |
| MACREL | 2020 | 22 | relative position of the first occurrence of residues in three groups of amino acids defined by their free energy of transition in a peptide from a random coil in aqueous environment to an organized helical structure in a lipid phase, solvent accessibility, AAC, charge and solubility, instability, aliphaticity, propensity to bind to membranes, hydrophobicity | none | RF | [54] | |
| AmpGram | 2020 | 32 835–33 612 | n-grams | QuiPT | RF | [18] | |
| ampir | 2020 | 27 | PseAAC, amphiphilicity, hydrophobicity, isoelectric point, molecular weight, net charge | none | SVM | [24] |

