Evidence map›Paper›PMID 33019775›Full record

ArticleInternational journal of molecular sciences2020

SPOTONE: Hot Spots on Protein Complexes with Extremely Randomized Trees via Sequence-Only Features.

A J Preto, Irina S Moreira

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Extremely Randomized Trees to Determine Binding Affinity.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  3. Article
  4. Predicting interacting hotspots for nanobodies' binding using triplets of residues.Protein science : a publication of the Protein Society · 2025
    Article
  5. PPI-hotspoteLife · 2024
    Article
  6. Article
  7. SARS-CoV-2 Membrane Protein: From Genomic Data to Structural New Insights.International journal of molecular sciences · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

A J PretoCNC-Center for Neuroscience and Cell Biology, University of Coimbra, 3004-504 Coimbra, Portugal.ORCID 0000-0003-4203-2230
Irina S MoreiraDepartment of Life Sciences, Center for Neuroscience and Cell Biology, Coimbra University, 3000-456 Coimbra, Portugal.
Centro de Neurociências e Biologia Celular · PTUniversity of Coimbra · PT

Funding

Fundação para a Ciência e a Tecnologia POCI-01-0145-FEDER-031356Fundação para a Ciência e a Tecnologia SFRH/BD/144966/2019Fundação para a Ciência e a Tecnologia UIDB/04539/2020
6 · The paper itself

Abstract

Protein Hot-Spots (HS) are experimentally determined amino acids, key to small ligand binding and tend to be structural landmarks on protein-protein interactions. As such, they were extensively approached by structure-based Machine Learning (ML) prediction methods. However, the availability of a much larger array of protein sequences in comparison to determined tree-dimensional structures indicates that a sequence-based HS predictor has the potential to be more useful for the scientific community. Herein, we present SPOTONE, a new ML predictor able to accurately classify protein HS via sequence-only features. This algorithm shows accuracy, AUROC, precision, recall and F1-score of 0.82, 0.83, 0.91, 0.82 and 0.85, respectively, on an independent testing set. The algorithm is deployed within a free-to-use webserver at http://moreiralab.com/resources/spotone, only requiring the user to submit a FASTA file with one or more protein sequences.

Indexed as

Machine LearningAmino AcidsAmino Acid SequenceBinding SitesComputational BiologyDatabases, ProteinDatasets as TopicHumansProtein BindingProtein Interaction MappingProteinsAmino AcidsProteinsbig-datahot-spotsmachine learningprotein–protein complexesstructural biology

Identifiers

PMID33019775
PMCPMC7582262
OpenAlexW3090648695

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.