Evidence map›Paper›PMID 33233636›Full record

ArticleInternational journal of molecular sciences2020

Structural and Functional Enrichment Analyses for Antimicrobial Peptides.

Sheng C Lo, Zhong-Ru Xie, Kuan Y Chang

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Creation of New Antimicrobial Peptides.International journal of molecular sciences · 2023
    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

3 authors at 2 institutions in 2 countries.

Sheng C LoComputational Biology Laboratory, Department of Computer Science and Engineering, National Taiwan Ocean University, Keelung 202, Taiwan.
Zhong-Ru XieSchool of Electrical and Computer Engineering, College of Engineering, University of Georgia, Athens, GA 30602, USA.ORCID 0000-0002-1539-5100
Kuan Y ChangComputational Biology Laboratory, Department of Computer Science and Engineering, National Taiwan Ocean University, Keelung 202, Taiwan.ORCID 0000-0002-2262-5218
National Taiwan Ocean University · TWUniversity of Georgia · US

Funding

National Taiwan Ocean University NTOU-107-009
6 · The paper itself

Abstract

Whether there is any inclination between structures and functions of antimicrobial peptides (AMPs) is a mystery yet to be unraveled. AMPs have various structures associated with many different antimicrobial functions, including antibacterial, anticancer, antifungal, antiparasitic and antiviral activities. However, none has yet reported any antimicrobial functional tendency within a specific category of protein/peptide structures nor any structural tendency of a specific antimicrobial function with respect to AMPs. Here, we examine the relationships between structures categorized by three structural classification methods (CATH, SCOP, and TM) and seven antimicrobial functions with respect to AMPs using an enrichment analysis. The results show that antifungal activities of AMPs were tightly related to the two-layer sandwich structure of CATH, the knottin fold of SCOP, and the first structural cluster of TM. The associations with knottin and TM Cluster 1 even sustained through the AMPs with a low sequence identity. Moreover, another significant mutual enrichment was observed between the third cluster of TM and anti-Gram-positive-bacterial/anti-Gram-negative-bacterial activities. The findings of the structure-function inclination further our understanding of AMPs and could help us design or discover new therapeutic potential AMPs.

Indexed as

Amino Acid SequenceAnimalsAnti-Bacterial AgentsAntifungal AgentsAntimicrobial Cationic PeptidesAntineoplastic AgentsAntiparasitic AgentsAntiviral AgentsBinding SitesFungiGram-Negative BacteriaGram-Positive BacteriaHumansProtein BindingProtein Conformation, alpha-HelicalProtein Conformation, beta-StrandAnti-Bacterial AgentsAntifungal AgentsAntimicrobial Cationic PeptidesAntineoplastic AgentsAntiparasitic AgentsAntiviral Agentsantifungal activitiesenrichment analysisknottinstructure–function relationshipstwo-layer sandwich architecture

Identifiers

PMID33233636
PMCPMC7699717
OpenAlexW3044818647

What OpenQuestion 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 OpenQuestion graph.