Evidence map›Paper›PMID 36304304›Full record

ArticleFrontiers in bioinformatics2022

ChanFAD: A Functional Annotation Database for Ion Channels.

Elizabeth V Castro, John W Shepherd, Ryan S Guggenheim, Manimone Sengvoravong, Bailey C Hall, McKenzie K Chappell, Jessica A Hearn, Olivia N Caraccio, Cora Bissman, Sydney Lantow and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

16 authors at 1 institution in 1 country.

Elizabeth V CastroDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
John W ShepherdDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
Ryan S GuggenheimDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
Manimone SengvoravongDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
Bailey C HallDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
McKenzie K ChappellDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
Jessica A HearnDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
Olivia N CaraccioDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
Cora BissmanDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
Sydney LantowDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
Damian BuehnerDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
Harry R CostlowDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
David M PratherDepartment of Chemistry, Baldwin Wallace University, Berea, OH, United States.
Abigail M ZonzaDepartment of Biology and Geology, Baldwin Wallace University, Berea, OH, United States.
Mallory WittDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
Jeffrey A ZahratkaDepartment of Neuroscience, Baldwin Wallace University, Berea, OH, United States.
Baldwin–Wallace College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ion channels are integral membrane protein complexes critical for regulation of membrane potential, cell volume, and other signaling events. As complex molecular assemblies with many interacting partners, ion channels have multiple structural and functional domains. While channel sequence and functional data are readily available across multiple online resources, there is an unmet need for functional annotation directly relating primary sequence information, 2D interactions, and three-dimensional protein structure. To this end, we present ChanFAD (Channel Functional Annotation Database), to provide the research community with a centralized resource for ion channel structure and functional data. ChanFAD provides functional annotation of PDB structures built on the National Center for Biotechnology Information's iCn3D structure viewing tool while providing additional information such as primary sequence, organism, and relevant links to other databases. Here we provide a brief tour of ChanFAD functionality while showing example use cases involving drug-channel interactions and structural changes based on mutation. ChanFAD is freely available and can be accessed at https://www.chanfad.org/.

Indexed as

databasefunctional annotationion channelsprotein structureproteomics

Identifiers

PMID36304304
PMCPMC9580856
OpenAlexW4287147530

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.