ArticleNucleic acids research2003
Active Sequences Collection (ASC) database: a new tool to assign functions to protein sequences.
Article in Nucleic acids research, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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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.
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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.
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Who cites it
7 citing papers in PubMed, 28 citations in OpenAlex.
- Biocatalysis by Transglutaminases: A Review of Biotechnological Applications.Micromachines · 2018Review
- Antibodies to age-β2 glycoprotein I in patients with anti-phospholipid antibody syndrome.Clinical and experimental immunology · 2016Article
- Resveratrol prevents dendritic cell maturation in response to advanced glycation end products.Oxidative medicine and cellular longevity · 2013Article
- High mobility group box 1 is a novel substrate of dipeptidyl peptidase-IV.Diabetologia · 2012Article
- Substrate specificity of microbial transglutaminase as revealed by three-dimensional docking simulation and mutagenesis.Protein engineering, design & selection : PEDS · 2009Article
- Phage display selection of efficient glutamine-donor substrate peptides for transglutaminase 2.Protein science : a publication of the Protein Society · 2006Article
- ELM server: A new resource for investigating short functional sites in modular eukaryotic proteins.Nucleic acids research · 2003Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Active Sequences Collection (ASC) is a collection of amino acid sequences, with an unique feature: only short sequences are collected, with a demonstrated biological activity. The current version of ASC consists of three sections: DORRS, a collection of active RGD-containing peptides; TRANSIT, a collection of protein regions active as substrates of transglutaminase enzyme (TGase), and BAC, a collection of short peptides with demonstrated biological activity. Literature references for each entry are reported, as well as cross references to other databases, when available. The current version of ASC includes more than 800 different entries. The main scope of this collection is to offer a new tool to investigate the structural features of protein active sites, additionally to similarity searches against large protein databases or searching for known functional patterns. ASC database is available at the web address http://crisceb.unina2.it/ASC/ which also offers a dedicated query interface to compare user-defined protein sequences with the database, as well as an updating interface to allow contribution of new referenced active sequences.
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Registered trials
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.