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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
libswiss-perl
 
Resource Report
Resource Website
libswiss-perl (RRID:SCR_024356) software toolkit, software library, software resource Software object oriented Perl library to handle Swiss-Prot entries object oriented Perl library, handle Swiss-Prot entries, is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/libswiss-perl/ SCR_024356 2026-08-05 10:48:03 0
VolPack
 
Resource Report
Resource Website
VolPack (RRID:SCR_024367) software toolkit, software library, software resource Portable software library for volume rendering. library for volume rendering, is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/libvolpack1-dev/ SCR_024367 volpack 2026-08-05 10:48:03 0
rSNP Guide
 
Resource Report
Resource Website
1+ mentions
rSNP Guide (RRID:SCR_000087) data or information resource, database A system of databases which stores information on the influence of mutations in regulatory gene regions . This tool helps recognize protein binding sites that are being altered by mutation. It has four cross-linked sub databases that focus on specific aspects including: (1) the effect of single nucleotide mutations in regulatory gene regions and their interaction with nuclear proteins; (2) references to original publications on the subject; (3) the experimental details of these publications; and (4) the protocols of these experiments. This resource is aimed at providing information to further research on the influence of specific sequence alterations on disease susceptibility, drug resistance and healthcare. database, single nucleotide mutations, RNA, DNA, nuclear proteins, protein binding sites, drug resistance, disease susceptibility, health care, regulatory gene regions, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: Siberian Branch of the Russian Academy of Sciences; Novosibirsk; Russia
Open Source nif-0000-03428, biotools:rsnp_guide https://bio.tools/rsnp_guide SCR_000087 rSNP Guide 2026-08-05 10:43:06 1
Interolog/Regulog Database
 
Resource Report
Resource Website
1+ mentions
Interolog/Regulog Database (RRID:SCR_000755) data or information resource, database Interolog/Regulog quantitatively assess the degree to which interologs can be reliably transferred between species as a function of the sequence similarity of the corresponding interacting proteins. interacting, interolog, protein, regulog, sequence, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: Yale University; Connecticut; USA
PMID:15173116 nif-0000-20863, biotools:interolog https://bio.tools/interolog SCR_000755 Interolog 2026-08-05 10:43:14 2
ProGlycProt
 
Resource Report
Resource Website
1+ mentions
ProGlycProt (RRID:SCR_000622) ProGlycProt data or information resource, database Manually curated, comprehensive repository of experimentally characterized bacterial glycoproteins and archaeal glycoproteins, generated from an exhaustive literature search. This is the focused effort to provide concise relevant information derived from rapidly expanding literature on prokaryotic glycoproteins, their glycosylating enzyme(s), glycosylation linked genes, and genomic context thereof, in a cross-referenced manner. The database is arranged into two sections namely, ProCGP and ProUGP. ProCGP is the main section containing characterized prokaryotic glycoproteins, defined as entries with at least one experimentally known glycosylated residue (glycosite). Whereas, ProUGP is the supplementary section, presenting uncharacterized prokaryotic glycoproteins, defined as entries with experimentally identified glycosylation but unidentified glycosites. The ProGlycProt has been developed with to aid and advance the emerging scientific interests in understanding the mechanisms, implications, and novelties of protein glycosylation in prokaryotes that include many pathogenic as well as economically important bacterial species. The website supports a dedicated structure gallery of homology models and crystal structures of characterized glycoproteins in addition to two new tools developed in view of emerging information about prokaryotic sequons (conserved sequences of amino acids around glycosites) that are never or rarely seen in eukaryotic glycoproteins. ProGlycProt provides an extensive compilation of experimentally identified glycosites (334) and glycoproteins (340) of prokaryotes that could serve as an information resource for research and technology applications in glycobiology. A general data update policy is once in three months. Existing entries are updated in real-time. glycoprotein, glycosite, glycosylation, coding gene, protein, glycosylation type, attached glycan, oligosaccharyl transferase, glycosyl transferase, glycobiology, glycosylating enzyme, glycosylation linked gene, crystal structure, homology, homology model, blast, predict, bacteria, archaea, image collection, structure, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: Institute of Microbial Technology; Chandigarh; India
Institute of Microbial Technology; Chandigarh; India OLP0063;
Council of Scientific and Industrial Research; New Delhi; India SIP10AA
PMID:22039152 nlx_151583, biotools:proglycprot https://bio.tools/proglycprot SCR_000622 Prokaryotic Glycoproteins, ProGlycProt - A Repository of Experimentally Characterized GlycoProteins of Prokaryotes 2026-08-05 10:43:12 1
dbSTS
 
Resource Report
Resource Website
1+ mentions
dbSTS (RRID:SCR_000400) dbSTS data or information resource, database THIS RESOURCE IS NO LONGER IN SERVICE, as of October 1, 2013; however, the site is still accessible. NCBI resource that contains sequence and mapping data on short genomic landmark sequences or Sequence Tagged Sites. STS sequences are incorporated into the STS Division of GenBank. The dbSTS database offers a route for submission of STS sequences to GenBank. It is designed especially for the submission of large batches of STS sequences. genomic, mapping, sequence, gold standard, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: NCBI
NIH PMID:2781285 THIS RESOURCE IS NO LONGER IN SERVICE biotools:dbsts, nif-0000-20939, r3d100010649 https://bio.tools/dbsts, https://doi.org/10.17616/R39P5C SCR_000400 NCBI dbSTS: database of Sequence Tagged Sites, Sequence Tagged Sites Database, NCBI dbSTS, dbSTS: database of Sequence Tagged Sites, Database of Sequence Tagged Sites 2026-08-05 10:43:09 3
HOMOZYGOSITYMAPPER
 
Resource Report
Resource Website
100+ mentions
HOMOZYGOSITYMAPPER (RRID:SCR_001714) HomozygosityMapper data analysis service, production service resource, service resource, analysis service resource A web-based approach of homozygosity mapping that can handle tens of thousands markers. User can upload their own SNP genotype files to the database. Intuitive graphic interface is provided to view the homozygous stretches, with the ability of zooming into single chromosomes or user-defined chromosome regions. The underlying genotypes in all samples are displayed. The software is also integrated with our candidate gene search engine, GeneDistiller, so that users can interactively determine the most promising gene. (entry from Genetic Analysis Software) gene, genetic, genomic, perl, genotype, homozygosity score, homozygosity, bio.tools, FASEB list is listed by: OMICtools
is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
has parent organization: Charite - Universitatsmedizin Berlin; Berlin; Germany
PMID:19465395 Free, Freely Available nlx_154069, biotools:homozygositymapper, OMICS_00123 https://bio.tools/homozygositymapper SCR_001714 2026-08-05 10:43:26 121
AnimalTFDB
 
Resource Report
Resource Website
100+ mentions
AnimalTFDB (RRID:SCR_001624) AnimalTFDB data or information resource, database A comprehensive transcription factor (TF) database in which they identified and classified all the genome-wide TFs in 50 sequenced animal genomes (Ensembl release version 60). In addition to TFs, it also collects transcription co-factors and chromatin remodeling factors of those genomes, which play regulatory roles in transcription. Here they defined the TFs as proteins containing a sequence-specific DNA-binding domain (DBD) and regulating target gene expression. Currently, the AnimalTFDB classifies all the animal TFs into 72 families according to their conserved DBDs. Gene lists of transcription factors, transcription co-factors and chromatin remodeling factors of each species are available for downloading., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. transcription factor, dna-binding domain, transcription co-factor, chromatin remodeling factor, gene structure, functional domain, go annotation, protein interaction, ortholog, paralog, 3d structure, pathway, protein-protein interaction, binding site, target, data set, image collection, 3d spatial image, bio.tools, FASEB list is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
is related to: Ensembl
has parent organization: Huazhong University of Science and Technology; Wuhan; China
Huazhong University of Science and Technology; Wuhan; China ;
Fundamental Research Funds for the Central Universities 2010MS045;
National Natural Science Foundation of China 31171271
PMID:22080564 THIS RESOURCE IS NO LONGER IN SERVICE nlx_153892, OMICS_01856, biotools:animal_tfdb https://bio.tools/animal_tfdb SCR_001624 Animal Transcription Factor Database 2026-08-05 10:43:25 289
Human Gene Mutation Database
 
Resource Report
Resource Website
1000+ mentions
Human Gene Mutation Database (RRID:SCR_001621) HGMD data or information resource, database Curated database of known (published) gene lesions responsible for human inherited disease. gene, disease, gene lesion, mutation, deletion, insertion, duplication, rearrangement, nuclear gene, functional polymorphism, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: BIOBASE Corporation
has parent organization: Cardiff University; Wales; United Kingdom
Inherited disease PMID:22948725
PMID:20368137
PMID:20038494
PMID:19348700
PMID:18428754
PMID:18245393
PMID:12754702
PMID:10612821
PMID:9399854
PMID:9066272
PMID:8882888
Free, Freely available nlx_153887, SCR_001888, biotools:hgmd, nif-0000-10459, OMICS_00281 http://www.hgmd.cf.ac.uk/ac/index.php, https://bio.tools/hgmd, SCR_001621 The Human Gene Mutation Database, The Human Gene Mutation Database at the Institute of Medical Genetics in Cardiff 2026-08-05 10:43:25 2462
COSMIC - Catalogue Of Somatic Mutations In Cancer
 
Resource Report
Resource Website
1000+ mentions
COSMIC - Catalogue Of Somatic Mutations In Cancer (RRID:SCR_002260) COSMIC data or information resource, database Database to store and display somatic mutation information and related details and contains information relating to human cancers. The mutation data and associated information is extracted from the primary literature. In order to provide a consistent view of the data a histology and tissue ontology has been created and all mutations are mapped to a single version of each gene. The data can be queried by tissue, histology or gene and displayed as a graph, as a table or exported in various formats.
Some key features of COSMIC are:
* Contains information on publications, samples and mutations. Includes samples which have been found to be negative for mutations during screening therefore enabling frequency data to be calculated for mutations in different genes in different cancer types.
* Samples entered include benign neoplasms and other benign proliferations, in situ and invasive tumours, recurrences, metastases and cancer cell lines.
cancer, mutation, somatic mutation, tumor, cancer genome, genome, gene, dna, tissue, histology, bio.tools, FASEB list is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
Cancer Wellcome Trust 077012/Z/05/Z PMID:20952405 Free nif-0000-02690, biotools:cosmic, OMICS_00082 http://www.sanger.ac.uk/perl/CGP/cosmic, https://bio.tools/cosmic SCR_002260 Catalogue Of Somatic Mutations In Cancer 2026-08-05 10:43:36 4486
WebGeSTer DB
 
Resource Report
Resource Website
1+ mentions
WebGeSTer DB (RRID:SCR_002165) WebGeSTer DB data or information resource, database Database of intrinsic terminators of transcription that is comprized of >2,200,000 bacterial terminators identified from a total of 2036 chromosomes and 1508 plasmids. Information about structural parameters of individual terminators such as sequence, length of stem and loop, mismatches and gaps, U-trail, genomic coordinates and gene name and accession number is available in both tabular form and as a composite figure. Summary statistics for terminator profiles of whole genome can be also obtained. Raw data files for individual genomes can be downloaded (.zip files) for detailed investigations. Data is organized into different tiers such that users can fine-tune their search by entering name of the species, or taxon ID or genomes with a certain number of terminators. To visualize the occurrence of the terminators, an interactive map, with the resolution to single gene level, has been developed. genome, terminator, transcription, plasmid, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:20972211 THIS RESOURCE IS NO LONGER IN SERVICE biotools:webgester_db, OMICS_01862 https://bio.tools/webgester_db SCR_002165 WebGesTer Database, Web Genome Scannner for Terminators Database, WebGeSTer DB - A Transcription Terminator Database 2026-08-05 10:43:34 5
PubGene
 
Resource Report
Resource Website
10+ mentions
PubGene (RRID:SCR_002119) data or information resource, database It helps users retrieve information on genes and proteins. The underlying structure of PubGene can be viewed as a gene-centric database. Gene and protein names are cross-referenced to each other and to terms that are relevant to understanding their biological function, importance in disease and relationship to chemical substances. The result is a literature network organizing information in a form that is easy to navigate. gene, information, protein, bio.tools, FASEB list is listed by: bio.tools
is listed by: Debian
is parent organization of: Coremine Medical
Free, Freely Available biotools:pubgene, nif-0000-20908 https://bio.tools/pubgene SCR_002119 PubGene 2026-08-05 10:43:33 39
VIRsiRNAdb
 
Resource Report
Resource Website
1+ mentions
VIRsiRNAdb (RRID:SCR_006108) VIRsiRNAdb data or information resource, data repository, storage service resource, database, data analysis service, production service resource, service resource, analysis service resource VIRsiRNAdb is a curated database of experimentally validated viral siRNA / shRNA targeting diverse genes of 42 important human viruses including influenza, SARS and Hepatitis viruses. Submissions are welcome. Currently, the database provides detailed experimental information of 1358 siRNA/shRNA which includes siRNA sequence, virus subtype, target gene, GenBank accession, design algorithm, cell type, test object, test method and efficacy (mostly quantitative efficacies). Further, wherever available, information regarding alternative efficacies of above 300 siRNAs derived from different assays has also been incorporated. The database has facilities like search, advance search (using Boolean operators AND, OR) browsing (with data sorting option), internal linking and external linking to other databases (Pubmed, Genbank, ICTV). Additionally useful siRNA analysis tools are also provided e.g. siTarAlign for aligning the siRNA sequence with reference viral genomes or user defined sequences. virsiRNAdb would prove useful for RNAi researchers especially in siRNA based antiviral therapeutics development. virus, sirna, shrna, gene, influenza, sars, hepatitis, sirna sequence, virus subtype, target gene, genbank accession, design algorithm, cell type, efficacy, target genome region, target object, experimental assay, off-target, sirna matching, reference viral sequence, influenza virus, hepatitis b virus, hpv, sars corona virus, viral genome, reference genome, align, sirna sequence, fasta, blast, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: Institute of Microbial Technology; Chandigarh; India
Influenza, SARS, Hepatitis, Infectious disease Council of Scientific and Industrial Research; New Delhi; India PMID:22139916 Open unspecified license / Freely available nlx_151610, biotools:virsirnadb https://bio.tools/virsirnadb SCR_006108 VIRsiRNAdb - Database of Viral siRNA / shRNA, Viral siRNA Database, Viral siRNA Database (VIRsiRNAdb) 2026-08-05 10:44:25 4
qrqc
 
Resource Report
Resource Website
1+ mentions
qrqc (RRID:SCR_006867) qrqc data processing software, software application, sequence analysis software, data analysis software, software resource Software R package to quickly scan reads and gather statistics on base and quality frequencies, read length, k-mers by position, and frequent sequences. Produces graphical output of statistics for use in quality control pipelines, and an optional HTML quality report. S4 SequenceSummary objects allow specific tests and functionality to be written around the data collected. Quickly scan reads, read length, k-mers, position, frequent sequences, quality control pipeline, HTML quality report, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
Free, Available for download, Freely available biotools:qrqc, OMICS_01071 https://github.com/vsbuffalo/qrqc, https://bio.tools/qrqc SCR_006867 quick read quality control, Quick Read Quality Control 2026-08-05 10:44:33 2
SPM
 
Resource Report
Resource Website
5000+ mentions
Issue
SPM (RRID:SCR_007037) SPM data processing software, image analysis software, software application, data analysis software, software resource Software package for analysis of brain imaging data sequences. Sequences can be a series of images from different cohorts, or time-series from same subject. Current release is designed for analysis of fMRI, PET, SPECT, EEG and MEG. analysis, brain, imaging, data, sequence, fMRI, PET, SPECT, EEG, MEG, bio.tools uses: Neuroimaging Data Model
uses: imcalc: SPM batch image calculator
is used by: rsfMRI_fconn calculation
is used by: Automatic Analysis
is used by: auto_acpc_reorient
is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: 3DVC
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
is affiliated with: Clinical Toolbox for SPM
is affiliated with: Statistical non-Parametric Mapping
is related to: WFU Biological Parametric Mapping Toolbox
is related to: vis: SPM Visualized Statistics toolbox
is related to: LEAD-DBS
is related to: CCHMC Pediatric Brain Templates
is related to: IBMA toolbox
is related to: ArtRepair for robust fMRI
is related to: ASL data processing tool box
is related to: BrainVISA / Anatomist
is related to: MRIcro Software
is related to: xjView: A Viewing Program For SPM
is related to: BrainMagix SPM Viewer
is related to: MarsBaR region of interest toolbox for SPM
is related to: NIRS-SPM
is related to: SPM SS - fMRI functional localizers
is related to: Wisconsin White Matter Hyperintensities Segmentation Toolbox
is related to: Dementia-specific FDG PET Template for SPM analyses
is related to: SPM Anatomy Toolbox
is related to: MIPAV: Medical Image Processing and Visualization
is related to: MATLAB
is related to: hMRI-toolbox
is related to: Sandwich Estimator Toolbox
has parent organization: University College London; London; United Kingdom
is required by: MRTool
provides: TSDiffAna
has plug in: ICN_Atlas
works with: UManitoba - JHU Functionally Defined Human White Matter Atlas
works with: NIAG Addiction Data
works with: ICN_Atlas
works with: spm_auto_reorient_coregister
works with: Computational Anatomy Toolbox for SPM
works with: FieldTrip
works with: POAS4SPM
Free, Available for download, Freely available biotools:SPM https://github.com/spm/spm12, https://bio.tools/SPM https://www.fil.ion.ucl.ac.uk/spm/ SCR_007037 Statistical Parametric Mapping, SPM5, SPM2, SPM12, Statistical Parametric Mapping Software, SPM99, SPM8, SPM, SPM96 2026-08-05 10:44:35 8694
SoyBase
 
Resource Report
Resource Website
500+ mentions
SoyBase (RRID:SCR_005096) SoyBase data or information resource, data repository, controlled vocabulary, storage service resource, database, data analysis service, ontology, production service resource, service resource, analysis service resource Professionally curated repository for genetics, genomics and related data resources for soybean that contains the most current genetic, physical and genomic sequence maps integrated with qualitative and quantitative traits. SoyBase includes annotated Williams 82 genomic sequence and associated data mining tools. The genetic and sequence views of the soybean chromosomes and the extensive data on traits and phenotypes are extensively interlinked. This allows entry to the database using almost any kind of available information, such as genetic map symbols, soybean gene names or phenotypic traits. The repository maintains controlled vocabularies for soybean growth, development, and traits that are linked to more general plant ontologies. Contributions to SoyBase or the Breeder''s Toolbox are welcome. soybean, gene, genetic map, genome, data set, trait, phenotype, molecular biology, sequence, chromosome, quantitative trait locus, php, genetics, genomics, legume, bio.tools, FASEB list is listed by: 3DVC
is listed by: re3data.org
is listed by: Debian
is listed by: bio.tools
has parent organization: Iowa State University; Iowa; USA
is parent organization of: Soybean Ontologies
is parent organization of: Soy Ontology
USDA Agricultural Research Service PMID:20008513 The community can contribute to this resource nif-0000-03483, r3d100010846, biotools:soybase https://bio.tools/soybase, https://doi.org/10.17616/R3S032 SCR_005096 SoyBase and the Soybean Breeder''s Toolbox, SoyBase and the Soybean Breeder''s Toolbox: Integrating Genetics and Molecular Biology for Soybean Researchers 2026-08-05 10:44:10 646
Generic GO Term Mapper
 
Resource Report
Resource Website
10+ mentions
Generic GO Term Mapper (RRID:SCR_005806) GOTermMapper, GO Term Mapper data processing software, software application, software resource, data analysis service, production service resource, service resource, analysis service resource The Generic GO Term Mapper finds the GO terms shared among a list of genes from your organism of choice within a slim ontology, allowing them to be binned into broader categories. The user may optionally provide a custom gene association file or slim ontology, or a custom list of slim terms. The implementation of this Generic GO Term Mapper uses map2slim.pl script written by Chris Mungall at Berkeley Drosophila Genome Project, and some of the modules included in the GO-TermFinder distribution written by Gavin Sherlock and Shuai Weng at Stanford University, made publicly available through the GMOD project. GO Term Mapper serves a different function than the GO Term Finder. GO Term Mapper simply bins the submitted gene list to a static set of ancestor GO terms. In contrast, GO Term Finder finds the GO terms significantly enriched in a submitted list of genes. Platform: Online tool, Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible gene ontology, gene, gene association, slim ontology, slimmer-type tool, term enrichment, gene annotation, genomics, ontology, process, function, component, bio.tools is listed by: Gene Ontology Tools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
is related to: Generic Model Organism Database Project
has parent organization: Princeton University; New Jersey; USA
Free for academic use nlx_149294, biotools:go_term_mapper https://bio.tools/go_term_mapper SCR_005806 Generic Gene Ontology Term Mapper, Generic Gene Ontology (GO) Term Mapper 2026-08-05 10:44:20 44
SOURCE
 
Resource Report
Resource Website
50+ mentions
SOURCE (RRID:SCR_005799) SOURCE data or information resource, database, data analysis service, production service resource, service resource, analysis service resource SOURCE compiles information from several publicly accessible databases, including UniGene, dbEST, UniProt Knowledgebase, GeneMap99, RHdb, GeneCards and LocusLink. GO terms associated with LocusLink entries appear in SOURCE. The mission of SOURCE is to provide a unique scientific resource that pools publicly available data commonly sought after for any clone, GenBank accession number, or gene. SOURCE is specifically designed to facilitate the analysis of large sets of data that biologists can now produce using genome-scale experimental approaches Platform: Online tool genomic, functional annotation, ontology, gene expression, gene, genome, statistical analysis, bio.tools, FASEB list is listed by: Gene Ontology Tools
is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
has parent organization: SMD
NIGMS ;
NCI CA85129-04;
NIGMS GM07365
PMID:12519986 Restricted biotools:source, nlx_149287 https://login.stanford.edu/idp/profile/SAML2/Redirect/SSO?execution=e1s1, https://bio.tools/source SCR_005799 2026-08-05 10:44:21 69
SEECER
 
Resource Report
Resource Website
10+ mentions
SEECER (RRID:SCR_005274) SEECER data processing software, algorithm resource, software application, data analysis software, sequence analysis software, software resource Algorithm for sequencing error correction of RNA-seq data sets. SEECER removes mismatch and indel errors from the raw reads and improves downstream analysis of the data. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Carnegie Mellon University; Pennsylvania; USA
PMID:23558750 Free, Available for download OMICS_01236, biotools:seecer https://bio.tools/seecer SCR_005274 SEECER - SEquencing Error CorrEction for Rna reads 2026-08-05 10:44:12 12
IDEAL - Intrinsically Disordered proteins with Extensive Annotations and Literature
 
Resource Report
Resource Website
10+ mentions
IDEAL - Intrinsically Disordered proteins with Extensive Annotations and Literature (RRID:SCR_006027) IDEAL data or information resource, database, data analysis service, production service resource, service resource, analysis service resource IDEAL, Intrinsically Disordered proteins with Extensive Annotations and Literature, is a collection of knowledge on experimentally verified intrinsically disordered proteins (IDPs) or intrinsically disordered regions (IDRs). IDEAL contains manually curated annotations on IDPs in locations, structures, and functional sites such as protein binding regions and posttranslational modification sites together with references and structural domain assignments. Protean segment One of the unique phenomena seen in IDPs is so-called the coupled folding and binding, where a short flexible segment can bind to its binding partner with forming a specific structure to act as a molecular recognition element. IDEAL explicitly annotates these regions as protean segment (ProS) when unstructured and structured information are both available in the region. Access to the data All the entries are tabulated in the list and individual entries can be retrieved by using the search tool at the upper-right corner in this page. IDEAL also provides the BLAST search, which can find homologs in IDEAL. All the information in IDEAL can be downloaded in the XML file. intrinsically disordered protein, protein, intrinsically disordered region, region, location, structure, functional site, protein binding region, binding region, posttranslational modification site, reference, structural domain assignment, blast, homolog, simian virus 40, epstein-barr virus, human herpesvirus 1, residue, protean segment, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: Nagoya University; Nagoya; Japan
Japanese Ministry of Education Culture Sports Science and Technology MEXT PMID:22067451 biotools:ideal, nlx_151427 https://bio.tools/ideal SCR_006027 IDEAL - Intrinsically Disordered proteins with Extensive Annotations Literature, Intrinsically Disordered proteins with Extensive Annotations and Literature 2026-08-05 10:44:25 10

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