These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. HPMV: human protein mutation viewer - relating sequence mutations to protein sequence architecture and function changes. Sherman WA; Kuchibhatla DB; Limviphuvadh V; Maurer-Stroh S; Eisenhaber B; Eisenhaber F J Bioinform Comput Biol; 2015 Oct; 13(5):1550028. PubMed ID: 26503432 [TBL] [Abstract][Full Text] [Related]
4. The visualCMAT: A web-server to select and interpret correlated mutations/co-evolving residues in protein families. Suplatov D; Sharapova Y; Timonina D; Kopylov K; Švedas V J Bioinform Comput Biol; 2018 Apr; 16(2):1840005. PubMed ID: 29361894 [TBL] [Abstract][Full Text] [Related]
5. The ProFunc Function Prediction Server. Laskowski RA Methods Mol Biol; 2017; 1611():75-95. PubMed ID: 28451973 [TBL] [Abstract][Full Text] [Related]
6. Pathogenic missense protein variants affect different functional pathways and proteomic features than healthy population variants. Laddach A; Ng JCF; Fraternali F PLoS Biol; 2021 Apr; 19(4):e3001207. PubMed ID: 33909605 [TBL] [Abstract][Full Text] [Related]
7. Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic Database. Zlotogora J; van Baal S; Patrinos GP Hum Mutat; 2007 Oct; 28(10):944-9. PubMed ID: 17492749 [TBL] [Abstract][Full Text] [Related]
9. 3D-GENOMICS: a database to compare structural and functional annotations of proteins between sequenced genomes. Fleming K; Müller A; MacCallum RM; Sternberg MJ Nucleic Acids Res; 2004 Jan; 32(Database issue):D245-50. PubMed ID: 14681404 [TBL] [Abstract][Full Text] [Related]
10. PRISMOID: a comprehensive 3D structure database for post-translational modifications and mutations with functional impact. Li F; Fan C; Marquez-Lago TT; Leier A; Revote J; Jia C; Zhu Y; Smith AI; Webb GI; Liu Q; Wei L; Li J; Song J Brief Bioinform; 2020 May; 21(3):1069-1079. PubMed ID: 31161204 [TBL] [Abstract][Full Text] [Related]
11. Bioinformatics Tools and Resources for Analyzing Protein Structures. Paxman JJ; Heras B Methods Mol Biol; 2017; 1549():209-220. PubMed ID: 27975294 [TBL] [Abstract][Full Text] [Related]
12. Identification of similar regions of protein structures using integrated sequence and structure analysis tools. Peters B; Moad C; Youn E; Buffington K; Heiland R; Mooney S BMC Struct Biol; 2006 Mar; 6():4. PubMed ID: 16526955 [TBL] [Abstract][Full Text] [Related]
13. The functional importance of disease-associated mutation. Mooney SD; Klein TE BMC Bioinformatics; 2002 Sep; 3():24. PubMed ID: 12220483 [TBL] [Abstract][Full Text] [Related]
14. F-SNP: computationally predicted functional SNPs for disease association studies. Lee PH; Shatkay H Nucleic Acids Res; 2008 Jan; 36(Database issue):D820-4. PubMed ID: 17986460 [TBL] [Abstract][Full Text] [Related]
15. ABCMdb: a database for the comparative analysis of protein mutations in ABC transporters, and a potential framework for a general application. Gyimesi G; Borsodi D; Sarankó H; Tordai H; Sarkadi B; Hegedűs T Hum Mutat; 2012 Nov; 33(11):1547-56. PubMed ID: 22693078 [TBL] [Abstract][Full Text] [Related]
16. VarSite: Disease variants and protein structure. Laskowski RA; Stephenson JD; Sillitoe I; Orengo CA; Thornton JM Protein Sci; 2020 Jan; 29(1):111-119. PubMed ID: 31606900 [TBL] [Abstract][Full Text] [Related]
17. Integrating genomic information with protein sequence and 3D atomic level structure at the RCSB protein data bank. Prlic A; Kalro T; Bhattacharya R; Christie C; Burley SK; Rose PW Bioinformatics; 2016 Dec; 32(24):3833-3835. PubMed ID: 27551105 [TBL] [Abstract][Full Text] [Related]
18. The SAAP pipeline and database: tools to analyze the impact and predict the pathogenicity of mutations. Al-Numair NS; Martin AC BMC Genomics; 2013; 14 Suppl 3(Suppl 3):S4. PubMed ID: 23819919 [TBL] [Abstract][Full Text] [Related]
19. Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information. Capriotti E; Calabrese R; Casadio R Bioinformatics; 2006 Nov; 22(22):2729-34. PubMed ID: 16895930 [TBL] [Abstract][Full Text] [Related]
20. Atlas - a data warehouse for integrative bioinformatics. Shah SP; Huang Y; Xu T; Yuen MM; Ling J; Ouellette BF BMC Bioinformatics; 2005 Feb; 6():34. PubMed ID: 15723693 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]