This web resource is supported by a Research Resource from the National Institute of General Medical Sciences (R24GM141196-01).
The tools are available without charge or license to both academic and commercial users.
RadicalSAM.org, our resource for investigating sequence-function space in the radical SAM superfamily, has been updated with sequences from the UniProt Release 2024_01 and InterPro Release 98 databases (January 24, 2024) !!
Levin, B. J., Huang, Y. Y., Peck, S. C., Wei, Y., MartÃnez-del Campo, A., Marks, J. A., Franzosa, E. A., Huttenhower, C., Balskus, E. P.
A prominent glycyl radical enzyme in human gut microbiomes metabolizes trans-4-hydroxy-l-proline.
Science355, eaai8386 (2017).
(DOI: 10.1126/science.aai8386)
For more information on ShortBRED, see
Kaminski J., Gibson M. K., Franzosa E. A., Segata N., Dantas G., Huttenhower C.
High-specificity targeted functional profiling in microbial communities with ShortBRED.
PLoS Comput Biol. 2015 Dec 18;11(12):e1004557. DOI: 10.1371/journal.pcbi.1004557
Nayfach, S. and Pollard, K.S.
Average genome size estimation improves comparative metagenomics and sheds light on the functional ecology of the human microbiome.
Genome Biology 2015;16(1):51.
The Human Microbiome Project Consortium. Structure, function and diversity of the healthy human microbiome.
Nature486, 207-214 (14 June 2012). DOI: 10.1038/nature11234
The Human Microbiome Project Consortium.
A framework for human microbiome research.
Nature486, 215-221 (14 June 2012). DOI: 10.1038/nature11209