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.
Important Notice
The UniProtKB database used by the EFI tools is undergoing major reorganization starting with the 2025_04 release
(https://www.uniprot.org/release-notes/forthcoming-changes).
When the reorganization is fully implemented (2026_02 release, Spring 2026), the number of proteins in UniProtKB is expected to decrease from ~253M accessions in the current 2025_03 release to ~141M accessions in the 2026_02 release.
In response to these changes, we are planning to provide the current 2025_03 release until the 2026_02 release is available.
More information about the changes is located here.
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