# *Bacillus subtilis* 168_trypsin

| iPtgxDB Release     ||
| ------: | :--------: |
| Version | 2          |
| Date    | 06.02.2020 |

## Downloaded from
[/database/annotations/b-subtilis-168](/database/annotations/b-subtilis-168)

*Bacillus subtilis* strain 168 (Genbank #[NC_00964.3](https://www.ncbi.nlm.nih.gov/nuccore/NC_000964.3/)) is one of the well studied bacterial strain for this widely used Gram-positive prokaryotic model organism [1].

iPtgxDB was created by hierarchically integrating protein coding sequences from the following annotation resources:

| Hierarchy | Resource | Link |
| :---: | :--- | :--- |
| 1 | NCBI RefSeq 2018 | [GCA_000009045.1_ASM904v1](ftp://ftp.ncbi.nlm.nih.gov/genomes/genbank/bacteria/Bacillus_subtilis/latest_assembly_versions/GCA_000009045.1_ASM904v1); from 15/01/2018 |
| 2 | NCBI RefSeq 2017 | [GCF_000009045.1_ASM904v1](ftp://ftp.ncbi.nlm.nih.gov/genomes/refseq/bacteria/Bacillus_subtilis/latest_assembly_versions/GCF_000009045.1_ASM904v1); from 21/05/2017 |
| 3 | Genoscope [2] | v2.7.3, accessed 17/07/2018 |
| 4 | IMG [3] | Integrated Microbial Genomes (IMG) initiative of the Joint Genome Institute (JGI); Taxon ID: 646311909, from 17/07/2018 |
| 5 | Prodigal [4] | *Ab initio* gene predictions from Prodigal (v2.6) |
| 6 | ChemGenome [5] | *Ab initio* gene predictions from ChemGenome (v2.0, http://www.scfbio-iitd.res.in/chemgenome/chemgenomenew.jsp; with parameters: method, Swissprot space; length threshold, 70 nt; initiation codons, ATG, CTG, TTG, GTG) |
| 7 | *in silico* ORFs |  The *in silico* ORF annotations were generated as described by Omasits and Varadarajan et al., 2017 [6] |

Only ORFs above a selectable length threshold (here 18 aa) were considered. The iPtgxDB was created using the hierarchy RefSeq 2018 > RefSeq 2017 > Genoscope > JGI > Prodigal > ChemGenome > *in silico*. Files were parsed to extract the identifier, coordinates and sequences of bona fide protein-coding sequences (CDS) and pseudogene entries. For extensions or reductions to already annotated CDSs, sequences were only included up to the first tryptic cleavage site, allowing to identify such proteins using the proteomics data obtained by using any of these alternative proteases. 

### References
1. Kunst, F., Ogasawara, N., Moszer, I., Albertini, A.M., Alloni, G. et al. 1997. The complete genome sequence of the gram-positive bacterium *Bacillus subtilis*. Nature 390:249-56.
2. Vallenet, D., Belda, E., Calteau, A., Cruveiller, S., Engelen, S., Lajus, A., Le Fevre, F., Longin, C., Mornico, D., Roche, D. et al. 2013. MicroScope--an integrated microbial resource for the curation and comparative analysis of genomic and metabolic data. Nucleic Acids Res 41: D636-647.
3. Markowitz, V.M., Mavromatis, K., Ivanova, N.N., Chen, I.M., Chu, K., and Kyrpides, N.C. 2009. IMG ER: a system for microbial genome annotation expert review and curation. Bioinformatics 25: 2271-2278.
4. Hyatt, D., Chen, G.L., Locascio, P.F., Land, M.L., Larimer, F.W., and Hauser, L.J. 2010. Prodigal: prokaryotic gene recognition and translation initiation site identification. BMC Bioinformatics 11: 119.
5. Singhal, P., Jayaram, B., Dixit, S.B., and Beveridge, D.L. 2008. Prokaryotic gene finding based on physicochemical characteristics of codons calculated from molecular dynamics simulations. Biophys J 94: 4173-4183.
6. Omasits, U., Varadarajan, A. R., Schmid, M., Goetze, S., Melidis, D., Bourqui, M., Nikolayeva, O., Quebatte, M., Patrignani, A., Dehio, C., Frey, J. E., Robinson, M. D., Wollscheid, B., and Ahrens., C. H. 2017. An integrative strategy to identify the entire protein coding potential of prokaryotic genomes by proteogenomics. Genome Research. 27: 2083-2095.
