Align 3-phosphoshikimate 1-carboxyvinyltransferase (EC 2.5.1.19) (characterized)
to candidate GFF2521 PS417_12855 3-phosphoshikimate 1-carboxyvinyltransferase
Query= BRENDA::A1Z0H6 (444 letters) >FitnessBrowser__WCS417:GFF2521 Length = 418 Score = 790 bits (2041), Expect = 0.0 Identities = 395/417 (94%), Positives = 408/417 (97%) Query: 27 LSSQKTVTVTPPNFPLTGKVAPPGSKSITNRALLLAALAKGTSRLSGALKSDDTRHMSVA 86 +SSQKTVTVTPPNFPL GKVAPPGSKSITNRALLLAALA GTSRLSGALKSDDTRHMSVA Sbjct: 1 MSSQKTVTVTPPNFPLNGKVAPPGSKSITNRALLLAALANGTSRLSGALKSDDTRHMSVA 60 Query: 87 LRQMGVTIDEPDDTTFVVTSQGSLQLPAQPLFLGNAGTAMRFLTAAVATVQGTVVLDGDE 146 LRQMGVTIDEPDDTTFVVT QG LQLP+QPLFLGNAGTAMRFLTAAVATV+GTVVLDGD+ Sbjct: 61 LRQMGVTIDEPDDTTFVVTGQGKLQLPSQPLFLGNAGTAMRFLTAAVATVEGTVVLDGDD 120 Query: 147 YMQKRPIGPLLATLGQNGIQVDSPTGCPPVTVHGMGKVQAKRFEIDGGLSSQYVSALLML 206 YMQKRPIGPLLATLGQNGI VDSPTGCPPVTVHG+GK++AKRFEIDGGLSSQYVSALLML Sbjct: 121 YMQKRPIGPLLATLGQNGILVDSPTGCPPVTVHGVGKIKAKRFEIDGGLSSQYVSALLML 180 Query: 207 AACGEAPIEVALTGKDIGARGYVDLTLDCMRAFGAQVDAVDDTTWRVAPTGYTAHDYLIE 266 AACGEAPIEVALTGKDIGARGYVDLTLDCMRAFGAQV+AVDDTTWRVAPTGYTAHDYLIE Sbjct: 181 AACGEAPIEVALTGKDIGARGYVDLTLDCMRAFGAQVEAVDDTTWRVAPTGYTAHDYLIE 240 Query: 267 PDASAATYLWAAEVLTGGRIDIGVAAQDFTQPDAKAQAVIAQFPNMQATVVGSQMQDAIP 326 PDASAATYLWAAEVLTGGRIDIGVAAQDFTQPDAKAQAVIAQFPNMQATVVGSQMQDAIP Sbjct: 241 PDASAATYLWAAEVLTGGRIDIGVAAQDFTQPDAKAQAVIAQFPNMQATVVGSQMQDAIP 300 Query: 327 TLAVLAAFNNTPVRFTELANLRVKECDRVQALHDGLNEIRPGLATIEGDDLLVASDPALA 386 TLAVLAAFNNTPVRFTELANLRVKECDRVQALHDGLNEIRPGLATIEGDDLLVASDPALA Sbjct: 301 TLAVLAAFNNTPVRFTELANLRVKECDRVQALHDGLNEIRPGLATIEGDDLLVASDPALA 360 Query: 387 GTACTALIDTHADHRIAMCFALAGLKVSGVRIQDPDCVAKTYPDYWKAWPSLGVHLN 443 GT+C ALIDTHADHRIAMCFALAGLKV+G+RIQDPDCVAKTYP+YWKA SLGV L+ Sbjct: 361 GTSCNALIDTHADHRIAMCFALAGLKVAGIRIQDPDCVAKTYPEYWKALGSLGVQLS 417 Lambda K H 0.318 0.134 0.400 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 760 Number of extensions: 13 Number of successful extensions: 1 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 444 Length of database: 418 Length adjustment: 32 Effective length of query: 412 Effective length of database: 386 Effective search space: 159032 Effective search space used: 159032 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory