Align Salicylate synthase; Chorismate mutase; CM; EC 5.4.99.5; Isochorismate synthase/isochorismate lyase; EC 4.2.99.21; EC 5.4.4.2; Mycobactin synthase protein (uncharacterized)
to candidate Dsui_0219 Dsui_0219 anthranilate synthase component I
Query= curated2:Q73XV3 (450 letters) >FitnessBrowser__PS:Dsui_0219 Length = 491 Score = 141 bits (355), Expect = 5e-38 Identities = 84/252 (33%), Positives = 129/252 (51%), Gaps = 1/252 (0%) Query: 187 YRDRVASAVAEIAAGRYHKVILSRCLQVPFAVDFPSTYRLARRHNTPVRSFLLRLGGIRA 246 ++ VA A I G +V+LS+ + PF+ S YR R N + Sbjct: 221 FKQAVAKAKEYITEGDIMQVVLSQRMTKPFSASPLSLYRALRTLNPSPYMYYFDFEDFHV 280 Query: 247 VGYSPELVAAVRHDGVVVTEPLAGTRAFGRGALHDRQARDDLESNSKEIVEHAISVRSSL 306 VG SPE++ + D V V P+AGTR G D +DL ++ KEI EH + Sbjct: 281 VGASPEILTRLEGDTVTV-RPIAGTRKRGATPEEDAALAEDLLADQKEIAEHVQLLDLGR 339 Query: 307 QEMAEIAEPGTAVVTDFMTVRERGSVQHLGSTVSGRLGTSNDRMDALEALFPAVTASGIP 366 ++ +A+ G+ +T+ M++ V H+ S V G+L +D L+A FPA T SG P Sbjct: 340 NDVGRVAQTGSVKLTERMSIERYSHVMHIVSNVEGKLQAGLSALDVLKAAFPAGTLSGAP 399 Query: 367 KAGGVEAILRLDEGPRGLYSGAVVMVSADGALDAALTLRAAYEHDGKTWLRAGAGIIEES 426 K +E I L+ RG+Y GA+ + +G +D A+ +R A DG+ ++AGAGI+ +S Sbjct: 400 KVRAMEIIDELEPVKRGIYGGAIGYLGFNGDMDLAIAIRTAVIKDGQLHVQAGAGIVADS 459 Query: 427 TPEREFEETCEK 438 P E++ET K Sbjct: 460 DPTSEWQETQNK 471 Lambda K H 0.318 0.135 0.391 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: 427 Number of extensions: 22 Number of successful extensions: 2 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: 450 Length of database: 491 Length adjustment: 33 Effective length of query: 417 Effective length of database: 458 Effective search space: 190986 Effective search space used: 190986 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