Align L-threonine ammonia-lyase; L-serine ammonia-lyase; Threonine dehydratase; EC 4.3.1.19; EC 4.3.1.17 (characterized)
to candidate WP_012991597.1 THAL_RS02775 threonine synthase
Query= SwissProt::Q9WYJ1 (401 letters) >NCBI__GCF_000025605.1:WP_012991597.1 Length = 352 Score = 90.1 bits (222), Expect = 9e-23 Identities = 92/298 (30%), Positives = 134/298 (44%), Gaps = 24/298 (8%) Query: 21 TALAYSSVLSEVTG--GEIYLKMENLQKTGSFKIRGAYNKIAHLSEEERKRGVVAASAGN 78 T L + L+ + G GE+YLK E L TGSFK RG I+ + EE KR V+ AS GN Sbjct: 31 TPLIKADNLARLVGFRGELYLKYEGLNPTGSFKDRGMTVAISK-ALEEGKRAVICASTGN 89 Query: 79 HAQGVALAAQIFGIPATIVMPRYA-PLSKITKTRNLGAQVILEGNIFDEAYEAALRIQEK 137 + A A G+ A +++PR A L K+++ GA+V+ FD+A +I + Sbjct: 90 TSASAAAYAARAGLKAYVLLPRGAVALGKLSQAVMYGAKVLAVKGTFDDALYIVRKIGQM 149 Query: 138 TGAVFVHPFNDPHVIAGQGTIGLEIMEDLPDV-EVVVVPVGGGGLISGVSVAIKSMNPEV 196 V+ N P+ I GQ T EI + L + + +PVG G I+ K Sbjct: 150 LPVEVVNSVN-PYRIEGQKTAAFEICDALGEAPDYHFLPVGNAGNITAYWKGYKEYYQMG 208 Query: 197 KVIGVQTENMPSMIASLRRGRAERVEGKP-----TLADGIAVKKP--GDLTFELVKKYVD 249 K+ +P M+ G A V+G P T+A I + P E ++ Sbjct: 209 KI-----RKLPRMMGWQAEGAAPIVKGYPIKNPQTIASAIRIGNPYSWQSALEAAQESGG 263 Query: 250 EMVAVNEEEIADAILFLLEQAKVVAEGAGAVGVAAVLNKLDVKGKKVAIVISGGNIDV 307 ++ AV +EEI A + V E A A VA + KL +G SGG + V Sbjct: 264 KIDAVTDEEILYAYKLVASTEGVFCEPASAASVAGFI-KLVREG-----FFSGGEVVV 315 Lambda K H 0.317 0.136 0.367 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: 268 Number of extensions: 17 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: 401 Length of database: 352 Length adjustment: 30 Effective length of query: 371 Effective length of database: 322 Effective search space: 119462 Effective search space used: 119462 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 (21.6 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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:
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