Align Δ1-piperideine-6-carboxylate dehydrogenase (characterized)
to candidate WP_055437407.1 ASC41_RS13180 aldehyde dehydrogenase
Query= metacyc::MONOMER-12387 (496 letters) >NCBI__GCF_001418085.1:WP_055437407.1 Length = 500 Score = 175 bits (443), Expect = 4e-48 Identities = 122/401 (30%), Positives = 199/401 (49%), Gaps = 18/401 (4%) Query: 39 PLTGADLFGLRAHTPEDVDRAVEAAHTAFLTWRTTPAPVRGALVKRFGELLTEHKQDLAD 98 P+ G T ED+D A++AAH AF W T+ A R ++ + +++ ++ + LA Sbjct: 35 PVDGKVFTQAARSTQEDIDLALDAAHEAFPAWSTSSATERSNMLLKIAQVMEDNFEYLAT 94 Query: 99 LVTIEAGK-IRSEALGEVQEMIDICDFAVGLSRQLYGRTMPSERPGHRLMETWHPLGVVG 157 L TI+ GK IR ++ ID + G+ R G ++ ++ P+GVVG Sbjct: 95 LETIDNGKPIRESRAADIPYCIDHFRYFAGVIRADEGSISEHDKDTVSIV-LHEPVGVVG 153 Query: 158 VISAFNFPVAVWAWNAAVALVCGDTVVWKPSELTPLNRAACAALLDLAIADAGAPKGLNQ 217 I +NFP+ + AW A AL G T V KP+E TP + L++L I D P G+ Sbjct: 154 EIIPWNFPMLMLAWKIAPALAAGCTAVVKPAEQTP---TSVIMLMEL-IGDI-LPAGVLN 208 Query: 218 VVVG-AADVGERLVDSPRVPLVSATGSTRMGRAVGPRVAARFGRTILELGGNNAAVVTPS 276 +V G A+ G L S R+ +S TGST GR V A +ELGG + V PS Sbjct: 209 IVTGFGAEAGAALATSKRIAKLSFTGSTETGRKVLHNAAENIIPVTMELGGKSPNVFFPS 268 Query: 277 -ADLD------LTVNAAVFAAAGTAGQRCTTLRRLIVHEDIADTVVERLTAAFERLPIGD 329 AD D A +F+ G+ CT R++VHEDIAD +E++ + + G+ Sbjct: 269 VADHDDDFFSKAIEGALMFSL--NQGEICTAPSRILVHEDIADLFIEKMKVRLKAIKTGN 326 Query: 330 PFQDTTLVGPLVNEAAFGRMREAVERATAEGGTLCAGGER-QFPDAAPGAYYVRPALVRM 388 P T++G V++ + ++ + ++ EG + AGG+ + YY++P +++ Sbjct: 327 PLDPETMIGSQVSKPQYDKILDYIKIGKDEGAEVVAGGDAGNYEGELSEGYYIQPTVLKG 386 Query: 389 PAQTAVVREETFAPILYVLTYRDLDEAIRLNNEVPQACRQG 429 + + +EE F P++ + T+ +EAI + N+ P G Sbjct: 387 NNKMRIFQEEIFGPVVALTTFSSTEEAIAIANDTPYGLGAG 427 Score = 25.0 bits (53), Expect = 0.006 Identities = 20/64 (31%), Positives = 26/64 (40%), Gaps = 4/64 (6%) Query: 33 TPHGPHPLTGADLFGLRAHTPEDVDRAVEAAHTAFLTWRTTPAPVRGALVKRFGELLTEH 92 TP+G GA ++ AH V RA++A + T PA VK G H Sbjct: 420 TPYG----LGAGVWSRDAHELYQVPRAIQAGRVWVNQYHTYPAHAPFGGVKESGFGRENH 475 Query: 93 KQDL 96 K L Sbjct: 476 KMAL 479 Lambda K H 0.320 0.135 0.406 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: 439 Number of extensions: 22 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 496 Length of database: 500 Length adjustment: 34 Effective length of query: 462 Effective length of database: 466 Effective search space: 215292 Effective search space used: 215292 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 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:
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