Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_013419459.1 RVAN_RS09190 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-16244 (495 letters) >NCBI__GCF_000166055.1:WP_013419459.1 Length = 506 Score = 341 bits (874), Expect = 4e-98 Identities = 202/490 (41%), Positives = 291/490 (59%), Gaps = 15/490 (3%) Query: 16 TYEQPTGLFINNEFVQSKSKKTFGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFHSSW 75 T+++ FI E+ + F +V+P T + QV + +EDI+ A++AA AA W Sbjct: 14 TFKERYDNFIGGEWRSPLGGQYFESVTPITGKPFAQVARSQAEDIELALDAAHAAAER-W 72 Query: 76 STSDPQVRMKVLYKLADLIDEHADTLAHIEALDNGKSLMCS-KGDVALTAAYFRSCAGWT 134 + R +L ++AD ++++ + LA+ E++DNGK + + D+ L +FR A Sbjct: 73 GHTSVAERSLILNRIADRMEQNLEKLAYAESVDNGKPIRETLAADIPLAIDHFRYFASCI 132 Query: 135 DKIKGSVIETGDTHFNYTRREPIGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAES 194 +G++ + + Y +EP+GV GQIIPWNFP+LMA+WKL P L G VLK AE Sbjct: 133 RAQEGTLGQVDEDTVAYHFQEPLGVVGQIIPWNFPILMAAWKLAPALAAGNCVVLKPAEQ 192 Query: 195 TPLSALYLASLIKEAGAPPGVVNVVSGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMKA 254 TP+ L A +I + P GV+N+V+GFG AG P++S P+I K+AFTG T+TGR IM+ Sbjct: 193 TPIGILVWAEIIGDL-LPKGVLNIVNGFGLEAGKPLASSPRIAKIAFTGETSTGRLIMQY 251 Query: 255 AAESNLKKVTLELGGKSPNIVFDD---ADVKSTIQHLVTGIFY--NTGEVCCAGSRIYVQ 309 A++ NL VTLELGGKSPNI FDD AD + + + + + N GEVC SR VQ Sbjct: 252 ASQ-NLIPVTLELGGKSPNIFFDDVAAADDEFFDKAIEGFVMFALNQGEVCTCPSRALVQ 310 Query: 310 EGIYDKIVSEFKNAAESLKIGDPFKEDTFMGAQTSQLQLDKILKYIDIGKKEGATVITGG 369 E + D+ V S+K G+P DT +GAQ SQ QL KIL Y++IG +EGA + GG Sbjct: 311 ESLRDRFVDRALARVASIKQGNPLDTDTMIGAQASQEQLHKILSYVNIGLEEGAKCLIGG 370 Query: 370 ER--FGNK---GYFIKPTIFGDVKEDHQIVRDEIFGPVVTITKFKTVEEVIALANDSEYG 424 ER G + G++++PT+F + +I ++EIFGPVV +T FK + + LAND+ YG Sbjct: 371 ERAYLGGELDTGFYVRPTVF-EGNNSMRIFQEEIFGPVVALTTFKDEADALHLANDTVYG 429 Query: 425 LAAGVHTTNLSTAISVSNKINSGTIWVNTYNDFHPMVPFGGYSQSGIGREMGEEALDNYT 484 L AGV T + + A I +G +W N Y+ + FGGY QSGIGRE LD+Y Sbjct: 430 LGAGVWTRDGNRAYRFGRGIKAGRVWTNCYHLYPAHAAFGGYKQSGIGRETHHMMLDHYQ 489 Query: 485 QVKAVRIGLS 494 Q K + + S Sbjct: 490 QTKNLLVSYS 499 Lambda K H 0.316 0.133 0.389 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: 613 Number of extensions: 29 Number of successful extensions: 7 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: 495 Length of database: 506 Length adjustment: 34 Effective length of query: 461 Effective length of database: 472 Effective search space: 217592 Effective search space used: 217592 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: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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