Align Aldehyde dehydrogenase family 7 member B4; Antiquitin-1; Turgor-responsive ALDH; EC 1.2.1.3 (characterized)
to candidate WP_078210708.1 BXU11_RS01185 aldehyde dehydrogenase family protein
Query= SwissProt::Q9SYG7 (508 letters) >NCBI__GCF_002017945.1:WP_078210708.1 Length = 517 Score = 499 bits (1284), Expect = e-145 Identities = 255/504 (50%), Positives = 345/504 (68%), Gaps = 5/504 (0%) Query: 9 EFLSEIGLTSHNLGSYVAGKWQANGPLVSTLNPANNQPIAQVVEASLEDYEQGLKACEEA 68 E L+++G+ + N G+ + A+G L+ + +P + Q IA V +S DYE+ ++ A Sbjct: 12 EALAQLGIKAVNEGTSTGTQHFASGSLLESYSPVDGQLIASVTTSSAADYEKVMQTATAA 71 Query: 69 AKIWMQVTAPKRGDIVRQIGDALRSKLDYLGRLLSLEMGKILAEGIGEVQEVIDMCDFAV 128 K + + AP+RG+IVRQ G+ LR + LG+L+S EMGK L EG GEVQE+ID+CDFAV Sbjct: 72 FKTFRLMPAPQRGEIVRQFGEKLRKNKEALGKLVSYEMGKSLQEGYGEVQEMIDICDFAV 131 Query: 129 GLSRQLNGSVIPSERPNHMMLEMWNPLGIVGVITAFNFPCAVLGWNACIALVCGNCVVWK 188 GLSRQL+G + SERP H M E ++ LG+VG+I+AFNFP AV WN +A +CG+ VWK Sbjct: 132 GLSRQLHGLTMHSERPGHRMYEQYHSLGVVGIISAFNFPVAVWAWNTALAWICGDVCVWK 191 Query: 189 GAPTTPLITIAMTKLVAEVLEKNNLPGAIFTAMCGGAEIGEAIAKDTRIPLVSFTGSSRV 248 + TPL +A ++AEVL++NNLP I + G IGE + KDTR+PL+S TGS+R+ Sbjct: 192 PSEKTPLCGVACQNIIAEVLKENNLPEGISCLINGDYTIGEMLTKDTRVPLISATGSTRM 251 Query: 249 GSMVQQTVNARSGKTLLELSGNNAIIVMDDADIQLAARSVLFAAVGTAGQRCTTCRRLLL 308 G +V QTV R GK+LLEL GNNAIIV DADI++ +F AVGTAGQRCT+ RRL++ Sbjct: 252 GKIVAQTVAGRLGKSLLELGGNNAIIVTPDADIKMTVIGAVFGAVGTAGQRCTSTRRLII 311 Query: 309 HESVYDKVLEQLLTSYKQVKIGNPLEKGTLLGPLHTPESKKNFEKGIEVIKSQGGKILTG 368 HES+YDKV + ++ +Y Q++IGNPL++ +GPL ++ + + + + + ++GGKIL Sbjct: 312 HESMYDKVKDTIVAAYGQLRIGNPLDEKNHVGPLIDKQAVEMYNQALTKVVAEGGKILVE 371 Query: 369 GKAVEGEGN----FVEPTIIEISADAAVVKEELFAPVLYVLKFK-SFGEAVAINNSVPQG 423 G + GEG +V+P I E +V+ E FAPVLY+LK+ A+ + N V QG Sbjct: 372 GGVLSGEGYESGCYVKPAIAEAQNSFEIVQHETFAPVLYLLKYSGDVDNAIKLQNGVAQG 431 Query: 424 LSSSIFTRNPENIFRWIGPLGSDCGIVNVNIPTNGAEIGGAFGGEKATGGGREAGSDSWK 483 LSS+I T N R++ GSDCGI NVNI T+GAEIGGAFGGEK TGGGRE+GSD+WK Sbjct: 432 LSSAIMTNNLREAERFLSVAGSDCGIANVNIGTSGAEIGGAFGGEKETGGGRESGSDAWK 491 Query: 484 QYMRRSTCTINYGNELPLAQGINF 507 YMRR T TINY LPLAQGI F Sbjct: 492 VYMRRQTNTINYTTNLPLAQGIKF 515 Lambda K H 0.317 0.135 0.398 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: 695 Number of extensions: 32 Number of successful extensions: 3 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: 508 Length of database: 517 Length adjustment: 35 Effective length of query: 473 Effective length of database: 482 Effective search space: 227986 Effective search space used: 227986 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 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