Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_090219935.1 CV091_RS15630 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_002796795.1:WP_090219935.1 Length = 490 Score = 520 bits (1339), Expect = e-152 Identities = 259/474 (54%), Positives = 345/474 (72%), Gaps = 3/474 (0%) Query: 46 LLRGDSFVGGRWLPTPATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEISV 105 LL ++VGG ++ T TF V +PA G + V D + AA+ +A A W + Sbjct: 17 LLETRAYVGGEFISTQNTFDVINPARGDVVAQVTDLTRADVAAAIASAETAQKEWATWTG 76 Query: 106 KERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVYGD 165 KERS++LR W++L+++N+++LA I+TAE GKPL E++GEI Y A FLE+F+EEA+R+YG+ Sbjct: 77 KERSAVLRNWFNLIMENQEDLALILTAEMGKPLTESRGEIAYGASFLEYFAEEAKRIYGE 136 Query: 166 IIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPYSA 225 I +DKR V+KQP+GVA+ ITPWNFP+AMITRK G ALAAGC V +PAE TP SA Sbjct: 137 TIPGHQRDKRITVIKQPIGVAASITPWNFPNAMITRKAGPALAAGCAFVARPAELTPLSA 196 Query: 226 LALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHHAA 285 ALA LA +AG+P GV++V+ S A E G+ C +P V KI+FTGSTA G+ILL AA Sbjct: 197 TALAVLAERAGLPSGVFSVVTTS--DASETGKEFCENPTVRKITFTGSTAVGRILLQQAA 254 Query: 286 NSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDSFV 345 VK+ SMELGG APFIVFD A++D AV GA+ KFRN GQTCVC+NR VQ G++D+F Sbjct: 255 GQVKKCSMELGGNAPFIVFDDADLDAAVEGAIMCKFRNNGQTCVCANRIYVQAGVYDAFA 314 Query: 346 TKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQSGG 405 K +A ++VG+GFE+GT GPLIN KA+EKV+ H+ DA AKG ++ GG + GG Sbjct: 315 EKL-KARVADMKVGDGFEDGTVFGPLINAKAMEKVKSHLTDATAKGGEIILGGNPSELGG 373 Query: 406 NFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDPAQ 465 FFEPT+++ T DM TEETFGP+AP+ KF+ E+E +A+AN GLA YFY++D ++ Sbjct: 374 TFFEPTIVTGATTDMAFSTEETFGPLAPLFKFEDEDEVIALANDTIFGLASYFYAKDLSR 433 Query: 466 IWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVC 519 +++VAE LE G+VGVN GLIS+ PFGG+KQSGLGREGS +GI+E+LE+KY+C Sbjct: 434 VYKVAEALEYGIVGVNTGLISTEVAPFGGIKQSGLGREGSHHGIEEFLEMKYIC 487 Lambda K H 0.318 0.135 0.400 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: 614 Number of extensions: 23 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: 523 Length of database: 490 Length adjustment: 34 Effective length of query: 489 Effective length of database: 456 Effective search space: 222984 Effective search space used: 222984 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: 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