Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_055436134.1 ASC41_RS08085 aldehyde dehydrogenase family protein
Query= BRENDA::Q8VWZ1 (503 letters) >NCBI__GCF_001418085.1:WP_055436134.1 Length = 517 Score = 200 bits (508), Expect = 1e-55 Identities = 145/481 (30%), Positives = 236/481 (49%), Gaps = 26/481 (5%) Query: 25 IPNINPSTENIIGDIPAATKEDVDLAVDAAKRAISRKNGRDWSAASGSLRARYLRAIAAK 84 I + +P+ ++IG + TK D + +++A A + + A R +R K Sbjct: 39 ISSYSPTDGSLIGKVTTTTKADYEKVMESATAAFT-----SFRAMPAPQRGEIVRQFGNK 93 Query: 85 IKEKKDELGKLESIDCGKPLEEALADLDDVVACFEYYAGLAEELDSKQKAPISLPMDTFK 144 ++E K+ LGKL S + GK L+E ++ +++ ++ GL+ +L+ Q P P Sbjct: 94 LRELKEPLGKLVSYEMGKSLQEGYGEVQEMIDICDFAVGLSRQLNG-QTIPSERP----- 147 Query: 145 SYILKEP---IGVVALITPWNYPFLMATWKIAPALAAGCAAILKPSE---LASVTCLEL- 197 ++++E IGVV +I+ +N+P + W A A G + K SE L S+ C + Sbjct: 148 GHVMREQWHSIGVVGIISAFNFPVAVWAWNTALAWVCGDVCVWKGSEKAPLCSIACQNII 207 Query: 198 GEICKEVGLPRGVLNIVTGLGHEAGASLASHPDVDKISFTGSSATGSKIMTTAAQLVKPV 257 + KE LP G+ I+ G ++ G + + + IS TGS+ G + T A+ Sbjct: 208 ATVLKENNLPEGISCIING-DYKVGEMMTTDHRIPLISATGSTRMGRIVGATVAERFGKS 266 Query: 258 SLELGGKSPIVVFEDVDLDKVAEWTVFGCFFTNGQICSATSRLIVHESIAVEFVDKLVKW 317 LELGG + I++ DL V VFG T GQ C++T RLI+HES+ + D +V Sbjct: 267 LLELGGNNAIIITPTADLKVVVPGAVFGAVGTCGQRCTSTRRLIIHESVYDKVRDAIVGA 326 Query: 318 AENIKISDPLEEGCRLGPIVSEAQYKKVLNCISSAKSEGATILTGG--RRPEHLKKGYFV 375 + I +PL+E +GP++ + L I AK+EG +L G E + G +V Sbjct: 327 YGQLTIGNPLDEKNHIGPLIDKDSVNTYLAAIEKAKAEGGNVLVEGGVLEGEGYESGCYV 386 Query: 376 EPTIITDVTTSMQIWREEVFGPVLAVKTFSTE-EEAINLANDTHYGLGSAVMSNDLERCE 434 +P II + +I + E F PVL + +S + E AI + N GL SA+M+N+L+ E Sbjct: 387 KPAII-EAKNDFEIVQSETFAPVLYLIKYSGDVENAIGVQNGVAQGLSSAIMTNELKEAE 445 Query: 435 RLSK--ALQAGIVWINC-AQPSFIQAPWGGIKRSGFGRELGEWGLENYLSVKQVTRYTSD 491 + GI +N + I +GG K +G GRE G + Y+ + T SD Sbjct: 446 KFLSFAGSDCGIANVNIGTSGAEIGGAFGGEKETGGGRESGSDAWKVYMRRQTNTVNYSD 505 Query: 492 E 492 E Sbjct: 506 E 506 Lambda K H 0.317 0.134 0.402 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: 545 Number of extensions: 22 Number of successful extensions: 5 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: 503 Length of database: 517 Length adjustment: 34 Effective length of query: 469 Effective length of database: 483 Effective search space: 226527 Effective search space used: 226527 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