Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_003466863.1 J416_RS06115 aldehyde dehydrogenase family protein
Query= BRENDA::Q8VWZ1 (503 letters) >NCBI__GCF_000359605.1:WP_003466863.1 Length = 486 Score = 250 bits (639), Expect = 7e-71 Identities = 151/481 (31%), Positives = 258/481 (53%), Gaps = 21/481 (4%) Query: 11 FIDGEWRVPILNKRIPNINPSTENIIGDIPAATKEDVDLAVDAAKRAISRKNGRDWSAAS 70 +IDG+W+ + N NP + + AA+K D+D A A++A + W + Sbjct: 11 YIDGQWKEGNSQLSMKNQNPYNQETLTTYQAASKTDIDHAYQVAQKAQKK-----WQQQN 65 Query: 71 GSLRARYLRAIAAKIKEKKDELGKLESIDCGKPLEEALADLDDVVACFEYYAGLAEELDS 130 + + I++ + + ++ + + G +A ++ V + + +D Sbjct: 66 PTFQRGIFEQAVHVIEDHHEAIVEVINKEIGGTRLKAEFEISLVKNMLKEASTFPFRMDG 125 Query: 131 KQKAPISLPMDTFKSYILKEPIGVVALITPWNYPFLMATWKIAPALAAGCAAILKPSELA 190 K ++ D ++ + + PIGVV +I+P+N+PF ++ IAPALA G ++KP E Sbjct: 126 KILPSMT---DGKENQVYRIPIGVVGVISPFNFPFFLSMKSIAPALATGNGVVVKPHEHT 182 Query: 191 SVTC-LELGEICKEVGLPRGVLNIVTGLGHEAGASLASHPDVDKISFTGSSATGSKIMTT 249 +T + +I +E GLP+G+LNIVT E G + HP ISFTGS+A G I + Sbjct: 183 VITGGTMIAKIFEEAGLPQGLLNIVTTEISEIGDAFVEHPIPQSISFTGSTAIGRHIGSI 242 Query: 250 AAQLVKPVSLELGGKSPIVVFEDVDLDKVAEWTVFGCFFTNGQICSATSRLIVHESIAVE 309 A + +K V LELGG S ++V +D D+D +F F GQIC + +R+I+HE + Sbjct: 243 AGRELKDVHLELGGNSGLIVLDDADIDLAVSAAIFSRFTHQGQICMSANRIIIHEDVYDT 302 Query: 310 FVDKLVKWAENIKISDPLEEGCRLGPIVSEAQYKKVLNCISSAKSEGATILTGGRRPEHL 369 FV+K V + DP ++ +GP+++E Q + I + +EGA L G+ Sbjct: 303 FVEKYVAKVNELSCGDPCDDTTIIGPLINEKQVENTKQIIEAGINEGADPLVHGQ----- 357 Query: 370 KKGYFVEPTIITDVTTSMQIWREEVFGPVLAVKTFSTEEEAINLANDTHYGLGSAVMSND 429 +G VEP + +VT +M + +EE+F PV+++ S+EEE +++ NDT YGL AV + + Sbjct: 358 VRGNVVEPVVFGNVTKNMTVAKEEMFAPVVSLFKASSEEEILDIVNDTSYGLSGAVHTQN 417 Query: 430 LERCERLSKALQAGIVWINCA----QPSFIQAPWGGIKRSGFGRELGEWGLENYLSVKQV 485 +ER +L+K ++ G++ IN +P+ +GG+K SG GR GEW L+ + + K + Sbjct: 418 IERGAQLAKQMETGMIHINDGTINDEPN---VAFGGMKNSGVGRLNGEWSLDAFTTTKWI 474 Query: 486 T 486 + Sbjct: 475 S 475 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: 530 Number of extensions: 23 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: 486 Length adjustment: 34 Effective length of query: 469 Effective length of database: 452 Effective search space: 211988 Effective search space used: 211988 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