Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_010529728.1 ON01_RS04100 betaine-aldehyde dehydrogenase
Query= BRENDA::Q93YB2 (503 letters) >NCBI__GCF_000224785.1:WP_010529728.1 Length = 489 Score = 420 bits (1080), Expect = e-122 Identities = 211/492 (42%), Positives = 311/492 (63%), Gaps = 8/492 (1%) Query: 8 RQLFINGDWKAPVLNKRIPVINPATQNIIGDIPAATKEDVDVAVAAAKTALTRNKGADWA 67 ++ I+G W + +INP Q I+ + + + D A+ AA+ A + DWA Sbjct: 4 KKQLIDGSWVTSNSDAVRDIINPFNQKIVATVTESDESDTKAAITAARKAFDQG---DWA 60 Query: 68 TASGAVRARYLRAIAAKVTEKKPELAKLESIDCGKPLDEAAWDIDDVAGCFEYYADLAEK 127 T A R + + IA + + ELA+LES+D GK ++E+ D+DD+AG F Y+A++A+K Sbjct: 61 TTPAAERGKIVHKIADLIERDREELAELESLDTGKTVEESLGDMDDIAGVFRYFAEMADK 120 Query: 128 LDARQKAPVSLPMDTFKSHVLREPIGVVGLITPWNYPMLMATWKVAPALAAGCAAILKPS 187 D + +P T K V+ EP+GV G ITPWNYP+L A+WK+APALAAG ++KPS Sbjct: 121 -DGGEIIESPIPNSTSK--VVHEPVGVCGQITPWNYPLLQASWKLAPALAAGNTLVMKPS 177 Query: 188 ELASLTCLELGEICKEVGLPPGVLNILTGLGPEAGAPLATHPDVDKVAFTGSSATGSKIM 247 E+ LT +++ E+ E G+P GV+N++ G G GA L+ + +VD ++FTG TG KIM Sbjct: 178 EITPLTSIKVFELMAEAGVPAGVVNLVLGPGDSVGAELSANDNVDLISFTGGIHTGKKIM 237 Query: 248 TAAAQLVKPVSLELGGKSPLVVFEDVDLDKAAEWAIFGCFWTNGQICSATSRLILHESIA 307 AA+ VK ++LELGGK+P +VF D D + A + A+ F+ GQICSA +RLI+ ESI Sbjct: 238 QAASSNVKNLALELGGKNPNIVFADADFETAVDQAMNAVFFHAGQICSAGTRLIIEESIH 297 Query: 308 TEFLNRIVKWIKNIKISDPLEEGCRLGPVVSEGQYEKILKFVSNAKSEGATILTGGSRPE 367 F++ IV +KNIK+ +E ++GP++SE K++ +V N K EGAT+ GGSRP+ Sbjct: 298 DAFVSAIVDRVKNIKLGSGFDESTQMGPLISEDHLNKVVNYVENGKQEGATVAVGGSRPD 357 Query: 368 --HLKKGFFIEPTIITDVTTNMQIWREEVFGPVLCVKTFSTEEEAIDLANDTVYGLGAAV 425 L+ G F PTI+T T++M++ ++E FGPV+ V+ F+TEEEA+ LAND++YGL V Sbjct: 358 DPELQNGLFYLPTILTGCTSDMRVVQDEGFGPVITVEKFTTEEEAVRLANDSIYGLSGGV 417 Query: 426 ISNDLERCERVTKAFKAGIVWVNCSQPCFTQAPWGGVKRSGFGRELGEWGLDNYLSVKQV 485 +ND+ + ER + G VW+N F APWGG K+SG GRELG+ GL+ Y K + Sbjct: 418 FTNDIAKAERCVAKLRMGTVWINDVNLYFPHAPWGGYKQSGIGRELGKTGLEEYQETKHI 477 Query: 486 TQYISEEPWGWY 497 Q + EP W+ Sbjct: 478 FQNLKPEPVNWF 489 Lambda K H 0.318 0.135 0.416 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: 21 Number of successful extensions: 4 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: 489 Length adjustment: 34 Effective length of query: 469 Effective length of database: 455 Effective search space: 213395 Effective search space used: 213395 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