Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_047214813.1 PATSB16_RS14485 aldehyde dehydrogenase
Query= BRENDA::A0A0E3T3B5 (503 letters) >NCBI__GCF_001931675.1:WP_047214813.1 Length = 498 Score = 348 bits (893), Expect = e-100 Identities = 200/492 (40%), Positives = 276/492 (56%), Gaps = 10/492 (2%) Query: 7 SRQLFIDGEWREPVLKKRIPIINPATEQIIGDIPAATAEDVEIAVEAARKALARNKGRDW 66 S + + G+WR R + PA E + +I AA A D AVEAA A R DW Sbjct: 11 SSDILVGGQWRAG-RGARYASLYPADESVNAEIAAADASDAAEAVEAADAAWRR---ADW 66 Query: 67 ALAPGAVRAKYLRAIAAKIAERKSEIAKLEAIDCGKPLDEAAWDIDDVSGCFEYYADLAE 126 + RA L IA I R +A L+ D GKP+ E + +G F Y+A E Sbjct: 67 SGLKPHQRAAVLHRIADLIQARAEPLAHLQRRDNGKPISETRALVASAAGTFRYFAACLE 126 Query: 127 GLDAQQKTPISLPMEQFKSHVLKEPIGVVGLITPWNYPLLMATWKVAPALAAGCAAILKP 186 L+ + TP + S + EP+GV+ ITPWN P+ K+APALAAG A +LKP Sbjct: 127 TLE-ENLTP---QRGDYLSMSVHEPLGVIAAITPWNSPIASDAQKLAPALAAGNAVVLKP 182 Query: 187 SELASVTCLELADVCREVGLPPGVLNILTGLGHEAGAPLASHPHVDKIAFTGSTMTGSKI 246 +E+ + LEL +C E G+PPGVL++L G G G L HP V K+AFTG T G I Sbjct: 183 AEVTPLVSLELGRICLEAGVPPGVLSVLPGKGSIIGDALVRHPKVKKVAFTGGTEVGRGI 242 Query: 247 MTAAAQLVKPVSLELGGKSPIVVFDDVDIDKAAEWTAFGIFWTNGQICSATSRLIIHENI 306 AA + PVSLELGGKSP +VF D D+D A +GIF ++G+ C A SRL +H ++ Sbjct: 243 ARLAADKLMPVSLELGGKSPTMVFADADLDHAVAGVLYGIFSSSGESCIAGSRLFVHTSV 302 Query: 307 AAKFLDRLVQWCKNIKIADPLEEGCRLGPVVSGGQYEKILKFIATAKSEGARVLSGGARP 366 F++RLV + +++ DPL E ++GP+V+G I +++ +EG R+L GGARP Sbjct: 303 HDAFVERLVAGARALRVGDPLREDTQMGPLVTGAHRASIERYVELGLAEGGRLLCGGARP 362 Query: 367 --EHLKKGFFIEPTIITDVTTSMQIWREEVFGPVLCVKTFSSEDEALELANDSHYGLGAA 424 E KG+F PTI+ + ++ REE+FGPVL V F E + L ANDS YGL A Sbjct: 363 AGEGRDKGYFYLPTILAGLNNEARMCREEIFGPVLAVMAFDDEADLLRQANDSVYGLAAG 422 Query: 425 VISKDLERCERVSKALQAGIVWINCSQPCFCQAPWGGNKRSGFGRELGKWGLDNYLTVKQ 484 + ++D +R RV++AL+ G VWIN + P+GG K SG GRE G+ GL Y K Sbjct: 423 IWTRDYKRAWRVARALETGTVWINTYKQFSISTPFGGWKESGVGREKGRLGLLEYTQQKS 482 Query: 485 VTEYVSDDPWGW 496 + +++ P W Sbjct: 483 LYWGLNEAPLPW 494 Lambda K H 0.319 0.136 0.419 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: 658 Number of extensions: 24 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: 503 Length of database: 498 Length adjustment: 34 Effective length of query: 469 Effective length of database: 464 Effective search space: 217616 Effective search space used: 217616 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 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