Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19); betaine-aldehyde dehydrogenase (EC 1.2.1.8) (characterized)
to candidate WP_068108446.1 I601_RS08960 aldehyde dehydrogenase family protein
Query= BRENDA::Q9STS1 (503 letters) >NCBI__GCF_001653335.1:WP_068108446.1 Length = 482 Score = 298 bits (763), Expect = 3e-85 Identities = 191/480 (39%), Positives = 263/480 (54%), Gaps = 21/480 (4%) Query: 8 RQLFIGGQWTEPVLRKTLPVVNPATEDIIGYIPAATSEDVELAVEAARKAFTRNNGKDWA 67 R +I G+W + +TLPV +PAT ++G + DV+ AV AAR A+ W Sbjct: 20 RGAYIDGRWWP--VEQTLPVHSPATGAVVGEVAVCGVADVDRAVAAARAAYP-----GWR 72 Query: 68 RATGAVRAKYLRAIAAKVIERKSELANLEAIDCGKPLDEAAWDMDDVA-GCFEYYADLAE 126 A RA L A+ + ER+ EL +L + G P+ A D++ +YA LA Sbjct: 73 DAGPEARADALDALLLALRERRDELVDLTVAEVGAPVAVAREAHIDLSLDIVAFYAGLAR 132 Query: 127 GLDAKQKTPLSLPMDTFKGYILKEPIGVVGMITPWNYPLLMAVWKVAPSLAAGCTAILKP 186 A+ +T + I +EP+GVV ITPWNYPL V K A ++AAGCT + KP Sbjct: 133 R-GAEVETVANTT-------IYREPVGVVAAITPWNYPLYQLVIKAAAAMAAGCTVVAKP 184 Query: 187 SELASLTCLELADICREVGLPPGVLNILTGLGTEAGAPLASHPHVDKIVFTGSTTTGSSI 246 +EL LT L A+ C GLPPGV N++ G G + G+ + HPHVD + FTGST GS+I Sbjct: 185 AELTPLTSLLFAEACTTSGLPPGVFNLVPGRGRQVGSAMVEHPHVDLVSFTGSTQVGSAI 244 Query: 247 MTSAAKLVKPVSLELGGKSPIIVFDDVDIDKAVEWTMFGCFWTNGQICSATSRLLVHERI 306 +AA VK VSLELGGKS +V D D+ AV T+ +GQ CSA +RLLV Sbjct: 245 AGAAALSVKRVSLELGGKSASVVLPDADLATAVRATVDSAMLNSGQTCSAWTRLLVPAER 304 Query: 307 ADEFLDKLVKWTKNIKISDPFEEGCRLGPVVSKGQYERVLKFVSNARNEGATVLCGGVRP 366 DE L + + DP +E LGPV+S Q + F+ A GA V G P Sbjct: 305 YDEALGLAADRLDALVVGDPEDEATELGPVISADQATSIEGFLERAAAGGAQVRRG---P 361 Query: 367 EHL-KKGYFVEPAIVSNVTTSMEIWREEVFGPALCVKTFSTEDEAIQLANDSQYGLAGAV 425 + G++V PA+V +V EI EEVFGP L V+ ++ D A+++AN + YGLAGAV Sbjct: 362 AYTGLPGHYVAPALVWDVEPDAEIALEEVFGPVLVVQAYTDVDHAVEIANATDYGLAGAV 421 Query: 426 LSNDLERCDRVSKAFQAGIVWVNCSQPCFCQAPWGGTKRSGFGRELGEWGLENYLSVKQV 485 S + V++ + G V +N ++ AP+GG K+SG+GRELG GL+ + VK V Sbjct: 422 WSASDQAALAVARRMRTGQVDLNGAE-FNLAAPFGGVKKSGYGRELGRHGLDEFTEVKAV 480 Lambda K H 0.318 0.135 0.421 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: 567 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: 482 Length adjustment: 34 Effective length of query: 469 Effective length of database: 448 Effective search space: 210112 Effective search space used: 210112 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