Align long-chain-aldehyde dehydrogenase (EC 1.2.1.48) (characterized)
to candidate 8501918 DvMF_2633 Aldehyde Dehydrogenase (RefSeq)
Query= BRENDA::P51648 (485 letters) >FitnessBrowser__Miya:8501918 Length = 460 Score = 224 bits (571), Expect = 5e-63 Identities = 146/464 (31%), Positives = 235/464 (50%), Gaps = 22/464 (4%) Query: 9 RQAFL-SGRSRPLRFRLQQLEALRRMVQEREKDILTAIAADLCKSEFNVYSQEVITVLGE 67 ++AF+ SG P R+ L LR VQ + AI AD + E +EV+ VL E Sbjct: 8 QKAFIASGAVLPSGARVDALRRLREGVQGYRDRLADAIRADYGRPEHPFLVREVVPVLHE 67 Query: 68 IDFMLENLPEWVTAKPVKKNVLTMLDEAYIQPQPLGVVLIIGAWNYPFVLTIQPLIGAIA 127 ID++++ +P + + V ++ +Y++ QPLG V+ W PF + PL AI Sbjct: 68 IDWLIKAVPGFCGGRRVLPSLGQFKARSYVRRQPLGRVVAYAHWADPFRSLLVPLADAIG 127 Query: 128 AGNAVIIKPSELSENTAKILAKLLPQYLDQDLYIVINGGVEETTELLKQRFDHIFYTGNT 187 AGNAV+++PS + TA+++ +++ QY + + V+ GG E LL D ++Y G+ Sbjct: 128 AGNAVVLRPSAEAPATAEMVTRMVRQYFEPEHVAVVGGGAETDEALLATAPDFVWYDGDA 187 Query: 188 AVGKIVMEAAAKHLTPVTLELGGKSPCYIDKDCDLDIVCRRITWGKYMNCGQTCIAPDYI 247 + + AA LTP GG S + D D+ + RRI W K+++ GQ APD + Sbjct: 188 RGARTIAVLAAPTLTPYAAITGGPSAALVHGDADMAMAARRIVWAKFLHAGQLRAAPDVL 247 Query: 248 LCEASLQNQIVWKIKETVKEFYGENIKESPDYERIINLRHFKRILSLLE-GQKIAFG--- 303 L + ++ ++++ ++ ++ +G + S D+ R+++ F R L G+ + FG Sbjct: 248 LVQRTVLDRVLDALRTELERAFGPQPRTSADFGRMVSAAGFARQAERLAIGRALPFGPGD 307 Query: 304 --GETDEATRYIAPTVLTDVDPKTKVMQEEIFGPILPIVPVKNVDEAINFINEREKPLAL 361 + D A+ Y+ PT+LTDV + V++EE FGP+L + P +DEA F+ AL Sbjct: 308 AANQPDRASLYVPPTLLTDVPDDSPVLREEGFGPVLVVRPYTRLDEATAFLAGLPALTAL 367 Query: 362 YVFSHNHKLIKRMIDETSSGGVTGNDVIMHFTLNSFPFGGVGSSGMGAYHGKHSFDTFSH 421 Y F+ H +R+++ T +G V ND H P GGVG +G GA G TFS Sbjct: 368 YAFTTAHARGERLMENTRAGAVLINDAATHLANPRLPQGGVGETGHGAMAGPAGLATFSA 427 Query: 422 QRPCLLKSLKREGAN----KLRYPPNSQSKVDWGKFFLLKRFNK 461 R + G+N LR+ P S K+ +LKR K Sbjct: 428 PRATAV------GSNFFDIPLRFAPGSDLKLK-----VLKRLYK 460 Lambda K H 0.321 0.139 0.411 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: 419 Number of extensions: 19 Number of successful extensions: 2 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: 485 Length of database: 460 Length adjustment: 33 Effective length of query: 452 Effective length of database: 427 Effective search space: 193004 Effective search space used: 193004 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 (21.9 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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