Align long-chain-aldehyde dehydrogenase (EC 1.2.1.48) (characterized)
to candidate Echvi_1497 Echvi_1497 NAD-dependent aldehyde dehydrogenases
Query= BRENDA::P51648 (485 letters) >lcl|FitnessBrowser__Cola:Echvi_1497 Echvi_1497 NAD-dependent aldehyde dehydrogenases Length = 469 Score = 336 bits (861), Expect = 1e-96 Identities = 180/446 (40%), Positives = 271/446 (60%), Gaps = 9/446 (2%) Query: 5 VRRVRQAFLSGRSRPLRFRLQQLEALRRMVQEREKDILTAIAADLCKSEFNVYSQEVITV 64 V+ +Q L + L R+++LE L+ ++ +K+I A+ ADL K V E V Sbjct: 6 VQAQKQKALKNQQSTLSSRIKKLEQLKEWIKSNQKEIEKALYADLRKPAAEVAVTETSFV 65 Query: 65 LGEIDFMLENLPEWVTAKPVKKNVLTMLDEAYIQPQPLGVVLIIGAWNYPFVLTIQPLIG 124 + EI+ L+ LP+W V + + + +AY+Q +P G VLII WNYPF L++ PL+ Sbjct: 66 VMEINAALKQLPKWTAPTKVGQPIHMLGTQAYLQAEPKGAVLIISPWNYPFNLSVAPLVS 125 Query: 125 AIAAGNAVIIKPSELSENTAKILAKLLPQYLDQDLYIVINGGVEETTELLKQRFDHIFYT 184 AIAAG + +KPSE S +T+ +L +++ + + + GGV T+ELL+Q FDHIF+T Sbjct: 126 AIAAGCSACLKPSEHSPHTSALLRRMVTELFAVEDVTIFEGGVPVTSELLEQPFDHIFFT 185 Query: 185 GNTAVGKIVMEAAAKHLTPVTLELGGKSPCYIDKDCDLDIVCRRITWGKYMNCGQTCIAP 244 G+T VGKIVM+AAAK+LT VTLELGGKSP ID+ DL+ ++I GK++N GQTCIAP Sbjct: 186 GSTEVGKIVMKAAAKNLTSVTLELGGKSPAIIDQGFDLEDAAKKIAIGKFINSGQTCIAP 245 Query: 245 DYILCEASLQNQIVWKIKETVKEFY---GENIKESPDYERIINLRHFKRILSLL-----E 296 DY+ S + + +K V Y G+ +PDY RII+ H R+ ++L + Sbjct: 246 DYLFVHESQKQDFIETLKAQVNRMYNANGKGFDRNPDYGRIIHAPHIVRLQNMLKDAQTK 305 Query: 297 GQKIAFGGETDEATRYIAPTVLTDVDPKTKVMQEEIFGPILPIVPVKNVDEAINFINERE 356 G + FGG+ +++ PTV+++V +M+EEIFGPILPI+ +D+ I I + Sbjct: 306 GAHVEFGGKNSLDQQFMEPTVVSNVSEAMDLMKEEIFGPILPIITYHQLDDVIQLIQLKP 365 Query: 357 KPLALYVFSHNHKLIKRMIDETSSGGVTGNDVIMHFTLNSFPFGGVGSSGMGAYHGKHSF 416 KPLA+Y F+ + ++I+++ TSSG + ND + F + PFGG+G+SGMG HG F Sbjct: 366 KPLAVYAFTTDDRIIEQLSKNTSSGALVINDCAIQFLHSELPFGGIGASGMGRSHGHAGF 425 Query: 417 DTFSHQRPCLLKSLKREGANKLRYPP 442 FS+++ +LK + KL YPP Sbjct: 426 LAFSNEK-AILKQRTGKTLPKLLYPP 450 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: 503 Number of extensions: 25 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: 485 Length of database: 469 Length adjustment: 33 Effective length of query: 452 Effective length of database: 436 Effective search space: 197072 Effective search space used: 197072 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