Align gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate Echvi_3822 Echvi_3822 NAD-dependent aldehyde dehydrogenases
Query= reanno::WCS417:GFF5420 (497 letters) >FitnessBrowser__Cola:Echvi_3822 Length = 453 Score = 230 bits (587), Expect = 7e-65 Identities = 141/457 (30%), Positives = 236/457 (51%), Gaps = 9/457 (1%) Query: 40 ISPVDGRLLATVASCDAADAQRAVENARATFNSGVWSRLAPAKRKSAMLRFAALLKANAE 99 I+P G LL + A++ + + S W L ++R M + +L+ N + Sbjct: 4 INPYTGELLEEFTDHTEQQVEAAIQKGQEAYLS--WRELPISQRADLMKKAGQVLRDNTD 61 Query: 100 ELALLETLDMGKPISDSLNIDVPGAANALSWSGE-AIDKIYDEVAATPHDQLGLVTREPV 158 + + +L+MGK I++S + +V A + E A + + D A P + V P+ Sbjct: 62 KYGKIISLEMGKVITESKS-EVEKCAWVCEYYAENAEEMLADAPIALPDGKEAKVVYNPL 120 Query: 159 GVVGAIVPWNFPLMMACWKLGPALSTGNSVILKPSEKSPLTAIRIAALAVEAGIPKGVFN 218 G+V A++PWNFP P L+ GN +LK + P A+ I + +AG P+GVF Sbjct: 121 GIVLAVMPWNFPFWQVFRFAAPNLTAGNVGLLKHASNVPQCALAIEEVFTQAGFPEGVFQ 180 Query: 219 VLPGYGHTVGNALALHMDVDTLVFTGSTKIAKQLLIRSGESNMKRVWLEAGGKSPNIVFA 278 L V N +A H DV TGS K +++ ++GE +K+ LE GG P IV Sbjct: 181 SLLIGSDKVANIIA-HPDVKAATLTGSEKAGQKIAAQAGEQ-IKKTVLELGGSDPFIVLK 238 Query: 279 DAPDLQAAAESAAGAIAFNQGEVCTAGSRLLVERSIKDKFLPLVIEALKGWKPGNPLDPA 338 DA D++ AA++AA N G+ C A R ++E+ + D+F+ A++ + PG+PLD Sbjct: 239 DA-DVKEAAKTAAKGRMINFGQSCIAAKRFIIEQEVYDEFITHFKSAIESYVPGDPLDEK 297 Query: 339 TNVGALVDTQQMNTVLSYIEAGHADGAKLVAGGKRTLEETGGTYVEPTIFDGVTNAMKIA 398 + + +EA GA+++ G T E G +++P I +T M Sbjct: 298 AGYACMARPDLAMELYEQVEASIQKGAEVILEG--TKPEKGKAFIKPYILGKLTPDMPAY 355 Query: 399 KEEIFGPVLSVITFDSAEEAVAIANDTIYGLAAAVWTADISKAHLTAKALRAGSVWVNQY 458 +EE+FGPV SV + +EA+AIAND+ +GL A++WT D KA + ++ + +G+V++N Sbjct: 356 REELFGPVASVFKANDVDEAIAIANDSAFGLGASLWTQDPQKADILSRKIESGAVFINSM 415 Query: 459 DGGDMTAPFGGFKQSGNGRDKSLHAFDKYTELKATWI 495 + PFGG K+SG GR+ + + ++ +K ++ Sbjct: 416 VASNPYLPFGGIKKSGYGRELAENGIKEFMNIKTVYL 452 Lambda K H 0.316 0.132 0.386 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: 478 Number of extensions: 18 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: 497 Length of database: 453 Length adjustment: 33 Effective length of query: 464 Effective length of database: 420 Effective search space: 194880 Effective search space used: 194880 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 (21.6 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