Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_013419913.1 RVAN_RS11630 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-15203 (503 letters) >NCBI__GCF_000166055.1:WP_013419913.1 Length = 517 Score = 197 bits (502), Expect = 6e-55 Identities = 152/484 (31%), Positives = 235/484 (48%), Gaps = 26/484 (5%) Query: 24 EVTNPATGQVTGQVALASQADVDSAVAAAQAAFPAWSDTPPIRRARVMFKFLELLNAHKD 83 E P TG++ G+V L AD+++AV AA AAF AW P R ++ F E L A+K Sbjct: 34 EAKTPITGEIIGRVRLGGAADMNAAVDAAHAAFLAWRSVPAPVRGELVRLFGEELRANKP 93 Query: 84 ELAEAITREHGKVFTDAQGEVARGIDIVEFACGIPQLLKGDYTEQVSTGIDNWTTRQPLG 143 L +T E GK+ ++ GEV IDI +FA G+ + L G T PLG Sbjct: 94 ALGRLVTIETGKIVSEGLGEVQEMIDICDFAVGLSRQLYGLTIASERADHRMMETWHPLG 153 Query: 144 VVAGITPFNFPVMVPMWMFPLAIAAGNSFVLKPSPLDPSASLMMADLLKQAGL------- 196 VV I+ FNFPV V W LA+ GN+ V KPS P +L + ++A Sbjct: 154 VVGIISAFNFPVAVWAWNASLALVCGNACVWKPSEKTPLTALATQAIFERAVARYRKAGH 213 Query: 197 --PDGVFNVVQGDKDSVEALIDHPDVKALSFVGSTPIANLIYER-GARSGKRIQALGGAK 253 PDG+ VV G +++ EAL+D+P V +S GST + + R +R + I LGG Sbjct: 214 IAPDGLSAVVIGAREAGEALVDNPRVPLVSATGSTAMGRAVGPRLASRFARAILELGG-N 272 Query: 254 NHMVVMPDANLDKAVDALIGAAYGSAGERCMAISVAVLVGDVADKIVPRLAERARDLKIK 313 N +V P A++D ++ A+ AA G+AG+RC ++ + V K+VPRL + +K+ Sbjct: 273 NAAIVCPTADIDLSLRAVAFAAMGTAGQRCTSLRRLFVHNSVYHKLVPRLKQAYATVKVG 332 Query: 314 NGLELDAEMGPIVTSQAHQRITGYIEKGVAEGAEMVVDGRDFDSSVTGEGCADGFWMGGT 373 N L+ +GP++ A+ + E+ A G + G + V EG G ++ T Sbjct: 333 NPLDDGTLVGPLIDEAAYAGMYKAFEEAKASGGSLFTGGERIRAGVP-EG---GVYVQPT 388 Query: 374 LFDHVTPEMTIYREEIFGPVLACVRVPDVATAIQLINDHEFGNGVSCFTESGSVAREF-- 431 L + + ++ +E F P+L +R ++ AI+L N+ G S FT A F Sbjct: 389 LIE-MPEQVGPVLKETFAPILYVIRYNELEEAIRLNNEVPQGLSSSIFTNDLREAERFLS 447 Query: 432 GRRIQVGMVGINVPIPVPMAWHGFGGWKRSMFGDTHAYGEEGVRFYTKQKSIMQRWSDSI 491 R G+ +N+ FGG K + G G + + Y M+R +++I Sbjct: 448 ARGSDCGIANVNIGPSGAEIGGAFGGEKET--GGGREAGSDSWKAY------MRRATNTI 499 Query: 492 DAGA 495 + G+ Sbjct: 500 NYGS 503 Lambda K H 0.319 0.136 0.406 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: 617 Number of extensions: 26 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: 503 Length of database: 517 Length adjustment: 34 Effective length of query: 469 Effective length of database: 483 Effective search space: 226527 Effective search space used: 226527 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 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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