Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate GFF3650 PGA1_262p00540 succinate-semialdehyde dehdyrogenase GabD
Query= BRENDA::A6T8Z5 (462 letters) >FitnessBrowser__Phaeo:GFF3650 Length = 459 Score = 375 bits (963), Expect = e-108 Identities = 200/449 (44%), Positives = 282/449 (62%), Gaps = 2/449 (0%) Query: 11 SVNPTTGEVVSSLPWASEREVDAAITLAAAGYRQWRQTPLADRADALRRIGAALRARGEE 70 +VNPTTG+ + + S + ++ A+ + WR T + DRA+ ++ IGAALR R +E Sbjct: 7 TVNPTTGKTLDTYNVLSGKALEDAVQRCHNAFLDWRLTSVEDRANTIKAIGAALRDRKDE 66 Query: 71 VAQMITLEMGKPIAQARGEVAKSANLCDWYAEHGPAMLATEATLVENNQ-AVIEYRPLGA 129 +A+++T EMGK + Q+ E+ A +CD+ A PA A E +E + I Y P+G Sbjct: 67 LAELMTKEMGKLLKQSHQEIDLCAAICDYSAAEAPAAFAPEERDIEGGEKGHIFYSPIGV 126 Query: 130 ILAVMPWNFPVWQVMRGAVPILLAGNSYLLKHAPNVMGSARLLGEIFAAAGLPDGVFGWV 189 + + PWNFP +QV+R ++ L+AGN LLKHA NV GS ++L EI+ AAGLP G+F + Sbjct: 127 VYGIQPWNFPAYQVVRYSIASLIAGNGVLLKHASNVTGSGQMLQEIYEAAGLPKGLFQAL 186 Query: 190 NATNDGVSQIINDDRIAAVTVTGSVRAGKAIGAQAGAALKKCVLELGGSDPFIVLNDADL 249 ++D +I+ D + VT+TGS AG+ +GA+A A+KK VLELG +D +IVL DAD+ Sbjct: 187 VISHDQSDTLISHDLVRGVTLTGSDGAGRKVGAKAAEAVKKTVLELGSNDAYIVLEDADI 246 Query: 250 DEAVKAAVTGRYQNSGQVCAASKRFILEAGIAEAFTRKFVDAVAALKMGDPRDEQNYVGP 309 D AV+ VTGR N+G+ C A+KRFI+ I F +V A+ + +GDP E +GP Sbjct: 247 DAAVQTCVTGRTYNNGETCIAAKRFIVVDAIYNQFRDAYVAAMKRVTLGDPMGEDADIGP 306 Query: 310 MARFDLRDELHQQVTATLDEGATLLLGAEKIEGAGNYYAPTVLGNVTAGMTGFRQELFGP 369 MAR DLRD+LHQQV +L+ GA LL G E + G +Y TVL NV G + ELFGP Sbjct: 307 MARKDLRDDLHQQVKDSLEGGAKLLCGGEMPDTDGFFYPATVLENVAPGQPAYDDELFGP 366 Query: 370 VATLTTARDADHALALANDSEFGLSATVYTTDEAQAQRFARE-LECGGVFLNGYCASDAR 428 VA L A+DAD A+ +ANDS FGL + T D +A AR+ + G VF+NG+ + Sbjct: 367 VAALIRAQDADDAMRIANDSRFGLGGGIMTKDTEKALALARDYFDTGMVFINGFGLAIPN 426 Query: 429 VAFGGVKKSGFGRELSHFGLHEFCNAQTV 457 + FGGVK SG+GRE FG+ EF N ++V Sbjct: 427 MPFGGVKDSGYGREHGGFGMKEFVNVKSV 455 Lambda K H 0.319 0.133 0.392 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: 505 Number of extensions: 24 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: 462 Length of database: 459 Length adjustment: 33 Effective length of query: 429 Effective length of database: 426 Effective search space: 182754 Effective search space used: 182754 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: 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