Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate GFF3555 PS417_18205 aldehyde dehydrogenase
Query= BRENDA::Q9K9B2 (515 letters) >FitnessBrowser__WCS417:GFF3555 Length = 492 Score = 243 bits (620), Expect = 1e-68 Identities = 152/444 (34%), Positives = 242/444 (54%), Gaps = 13/444 (2%) Query: 51 KIQSWNPARKDQLVGSVSKANQDLAEKAIQSADEAFQTWRNVNPEERANILVKAAAIIRR 110 ++ NP ++L+ + DL + A Q+A A W ++P +R+ L K A +I+ Sbjct: 29 RLDDRNPFNGERLLEMPLASVVDL-DDAYQAAQRAQTDWAALHPTQRSAQLEKLAQVIQD 87 Query: 111 RKHEFSAWLVHEAGKPWKEADADTAEAIDFLEYYARQMIELNRGKEILS-RPGEQNRYFY 169 R E WL+ E+G +A + ++ + A +++ G+ + S +PGEQ+ F Sbjct: 88 RSEEIIDWLIRESGSTRIKAGMEWQFTLNLVRECATLPMQVE-GRILSSYKPGEQSFVFR 146 Query: 170 TPMGVTVTISPWNFALAIMVGTAVAPIVTGNTVVLKPASTTPVVAAKFV-EVLEDAGLPK 228 P+GV ISPWNF L + + + V + GNTVVLKPAS T V + + E+AG P Sbjct: 147 EPLGVVGVISPWNFPLYLSMRSVVPALALGNTVVLKPASDTAVTGGLLIAHLFEEAGFPA 206 Query: 229 GVINYVPGSGAEVGDYLVDHPKTSLITFTGSKDVGVRLYERAAVVRPGQNHLKRVIVEMG 288 G +N V G+G+E+GD V+HP SLI+FTGS DVG R R A+ G H+KRV +E+G Sbjct: 207 GALNVVVGAGSEIGDAFVEHPIPSLISFTGSTDVG-RNVGRIAI---GGKHIKRVALELG 262 Query: 289 GKDTVVVDRDADLDLAAESILVSAFGFSGQKCSAGSRAVIHKDVYDEVLEKTVALAKNLT 348 G +VV DAD+++AA + +V F GQ C + +R ++ + +Y + V NL Sbjct: 263 GNAPLVVLDDADIEIAAHAAVVGRFLHQGQICMSVNRVIVDRSLYADFAALVVERVLNLK 322 Query: 349 VGDPTNRDNYMGPVIDEKAFEKIMSYIEIGKKEG-RLMTGGEGDSSTGFFIQPTIIADLD 407 GDP D +GPV+++ + ++ I+ ++ G + + GG+ + G + + ++ Sbjct: 323 TGDPAKPDTVIGPVVNQSQLDGLLGKIDAAERAGLKQLCGGQ---AQGLVLPAHVFGEVG 379 Query: 408 PEAVIMQEEIFGPVVAFSKANDFDHALEIANNTEYGLTGAVITRNRAHIEQAKREFHVGN 467 PE + ++E FGP++ A++ HALE+AN +EYGL+ AV TR+ A R G Sbjct: 380 PEQALARDETFGPLLPLMIAHNQAHALELANASEYGLSSAVFTRDMARGLSFARGIVAGM 439 Query: 468 LYFNRNCTGAIVGYHPFGGFKMSG 491 + N + T PFGG K SG Sbjct: 440 THIN-DITVDDQPNAPFGGEKNSG 462 Lambda K H 0.316 0.134 0.388 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: 602 Number of extensions: 33 Number of successful extensions: 5 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: 515 Length of database: 492 Length adjustment: 34 Effective length of query: 481 Effective length of database: 458 Effective search space: 220298 Effective search space used: 220298 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: 52 (24.6 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