Align aminomuconate-semialdehyde dehydrogenase (EC 1.2.1.32) (characterized)
to candidate GFF2135 PGA1_c21670 betaine aldehyde dehydrogenase BetB
Query= BRENDA::Q83XU8 (485 letters) >FitnessBrowser__Phaeo:GFF2135 Length = 485 Score = 313 bits (801), Expect = 1e-89 Identities = 173/455 (38%), Positives = 262/455 (57%), Gaps = 13/455 (2%) Query: 31 IAKVHEAGRAEVDAAVAAAQAALKGAWGRMSLAQRVEVLYAVADGINRRFDDFLAAEVED 90 IA VH A A V+ A++ A+AA K AW RM+ +R +L AD + R D E D Sbjct: 37 IATVHAATPAIVEQALSTAKAAQK-AWARMTGTERGRILRRAADIMRERNHDLSVLETYD 95 Query: 91 TGKPMSLARHVDIPRGAANFKIFADVVKNVPTEFFEMPTPDGVGAINYAVRRPVGVVGVI 150 TGKP+ D GA + F + ++ E + D V Y R +G+ I Sbjct: 96 TGKPLQETLVADATSGADALEYFGGLAASLTGEHIPLGE-DWV----YTKREALGLCVGI 150 Query: 151 CPWNLPLLLMTWKVGPALACGNTVVVKPSEETPQTAALLGEVMNTAGVPPGVYNVVHGFG 210 WN P + WK PALACGN++V KPSE TP A + E++ AG P GV+NVV G G Sbjct: 151 GAWNYPTQIACWKGAPALACGNSMVFKPSETTPLCALKVAEILIEAGAPAGVFNVVQGMG 210 Query: 211 PNSTGEFLTSHPDVNAITFTGETGTGEAIMKAAADGARPVSLELGGKNAAIVFADCDLDK 270 G L + P V+ ++ TG TG+ + AAA+G + V++ELGGK+ I+F D D+D Sbjct: 211 --EVGGALVTDPRVDKVSLTGSVPTGKKVYAAAAEGMKHVTMELGGKSPLIIFDDADIDN 268 Query: 271 AIEGTLRSCFANCGQVCLGTERVYVERPIFDRFVSRLKKGAEGMQLGRPEDLATGMGPLI 330 A+ G + F + GQVC RV+V++ I ++F++RL + LG P D AT GP++ Sbjct: 269 AVGGAINGNFYSSGQVCSNGTRVFVQKGIKEKFLARLAERTGNAILGDPMDEATSFGPMV 328 Query: 331 SQEHREKVLSYYKKAVEAGATVVTGGGVPEMPEALKGGAWVQPTIWTGLGDDSVVAREEI 390 ++ VL Y +K E GA ++ GG +M G +++PT++ + DD +AREEI Sbjct: 329 TENQMNIVLGYIEKGKEEGARLICGGRRADM-----DGYFIEPTVFADVTDDMTIAREEI 383 Query: 391 FGPCALVMPFDSEEEVIRRANDNDYGLARRIWTTNLSRAHRVAGAIEVGIAWVNSWFLRD 450 FGP V+ FD+EEEV+ RAND ++GL+ ++T + +RAHRV G +E G ++NS+ Sbjct: 384 FGPVMSVLDFDTEEEVVARANDTEFGLSAGVFTKDFTRAHRVIGNLEAGSCFINSYNDAP 443 Query: 451 LRTAFGGSKQSGIGREGGVHSLEFYTELKNVCIKL 485 + FGG K SG+GRE +++ ++++K+V +++ Sbjct: 444 VEAPFGGVKASGVGRENSKEAIKHFSQVKSVYVRM 478 Lambda K H 0.318 0.135 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: 578 Number of extensions: 29 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: 485 Length of database: 485 Length adjustment: 34 Effective length of query: 451 Effective length of database: 451 Effective search space: 203401 Effective search space used: 203401 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 (21.7 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