Align gamma-glutamylputrescine oxidase (EC 1.4.3.-) (characterized)
to candidate BPHYT_RS23125 BPHYT_RS23125 FAD-dependent oxidoreductase
Query= reanno::pseudo5_N2C3_1:AO356_21495 (427 letters) >lcl|FitnessBrowser__BFirm:BPHYT_RS23125 BPHYT_RS23125 FAD-dependent oxidoreductase Length = 430 Score = 360 bits (924), Expect = e-104 Identities = 193/425 (45%), Positives = 261/425 (61%), Gaps = 4/425 (0%) Query: 2 ANTPYPESYYAASANPVPPRPALQDDVETDVCVIGAGYTGLSSALFLLENGFKVTVLEAA 61 +N P+ SYYAA+AN PAL + + DVCVIGAG TG+S+AL L E G V VLEA+ Sbjct: 5 SNQPHVASYYAATANDSTRHPALDETISVDVCVIGAGLTGISTALNLAERGHSVAVLEAS 64 Query: 62 KVGFGASGRNGGQIVNSYSRDIDVIERSVGPQQAQLLGNMAFEGGRIIRERVAKYQIQCD 121 KVG+ ASGRNGGQ++ ++ DID + + + + +M E I++ERVAK+QI CD Sbjct: 65 KVGWAASGRNGGQLIGGFACDIDTFAKYLPADDVKRVWDMGIETLDIVKERVAKHQIDCD 124 Query: 122 LKDGGVFAALTAKQMGHLESQK-RLWERFGHTQLELLDQRRIREVVACEEYVGGMLDMSG 180 L G + AA + L+ + RFG+ +L +D + V + Y+GG+ D Sbjct: 125 LTIGYLTAANKPRDTDALQKWRDEAQRRFGYDRLSYVDADGVGNYVQSQRYLGGLFDADS 184 Query: 181 GHIHPLNLALGEAAAVESLGGVIYEQS--PAVRIERGASPVVHTPQGKVRAKFIIVAGNA 238 GH+HPLN LG A A G I+E S A+R E G V T +G+V+A+F+++A N Sbjct: 185 GHLHPLNYTLGLARAAREAGVQIFEDSCVTALREEDGRH-VAETARGRVQARFVVLACNT 243 Query: 239 YLGNLVPELAAKSMPCGTQVIATEPLGDELAHSLLPQDYCVEDCNYLLDYYRLTGDKRLI 298 YLG L P++A K MP GT VIATEPL + A +L+P V D ++LDY+R D RL+ Sbjct: 244 YLGQLAPDVANKIMPVGTYVIATEPLDPDRAEALMPAKAAVCDSRFVLDYFRPAPDHRLL 303 Query: 299 FGGGVVYGARDPANIEAIIRPKMLKAFPQLKDVKIDYAWTGNFLLTLSRLPQVGRLGDNI 358 +GG V Y P N+ +R MLK FPQL DVKIDYAW G +T++R P GRL + Sbjct: 304 WGGKVSYSKLAPRNLGEAMRRDMLKTFPQLDDVKIDYAWGGFVDITMNRAPHFGRLSPTV 363 Query: 359 YYSQGCSGHGVTYTHLAGKVLAEALRGQAERFDAFADLPHYPFPGGQLLRTPFAAMGAWY 418 Y++QG SGHGV T LAGK++AEA+ GQA RFD F + H FPGG LRTP + + Sbjct: 364 YFAQGFSGHGVNTTGLAGKLIAEAIDGQASRFDLFGKIRHRDFPGGATLRTPALVLAMAW 423 Query: 419 YGLRD 423 Y ++D Sbjct: 424 YRMKD 428 Lambda K H 0.320 0.139 0.421 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: 546 Number of extensions: 21 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: 427 Length of database: 430 Length adjustment: 32 Effective length of query: 395 Effective length of database: 398 Effective search space: 157210 Effective search space used: 157210 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