Align gamma-glutamylputrescine oxidase (EC 1.4.3.-) (characterized)
to candidate AO356_00055 AO356_00055 oxidoreductase
Query= reanno::pseudo5_N2C3_1:AO356_21495 (427 letters) >FitnessBrowser__pseudo5_N2C3_1:AO356_00055 Length = 433 Score = 205 bits (521), Expect = 3e-57 Identities = 141/442 (31%), Positives = 220/442 (49%), Gaps = 26/442 (5%) Query: 1 MANTPYPE---SYYAASANPVPPRPALQDDVETDVCVIGAGYTGLSSALFLLENGFKVTV 57 MA +P+ S + ++A P PAL+ D DV V+G GYTGLS+A +L + G V Sbjct: 1 MAVSPFAADIASLWQSTAVDAPSFPALEGDRSYDVVVVGGGYTGLSTAHYLAKKGLATVV 60 Query: 58 LEAAKVGFGASGRNGGQIVNSYSRDIDVIERSVGPQQAQLLGNMAFEGGRIIRERVAKYQ 117 LEA+++G+GASGRNGG + Y + + G + AQ + ++ E + E VA Y Sbjct: 61 LEASRIGWGASGRNGGVVSAKYRISLSKVAARYGLEMAQTMRRLSLESVEHLEELVAVYS 120 Query: 118 IQCD--LKDGGVFAALTAKQMGH-LESQKRLWERFGHTQLELLDQRRIREVVACEEYVGG 174 ++ + G + A + + + + L E G + E+L +++E ++VGG Sbjct: 121 LEAAQYRRSGSLHCAHNEATLDYCVREAQWLHEHLGDSSFEVLCAGQMQEETGSGDFVGG 180 Query: 175 MLDMSGGHIHPLNLALGEAAAVESLGGVIYEQSPAVRIER-GASPVVHTPQGKVRAKFII 233 +LD GG +HPLN G A V + G I+E +P + I R G V TP G VRAK ++ Sbjct: 181 VLDRGGGLLHPLNFVRGLADGVSAAGVSIHEGAPVMGIRRMGTGVRVETPTGTVRAKQVV 240 Query: 234 VAGNAYLGNLVPELA---AKSMPCGTQVIATEPL-GDELAHSLLPQDYCVEDCNYLLDYY 289 +A N Y +L P A +P + ++ATEPL G +L LL + ++ ++ Sbjct: 241 LATNGY-SSLTPATAPVRKSVVPFRSAMLATEPLTGPQL--ELLRHGRSYTETRRMMRWF 297 Query: 290 RLTGDKRLIFGGGVVYGARDPANIEAIIRPKMLKAFPQLKDVKIDYAWTGNFLLTLSRLP 349 R+ D RL++GG +G D + M+K FP L I + W+G LT+ +P Sbjct: 298 RMAED-RLLYGGRGAFGTDDSEAAFNALHEAMVKQFPLLARATITHRWSGLVALTIDSVP 356 Query: 350 QVGRLGDNIYYSQGCSGHGVTYTHLAGKVLAEALRGQAERF-----DAFADLPHYPFPGG 404 VGR+ D + Y+ G +G GV + GK +A+ + G+ D +P Y Sbjct: 357 HVGRIDDRVVYAMGYNGTGVAMSSYIGKHVADVIVGRKPELGLMWADKIRRIPFYS---- 412 Query: 405 QLLRTPFAAMGAWYYGLRDKLG 426 LR P M A +Y D +G Sbjct: 413 --LRVPVVRMVAGWYQFLDAIG 432 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: 458 Number of extensions: 20 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: 427 Length of database: 433 Length adjustment: 32 Effective length of query: 395 Effective length of database: 401 Effective search space: 158395 Effective search space used: 158395 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