Align gamma-glutamylputrescine oxidase (EC 1.4.3.-) (characterized)
to candidate Pf1N1B4_4824 Gamma-glutamyl-putrescine oxidase (EC1.4.3.-)
Query= reanno::pseudo5_N2C3_1:AO356_21495 (427 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4824 Length = 433 Score = 359 bits (921), Expect = e-103 Identities = 184/426 (43%), Positives = 265/426 (62%), Gaps = 5/426 (1%) Query: 6 YPESYYAASANPVPPRPALQDDVETDVCVIGAGYTGLSSALFLLENGFKVTVLEAAKVGF 65 + SYYAASAN + P P L D+ DVCV+G G+TG+++A+ L + G V +LE ++G+ Sbjct: 8 HAHSYYAASANSLAPYPVLASDLTADVCVVGGGFTGVNTAIELAQRGLSVILLEGRRIGW 67 Query: 66 GASGRNGGQIVNSYSRDIDVIERSVGPQQAQLLGNMAFEGGRIIRERVAKYQIQCDLKDG 125 GASGRNGGQ++ D+ R VG + L E ++ R+ ++ I CDL+ G Sbjct: 68 GASGRNGGQLIRGIGHDVSGFARYVGQDGVRYLERAGIESVELVGNRIREHGIDCDLRWG 127 Query: 126 GVFAALTAKQMGHLESQKRLWERFGHT-QLELLDQRRIRE-VVACEEYVGGMLDMSGGHI 183 A T Q +++ + G++ + L+ +IR+ VV + Y GG++DM GH+ Sbjct: 128 FCELANTPAQYEAFKAELQNLAELGYSHETRLVGPEQIRQQVVGSDVYAGGLIDMGSGHL 187 Query: 184 HPLNLALGEAAAVESLGGVIYEQSPAVRIERGASPVVHTPQGKVRAKFIIVAGNAYLGNL 243 HPLNL LGEA ESLG I+EQSP + + G++ + G VRA +++A NA+L L Sbjct: 188 HPLNLVLGEARVAESLGVRIFEQSPVLELIHGSTVQIRCAGGTVRAGSLVLACNAHLEEL 247 Query: 244 VPELAAKSMPCGTQVIATEPLGDELAHSLLPQDYCVEDCNYLLDYYRLTGDKRLIFGGGV 303 P L+ K +P G+ +IATEPL E+A L+PQ+ + D LDYYRL+ D+RL+FGG Sbjct: 248 EPHLSGKVLPAGSYIIATEPLAPEVAAQLIPQNLALCDQKVGLDYYRLSADRRLLFGGAC 307 Query: 304 VYGARDPANIEAIIRPKMLKAFPQLKDVKIDYAWTGNFLLTLSRLPQVGRLGD--NIYYS 361 Y RDP +I A +RPKMLK FPQL DV+IDY W G +T +R PQ GRL N++Y+ Sbjct: 308 HYSGRDPGDIGAYMRPKMLKVFPQLADVRIDYQWGGMIGITANRFPQAGRLSQYPNVFYA 367 Query: 362 QGCSGHGVTYTHLAGKVLAEALR-GQAERFDAFADLPHYPFPGGQLLRTPFAAMGAWYYG 420 QG SGHG+ TH ++LAEA+ G ++ D F+ +PH FPGG+ LR+P A+G ++Y Sbjct: 368 QGYSGHGLNVTHWCARLLAEAIHAGHSKGLDVFSAVPHMTFPGGKALRSPLLALGMFWYR 427 Query: 421 LRDKLG 426 LR+ LG Sbjct: 428 LRELLG 433 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: 639 Number of extensions: 33 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: 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