Align Gamma-glutamylputrescine oxidoreductase; Gamma-Glu-Put oxidase; Gamma-glutamylputrescine oxidase; EC 1.4.3.- (characterized)
to candidate 7025953 Shewana3_3101 FAD dependent oxidoreductase (RefSeq)
Query= SwissProt::P37906 (426 letters) >FitnessBrowser__ANA3:7025953 Length = 435 Score = 347 bits (891), Expect = e-100 Identities = 175/423 (41%), Positives = 259/423 (61%), Gaps = 3/423 (0%) Query: 3 EHTSSYYAASANKYAPFDTLNESITCDVCVVGGGYTGLSSALHLAEAGFDVVVLEASRIG 62 ++ SYY +A + L ++ DVC++GGG++G+++A+ L + G +VV+LEA RIG Sbjct: 11 QYPQSYYVDTAKEIYAHPQLEGKVSTDVCIIGGGFSGINTAIELRQKGLNVVLLEAKRIG 70 Query: 63 FGASGRNGGQLVNSYSRDIDVIEKSYGMDTARMLGSMMFEGGEIIRERIKRYQIDCDYRP 122 +GASGRNGG+L+ D G + + M FE EI+R RI+ + IDCD + Sbjct: 71 WGASGRNGGELIRGIGHDPAQFINEIGQEGVSAIEQMGFEAVEIVRNRIQTHHIDCDLQM 130 Query: 123 GGLFVAMNDKQLATLEEQKENWERYGNK-QLELLDANAIRREVASDRYTGALLDHSGGHI 181 G +A+ + + LE++ ++ +R G + +++LL + + + SD Y GAL+D GH+ Sbjct: 131 GYCDLAVKPRHMLELEQEFDHLKRLGYQHEIKLLTQSQLGEVIGSDFYQGALVDMGSGHL 190 Query: 182 HPLNLAIGEADAIRLNGGRVYELSAVTQIQHTTPAVVRTAKGQVTAKYVIVAGNAYLGDK 241 HPLNLA+GEA R G +++E SA +I V TAKG+VT +YV++AGNAY+G K Sbjct: 191 HPLNLALGEARVARDLGAQLFEYSAAEKIIPRDKPRVLTAKGEVTCQYVVLAGNAYIGHK 250 Query: 242 VEPELAKRSMPCGTQVITTERLSEDLARSLIPKNYCVEDCNYLLDYYRLTADNRLLYGGG 301 + + + +P G+ ++ TE L+E +S+IP+N D LDY+ L+AD RLL+GG Sbjct: 251 LNSYIGGKVLPAGSYLLATEPLTEVQCQSIIPQNMAFADMRIALDYFHLSADRRLLFGGL 310 Query: 302 VVYGARDPDDVERLVVPKLLKTFPQLKGVKIDYRWTGNFLLTLSRMPQFGRLD--TNIYY 359 Y +DP D+E + P L K FPQLKGV+IDY W G + +RMPQ GRL +NI+Y Sbjct: 311 CTYSGKDPKDIEAALRPNLEKVFPQLKGVRIDYEWGGMIGIGANRMPQIGRLPDASNIFY 370 Query: 360 MQGYSGHGVTCTHLAGRLIAELLRGDAERFDAFANLPHYPFPGGRTLRVPFTAMGAAYYS 419 Q Y+GHGV TH+A +L+AE + A FD FA + H FPGG T R P A G Y+ Sbjct: 371 AQAYAGHGVNATHMAAKLLAEAICQQAGYFDVFAKIKHMTFPGGPTFRSPMLAAGMLYHR 430 Query: 420 LRD 422 +D Sbjct: 431 FKD 433 Lambda K H 0.320 0.138 0.411 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: 521 Number of extensions: 26 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: 426 Length of database: 435 Length adjustment: 32 Effective length of query: 394 Effective length of database: 403 Effective search space: 158782 Effective search space used: 158782 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