Align Gamma-glutamylputrescine oxidoreductase; Gamma-Glu-Put oxidase; Gamma-glutamylputrescine oxidase; EC 1.4.3.- (characterized)
to candidate AO356_25540 AO356_25540 FAD-dependent oxidoreductase
Query= SwissProt::P37906 (426 letters) >FitnessBrowser__pseudo5_N2C3_1:AO356_25540 Length = 432 Score = 252 bits (643), Expect = 2e-71 Identities = 142/420 (33%), Positives = 239/420 (56%), Gaps = 5/420 (1%) Query: 5 TSSYYAASANKYAPFDTLNESITCDVCVVGGGYTGLSSALHLAEAGF-DVVVLEASRIGF 63 T +YY A+ F TL + + DV V+GGG++G+++AL LAE G ++VVLEA +GF Sbjct: 6 TPTYYTATKKYNLSFPTLEQDVEADVVVIGGGFSGINTALELAEKGITNIVVLEARYLGF 65 Query: 64 GASGRNGGQLVNSYSRDIDVIEKSYGMDTARMLGSMMFEGGEIIRERIKRYQIDCDYRPG 123 G +GRNGGQ++ D++ I+K G D R + + G +II++RI +Y ID D+ G Sbjct: 66 GGTGRNGGQIMAGIGHDLEKIKKDVGEDGLRQVFEISDLGADIIKDRIAKYAIDADFCHG 125 Query: 124 GLFVAMNDKQLATLEEQKENWERYGNK-QLELLDANAIRREVASDRYTGALLDHSGGHIH 182 ++ N +Q TL +++++ +K ++ L + +++ + S Y+ ALL GGH+H Sbjct: 126 YGYMGFNARQEKTLRAWEKDFKSINSKHEIRFLGGSDVQQIIGSKAYSSALLHMGGGHVH 185 Query: 183 PLNLAIGEADAIRLNGGRVYELSAVTQIQHTTPAVVRTAKGQVTAKYVIVAGNAYLGDKV 242 LNL +GEA A+ +G R++E S ++ + VRT +G V A ++ A +++L +K+ Sbjct: 186 SLNLLLGEAKAVVSHGVRIFENSPALEVSYGERITVRTGRGSVRASKLLWACDSFL-NKL 244 Query: 243 EPELAKRSMPCGTQVITTERLSEDLARSLIPKNYCVEDCNYLLDYYRLTADNRLLYGGGV 302 EPEL + ++ + TE LS++L + + P D ++DYYR+T +NRLL+G Sbjct: 245 EPELHRSTINTYAFQMMTEPLSDELIQRISPIRGAYSDIRPVIDYYRVTNENRLLFGAAT 304 Query: 303 VYGARDPDDVERLVVPKLLKTFPQLKGVKIDYRWTGNFLLTLSRMPQFGRLD--TNIYYM 360 P D++ +LK FP LK VKID W G + + PQ G L +N +++ Sbjct: 305 PLVEHIPQDLKAWNRRLMLKIFPYLKDVKIDLAWGGPMACSPNLFPQIGTLPGRSNAFFV 364 Query: 361 QGYSGHGVTCTHLAGRLIAELLRGDAERFDAFANLPHYPFPGGRTLRVPFTAMGAAYYSL 420 QGYSG GVT +H+ +++AE + + R+D +++ G +R G +++ L Sbjct: 365 QGYSGFGVTPSHIICKVLAEGMSEGSARYDLVSSIHRPTIIGKDAIRPLLLTAGKSWHQL 424 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: 496 Number of extensions: 24 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: 426 Length of database: 432 Length adjustment: 32 Effective length of query: 394 Effective length of database: 400 Effective search space: 157600 Effective search space used: 157600 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