Align Gamma-glutamylputrescine oxidoreductase; Gamma-Glu-Put oxidase; Gamma-glutamylputrescine oxidase; EC 1.4.3.- (characterized)
to candidate WP_010441035.1 G7G_RS0110025 FAD-binding oxidoreductase
Query= SwissProt::P37906 (426 letters) >NCBI__GCF_000192475.1:WP_010441035.1 Length = 423 Score = 138 bits (348), Expect = 3e-37 Identities = 113/387 (29%), Positives = 169/387 (43%), Gaps = 5/387 (1%) Query: 1 MTEHTSSYYAASANKYAPFDTLNESITCDVCVVGGGYTGLSSALHLAEAGFDVVVLEASR 60 M ++ S + + + L+ +T D+ V+GGGYTG S+AL A+AG V +LEA Sbjct: 1 MPDYDQSLWRQTCGESIKTQKLSGDVTVDIAVIGGGYTGCSAALTAAKAGASVCLLEAHE 60 Query: 61 IGFGASGRNGGQLVNSYSRDIDVIEKSYGMDTARMLGSMMFEGGEIIRERIKRYQIDCD- 119 IG G SGRN G + D I G L ++ + I ++I C+ Sbjct: 61 IGHGGSGRNVGLVNAGLWLPPDQIRSHLGQVPGNRLIDLLANAPSEVFGLIDAHEIACEP 120 Query: 120 YRPGGLFVAMNDKQLATLEEQKENWERYGNKQLELLDANAIRREVASDRYTGALLDHSGG 179 R G L A + K L + G +ELLDAN R+ S GAL D G Sbjct: 121 VRHGTLHCAHSAKGFEDLHTRHSQLSVSG-APVELLDANTSRKRTGSPAVHGALFDPRAG 179 Query: 180 HIHPLNLAIGEADAIRLNGGRVYELSAVTQI-QHTTPAVVRTAKGQVTAKYVIVAGNAYL 238 I PL +G A A + G +Y S + + Q V+ G V AK +I A NAY Sbjct: 180 TIQPLAFVVGLARAAQDAGALIYTDSPIQSLRQEAGMWVLHGENGTVRAKSIIQATNAY- 238 Query: 239 GDKVEPELAKRSMPCGTQVITTERLSEDLARSLIPKNYCVEDCNYLLDYYRLTADNRLLY 298 + + A +P T LS +L S++P+ D ++ +RL + R + Sbjct: 239 -HQGIADTAPAYVPVYYFQYATAPLSHNLRASILPEGEGCWDTGLIMTSFRLDQEGRFII 297 Query: 299 GGGVVYGARDPDDVERLVVPKLLKTFPQLKGVKIDYRWTGNFLLTLSRMPQFGRLDTNIY 358 GG + + V KL+ +PQL + W G +T +P+ ++ N Sbjct: 298 GGMGDLNSVGGFAHKAWVSRKLVVLYPQLADQPLVEGWHGRIAMTSDHIPKIIQIGPNAL 357 Query: 359 YMQGYSGHGVTCTHLAGRLIAELLRGD 385 G+SG G+ + GRL+AE L D Sbjct: 358 AAHGFSGRGIGPGTVFGRLMAESLLND 384 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: 396 Number of extensions: 22 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: 426 Length of database: 423 Length adjustment: 32 Effective length of query: 394 Effective length of database: 391 Effective search space: 154054 Effective search space used: 154054 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 24 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:
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