Align Gamma-glutamylputrescine oxidoreductase; Gamma-Glu-Put oxidase; Gamma-glutamylputrescine oxidase; EC 1.4.3.- (characterized)
to candidate 5209538 Shew_2005 FAD dependent oxidoreductase (RefSeq)
Query= SwissProt::P37906 (426 letters) >FitnessBrowser__PV4:5209538 Length = 443 Score = 163 bits (413), Expect = 9e-45 Identities = 134/430 (31%), Positives = 211/430 (49%), Gaps = 20/430 (4%) Query: 7 SYYAASANKYAPFDTLNESITCDVCVVGGGYTGLSSALHLA-EAGFDVVVLEASRIGFGA 65 SY+A + ++ A L+ + DV +VGGG+TGL +A +LA E + VLEA++IGFGA Sbjct: 19 SYWATTVSRPARLPALSGRMQTDVAIVGGGFTGLLTAYYLASEFNIEARVLEANQIGFGA 78 Query: 66 SGRNGGQLVNSYSR-DIDVIEKSYGMDTARMLGSMMFEGGEIIRERIKRYQIDCDYRPGG 124 SGRN G ++ R + K +GM+T + + + + I++++I CD +P G Sbjct: 79 SGRNAGFVLKGSGRMGYSQMAKKWGMETTKGIYGEFTSAVRRVEQLIEQHEIACDAQPKG 138 Query: 125 -LFVAMNDKQLATLEEQKENWERYGNKQLELLDANAIRREVASDRYT-GALLDHSGGHIH 182 L +A N K +TL+ + + + L + ++ + GAL + G ++ Sbjct: 139 YLKIAHNAKAYSTLKGAADFIAEHLGDDAQFLTPSELKESYMDNHQAYGALRLNDGFGVN 198 Query: 183 PLNLAIGEADAIRLNGGRVYELSAVTQ-IQHTTPAVVRTAKGQVTAKYVIVAGNAYLGDK 241 PL L +G ++ G ++E S V + ++ + T KG++ AK V+ AGNAY + Sbjct: 199 PLKLCLGYKRVVQSLGVHLHEESCVREWLKEGPHHRLITDKGELIAKQVVSAGNAYTPKR 258 Query: 242 VEPELAKRSMPCGTQVITTERLSE-DLARSLIPKNYCVEDCNYLLDYYRLTADNRLLYGG 300 + R +P + +I T L++ L + + + V D L YYRL +DNRLL+GG Sbjct: 259 FNQAVDNRYLPILSNIIVTAPLTDAQLEATGLKTHQVVMDTRRLKYYYRLLSDNRLLFGG 318 Query: 301 -GVVYG--ARDPDDVERLVVPKLLKTFPQLKGVKIDYRWTGNFLLTLSRMPQFGRLDTNI 357 G + G A DP ERL + FP L V +D+ WTG L MP N+ Sbjct: 319 RGAISGADAGDPRYGERL-KSAMADCFPALAEVTVDHNWTGWIAAALDDMPHVFS-QGNM 376 Query: 358 YYMQGYSGHGVTCTHLAGRLIAELLRGDAERFDAFANLPHYPFPGGRTLRVPFTAMG-AA 416 Y GY G GV + A +A+ + G + LP Y P + +G +A Sbjct: 377 GYSLGYCGSGVAFSAQAAYRLAQHIAG-----ERLPELPLYQSPLPKFHFARLRRLGQSA 431 Query: 417 YYS---LRDR 423 YY LRDR Sbjct: 432 YYQYAWLRDR 441 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: 514 Number of extensions: 35 Number of successful extensions: 8 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: 443 Length adjustment: 32 Effective length of query: 394 Effective length of database: 411 Effective search space: 161934 Effective search space used: 161934 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