Align Succinylornithine transaminase; SOAT; Succinylornithine aminotransferase; EC 2.6.1.81 (characterized)
to candidate 17148 b3073 putrescine:2-oxoglutaric acid aminotransferase, PLP-dependent (RefSeq)
Query= SwissProt::Q8ZPV2 (408 letters) >lcl|FitnessBrowser__Keio:17148 b3073 putrescine:2-oxoglutaric acid aminotransferase, PLP-dependent (RefSeq) Length = 459 Score = 204 bits (518), Expect = 6e-57 Identities = 138/390 (35%), Positives = 201/390 (51%), Gaps = 23/390 (5%) Query: 28 GEGSRLWDQQGKEYIDFAGGIAVNALGHAHPALREALNEQANRFWHIGNGYTNEPALRLA 87 G + L D QG+E+ID GG + +GH +P + A+ Q + + LA Sbjct: 71 GSLNTLVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLRAMLA 130 Query: 88 KKLIDATFAERV--FFCNSGAEANEAALKLARKYAHDRVGNHKSGIVAFKNAFHGRTLFT 145 K L T + FFCNSG E+ EAALKLA+ Y R K +A AFHG++L Sbjct: 131 KTLAALTPGKLKYSFFCNSGTESVEAALKLAKAYQSPR---GKFTFIATSGAFHGKSLGA 187 Query: 146 VSAGGQPTYSQDFAPLPPDIRHAAYNDLNSASALID------DNTCAVIVEPVQGEGGVI 199 +SA + T+ + F PL P RH + ++ + ++ D+ AVI+EP+QGEGGVI Sbjct: 188 LSATAKSTFRKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQGEGGVI 247 Query: 200 PATKAFLQGLRELCDRHQALLIFDEVQTGVGRTGELYAYMHYGVTPDILTTAKALGGG-F 258 +L +R+LCD AL+I DEVQTG+GRTG+++A H V PDIL AKALGGG Sbjct: 248 LPPPGYLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGGGVM 307 Query: 259 PIGAMLTTQDYASVM--TPGTHGTTYGGNPLATAVAGKVLDIINTPEMQNGVRQRHDAFI 316 PIGA + T++ SV+ P H TT+GGNPLA A A ++++ + Q+ D + Sbjct: 308 PIGATIATEEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQKGDMLL 367 Query: 317 ERLNTLNVRF-GMFSEIRGLGLLLGCVLQTEFAG---KAKLIAQEAAKAGVMVLIAGGDV 372 + L + + E RG G+L+ G +++ Q AG + Sbjct: 368 DGFRQLAREYPDLVQEARGKGMLMAIEFVDNEIGYNFASEMFRQRVLVAGT---LNNAKT 424 Query: 373 VRFAPALNVSDE--EIATGLDRFALACERL 400 +R P L ++ E E+ R ALA R+ Sbjct: 425 IRIEPPLTLTIEQCELVIKAARKALAAMRV 454 Lambda K H 0.320 0.137 0.413 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: 477 Number of extensions: 22 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: 408 Length of database: 459 Length adjustment: 32 Effective length of query: 376 Effective length of database: 427 Effective search space: 160552 Effective search space used: 160552 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