Align Succinylornithine transaminase; SOAT; Succinylornithine aminotransferase; EC 2.6.1.81 (characterized)
to candidate BWI76_RS24630 BWI76_RS24630 putrescine aminotransferase
Query= SwissProt::Q8ZPV2 (408 letters) >FitnessBrowser__Koxy:BWI76_RS24630 Length = 468 Score = 209 bits (532), Expect = 1e-58 Identities = 142/385 (36%), Positives = 202/385 (52%), Gaps = 23/385 (5%) Query: 33 LWDQQGKEYIDFAGGIAVNALGHAHPALREALNEQANRFWHIGNGYTNEPALRLAKKLID 92 L D QG+E+ID GG + +GH +P + A+ Q + + LAK L Sbjct: 85 LVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVENQLAKQPLHSQELLDPLRAMLAKTLAA 144 Query: 93 ATFAERV--FFCNSGAEANEAALKLARKYAHDRVGNHKSGIVAFKNAFHGRTLFTVSAGG 150 T + FF NSG E+ EAALKLA+ Y R K VA AFHG++L +SA Sbjct: 145 LTPGKLKYSFFSNSGTESVEAALKLAKAYQSPR---GKFTFVATSGAFHGKSLGALSATA 201 Query: 151 QPTYSQDFAPLPPDIRHAAYNDLNSASALID------DNTCAVIVEPVQGEGGVIPATKA 204 + T+ + F PL P RH + D+N+ L+ D+ AVI+EP+QGEGGVI Sbjct: 202 KSTFRKPFMPLLPGFRHVPFGDINAMRTLLSECKKTGDDVAAVILEPIQGEGGVILPPPG 261 Query: 205 FLQGLRELCDRHQALLIFDEVQTGVGRTGELYAYMHYGVTPDILTTAKALGGG-FPIGAM 263 +L +R+LCD ALLI DEVQTG+GRTG+++A H V PDIL AKALGGG PIGA Sbjct: 262 YLPAVRKLCDEFGALLILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGGGVMPIGAT 321 Query: 264 LTTQDYASVM--TPGTHGTTYGGNPLATAVAGKVLDIINTPEMQNGVRQRHDAFIERLNT 321 + T++ SV+ P H TT+GGNPLA A A ++++ T + Q+ D ++ Sbjct: 322 IATEEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLTQNLPAQAEQKGDMLLDGFRQ 381 Query: 322 LNVRF-GMFSEIRGLGLLLGCVLQTEFAG---KAKLIAQEAAKAGVMVLIAGGDVVRFAP 377 L + + +E+RG G+L+ G +++ Q AG + +R P Sbjct: 382 LAREYPDLVNEVRGKGMLMAIEFVDNEIGYDFASEMFRQRVLVAGT---LNNARTIRVEP 438 Query: 378 ALNVSDEEIATGLD--RFALACERL 400 L ++ E+ L R ALA R+ Sbjct: 439 PLTLTLEQCEQVLKAARLALAALRV 463 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: 514 Number of extensions: 25 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: 468 Length adjustment: 32 Effective length of query: 376 Effective length of database: 436 Effective search space: 163936 Effective search space used: 163936 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