Align Succinylornithine transaminase; SOAT; Succinylornithine aminotransferase; EC 2.6.1.81 (characterized)
to candidate 3608039 Dshi_1446 aminotransferase class-III (RefSeq)
Query= SwissProt::Q8ZPV2 (408 letters) >lcl|FitnessBrowser__Dino:3608039 Dshi_1446 aminotransferase class-III (RefSeq) Length = 444 Score = 192 bits (489), Expect = 1e-53 Identities = 139/409 (33%), Positives = 202/409 (49%), Gaps = 49/409 (11%) Query: 26 VRGEGSRLWDQQGKEYIDFAGGIAVNALGHAHPALREALNEQANR--FWHIGNGYTNEPA 83 V G G + D GK Y+D +GG AV+ LGH HPA+R AL+ Q ++ F H G +T+EPA Sbjct: 17 VAGAGCYIIDADGKRYLDGSGGAAVSCLGHDHPAVRAALHAQIDKIAFAHTGF-FTSEPA 75 Query: 84 LRLAKKLIDAT--FAERVFFCNSGAEANEAALKLARKYAHDRVGNHKSGIVAFKNAFHGR 141 L LI A E+V+ + G+E+ EAALKLAR++ + + ++A + ++HG Sbjct: 76 EVLCDALIAAAPKGIEKVYLLSGGSESVEAALKLARQFFLETGEPRRHRVIARRQSYHGN 135 Query: 142 TLFTVSAGGQPTYSQDFAPLPPDI---------RHAAYNDLNSA-------------SAL 179 TL ++AGG + +APL + RH A + ++A L Sbjct: 136 TLGALAAGGNAWRREKYAPLLVETYHIDPCYAYRHQAVGESDAAYGRRAADALRTEIERL 195 Query: 180 IDDNTCAVIVEPVQGE-GGVIPATKAFLQGLRELCDRHQALLIFDEVQTGVGRTGELYAY 238 + A I EPV G G +P + + +RE+CD + LLI DEV G+GRTG L+A Sbjct: 196 GPETVMAFIAEPVVGATAGAVPPAPGYFERIREICDEYGVLLILDEVMCGMGRTGTLFAC 255 Query: 239 MHYGVTPDILTTAKALGGGF-PIGAMLTTQDYASVMTPGT----HGTTYGGNPLATAVAG 293 G++PDI+T AK LG G+ PIGAML + + G+ HG TY G+PLA A AG Sbjct: 256 EQDGISPDIVTIAKGLGAGYAPIGAMLASGRIYDAIAQGSGSFQHGHTYHGHPLAAAAAG 315 Query: 294 KVLDIINTPEMQNGVRQRHDAFIERLNTLNVRFGMFSEIRGLGLLLGCVL--------QT 345 V++ + P VR + RL + +IRG GL G L Sbjct: 316 AVVETLRAPGTMAQVRAKGATLQSRLEAALGQHSHVGDIRGRGLFRGIELVEDRDTKRPL 375 Query: 346 EFAGKAKLIAQEAAKAGVMVLIAG--------GDVVRFAPALNVSDEEI 386 + A K + AA A ++ G GD + AP + D++I Sbjct: 376 DPARKVSARIKAAAMARGLICYPGSGTIDGKHGDHILLAPPFIIEDKQI 424 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: 484 Number of extensions: 18 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: 408 Length of database: 444 Length adjustment: 32 Effective length of query: 376 Effective length of database: 412 Effective search space: 154912 Effective search space used: 154912 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 Aug 03 2021. The underlying query database was built on Aug 03 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, or see changes to Amino acid biosynthesis since the publication.
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