Align Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial; Beta-alanine-pyruvate aminotransferase 1; EC 2.6.1.44 (characterized)
to candidate GFF179 PS417_00900 4-aminobutyrate aminotransferase
Query= SwissProt::Q940M2 (476 letters) >lcl|FitnessBrowser__WCS417:GFF179 PS417_00900 4-aminobutyrate aminotransferase Length = 425 Score = 194 bits (494), Expect = 4e-54 Identities = 125/391 (31%), Positives = 188/391 (48%), Gaps = 8/391 (2%) Query: 78 PLNIVEGKMQYLYDESGRRYLDAFAGIVTVSCGHCHPDILNAITEQSKLLQHAT-TIYLH 136 P+ K + D GR ++D GI ++ GH HP I+ A+TEQ L H + + Sbjct: 25 PIFAESAKNATVTDVEGREFIDFAGGIAVLNTGHVHPKIIAAVTEQLNKLTHTCFQVLAY 84 Query: 137 HAIGDFAEALAAKMPGNL-KVVYFVNSGSEANELAMMMARLYTGSLEMISLRNAYHGGSS 195 + E + AK+PG+ K V +GSEA E A+ +AR TG +I+ AYHG + Sbjct: 85 EPYVELCEKINAKVPGDFAKKTLLVTTGSEAVENAVKIARAATGRAGVIAFTGAYHGRTM 144 Query: 196 NTIGLTAL---NTWKYPLPQGEIHHVVNPDPYRGVFGSDGSLYAKDVHDHIEYGTSGKVA 252 T+GLT + L G + + P+ GV SD A +A Sbjct: 145 MTLGLTGKVVPYSAGMGLMPGGVFRALFPNELHGV--SDDDAIASIERIFKNDAEPRDIA 202 Query: 253 GFIAETIQGVGGAVELAPGYLKSVYEIVRNAGGVCIADEVQTGFGRTGSHYWGFQTQDVV 312 I E +QG GG ++K + E+ G + IADEVQTG GRTG+ ++ + V Sbjct: 203 AIIIEPVQGEGGFYVAPKSFMKRLRELCDKHGILLIADEVQTGAGRTGT-FFAMEQMGVA 261 Query: 313 PDIVTMAKGIGNGLPLGAVVTTPEIASVLASKILFNTFGGNPVCSAGGLAVLNVIDKEKR 372 D+ T AK I G PL V E +A L T+ G+P+ A LAV+ V ++E Sbjct: 262 ADLTTFAKSIAGGFPLAGVCGKAEYMDAIAPGGLGGTYAGSPIACAAALAVMEVFEEEHL 321 Query: 373 QEHCAEVGSHLIQRLKDVQKRHDIIGDVRGRGLMVGIELVSDRKDKTPAKAETSVLFEQL 432 + C VG L+ LK +Q ++ +IG+VR G M+ +EL D P A + + + Sbjct: 322 LDRCKAVGERLVTGLKAIQAKYPVIGEVRALGAMIAVELFDDGDTHKPNAAAVASVVAKA 381 Query: 433 RELGILVGKGGLHGNVFRIKPPMCFTKDDAD 463 RE G+++ G +GNV R+ P+ + D Sbjct: 382 REKGLILLSCGTYGNVLRVLVPLTSPDEQLD 412 Lambda K H 0.320 0.138 0.412 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: 31 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: 476 Length of database: 425 Length adjustment: 33 Effective length of query: 443 Effective length of database: 392 Effective search space: 173656 Effective search space used: 173656 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