Align Alanine--glyoxylate aminotransferase 2 homolog 2, mitochondrial; Beta-alanine-pyruvate aminotransferase 2; EC 2.6.1.44 (characterized)
to candidate 200454 SO1276 4-aminobutyrate aminotransferase (NCBI ptt file)
Query= SwissProt::Q94AL9 (477 letters) >FitnessBrowser__MR1:200454 Length = 425 Score = 195 bits (496), Expect = 2e-54 Identities = 128/380 (33%), Positives = 185/380 (48%), Gaps = 12/380 (3%) Query: 91 LFDESGRRYLDAFAGIAVVNCGHCHPDVVEPVINQIKRLQHPTVLYLNH-AIADFSEALA 149 ++D GR ++D GIAV+N GH HP V V Q++ H + L + + E L Sbjct: 36 VWDVEGREFIDFAGGIAVLNTGHLHPKVKAAVAAQLEDFSHTCFMVLGYESYIQVCEKLN 95 Query: 150 SKLPGDL--KVVFFTNSGTEANELALMMAKLYTGCQDIVAVRNGYHGNAAATMGATGQSM 207 +PGD K FT SG+EA E A+ +A+ YT ++A +GYHG A + TG+ Sbjct: 96 QLVPGDFAKKTALFT-SGSEAVENAVKVARAYTKRAGVIAFTSGYHGRTMAALALTGKVA 154 Query: 208 ---WKFNVVQNSVHHALNPDPYRGVFGSDGEKYAKDLQDLIQYGTTGHIAGFICEAIQGV 264 ++ +V A P GV SD + A + IA I E +QG Sbjct: 155 PYSKGMGLMSANVFRAEFPCALHGV--SDDDAMASIERIFKNDAEPSDIAAIILEPVQGE 212 Query: 265 GGIVELAPGYLSAAYDTVKKAGGLFIADEVQSGFARTGNFWGFEAHNVVPDIVTMAKGIG 324 GG ++P ++ + G + IADEVQ+G RTG F+ E V DI T AK I Sbjct: 213 GGFYAVSPAFMQRLRALCDREGIMLIADEVQTGAGRTGTFFAMEQMGVSADITTFAKSIA 272 Query: 325 NGFPLGAVVTTPEIAGVLTRRSYFNTFGGNSVSTTAGLAVLNVIEKEKLQENAAMVGSYL 384 GFPL + ++ + T+GGN ++ A LAVL V E+EKL E A +G + Sbjct: 273 GGFPLSGITGRAQVMDAIGPGGLGGTYGGNPLACAAALAVLEVFEEEKLLERANAIGDRI 332 Query: 385 KEKLTQLKEKHEIIGDVRGRGLMLGVELVSDRKLKTPATAETLHIMDQMKELGVLIGKGG 444 K L ++ +H I DVRG G M +EL+ D K PA I+ + + G+++ G Sbjct: 333 KSALNTMQVEHPQIADVRGLGAMNAIELMEDGK---PAPQYCAQILAEARNRGLILLSCG 389 Query: 445 YFGNVFRITPPLCFTKDDAD 464 +GNV RI PL + D Sbjct: 390 TYGNVLRILVPLTVSDTQLD 409 Lambda K H 0.320 0.136 0.403 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: 490 Number of extensions: 27 Number of successful extensions: 3 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: 477 Length of database: 425 Length adjustment: 33 Effective length of query: 444 Effective length of database: 392 Effective search space: 174048 Effective search space used: 174048 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