Align Alanine--glyoxylate aminotransferase 2 homolog 2, mitochondrial; Beta-alanine-pyruvate aminotransferase 2; EC 2.6.1.44 (characterized)
to candidate Pf1N1B4_2980 Acetylornithine aminotransferase (EC 2.6.1.11)
Query= SwissProt::Q94AL9 (477 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_2980 Length = 391 Score = 194 bits (493), Expect = 4e-54 Identities = 132/395 (33%), Positives = 202/395 (51%), Gaps = 40/395 (10%) Query: 91 LFDESGRRYLDAFAGIAVVNCGHCHPDVVEPVINQIKRLQHPTVLYLNHAIADFSEALAS 150 L+D++GR YLDA AG+AV N GH HP +V + Q L H + LY D+ + LA Sbjct: 25 LWDQAGREYLDAVAGVAVTNVGHSHPRIVAAISEQAGLLLHTSNLYS----IDWQQRLAR 80 Query: 151 KLP--GDLKVVFFTNSGTEANELALMMAKLY---TGCQD--IVAVRNGYHGNAAATMGAT 203 KL + FF NSG EANE AL +A+LY G + +V + N +HG T+ A+ Sbjct: 81 KLVRLSGMDRAFFNNSGAEANETALKLARLYGWHKGIEQPLVVVMENAFHGRTLGTLSAS 140 Query: 204 GQSMWKFNVVQNSVHHALNPDPYRGVFGSDGEKYAKDLQDL--IQYGTTGHIAGFICEAI 261 + + L D + FG DL L +Q I + E + Sbjct: 141 DGPAVRLGF------NELPGDFIKVPFG--------DLAALEAVQQAHGPRIVAILMEPV 186 Query: 262 QGVGGIVELAPGYLSAAYDTVKKAGGLFIADEVQSGFARTGNFWGFEAHNVVPDIVTMAK 321 QG G+ PGYL A + + L + DE+Q+G RTG ++ F+ +VPD++T+AK Sbjct: 187 QGESGVQVAPPGYLKAVRELCNRRAWLLMLDEIQTGIGRTGQWFAFQHEGIVPDVMTLAK 246 Query: 322 GIGNGFPLGAVVTTPEIAGVLTRRSYFNTFGGNSVSTTAGLAVLNVIEKEKLQENAAMVG 381 G+GNG P+GA + + A + T S+ +TFGGN ++ G VL +IE++ L ENA + G Sbjct: 247 GLGNGIPIGACLARGKAADLFTPGSHGSTFGGNPLACRVGCTVLEIIEEQGLLENARLQG 306 Query: 382 SYLKEKL-TQLKEKHEIIGDVRGRGLMLGVELVSDRKLKTPATAETLHIMDQMKELGVLI 440 L +L +L + ++ +RG+GLM+G+E LK P TL ++ G+LI Sbjct: 307 ERLLARLRIELADDPNVLA-IRGQGLMIGIE------LKQPIRDLTL---IAARDHGLLI 356 Query: 441 GKGGYFGNVFRITPPLCFTKDDADFLVEAMDYSMS 475 G R+ PPL + + + +V + ++S Sbjct: 357 NVTR--GKTIRLLPPLTIDEREVEMIVRGVGRAVS 389 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: 424 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: 477 Length of database: 391 Length adjustment: 32 Effective length of query: 445 Effective length of database: 359 Effective search space: 159755 Effective search space used: 159755 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