Align Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial; Beta-alanine-pyruvate aminotransferase 1; EC 2.6.1.44 (characterized)
to candidate RR42_RS21370 RR42_RS21370 4-aminobutyrate aminotransferase
Query= SwissProt::Q940M2 (476 letters) >FitnessBrowser__Cup4G11:RR42_RS21370 Length = 420 Score = 179 bits (453), Expect = 2e-49 Identities = 131/396 (33%), Positives = 196/396 (49%), Gaps = 26/396 (6%) Query: 89 LYDESGRRYLDAFAGIVTVSCGHCHPDILNAITEQSKLLQH-ATTIYLHHAIGDFAEALA 147 ++D G+RY+D AGI ++ GH HP ++ A+ Q + H A I + + + AE + Sbjct: 34 IWDVEGKRYIDFAAGIAVLNTGHRHPRLVEAMQRQLERFTHTAYQIVPYASYIELAERIN 93 Query: 148 AKMPGN-LKVVYFVNSGSEANELAMMMARLYTGSLEMISLRNAYHGGSSNTIGLTA-LNT 205 + PG K F +G+EA E A+ +AR TG +I+ +HG + + LT + Sbjct: 94 QRAPGRGAKKTAFFTTGAEAVENAIKIARAATGRPGVIAFSGGFHGRTMMGMALTGKVVP 153 Query: 206 WKY---PLPQGEIHHVVNPDPYRGVFGSDG-----SLYAKDVHDHIEYGTSGKVAGFIAE 257 +K P P GE+ H P GV D L+ DV +VA I E Sbjct: 154 YKVGFGPFP-GEVFHAPYPCALHGVSVEDALKAMEHLFKADVDPK-------RVAAIIFE 205 Query: 258 TIQGVGGAVELAPGYLKSVYEIVRNAGGVCIADEVQTGFGRTGSHYWGFQTQDVVPDIVT 317 +QG GG P ++K++ I G + +ADEVQTGFGRTG + + DV PD+ T Sbjct: 206 PVQGEGGFNVAPPAFVKALRAICDEHGILLVADEVQTGFGRTGKLF-AMEHYDVAPDLTT 264 Query: 318 MAKGIGNGLPLGAVVTTPEIASVLASKILFNTFGGNPVCSAGGLAVLNVIDKEKRQEHCA 377 MAK + G+PL AV E+ A L T+ GNP+ A LAVL+V++ E+ A Sbjct: 265 MAKSLAGGMPLSAVCGRAEVMDAPAPGGLGGTYAGNPLAVASALAVLDVLEGEQLIPRGA 324 Query: 378 EVGSHLIQRLKDVQKRHDIIGDVRGRGLMVGIELVSDRKDKTPAKAETSVLFEQLRELGI 437 +G L+ RL+ ++ R I ++RG G MV +E R D P T + + E G+ Sbjct: 325 ALGQRLVARLEALKARVPQIAEIRGLGAMVAVEF--RRADGAPDAEFTREVQNRALEQGL 382 Query: 438 LVGKGGLHGNVFRIKPPMCFT----KDDADFLVDAL 469 L+ G++GNV R P+ + + D L D L Sbjct: 383 LLLSCGVYGNVIRFLFPLTISDAVMNEGLDILADVL 418 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: 528 Number of extensions: 36 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: 476 Length of database: 420 Length adjustment: 33 Effective length of query: 443 Effective length of database: 387 Effective search space: 171441 Effective search space used: 171441 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