Align LL-diaminopimelate aminotransferase; DAP-AT; DAP-aminotransferase; LL-DAP-aminotransferase; EC 2.6.1.83 (uncharacterized)
to candidate AZOBR_RS12970 AZOBR_RS12970 aspartate aminotransferase
Query= curated2:B1I544 (392 letters) >lcl|FitnessBrowser__azobra:AZOBR_RS12970 AZOBR_RS12970 aspartate aminotransferase Length = 401 Score = 173 bits (438), Expect = 9e-48 Identities = 122/401 (30%), Positives = 194/401 (48%), Gaps = 22/401 (5%) Query: 6 AKRIRNLPPYLFARIEQLIADKKAQGVDVISLGIGDPDVPTPDHIIEAAEKELKIPANHQ 65 A R+ + P + Q + A G DVI LG G+PD TPD+I +AA K ++ + + Sbjct: 5 ASRLSRIKPSPTIAVTQKARELAAAGRDVIGLGAGEPDFDTPDNIKDAAIKAIQA-GDTK 63 Query: 66 YPSSAGMPAYRRAVADWYARRFGVELDPQREVVSLIGSKEGIAHLPWCFVDPGDVVLVPD 125 Y + G PA ++A+ + R G++ P + V +G K+ + + + PGD V++P Sbjct: 64 YTAVDGTPALKKAICAKFERENGLKYAPDQITVG-VGGKQVLYNALMATLTPGDEVIIPA 122 Query: 126 PGYPVYAGGTILAGGIPHPVPLTAGNGFLPDLAAIPAETARRAKVMFINYPNNPTGAVAS 185 P + Y LA G P V A GF A + + K + +N P+NP+GA + Sbjct: 123 PYWVSYPDMVELAEGTPVFVSCPAEQGFKLQPADLEKAITPKTKWLILNSPSNPSGAAYT 182 Query: 186 KEFFARVVD-FAREYGILVCHDAAYSEIAFDG--YRPPSFLEVAGAREVGIEFHSVSKTY 242 ++ + D + + V D Y + +DG + P+ +E A + + + VSK+Y Sbjct: 183 RDEMKALTDVLVKHPQVWVMTDDMYEHLLYDGIEFVTPAQVEPA-LYDRTLTVNGVSKSY 241 Query: 243 NMTGWRAGWAAGNAGAVEALGRLKSNLDSGVFQVVQYAAIAALNGPQDGVQSLCEMYRER 302 MTGWR G+A G ++A+G ++S S + Q AA+ ALNGPQD + ++ +R Sbjct: 242 AMTGWRIGYAGGPKALIKAMGVIQSQSTSNPTSIAQAAAVEALNGPQDFIAERAAVFAQR 301 Query: 303 RDLVVDTLNDL-GWRLTRPRATFYIWAPVPAG------------HDASSFAEMVLEKAGV 349 RDLVV LN G +P FY++ P AG F +LE GV Sbjct: 302 RDLVVSMLNQAKGISCPKPEGAFYVY-PSCAGTIGKTTPDGKVIETDEDFVTYLLESEGV 360 Query: 350 VITPGTGYGTYGEGYFRISLTLPTPRLVEAMERLRGCLGRV 390 + G+ +G +FRIS T L EA +R++ G + Sbjct: 361 AVVQGSAFGL--APHFRISYATSTEALEEACKRIQRACGNL 399 Lambda K H 0.321 0.139 0.430 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: 322 Number of extensions: 18 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: 392 Length of database: 401 Length adjustment: 31 Effective length of query: 361 Effective length of database: 370 Effective search space: 133570 Effective search space used: 133570 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: 50 (23.9 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