Align Aromatic-amino-acid aminotransferase (EC 2.6.1.57) (characterized)
to candidate HSERO_RS15835 HSERO_RS15835 aspartate aminotransferase
Query= reanno::Cup4G11:RR42_RS33490 (400 letters) >lcl|FitnessBrowser__HerbieS:HSERO_RS15835 HSERO_RS15835 aspartate aminotransferase Length = 405 Score = 421 bits (1083), Expect = e-122 Identities = 210/397 (52%), Positives = 261/397 (65%), Gaps = 1/397 (0%) Query: 1 MFEHIDAYPGDPILSLNESFQLDPRTDKVNLSIGIYFDDEGRLPVMQAVREAEAALMADM 60 +F I+ P DPIL + E++ D K NL +G+Y+DD G++P+++ V++AEA L A + Sbjct: 9 LFSAIEMAPRDPILGVTEAYNADQNPAKTNLGVGVYYDDNGKVPLLECVKKAEAELAAKL 68 Query: 61 GPRPYLPMAGFAAYRDAVQALVFGQPCQARAEGRIATVQTLGGSGALRVGADFLKRYFP- 119 PR YLP+ G A Y AVQ LVFG E R TVQ LGG+GAL++GADFLK + P Sbjct: 69 APRTYLPIDGLATYDRAVQELVFGAGSAVVTEKRAITVQALGGTGALKLGADFLKHFSPA 128 Query: 120 DAQVWISDPSWENHRVIFERTGFTVNTYPYYDDATGGLKFDAMLDALRLIPKRSIVLLHA 179 +VWISDPSWENHR +FE GF VN YPYYD AT G+ F MLDAL+ + S+VLLHA Sbjct: 129 GTEVWISDPSWENHRALFEMAGFKVNAYPYYDPATRGVNFAGMLDALKTMKSGSVVLLHA 188 Query: 180 CCHNPTGVDLNHDQWRQLITLLKQHELLPFVDMAYQGFGAGLDDDAFAVRELVAQGVPCL 239 CCHNPTG DL DQW Q+I ++ L+PF+DMAYQGFG G+ +D VR G P Sbjct: 189 CCHNPTGADLTDDQWTQVIEVVTSRGLVPFLDMAYQGFGDGIAEDGQVVRRFAEAGGPLF 248 Query: 240 VANSFSKNFSLYGERCGGLSVVCDSAEETGRVLGQLTGAVRANYSNPPTHGARVVARVLT 299 V+NSFSK+FSLYGER G LS+ SAEE RVL QL VR NYSNPP HG +VVA L Sbjct: 249 VSNSFSKSFSLYGERVGALSIAAASAEEAARVLSQLKRVVRTNYSNPPIHGGQVVATALA 308 Query: 300 TPALRTIWERELAGKCERIAKMRAAIHKGLAAHVSGEALSRYLTQRGMFTYTGLTADQVD 359 +P LR +WE ELA RI +MR + L G + QRGMF+Y+GLT QVD Sbjct: 309 SPELRKLWEDELAEMRVRIREMRQLLVAKLKEKAPGHDFDFVIKQRGMFSYSGLTKAQVD 368 Query: 360 RLRTEHGVYLLRSGRMCVAGLNERNVTQVAQAIASVL 396 RLR E +Y + +GR+CVA LN +N+ V AIA VL Sbjct: 369 RLRNEFSIYAVDTGRICVAALNTKNIDVVVDAIAKVL 405 Lambda K H 0.323 0.137 0.417 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: 446 Number of extensions: 14 Number of successful extensions: 2 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: 400 Length of database: 405 Length adjustment: 31 Effective length of query: 369 Effective length of database: 374 Effective search space: 138006 Effective search space used: 138006 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 (21.9 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