Align Serine O-acetyltransferase; SAT; Homoserine O-acetyltransferase; HAT; Homoserine transacetylase; HTA; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate 7025621 Shewana3_2772 homoserine O-succinyltransferase (RefSeq)
Query= SwissProt::A0A1D3PCK2 (262 letters) >lcl|FitnessBrowser__ANA3:7025621 Shewana3_2772 homoserine O-succinyltransferase (RefSeq) Length = 313 Score = 145 bits (366), Expect = 1e-39 Identities = 85/258 (32%), Positives = 137/258 (53%), Gaps = 15/258 (5%) Query: 5 VKIGILNLMHDKLDTQSHFIKVLPNADLTFFYPRMHYQNRPIP----PEVNMTSEPLDIN 60 +K+ ILNLM +K++T++ +++L N L + ++ +N + Sbjct: 36 MKVLILNLMPNKIETETQLLRLLGNTPLQVDVDLLRIHDKESKHTSIDHMNTFYRDFEDV 95 Query: 61 RVSEFDGFIITGAPIDQIDFSKITYIEEIRYLLQALDNHKIQQLYFCWGAMAALNYFYGI 120 R +DG IITGAP+ QIDF ++TY + IR ++ H L+ CW A A L + YG+ Sbjct: 96 RHKNYDGLIITGAPLGQIDFEEVTYWDHIREIIDWSQQHVTSVLFLCWAAHAGLYHLYGL 155 Query: 121 KKKILAEKIFGVFPHLITEPH-PLLSGLSQGFMAPHARYAEMDKKQIMQDERLAINAVDD 179 +KIL +K GVF H T H PLL G F APH+R+AEMD +++ Q L + A D Sbjct: 156 NRKILQQKRSGVFVHRRTCQHFPLLRGFDDEFFAPHSRFAEMDIEELKQHSELQVLAQSD 215 Query: 180 NSHLFMVSAKDNPERN-FIFSHIEYGKDSLRDEYNREINAH-----PERHYKKPINYSMS 233 + ++V +++N RN F+ H EY K +L DEY+R++ P+ +Y+ + Sbjct: 216 EAGAYLVLSRNN--RNLFVMGHPEYQKSTLNDEYHRDLAQGLNPNVPQNYYRN--DDPKD 271 Query: 234 NPSFQWQDTQKIFFNNWL 251 + +W + +NWL Sbjct: 272 DAIARWHSHGSLLVSNWL 289 Lambda K H 0.322 0.138 0.420 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: 197 Number of extensions: 11 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: 262 Length of database: 313 Length adjustment: 26 Effective length of query: 236 Effective length of database: 287 Effective search space: 67732 Effective search space used: 67732 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: 47 (22.7 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