Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate WP_011320764.1 AVA_RS20670 homoserine O-acetyltransferase
Query= SwissProt::H8L374 (367 letters) >NCBI__GCF_000204075.1:WP_011320764.1 Length = 359 Score = 246 bits (627), Expect = 9e-70 Identities = 141/368 (38%), Positives = 207/368 (56%), Gaps = 26/368 (7%) Query: 1 MSDARRYHALPSPFPMKRGGQLQGARLAYETWGRLSPGCDNAVLILTGLSPSAHAASHPD 60 +S+ Y+ LP PF ++ GG L G ++AY TWG+L+ DN VLI L+ SA A Sbjct: 7 ISEQTEYYHLPVPFELEGGGVLTGVQVAYRTWGKLNSAGDNGVLICHALTGSADADE--- 63 Query: 61 GDTSPGWWEGMLGPGKAIDTDRWYVICVNSLGSDKGSTGPASPDPATGAPYRLSFPELAL 120 WWEG+LG KA+D+DR ++IC N LGS G+TG S +P TG PY SFP + + Sbjct: 64 ------WWEGLLGANKALDSDRDFIICSNILGSCYGTTGATSINPQTGIPYGASFPAITI 117 Query: 121 EDVASAAHDLVKALGIARLACLIGCSMGGMSALAYMLQYEGEVEAHISVDTAPQAQPFAI 180 D+ L++ LGI L +IG S+GGM L + L Y V+A + T+ + + I Sbjct: 118 RDMVRLQAALIQHLGIKSLQLVIGGSLGGMQVLEWALLYPEIVQAIAPIATSGRHSAWCI 177 Query: 181 AIRSLQREAIRLDPNWQDGHYTDAAYPETGMAMARKLGVITYRSAMEWNGRFARIRLDGD 240 + QR+AI DPNW+ G+YT P G+A+AR + + YRS + RF Sbjct: 178 GLSEAQRQAIYADPNWKGGNYTKEQPPSQGLAVARMMAMSAYRSWQSFTARFG------- 230 Query: 241 QRPDEPFAREFQVESYLEHHAQRFVRRFDPACYLYLTRASDWFDVAEYGE-GSVMQGLAR 299 R + A +F + SYL+HH Q+ V+RFD Y+ LT+A D DVA+ + SV+Q + Sbjct: 231 -RQYDAVADQFAIASYLQHHGQKLVQRFDANTYITLTQAMDSHDVAQGRDYKSVLQSIK- 288 Query: 300 IHVRRALVIGVSTDILFPLEQQQQIAEGLQAAGAEVDFVALDSPQGHDAFLVDIENYSAA 359 + ALV+ + +DIL+P +QQ++A+ + + L S GHDAFL+DI S Sbjct: 289 ---QPALVVAIDSDILYPPTEQQELADFI----PDAQLGWLQSSYGHDAFLIDIATLSQL 341 Query: 360 IGGFLRTL 367 + F ++L Sbjct: 342 VINFRQSL 349 Lambda K H 0.320 0.136 0.421 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: 384 Number of extensions: 22 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: 367 Length of database: 359 Length adjustment: 29 Effective length of query: 338 Effective length of database: 330 Effective search space: 111540 Effective search space used: 111540 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: 49 (23.5 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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:
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