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_093428353.1 BM272_RS08475 homoserine O-acetyltransferase
Query= SwissProt::S2KHP1 (367 letters) >NCBI__GCF_900112605.1:WP_093428353.1 Length = 384 Score = 245 bits (626), Expect = 1e-69 Identities = 137/354 (38%), Positives = 202/354 (57%), Gaps = 6/354 (1%) Query: 13 PVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAA--SSMADPSPGWWEYM 70 P+ + G LP + YET+G NA+L+ LS HAA +SM D PGWWE Sbjct: 23 PLELDCGRVLPEYELVYETYGTPNADRSNAILVCHALSGDHHAAGYNSMEDRKPGWWEAC 82 Query: 71 IGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAARGAC 130 IGPGKP+DT RFF++++N+LGSC GS+GP +INP TG+ + DFP ++V D V + Sbjct: 83 IGPGKPLDTNRFFIVSVNNLGSCKGSSGPNTINPETGRYWGPDFPIVTVRDWVHSHARLA 142 Query: 131 RALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQREAVR 190 LGI+ V G SLGGM + +A+ YP R + I+ A + IA + R+A+ Sbjct: 143 DELGIEQWAAVVGGSLGGMQVMQWAIDYPDRLRHAVIIAGAPRLSAQNIAFNEVARQAIM 202 Query: 191 ADPAWAGGNY-APGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANPFAMA 249 +DP + G Y G P+ G+ +AR LG +TY S E +F RE +D + + Sbjct: 203 SDPEFHDGYYLQKGTLPRRGLMLARMLGHITYLSDEAMRAKFGREL--RTDQINFGYDVD 260 Query: 250 FQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRALVAGV 309 FQV+SY+ + F DRFDAN YL +++A+D FD A D L AA+ + A R+LV Sbjct: 261 FQVESYLRYQGQSFVDRFDANTYLLMTRALDYFDPAAEHDDDLTAALAPVTA-RSLVVSF 319 Query: 310 TTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFL 363 T+DW F + R++ + L +V+Y E+ + QGHDAFL+ ++ + ++ Sbjct: 320 TSDWRFSPERSREIVKALLDGNKSVAYAEVQAHQGHDAFLMPIAQYMAVFRAYM 373 Lambda K H 0.320 0.135 0.414 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: 414 Number of extensions: 19 Number of successful extensions: 4 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: 384 Length adjustment: 30 Effective length of query: 337 Effective length of database: 354 Effective search space: 119298 Effective search space used: 119298 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 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