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_038202407.1 Q392_RS05130 homoserine O-acetyltransferase
Query= SwissProt::S2KHP1 (367 letters) >NCBI__GCF_000745855.1:WP_038202407.1 Length = 374 Score = 264 bits (674), Expect = 3e-75 Identities = 150/350 (42%), Positives = 207/350 (59%), Gaps = 5/350 (1%) Query: 13 PVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSMADP--SPGWWEYM 70 P+ + G L T+AYET+G L + NA+L+ L+ S H A A S GWW+ M Sbjct: 15 PLALRSGASLGDYTLAYETYGTLNAERSNAVLVCHALNASHHVAGRYAGQPKSEGWWDNM 74 Query: 71 IGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAARGAC 130 IGPGK +DT+RFFVI IN+LGSCFGSTGP +NPATG+ Y DFP ++VED V A Sbjct: 75 IGPGKAVDTDRFFVIGINNLGSCFGSTGPMHVNPATGRVYGADFPVVTVEDWVDAQARLL 134 Query: 131 RALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQREAVR 190 ALGID + V G SLGGM AL++ + YP R I++A + IA + R A+ Sbjct: 135 DALGIDTLAAVMGGSLGGMQALSWTLQYPERVRHAAVIASAPNLNAENIAFNEVARRAIV 194 Query: 191 ADPAWAGGN-YAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANPFAMA 249 DP + GG+ Y G PK G+R+AR +G +TY S + ++F RE EG + Sbjct: 195 TDPDFHGGHFYEHGVVPKRGLRIARMIGHITYLSDDVMNEKFGRELREGVVRYTTQ-DVE 253 Query: 250 FQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRALVAGV 309 FQ++SY+ KF++ FDAN YL +++A+D FD A G L AA+ R AK LV+ Sbjct: 254 FQIESYLRYQGDKFSEYFDANTYLLITRALDYFDPAGGHGGDLAAALARATAKFLLVS-F 312 Query: 310 TTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMV 359 +TDW F + R++ + L +VSY E+ + GHDAFL+D R+ +V Sbjct: 313 STDWRFSPQRSREIVKALLDNRRSVSYAEIDAPHGHDAFLLDDVRYLGVV 362 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: 401 Number of extensions: 19 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: 374 Length adjustment: 30 Effective length of query: 337 Effective length of database: 344 Effective search space: 115928 Effective search space used: 115928 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