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_013011985.1 DACET_RS13820 homoserine O-acetyltransferase
Query= SwissProt::S2KHP1 (367 letters) >NCBI__GCF_000025725.1:WP_013011985.1 Length = 369 Score = 263 bits (671), Expect = 7e-75 Identities = 144/350 (41%), Positives = 213/350 (60%), Gaps = 10/350 (2%) Query: 19 GGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAA--SSMADPSPGWWEYMIGPGKP 76 G L SVT+AYET+G+L DNA+L+ L+ +AHAA + D PGWW+ MIGPGK Sbjct: 24 GRVLSSVTVAYETYGKLNEARDNAILVCHALTGNAHAAGFNREDDQRPGWWDSMIGPGKA 83 Query: 77 IDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAARGACRALGID 136 DT+++FVI+ N LGSCFG+TGP+S++P T + Y L FP ++V D+V + LGI+ Sbjct: 84 FDTDKYFVISSNFLGSCFGTTGPSSVDPQTKKRYGLKFPVVTVRDMVKLQKKLIDHLGIE 143 Query: 137 HVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQREAVRADPAWA 196 +H+VAG S+GGM AL + +P + II I+A+A TP IA +I + A+ DP W Sbjct: 144 VLHSVAGGSMGGMQALEWGATFPYATKSIIPIAASAAVTPMAIAFNAIAKFAIMKDPNWR 203 Query: 197 GGNYAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRE--RLEGSDDSANPFAMAFQVQS 254 GG+Y P DG+ +AR G +TY S + +F R EG D F F+V++ Sbjct: 204 GGDYYDDVAPLDGLAIARMAGHITYMSDASFHSKFGRRYATFEGIYD----FKGLFEVEN 259 Query: 255 YMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRALVAGVTTDWL 314 Y+ N KF + +D N YLY+ +AMD+F++A +G L+ A+R I +K AL T+D+L Sbjct: 260 YLRYNGYKFTEFYDPNTYLYVLKAMDIFELA-YGRNGLKDALRLITSK-ALFITFTSDFL 317 Query: 315 FPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFLA 364 FP +Q ++ L++ G + + S GHDAFL++ E ++ FL+ Sbjct: 318 FPPYQTEELVTLMKEIGNEPRWENIESDYGHDAFLLEFEAQTEIIKNFLS 367 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: 344 Number of extensions: 16 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: 369 Length adjustment: 30 Effective length of query: 337 Effective length of database: 339 Effective search space: 114243 Effective search space used: 114243 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