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_004511679.1 GMET_RS13945 homoserine O-acetyltransferase
Query= SwissProt::S2KHP1 (367 letters) >NCBI__GCF_000012925.1:WP_004511679.1 Length = 369 Score = 279 bits (714), Expect = 8e-80 Identities = 152/352 (43%), Positives = 213/352 (60%), Gaps = 8/352 (2%) Query: 14 VRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAA--SSMADPSPGWWEYMI 71 +R+ G L +T+AYET+GEL NA+L+ + +AH A +S D PGWW+ ++ Sbjct: 17 LRLESGRILGPITLAYETYGELNADRSNAILVAHAWTGNAHLAGKNSEEDTKPGWWDAIV 76 Query: 72 GPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAARGACR 131 GPG+ +DT+R FVI N +GSC+GSTGPASINP TG+ Y L FP ++V D+V A Sbjct: 77 GPGRLLDTDRCFVICSNVIGSCYGSTGPASINPKTGKRYNLTFPVITVRDMVRAQALLLD 136 Query: 132 ALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQREAVRA 191 LGID + TV G S+GGM AL +A +P R I+++ + +P I+L ++ R A+ Sbjct: 137 HLGIDRLLTVLGGSMGGMQALEWATQFPDRIRSAIALATTSRPSPQAISLNAVARWAIFN 196 Query: 192 DPAWAGGNYAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANPFAMAFQ 251 DP W G Y + PKDG+ +AR +G +T+ S E Q+F R + D F F+ Sbjct: 197 DPTWKKGEYR--KNPKDGLALARGIGHITFLSDESMWQKFGRR--FNARDGLFDFFGQFE 252 Query: 252 VQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRALVAGVTT 311 V+ Y+ N F DRFD N +LYL++A+DL+D A G SLE A R+ A A T+ Sbjct: 253 VERYLSYNGYNFVDRFDTNSFLYLAKALDLYDTA-WGYESLEEAFSRVKAPIQFFA-FTS 310 Query: 312 DWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFL 363 DWL+P +Q ++A +L G V YH + S GHDAFL++ E FAPMV EFL Sbjct: 311 DWLYPPYQTEEMATILRSLGKPVEYHLIESAYGHDAFLLEHETFAPMVREFL 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: 398 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: 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