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_011937520.1 GURA_RS02975 homoserine O-acetyltransferase
Query= SwissProt::S2KHP1 (367 letters) >NCBI__GCF_000016745.1:WP_011937520.1 Length = 370 Score = 264 bits (674), Expect = 3e-75 Identities = 146/352 (41%), Positives = 207/352 (58%), Gaps = 8/352 (2%) Query: 14 VRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAAS--SMADPSPGWWEYMI 71 +R+ G L +T+AYET+GEL NA+L+ + +AH A S + PGWW ++ Sbjct: 17 LRLESGRILGPITLAYETYGELNAARSNAILVAHAWTGNAHLAGRYSENEQKPGWWNEIV 76 Query: 72 GPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAARGACR 131 GPGK +DT+R+F+I N +GSCFGSTGPASINP TG+ Y L FP ++V D+V A + Sbjct: 77 GPGKLLDTDRYFIICANVIGSCFGSTGPASINPKTGKKYNLSFPVITVRDMVRAQQLLID 136 Query: 132 ALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQREAVRA 191 LGID + +V G S+GGM AL +A +P I ++ + I+L ++ R A+ Sbjct: 137 HLGIDRLFSVMGGSMGGMQALEWATQFPERIASAIVLATTPRPSAQAISLNAVARWAIFN 196 Query: 192 DPAWAGGNYAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANPFAMAFQ 251 DP W G Y + PKDG+ +AR +G +T+ S E +F R R D + F F+ Sbjct: 197 DPTWKKGEYR--KNPKDGLALARGIGHITFLSDESMTAKFGR-RFSARDGQFDFFG-RFE 252 Query: 252 VQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRALVAGVTT 311 V+ Y+ N F DRFDAN +LYL++A+DL+D+A G SLE A ++ A A ++ Sbjct: 253 VERYLSYNGYNFVDRFDANSFLYLAKALDLYDVA-WGYESLEEAFAQVAAPIQFFA-FSS 310 Query: 312 DWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFL 363 DWL+P Q ++ LE G V YH + S GHDAFL++ E F PMV FL Sbjct: 311 DWLYPPAQTEEMVTTLEKLGKPVEYHLITSAYGHDAFLLEHETFTPMVRAFL 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: 380 Number of extensions: 21 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: 370 Length adjustment: 30 Effective length of query: 337 Effective length of database: 340 Effective search space: 114580 Effective search space used: 114580 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