Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate GFF5222 PS417_26740 homoserine acetyltransferase
Query= SwissProt::S2KHP1 (367 letters) >FitnessBrowser__WCS417:GFF5222 Length = 379 Score = 248 bits (634), Expect = 1e-70 Identities = 141/366 (38%), Positives = 208/366 (56%), Gaps = 8/366 (2%) Query: 1 MPDARRFIELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAAS--S 58 +P F E P+ + G LP+ + YET+G+L NA+L+ LS HAA S Sbjct: 14 VPQVAHFSE---PLALACGRALPAYDLIYETYGQLNATASNAVLICHALSGHHHAAGFHS 70 Query: 59 MADPSPGWWEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLS 118 + + PGWW+ IGPGKPIDT +FFV+++N+LG C GSTGP+SINP TG+P+ DFP L+ Sbjct: 71 VDERKPGWWDSCIGPGKPIDTNKFFVVSLNNLGGCNGSTGPSSINPETGKPFGADFPVLT 130 Query: 119 VEDIVAAARGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFT 178 VED V + LGI+ V G SLGGM AL + + YP R ++I++A + Sbjct: 131 VEDWVHSQARLADLLGINQWAAVIGGSLGGMQALQWTITYPDRVRHCLAIASAPKLSAQN 190 Query: 179 IALRSIQREAVRADPAWAGGNY-APGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLE 237 IA + R+A+ DP + GG++ G PK G+ +AR +G +TY S + ++F R L+ Sbjct: 191 IAFNEVARQAILTDPEFHGGSFQEAGVIPKRGLMLARMVGHITYLSDDSMGEKFGR-GLK 249 Query: 238 GSDDSANPFAMAFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVR 297 + + ++ FQV+SY+ +F+ RFDAN YL +++A+D FD A + D L Sbjct: 250 SEKLNYDFHSVEFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFDPAANFDDDLAKTFE 309 Query: 298 RIDAKRALVAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAP 357 AK V TTDW F + R++ + L A V Y E+ + QGHDAFL+ R+ Sbjct: 310 GATAK-FCVMSFTTDWRFSPARSRELVDALMAARKDVCYLEIDAPQGHDAFLIPIPRYLQ 368 Query: 358 MVAEFL 363 ++ Sbjct: 369 AFGNYM 374 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: 374 Number of extensions: 22 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: 379 Length adjustment: 30 Effective length of query: 337 Effective length of database: 349 Effective search space: 117613 Effective search space used: 117613 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