Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate PfGW456L13_1007 Homoserine O-acetyltransferase (EC 2.3.1.31)
Query= SwissProt::S2KHP1 (367 letters) >FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1007 Length = 379 Score = 245 bits (626), Expect = 1e-69 Identities = 140/365 (38%), Positives = 205/365 (56%), Gaps = 8/365 (2%) Query: 2 PDARRFIELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAAS--SM 59 P F E P+ + G LP+ + YET+G L NA+L+ LS HAA S Sbjct: 15 PQVAHFSE---PLALACGRSLPAYDLIYETYGTLNATASNAVLICHALSGHHHAAGYHSA 71 Query: 60 ADPSPGWWEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSV 119 D PGWW+ IGPGKPIDT +FFV+++N+LG C GSTGP+SINP TG+P+ DFP L+V Sbjct: 72 DDRKPGWWDSCIGPGKPIDTSKFFVVSLNNLGGCNGSTGPSSINPDTGKPFGADFPVLTV 131 Query: 120 EDIVAAARGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTI 179 ED V + LGI V G SLGGM A+ +++ YP R ++I++A + I Sbjct: 132 EDWVHSQARLADRLGIAQFAAVIGGSLGGMQAMQWSITYPDRIRHCLAIASAPKLSAQNI 191 Query: 180 ALRSIQREAVRADPAWAGGNYAPGEG-PKDGMRVARQLGILTYRSAEEWLQRFDRERLEG 238 A + R+A+ DP + GG++ PK G+ +AR +G +TY S + ++F R L+ Sbjct: 192 AFNEVARQAILTDPEFHGGSFQEHNVIPKRGLMLARMVGHITYLSDDSMGEKFGR-GLKS 250 Query: 239 SDDSANPFAMAFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRR 298 + + ++ FQV+SY+ +F+ RFDAN YL +++A+D FD A + D +L Sbjct: 251 EKLNYDFHSVEFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFDPAANFDDNLAKTFEG 310 Query: 299 IDAKRALVAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPM 358 AK V TTDW F + R++ + L A V Y E+ + QGHDAFL+ R+ Sbjct: 311 AKAK-FCVMSFTTDWRFSPARSRELVDALMAARKDVCYLEIDAPQGHDAFLIPIPRYLQA 369 Query: 359 VAEFL 363 ++ Sbjct: 370 FGNYM 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: 386 Number of extensions: 24 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 Aug 03 2021. The underlying query database was built on Aug 03 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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