Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate GFF285 HP15_284 homoserine O-acetyltransferase
Query= SwissProt::S2L5R8 (390 letters) >FitnessBrowser__Marino:GFF285 Length = 382 Score = 569 bits (1467), Expect = e-167 Identities = 272/381 (71%), Positives = 323/381 (84%), Gaps = 1/381 (0%) Query: 7 MPE-LPSDSVGLVAPQTAHFDVPLALACGKTLQSYDLVYETYGKLNASRSNAVLICHALS 65 MP+ LP+DSVG+V+PQT HFD P+ LACG++L++YDLV ETYG LNA SNAVLICHALS Sbjct: 1 MPDTLPADSVGIVSPQTYHFDAPIDLACGQSLENYDLVVETYGTLNADASNAVLICHALS 60 Query: 66 GHHHAAGYHSREDRKPGWWDAHIGPGKSIDTDRFFVISLNNLGGCHGSTGPCAINPDTGR 125 GHHHAAGYHS EDRKPGWWD+ IGPGK IDTDRFFV+SLNNLGGCHGSTGP +INP+TG+ Sbjct: 61 GHHHAAGYHSAEDRKPGWWDSCIGPGKPIDTDRFFVVSLNNLGGCHGSTGPNSINPETGK 120 Query: 126 QWGPDFPMMTVGDWVHSQARLADRLGIERFAAVIGGSLGGMQVLQWSLAYPERIANAVVI 185 +GP+FP++TVGDWV SQA LADRLGI+ +AAV+GGSLGGMQ LQWSL YP+R+ +AVVI Sbjct: 121 PFGPEFPVITVGDWVKSQALLADRLGIQCWAAVVGGSLGGMQALQWSLDYPDRLRHAVVI 180 Query: 186 AATPKLSAQNIAFNEVARQAIRSDPDFYDGWYAEHDTLPRRGLKLARMVGHITYLSEDAM 245 A+TP+L+AQNIAFNEVARQAI SD +F+DG Y + DT+PRRGL LARMVGHITYLS+ +M Sbjct: 181 ASTPRLTAQNIAFNEVARQAITSDREFHDGRYYDFDTVPRRGLMLARMVGHITYLSDASM 240 Query: 246 GSKFGRDLRSDDLNFGYDVEFQVESYLRYQGDTFSTSFDANTYLLMTKALDYFDPAAAHD 305 G KFGR+LR FGYD EFQVESYLRYQG+ FS SFDANTYLLMT+ALDYFDPA Sbjct: 241 GEKFGRELRDQAYKFGYDAEFQVESYLRYQGERFSESFDANTYLLMTRALDYFDPAYEFG 300 Query: 306 GDLAAAVAPASCPFLVVSFSTDWRFPPSRSRELVDALIRAGKPVSYVCIDSPHGHDAFLL 365 GDL+ A+A ASC +LV+SFSTDWRF P+RS E+V+A+I A + VSY +D+P GHDAFL+ Sbjct: 301 GDLSKALAAASCEYLVLSFSTDWRFTPARSEEMVNAMIGARRKVSYAEVDAPWGHDAFLI 360 Query: 366 PETRYQAIFASFMGRVAHDSG 386 P RY IF ++M RVA + G Sbjct: 361 PTPRYTDIFNAYMDRVAREVG 381 Lambda K H 0.321 0.136 0.428 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: 587 Number of extensions: 24 Number of successful extensions: 1 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: 390 Length of database: 382 Length adjustment: 30 Effective length of query: 360 Effective length of database: 352 Effective search space: 126720 Effective search space used: 126720 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