Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_093428353.1 BM272_RS08475 homoserine O-acetyltransferase
Query= SwissProt::S2L5R8 (390 letters) >NCBI__GCF_900112605.1:WP_093428353.1 Length = 384 Score = 551 bits (1421), Expect = e-162 Identities = 257/377 (68%), Positives = 313/377 (83%), Gaps = 1/377 (0%) Query: 7 MPE-LPSDSVGLVAPQTAHFDVPLALACGKTLQSYDLVYETYGKLNASRSNAVLICHALS 65 MPE LP+DSVGLV PQ+ HFD PL L CG+ L Y+LVYETYG NA RSNA+L+CHALS Sbjct: 1 MPESLPADSVGLVQPQSLHFDQPLELDCGRVLPEYELVYETYGTPNADRSNAILVCHALS 60 Query: 66 GHHHAAGYHSREDRKPGWWDAHIGPGKSIDTDRFFVISLNNLGGCHGSTGPCAINPDTGR 125 G HHAAGY+S EDRKPGWW+A IGPGK +DT+RFF++S+NNLG C GS+GP INP+TGR Sbjct: 61 GDHHAAGYNSMEDRKPGWWEACIGPGKPLDTNRFFIVSVNNLGSCKGSSGPNTINPETGR 120 Query: 126 QWGPDFPMMTVGDWVHSQARLADRLGIERFAAVIGGSLGGMQVLQWSLAYPERIANAVVI 185 WGPDFP++TV DWVHS ARLAD LGIE++AAV+GGSLGGMQV+QW++ YP+R+ +AV+I Sbjct: 121 YWGPDFPIVTVRDWVHSHARLADELGIEQWAAVVGGSLGGMQVMQWAIDYPDRLRHAVII 180 Query: 186 AATPKLSAQNIAFNEVARQAIRSDPDFYDGWYAEHDTLPRRGLKLARMVGHITYLSEDAM 245 A P+LSAQNIAFNEVARQAI SDP+F+DG+Y + TLPRRGL LARM+GHITYLS++AM Sbjct: 181 AGAPRLSAQNIAFNEVARQAIMSDPEFHDGYYLQKGTLPRRGLMLARMLGHITYLSDEAM 240 Query: 246 GSKFGRDLRSDDLNFGYDVEFQVESYLRYQGDTFSTSFDANTYLLMTKALDYFDPAAAHD 305 +KFGR+LR+D +NFGYDV+FQVESYLRYQG +F FDANTYLLMT+ALDYFDPAA HD Sbjct: 241 RAKFGRELRTDQINFGYDVDFQVESYLRYQGQSFVDRFDANTYLLMTRALDYFDPAAEHD 300 Query: 306 GDLAAAVAPASCPFLVVSFSTDWRFPPSRSRELVDALIRAGKPVSYVCIDSPHGHDAFLL 365 DL AA+AP + LVVSF++DWRF P RSRE+V AL+ K V+Y + + GHDAFL+ Sbjct: 301 DDLTAALAPVTARSLVVSFTSDWRFSPERSREIVKALLDGNKSVAYAEVQAHQGHDAFLM 360 Query: 366 PETRYQAIFASFMGRVA 382 P +Y A+F ++M VA Sbjct: 361 PIAQYMAVFRAYMDEVA 377 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: 531 Number of extensions: 16 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: 384 Length adjustment: 30 Effective length of query: 360 Effective length of database: 354 Effective search space: 127440 Effective search space used: 127440 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