Align Homoserine O-succinyltransferase; HST; EC 2.3.1.46; Homoserine transsuccinylase; HTS (uncharacterized)
to candidate WP_280949203.1 DL88_RS09745 alpha/beta fold hydrolase
Query= curated2:B1YPU9 (381 letters) >NCBI__GCF_000745425.1:WP_280949203.1 Length = 361 Score = 108 bits (269), Expect = 3e-28 Identities = 96/321 (29%), Positives = 141/321 (43%), Gaps = 41/321 (12%) Query: 9 PQTMHFAEPLRLQSGSVIGNYQLVVETYGELNAARSNAVLVCHALNASHHVAGVYADDPR 68 P +H P L++G I N QL T+GEL+AA NA+L + + + Sbjct: 26 PFEIHDLGPFLLENGGTIRNLQLAYATFGELSAAGDNAILFPTWYSGTTKILE------- 78 Query: 69 STGWWDNLVGPGKPLDTNRFFVIGVNNLGSCFGSTGPMSIDPSSGKPYGA-RFPVVTVED 127 +GPG+ LD +R+F+I VN +G+ G S ++ P+ A RFP+V++ D Sbjct: 79 -----QAYIGPGRALDPDRYFIILVNQIGN-----GLSSAPSNNPAPFNAARFPLVSIGD 128 Query: 128 WVHAQAR-VADAFGIERFAAVMGGSLGGMQALAWSLMYPERVAHCIDIASTPKLSAQNIA 186 V AQ R V + FG+ R V+GGS+G Q W++ YPE V IA T + SA N Sbjct: 129 DVRAQHRLVTEHFGLTRLQLVLGGSMGAQQTYEWAVRYPEFVRRAAPIAGTARASAHNQL 188 Query: 187 FNEVARSAILSDPDFHGGDYYAHGVKPKRGLRVARMIGHITYLSDDDMAEKFGRALRRAD 246 E AI SD + G +Y + RGLR + + AE+ R L Sbjct: 189 LVESFIEAITSDRAYDNG-WYDNAGDIHRGLRRHARLFATAAFTPRLYAEEGWRDL---- 243 Query: 247 GALDAYNFSFDVEFE---VESYLRYQGDKFADYFDANTYLLITRALDYFDPAKAFDGNLT 303 FS +F VE + Q D N +L+ R D + G++ Sbjct: 244 ------GFSSTEDFLTGFVEGHFLPQ--------DPNNLILLARKWQGGDVGRNSGGDIK 289 Query: 304 AALAHTQAKYLIASFSTDWRF 324 AL+H A + + D F Sbjct: 290 KALSHIIATTYVIAIDEDGLF 310 Lambda K H 0.321 0.136 0.415 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: 348 Number of extensions: 24 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 381 Length of database: 361 Length adjustment: 30 Effective length of query: 351 Effective length of database: 331 Effective search space: 116181 Effective search space used: 116181 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 (21.9 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