Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate WP_029933743.1 N746_RS0102275 homoserine O-acetyltransferase
Query= SwissProt::S2KHP1 (367 letters) >NCBI__GCF_000711195.1:WP_029933743.1 Length = 379 Score = 233 bits (594), Expect = 6e-66 Identities = 134/347 (38%), Positives = 188/347 (54%), Gaps = 7/347 (2%) Query: 13 PVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSM-ADPSPGWWEYMI 71 P+ + G LP + YET+G L + +NA+L+ LS H A D PGWW I Sbjct: 18 PLALVSGAVLPQYDLVYETYGSLNAEANNAILICHALSGDHHVAGFYEGDDKPGWWNDYI 77 Query: 72 GPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAARGACR 131 GPGKPIDT FFV+ N+LGSC GSTGP S+NP TG+ + DFP ++ D V + + Sbjct: 78 GPGKPIDTNEFFVVCSNNLGSCRGSTGPTSLNPETGKVFGSDFPIVTCRDWVHSQNQLRQ 137 Query: 132 ALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQREAVRA 191 LGI+ + G S+GGM + +A+ YP R + I+AA + IA + R A+ Sbjct: 138 HLGIEQWAAIVGGSMGGMQVMQWAIDYPDKLRHAVVIAAAPKLSAQNIAFNEVARRAIMT 197 Query: 192 DPAWAGGNY-APGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANPFAMAF 250 DP + G + G PK G+ +AR LG LTY S + +F RE +D F + F Sbjct: 198 DPEFHEGRFIEAGTIPKGGLALARMLGHLTYLSDDMMGAKFGREL--RADKLKYSFEVEF 255 Query: 251 QVQSYMEANARKFADR--FDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRALVAG 308 QV+SY+ KFA + FDAN YL +++A+D FD A D L A A + LV Sbjct: 256 QVESYLRYQGEKFATKQNFDANTYLLMTKALDYFDPASEFDNDLSQAFANTKA-QFLVIS 314 Query: 309 VTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERF 355 T+DW F + R++ L ++VSY E+ S GHDAFL+ + + Sbjct: 315 FTSDWRFSPARSREIVRALLDNDLSVSYAEVVSEHGHDAFLLPNTHY 361 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: 373 Number of extensions: 20 Number of successful extensions: 6 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