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_024850420.1 N745_RS0101730 homoserine O-acetyltransferase
Query= SwissProt::S2KHP1 (367 letters) >NCBI__GCF_000526715.1:WP_024850420.1 Length = 386 Score = 227 bits (578), Expect = 5e-64 Identities = 134/360 (37%), Positives = 192/360 (53%), Gaps = 7/360 (1%) Query: 8 IELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAAS-SMADPSPGW 66 + + P+ M G LP +A+ET+GEL NA+L+ LS H A D GW Sbjct: 12 LHISTPLNMVCGSVLPEYDLAFETYGELNDDHSNAILICHALSGHQHVAGFHEGDKDAGW 71 Query: 67 WEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAA 126 W+ IGPGK IDT+RFFV+ N+LG C GS+GP SINP TGQ Y DFP ++ +D V + Sbjct: 72 WDSYIGPGKVIDTDRFFVVCSNNLGGCHGSSGPTSINPETGQVYGPDFPIVTCKDWVNSQ 131 Query: 127 RGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQR 186 + L I+ + G S+GGM + +A+ YP + + I++A + IA + R Sbjct: 132 NELRKYLKIEAWAAIIGGSMGGMQVMQWAIDYPDKIKHAVVIASAPKLSAQNIAFNEVAR 191 Query: 187 EAVRADPAWAGGNY-APGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANP 245 A+ DP + G + PK G+ +AR LG LTY S + +F RE EG + Sbjct: 192 RAIMTDPDFLDGRFIEKNTTPKRGLALARMLGHLTYLSDDLMGTKFGRELREGKLN--YN 249 Query: 246 FAMAFQVQSYMEANARKFADR--FDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKR 303 + + FQV+SY+ KFA + FDAN YL +++A+D FD A D L A+ AK Sbjct: 250 YEVEFQVESYLRYQGEKFATKQNFDANTYLLMTKALDYFDPASEYDNDLTKALSHAKAK- 308 Query: 304 ALVAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFL 363 LV TTDW F + ++ + L VSY E+ S GHDAFL+ + + + +L Sbjct: 309 FLVISFTTDWRFAPERSHEIVKALLDNDADVSYAEIESKHGHDAFLLPNPHYENVFRAYL 368 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: 368 Number of extensions: 18 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: 386 Length adjustment: 30 Effective length of query: 337 Effective length of database: 356 Effective search space: 119972 Effective search space used: 119972 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