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_011391014.1 RRU_RS16855 homoserine O-acetyltransferase
Query= SwissProt::A0A0I9RJ56 (370 letters) >NCBI__GCF_000013085.1:WP_011391014.1 Length = 391 Score = 253 bits (645), Expect = 8e-72 Identities = 145/355 (40%), Positives = 199/355 (56%), Gaps = 4/355 (1%) Query: 16 SPFPFKRGGALHGARVAYETWGTLAADASNAILIVTGLSPDAHAAA-NDANPAAGWWEGM 74 +P G L VAY+T G L A+ +NAILI L+ D H + GWWE + Sbjct: 21 APMRLDSGLELGPLTVAYQTIGRLNAERTNAILICHALTGDQHVIGPHPVTGRPGWWETL 80 Query: 75 VGPGKAIDTDRWFVVCVNSLGSCRGSTGPASLNPATGQPYRLDFPELSIEDGARAAIEVV 134 VGPGK IDTDR+F++C N LG C G+TGP +NPATG+P+ L FP ++I D RA ++ Sbjct: 81 VGPGKTIDTDRYFIICSNVLGGCLGTTGPKEINPATGKPWGLGFPVITIGDMVRAQALLL 140 Query: 135 RAQGIEQLACVVGNSMGGMTALAVLMLHPGIARSHVNISGSAQALPFSIAIRSLQREAIR 194 GIE+L C +G SMG M L + +P R+ V I+GS + +IA + R+AI Sbjct: 141 DHLGIERLFCAIGGSMGAMQVLQWAVSYPERVRAVVPIAGSWRHSAQNIAFHEVGRQAIM 200 Query: 195 LDPRWNGGHY-DDDAYPESGMRMARKLGVITYRSALEWDGRFGRVRLDSDQTDDDPFGLE 253 DP WNGG Y + P G+ +AR ITY S +FGR +L + F + Sbjct: 201 ADPDWNGGDYLNQGTVPRRGLAVARMTAHITYLSEPALQSKFGR-KLQDRASITYGFDAD 259 Query: 254 FQVESYLEGHARRFVRFFDPNCYLYLSRSMDWFDLAEYADGDVLAGLAKIRVEKALAIGA 313 FQVESYL FV+ FD N YLY++R+MD+FDLA DG VLA + + + Sbjct: 260 FQVESYLRHQGANFVKRFDANSYLYITRAMDYFDLAAEHDG-VLARAFQGTKVRFCVVSF 318 Query: 314 NTDILFPVQQQQQVADGLRAGGADARFIGLESPQGHDAFLVDFERFCPAVRGFLD 368 +D LFP + + V + A AD F+ + + +GHDAFL+D F ++GFLD Sbjct: 319 TSDWLFPTAESRAVVRAMNAAAADVSFVEVTTDKGHDAFLLDEPEFHDTLQGFLD 373 Lambda K H 0.322 0.138 0.432 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: 387 Number of extensions: 17 Number of successful extensions: 5 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: 370 Length of database: 391 Length adjustment: 30 Effective length of query: 340 Effective length of database: 361 Effective search space: 122740 Effective search space used: 122740 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: 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