Align Serine O-succinyltransferase; SST; EC 2.3.1.- (characterized)
to candidate WP_042444600.1 AZL_RS18255 homoserine O-acetyltransferase
Query= SwissProt::A0A1D3PCM3 (517 letters) >NCBI__GCF_000010725.1:WP_042444600.1 Length = 404 Score = 178 bits (451), Expect = 4e-49 Identities = 100/275 (36%), Positives = 147/275 (53%), Gaps = 10/275 (3%) Query: 112 GGLLPEFDIAYETWGQLNEKKDNVILLHTGLSASSHAHSTEA--NPKPGWWEKFIGPGKT 169 GG + I +E++G+LNE KDN IL+ S SSHA + PG+W+ IGPGK Sbjct: 51 GGTIKNVRIGWESYGKLNEAKDNAILITHFFSGSSHAAGKYKADDAAPGYWDSIIGPGKP 110 Query: 170 LDTDKYFVICTNVLGGCYG------STGPSTVDPSDGKKYATRFPILTIEDMVRAQFRLL 223 LDTDKYF++ ++ L +TGP++++P GK Y FPI+TI+D V Q L+ Sbjct: 111 LDTDKYFILSSDTLVNLSPKDPNVITTGPASINPDTGKPYGMSFPIVTIQDFVNVQKALV 170 Query: 224 DHLGVRKLYASVGSSMGGMQSLAAGVLFPERVGKIVSISGCARSHPYSIAMRHTQRQVLM 283 D LG++ L A +G SMG +Q+ G PE V ++++ G + P+ I + + Sbjct: 171 DSLGIKTLQAVMGGSMGSLQAFEWGADHPEMVKRVIAAIGGPEADPFLIGWLNLWAAPIK 230 Query: 284 MDPNWARGFYYDSIPPHSGMKLAREIATVTYRSGPEWEKRFGRKRADPSKQP--ALCPDF 341 +DPNW G YY P +G+ A ++ T+ R + FGRK A+ K P ++ + Sbjct: 231 LDPNWNNGDYYGKAEPKAGLTEALKLVTLQARHWKWADAAFGRKWAEEGKDPKASMANQY 290 Query: 342 LIETYLDHAGEKFCLEYDANSLLYISKAMDLFDLG 376 IE +LD A DAN LY+ KA F G Sbjct: 291 AIEAWLDKAAAGRAAVSDANHFLYLVKANQTFVTG 325 Lambda K H 0.316 0.132 0.397 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: 539 Number of extensions: 24 Number of successful extensions: 4 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: 517 Length of database: 404 Length adjustment: 33 Effective length of query: 484 Effective length of database: 371 Effective search space: 179564 Effective search space used: 179564 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 51 (24.3 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