Align Homoserine O-succinyltransferase; HST; EC 2.3.1.46; Homoserine transsuccinylase; HTS (uncharacterized)
to candidate WP_042444600.1 AZL_RS18255 homoserine O-acetyltransferase
Query= curated2:A0LCI7 (394 letters) >NCBI__GCF_000010725.1:WP_042444600.1 Length = 404 Score = 201 bits (510), Expect = 4e-56 Identities = 108/280 (38%), Positives = 157/280 (56%), Gaps = 14/280 (5%) Query: 31 GGTLLHSVDVSYETYGTLNQERSNAVLICHALSGNAHAAGYHSKDDKRPGWWDHYIGPGK 90 GG + +V + +E+YG LN+ + NA+LI H SG++HAAG + DD PG+WD IGPGK Sbjct: 50 GGGTIKNVRIGWESYGKLNEAKDNAILITHFFSGSSHAAGKYKADDAAPGYWDSIIGPGK 109 Query: 91 PFDTNRYFVIASNNLGGCDG------TTGPSSIDPATGMPYGLNFPMITIGDIVRVQHAL 144 P DT++YF+++S+ L TTGP+SI+P TG PYG++FP++TI D V VQ AL Sbjct: 110 PLDTDKYFILSSDTLVNLSPKDPNVITTGPASINPDTGKPYGMSFPIVTIQDFVNVQKAL 169 Query: 145 VRQLGIERLMAVVGGSMGGMQALQWALDYPHMVPASVIIAAAPRLTAQNIAFNAVARQAI 204 V LGI+ L AV+GGSMG +QA +W D+P MV + P I + + I Sbjct: 170 VDSLGIKTLQAVMGGSMGSLQAFEWGADHPEMVKRVIAAIGGPEADPFLIGWLNLWAAPI 229 Query: 205 MADPHFNGGDYYTLPGDPTTKARPESGLALARMMAHITYLSEQGLHERFGRR-LQDRDAL 263 DP++N GDYY KA P++GL A + + + FGR+ ++ Sbjct: 230 KLDPNWNNGDYY-------GKAEPKAGLTEALKLVTLQARHWKWADAAFGRKWAEEGKDP 282 Query: 264 SYGFETDFAVESYLSYQGSSFVKRFDANSYLYITKAMDYF 303 +A+E++L + DAN +LY+ KA F Sbjct: 283 KASMANQYAIEAWLDKAAAGRAAVSDANHFLYLVKANQTF 322 Lambda K H 0.320 0.136 0.417 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: 463 Number of extensions: 22 Number of successful extensions: 3 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: 394 Length of database: 404 Length adjustment: 31 Effective length of query: 363 Effective length of database: 373 Effective search space: 135399 Effective search space used: 135399 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