Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate GFF5222 PS417_26740 homoserine acetyltransferase
Query= SwissProt::Q4ZZ78 (379 letters) >FitnessBrowser__WCS417:GFF5222 Length = 379 Score = 736 bits (1899), Expect = 0.0 Identities = 353/379 (93%), Positives = 367/379 (96%) Query: 1 MPTVFPHDSVGLVTPQTAHFSEPLALACGRSLPAYDLIYETYGQLNAARSNAVLICHALS 60 MPT FP DSVGLV PQ AHFSEPLALACGR+LPAYDLIYETYGQLNA SNAVLICHALS Sbjct: 1 MPTAFPPDSVGLVVPQVAHFSEPLALACGRALPAYDLIYETYGQLNATASNAVLICHALS 60 Query: 61 GHHHAAGFHSADDRKPGWWDSCIGPGKPIDTTKFFVVSLNNLGGCNGSTGPSSIDPDTGK 120 GHHHAAGFHS D+RKPGWWDSCIGPGKPIDT KFFVVSLNNLGGCNGSTGPSSI+P+TGK Sbjct: 61 GHHHAAGFHSVDERKPGWWDSCIGPGKPIDTNKFFVVSLNNLGGCNGSTGPSSINPETGK 120 Query: 121 PFGANFPVVTVEDWVNSQARLADLLGIDTWAAVIGGSLGGMQALQWTISYPNRVRHCLAI 180 PFGA+FPV+TVEDWV+SQARLADLLGI+ WAAVIGGSLGGMQALQWTI+YP+RVRHCLAI Sbjct: 121 PFGADFPVLTVEDWVHSQARLADLLGINQWAAVIGGSLGGMQALQWTITYPDRVRHCLAI 180 Query: 181 ASAPKLSAQNIAFNEVARQAILTDPEFHGGSFQERGVIPKRGLMLARMVGHITYLSDDSM 240 ASAPKLSAQNIAFNEVARQAILTDPEFHGGSFQE GVIPKRGLMLARMVGHITYLSDDSM Sbjct: 181 ASAPKLSAQNIAFNEVARQAILTDPEFHGGSFQEAGVIPKRGLMLARMVGHITYLSDDSM 240 Query: 241 GEKFGRGLKSEKLNYDFHSVEFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFDPAANF 300 GEKFGRGLKSEKLNYDFHSVEFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFDPAANF Sbjct: 241 GEKFGRGLKSEKLNYDFHSVEFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFDPAANF 300 Query: 301 NDDLAKTFANATARFCVMSFTTDWRFSPARSRELVDALMAARKDVCYLEIDAPQGHDAFL 360 +DDLAKTF ATA+FCVMSFTTDWRFSPARSRELVDALMAARKDVCYLEIDAPQGHDAFL Sbjct: 301 DDDLAKTFEGATAKFCVMSFTTDWRFSPARSRELVDALMAARKDVCYLEIDAPQGHDAFL 360 Query: 361 IPIPRYLQAFGNYMNRISL 379 IPIPRYLQAFGNYMNRI++ Sbjct: 361 IPIPRYLQAFGNYMNRITV 379 Lambda K H 0.321 0.137 0.428 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: 608 Number of extensions: 18 Number of successful extensions: 1 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: 379 Length of database: 379 Length adjustment: 30 Effective length of query: 349 Effective length of database: 349 Effective search space: 121801 Effective search space used: 121801 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 Aug 03 2021. The underlying query database was built on Aug 03 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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