Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate Pf6N2E2_4597 Homoserine O-acetyltransferase (EC 2.3.1.31)
Query= SwissProt::Q4ZZ78 (379 letters) >FitnessBrowser__pseudo6_N2E2:Pf6N2E2_4597 Length = 363 Score = 711 bits (1834), Expect = 0.0 Identities = 341/362 (94%), Positives = 354/362 (97%) Query: 18 AHFSEPLALACGRSLPAYDLIYETYGQLNAARSNAVLICHALSGHHHAAGFHSADDRKPG 77 AHFSEPLALACGRSLPAYDLIYETYG LNA SNAVLICHALSGHHHAAG+HS DDRKPG Sbjct: 2 AHFSEPLALACGRSLPAYDLIYETYGTLNATASNAVLICHALSGHHHAAGYHSVDDRKPG 61 Query: 78 WWDSCIGPGKPIDTTKFFVVSLNNLGGCNGSTGPSSIDPDTGKPFGANFPVVTVEDWVNS 137 WWDSCIGPGKPIDT+KFFVVSLNNLGGCNGSTGPSS++PDTGKPFGA+FPV+TVEDWV+S Sbjct: 62 WWDSCIGPGKPIDTSKFFVVSLNNLGGCNGSTGPSSLNPDTGKPFGADFPVLTVEDWVHS 121 Query: 138 QARLADLLGIDTWAAVIGGSLGGMQALQWTISYPNRVRHCLAIASAPKLSAQNIAFNEVA 197 QARLAD LGI WAAVIGGSLGGMQALQWTI+YP+RVRHCLAIASAPKLSAQNIAFNEVA Sbjct: 122 QARLADRLGIGQWAAVIGGSLGGMQALQWTITYPDRVRHCLAIASAPKLSAQNIAFNEVA 181 Query: 198 RQAILTDPEFHGGSFQERGVIPKRGLMLARMVGHITYLSDDSMGEKFGRGLKSEKLNYDF 257 RQAILTDPEFHGGSFQE GVIPKRGLMLARMVGHITYLSDDSMGEKFGRGLKSEKLNYDF Sbjct: 182 RQAILTDPEFHGGSFQEHGVIPKRGLMLARMVGHITYLSDDSMGEKFGRGLKSEKLNYDF 241 Query: 258 HSVEFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFDPAANFNDDLAKTFANATARFCV 317 HSVEFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFDPAANF+D+LAKTFANATA+FCV Sbjct: 242 HSVEFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFDPAANFDDNLAKTFANATAKFCV 301 Query: 318 MSFTTDWRFSPARSRELVDALMAARKDVCYLEIDAPQGHDAFLIPIPRYLQAFGNYMNRI 377 MSFTTDWRFSPARSRELVDALMAARKDVCYLEIDAPQGHDAFLIPIPRYLQAFGNYMNRI Sbjct: 302 MSFTTDWRFSPARSRELVDALMAARKDVCYLEIDAPQGHDAFLIPIPRYLQAFGNYMNRI 361 Query: 378 SL 379 +L Sbjct: 362 TL 363 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: 569 Number of extensions: 15 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: 363 Length adjustment: 30 Effective length of query: 349 Effective length of database: 333 Effective search space: 116217 Effective search space used: 116217 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: 49 (23.5 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