Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_041101080.1 SUTH_RS17455 homoserine O-acetyltransferase
Query= SwissProt::A9I0E6 (424 letters) >NCBI__GCF_000828635.1:WP_041101080.1 Length = 372 Score = 517 bits (1331), Expect = e-151 Identities = 245/371 (66%), Positives = 294/371 (79%), Gaps = 4/371 (1%) Query: 26 VGIVTPQLIRFDTPLPLASGQSLQSYELAVETYGTLNAGRTNAVLVCHALNASHHVAGLA 85 VG+V+ Q+ F PL L G L +++L ETYGTLNA ++NA+LVCHAL+ HHVAG Sbjct: 4 VGLVSAQIAHFTQPLALKGGGLLPAFDLVYETYGTLNAAKSNAILVCHALSGHHHVAGHT 63 Query: 86 ADDPNDVGWWDNMVGPGKPLDTNRFFVIGVNNLGSCFGSTGPASINPATGHPWGAAFPVL 145 +P ++GWWDN+VGPG+PLDT RFF++GVNNLG C GSTGPAS NPATG PWGA FPV+ Sbjct: 64 EGNPANIGWWDNIVGPGRPLDTERFFIVGVNNLGGCHGSTGPASTNPATGKPWGADFPVV 123 Query: 146 TVEDWVHAQARLADHFGIERFAAVMGGSLGGMQALSWAITCPERVAHCIVIASTPRLSAQ 205 TVEDWV AQARLADH GI +AAVMGGSLGGMQAL W ++ P+RV H +VIA+ P+LSA+ Sbjct: 124 TVEDWVDAQARLADHLGIGAWAAVMGGSLGGMQALQWTLSFPDRVRHALVIAAAPKLSAE 183 Query: 206 NIGFNEVARRAIITDPDFHGGDYYAHNTVPRRGLSVARMIGHITYLSDDDMAEKFGRTQR 265 NI FN+VAR+AI+TDPDFHGG +Y H P RGL +ARM+GHITYLSDD MAEKFGR R Sbjct: 184 NIAFNDVARQAILTDPDFHGGHFYEHGVRPVRGLRLARMLGHITYLSDDQMAEKFGRRLR 243 Query: 266 EPAEGGAYRYGYDVEFEVESYLRYQGEKFSRYFDANTYLLITRALDYFDPARGTGGDLAR 325 GA YG+DVEFE+ESYLRYQG+KF+ FDANTYL +T+ALDYFDPA+ DLAR Sbjct: 244 T----GAGSYGFDVEFEIESYLRYQGDKFAGVFDANTYLRMTKALDYFDPAQDFDDDLAR 299 Query: 326 ALKPAQADFLLVSFSTDWRFPPERSREIVRALLKNGSPVTYAEIDAPHGHDAFLLDDARY 385 AL A+A FL+V+FSTDWRF PERSREIV AL+ NG V YAEID+ HGHD+FL+D+ Y Sbjct: 300 ALARARAKFLVVAFSTDWRFSPERSREIVHALVHNGQAVAYAEIDSAHGHDSFLMDEPHY 359 Query: 386 HAVVRGYYERI 396 HAVV Y +R+ Sbjct: 360 HAVVDTYLKRV 370 Lambda K H 0.320 0.137 0.427 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: 615 Number of extensions: 26 Number of successful extensions: 2 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: 424 Length of database: 372 Length adjustment: 31 Effective length of query: 393 Effective length of database: 341 Effective search space: 134013 Effective search space used: 134013 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