Align Homoserine O-succinyltransferase; HST; EC 2.3.1.46; Homoserine transsuccinylase; HTS (uncharacterized)
to candidate WP_011391014.1 RRU_RS16855 homoserine O-acetyltransferase
Query= curated2:A0LCI7 (394 letters) >NCBI__GCF_000013085.1:WP_011391014.1 Length = 391 Score = 390 bits (1002), Expect = e-113 Identities = 197/358 (55%), Positives = 249/358 (69%), Gaps = 8/358 (2%) Query: 26 PLQLDGGTLLHSVDVSYETYGTLNQERSNAVLICHALSGNAHAAGYHSKDDKRPGWWDHY 85 P++LD G L + V+Y+T G LN ER+NA+LICHAL+G+ H G H RPGWW+ Sbjct: 22 PMRLDSGLELGPLTVAYQTIGRLNAERTNAILICHALTGDQHVIGPHPVTG-RPGWWETL 80 Query: 86 IGPGKPFDTNRYFVIASNNLGGCDGTTGPSSIDPATGMPYGLNFPMITIGDIVRVQHALV 145 +GPGK DT+RYF+I SN LGGC GTTGP I+PATG P+GL FP+ITIGD+VR Q L+ Sbjct: 81 VGPGKTIDTDRYFIICSNVLGGCLGTTGPKEINPATGKPWGLGFPVITIGDMVRAQALLL 140 Query: 146 RQLGIERLMAVVGGSMGGMQALQWALDYPHMVPASVIIAAAPRLTAQNIAFNAVARQAIM 205 LGIERL +GGSMG MQ LQWA+ YP V A V IA + R +AQNIAF+ V RQAIM Sbjct: 141 DHLGIERLFCAIGGSMGAMQVLQWAVSYPERVRAVVPIAGSWRHSAQNIAFHEVGRQAIM 200 Query: 206 ADPHFNGGDYYTLPGDPTTKARPESGLALARMMAHITYLSEQGLHERFGRRLQDRDALSY 265 ADP +NGGDY P GLA+ARM AHITYLSE L +FGR+LQDR +++Y Sbjct: 201 ADPDWNGGDYL------NQGTVPRRGLAVARMTAHITYLSEPALQSKFGRKLQDRASITY 254 Query: 266 GFETDFAVESYLSYQGSSFVKRFDANSYLYITKAMDYFDPFPDAETTVQR-LTGVESHFL 324 GF+ DF VESYL +QG++FVKRFDANSYLYIT+AMDYFD + + + R G + F Sbjct: 255 GFDADFQVESYLRHQGANFVKRFDANSYLYITRAMDYFDLAAEHDGVLARAFQGTKVRFC 314 Query: 325 VMSFDTDWRFDTSRSKELVRILHRSLKDCTFQEFSSPAGHDAFLLPHPSYEKSLGSFL 382 V+SF +DW F T+ S+ +VR ++ + D +F E ++ GHDAFLL P + +L FL Sbjct: 315 VVSFTSDWLFPTAESRAVVRAMNAAAADVSFVEVTTDKGHDAFLLDEPEFHDTLQGFL 372 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: 508 Number of extensions: 28 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: 394 Length of database: 391 Length adjustment: 31 Effective length of query: 363 Effective length of database: 360 Effective search space: 130680 Effective search space used: 130680 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