Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate WP_011737308.1 PPRO_RS17420 homoserine O-acetyltransferase
Query= SwissProt::S2KHP1 (367 letters) >NCBI__GCF_000015045.1:WP_011737308.1 Length = 371 Score = 259 bits (662), Expect = 8e-74 Identities = 138/358 (38%), Positives = 205/358 (57%), Gaps = 8/358 (2%) Query: 8 IELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAASSMA--DPSPG 65 I + +R+ G L +TIAYET+G L NA+L+ + SAH A + D PG Sbjct: 11 ITISDGIRLDSGRILAPITIAYETYGTLNTDASNAILVEHAWTGSAHLAGKQSENDTKPG 70 Query: 66 WWEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAA 125 WW+ ++GPG+ +DT+R+FVI N +GSCFGSTGPASINP TG+ Y L FP +++ D+V A Sbjct: 71 WWDAIVGPGRLLDTDRYFVICSNVIGSCFGSTGPASINPKTGKRYNLTFPVITIRDMVRA 130 Query: 126 ARGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQ 185 + LGI + +V G S+GGM L + YP + ++ +P I++ +I Sbjct: 131 QKLLIEMLGIRRLLSVMGGSMGGMQTLEWITQYPDAIASAVLLATTPRPSPLAISMNAIA 190 Query: 186 REAVRADPAWAGGNYAPGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANP 245 R ++ DP W G Y PKDG+ +AR +G +T+ S E +F R+ + D Sbjct: 191 RWSIFNDPTWRKGEYK--NNPKDGLALARAIGHITFLSDESMQAKFGRK--FSARDGQFD 246 Query: 246 FAMAFQVQSYMEANARKFADRFDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKRAL 305 F F+V+ Y++ N F RFDAN +LYL++A+DL+D++ G S+ A R+ A Sbjct: 247 FFGQFEVERYLDYNGYSFVSRFDANSFLYLAKALDLYDVS-WGYESMAEAFARVSAPLQF 305 Query: 306 VAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFL 363 A ++DWL+P Q ++ L G V YH + S GHDAFL++ E F+P+V FL Sbjct: 306 FA-FSSDWLYPPGQTEEMVSCLRKLGKEVEYHLISSSYGHDAFLLEHEAFSPLVKRFL 362 Lambda K H 0.320 0.135 0.414 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: 371 Number of extensions: 18 Number of successful extensions: 5 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: 367 Length of database: 371 Length adjustment: 30 Effective length of query: 337 Effective length of database: 341 Effective search space: 114917 Effective search space used: 114917 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: 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