Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate WP_013644807.1 METBO_RS06075 homoserine O-acetyltransferase
Query= SwissProt::D2Z028 (374 letters) >NCBI__GCF_000191585.1:WP_013644807.1 Length = 489 Score = 257 bits (656), Expect = 5e-73 Identities = 138/365 (37%), Positives = 212/365 (58%), Gaps = 10/365 (2%) Query: 9 SRFIELPDGFAMRRGGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAASRPD-DPT 67 +++ L D + G L ++AYET+G LN + NA+LV L+ DAH A + D Sbjct: 11 TKYHSLSDDLILESGEKLKNVQVAYETYGKLNKEKSNAILVCHALTGDAHVAGWYEGDKK 70 Query: 68 PGWWEAMVGPGKPVDTDLWHVICVNSLGSCKGSTGPASTDPRTGEPYRLSFPELSIEDIA 127 PGWW+ ++GPGK +DT+ + +IC N +G CKGSTGP+S +P T +PY L FP ++I+D+ Sbjct: 71 PGWWDVIIGPGKCLDTEKYFIICSNVIGGCKGSTGPSSINPETNKPYGLDFPIITIKDMV 130 Query: 128 DAAAHTVRALGISRLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFSIAVRS 187 +A V ++G+++L V+G SMGGM L +P++ R+ I ++ + P IA Sbjct: 131 NAQKKLVNSMGVTQLFAVIGGSMGGMQVLQWCVSYPDMVRSAIPIATTAFSSPQQIAFNE 190 Query: 188 LQREAIRSDPGWLQGHYDEGEGPRRGMLTARKLGMMTYRSAQEWDCRFGRTRIGERRRAD 247 + R AI SDP W G Y + E P G+ AR + +TY S + +FGR R+ ++ D Sbjct: 191 VGRRAIISDPNWNNGQYYDSEVPTEGLALARMIAHITYLSNESMYQKFGR-RLQDKE--D 247 Query: 248 QG-RFGPEFEVESYLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAPGALSRM 306 G F +FEVESYL + F RFD NSYLY++ A+D FDL G G + Sbjct: 248 YGFDFETDFEVESYLHYQGNSFTKRFDANSYLYITKAVDYFDL----AGEGSLAETFYGL 303 Query: 307 RVERALVMGARTDILFPLSQQQEIADGLSAGGADVSFLPVDTPAGHDAFLVDIERFGPPV 366 ++ + LV+ +D L+P S ++I GL+A +VS+ + + GHDAFL++ + + Sbjct: 304 KI-KFLVISVDSDWLYPPSLSRDIVMGLNANDINVSYCEIKSSYGHDAFLIEAGQLNYLI 362 Query: 367 AKFLA 371 A FL+ Sbjct: 363 AGFLS 367 Lambda K H 0.321 0.138 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: 428 Number of extensions: 15 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: 374 Length of database: 489 Length adjustment: 32 Effective length of query: 342 Effective length of database: 457 Effective search space: 156294 Effective search space used: 156294 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: 51 (24.3 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