Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate WP_092345255.1 BLU87_RS04830 homoserine O-acetyltransferase
Query= SwissProt::D2Z028 (374 letters) >NCBI__GCF_900107645.1:WP_092345255.1 Length = 370 Score = 241 bits (614), Expect = 3e-68 Identities = 135/367 (36%), Positives = 208/367 (56%), Gaps = 15/367 (4%) Query: 9 SRFIELPDGFAMRRGGALYGARIAYETFGSLNAARDNAVLVLTGLSPDAHAASR--PDDP 66 +++ E + G L +AYET+G LNA N +LV + +AHAA R +D Sbjct: 10 TKYAEFDVELRLESGRLLGPLTLAYETYGELNADASNVILVTHAWTGNAHAAGRHSEEDR 69 Query: 67 TPGWWEAMVGPGKPVDTDLWHVICVNSLGSCKGSTGPASTDPRTGEPYRLSFPELSIEDI 126 PGWW+ M+GPGK +DT+ + ++ N++GSCKGSTGP S +PRT +PYRLSFP + I D+ Sbjct: 70 KPGWWDNMIGPGKVLDTNRYFILSSNTIGSCKGSTGPTSINPRTRKPYRLSFPVIMIRDM 129 Query: 127 ADAAAHTVRALGISRLACVVGASMGGMSALALLARHPELARTHISLSGAVHALPFSIAVR 186 A + LGI+ LA +VG SMG M A+ +P++ R + ++G P +IA+ Sbjct: 130 VRAQKLLLDHLGITSLAAIVGGSMGAMQAIEWAIHYPDMVRAIVPIAGTGKTAPMAIALN 189 Query: 187 SLQREAIRSDPGWLQGHYDEGEGPRRGMLTARKLGMMTYRSAQEWDCRFGRTRIGERR-- 244 +L R+AI +DP W +G+Y P G AR +G +++ S +F ERR Sbjct: 190 ALARQAIFNDPLWKKGNYQPEHPPADGFSLARAVGHISFLSDISMQLKF------ERRFS 243 Query: 245 -RADQGRFGPEFEVESYLDFHAQRFADRFDPNSYLYLSHAMDQFDLGDGGGGGGGAPGAL 303 R F +FEVE YLD++ + F D+FDPNS+LYL+ A+D +D+ AL Sbjct: 244 VRDGMFDFFGKFEVERYLDYNGKNFVDQFDPNSFLYLAKALDLYDV---AWNFDSLSEAL 300 Query: 304 SRMRVERALVMGARTDILFPLSQQQEIADGLSAGGADVSFLPVDTPAGHDAFLVDIERFG 363 R++ ++ +D L+P Q +E+ + L V + +D+ GHD+FLV+ E++ Sbjct: 301 ERVQCP-SIWFAFNSDWLYPAQQTEELVEELQRLNKTVDYHLIDSDYGHDSFLVEPEKYI 359 Query: 364 PPVAKFL 370 P + +FL Sbjct: 360 PLLKEFL 366 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: 375 Number of extensions: 18 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: 370 Length adjustment: 30 Effective length of query: 344 Effective length of database: 340 Effective search space: 116960 Effective search space used: 116960 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