Align L-serine/homoserine O-acetyltransferase; Homoserine O-trans-acetylase; EC 2.3.1.30; EC 2.3.1.31 (characterized)
to candidate WP_027490865.1 LRK54_RS05310 homoserine O-succinyltransferase
Query= SwissProt::D2Z028 (374 letters) >NCBI__GCF_021560695.1:WP_027490865.1 Length = 340 Score = 137 bits (344), Expect = 6e-37 Identities = 111/331 (33%), Positives = 157/331 (47%), Gaps = 48/331 (14%) Query: 41 AARDNAVLVLTGLSPDAHAASRPDDPTPGWWEAMVGPGKPVDTDLWHVICVNSLGSCKGS 100 AA V+V G+S D + D PGWW+A+VG G VD + W V+ ++ L Sbjct: 58 AAGAPTVIVQGGISADRDVTALDGDAAPGWWQALVGRGAAVDLERWRVLAIDWL------ 111 Query: 101 TGPASTDPRTGEPYRLSFPELSIEDIADAAAHTVRALGISRLACVVGASMGGMSALALLA 160 P +L +S ED ADA A +R LGI++ +G+S G M ALA A Sbjct: 112 -----------TPDQLGAGSVSSEDQADALAALLRELGIAQAHAFIGSSYGAMVALAFAA 160 Query: 161 RHPELARTHISLSGAVHALPFSIAVRSLQREAIRSDPGWLQGHYDEGEGPRRGMLTARKL 220 RHP + L+GA P S A RS+QR +R G G DE + AR+L Sbjct: 161 RHPRSVERLLLLAGAHRPHPLSTAQRSVQRGIVRL--GQASGQADE------ALALARQL 212 Query: 221 GMMTYRSAQEWDCRFGRTRIGERRRADQGRFGPEFEVESYLDFHAQRFADRFDPNSYLYL 280 + TYR + E+ RF G R + RF F VE YL +RF +RFD + +L L Sbjct: 213 AITTYRGSAEFGRRFAG---GPEWREE--RF--HFPVEDYLAHQGRRFVERFDADRFLAL 265 Query: 281 SHAMDQFDLGDGGGGGGGAPGALSRMRVERALVMGARTDILFPLSQQQEIADGLSAGGAD 340 S ++D D+ P + A ++G +D L PL+ E+ L G A Sbjct: 266 SESIDLHDI---------KPEQIP----TPATLIGFPSDRLVPLADLCELQRRLH-GPAT 311 Query: 341 VSFLPVDTPAGHDAFLVDIERFGPPVAKFLA 371 + V++P GHDAFL + E+ P + + LA Sbjct: 312 LEV--VESPYGHDAFLKEPEQLAPLLREALA 340 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: 374 Number of extensions: 20 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: 340 Length adjustment: 29 Effective length of query: 345 Effective length of database: 311 Effective search space: 107295 Effective search space used: 107295 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