Align serine O-acetyltransferase; EC 2.3.1.30 (characterized, see rationale)
to candidate WP_035239963.1 Q366_RS13785 serine acetyltransferase
Query= uniprot:Q72EB6_DESVH (323 letters) >NCBI__GCF_000745975.1:WP_035239963.1 Length = 327 Score = 262 bits (670), Expect = 7e-75 Identities = 135/296 (45%), Positives = 189/296 (63%), Gaps = 8/296 (2%) Query: 10 VSLTGMPE-LERIVESLCTPESYEAVYHQSLHGSPMPSLEALTELMARLRAALFPGYFGA 68 V T +P ++RI+ +L PE + + + +H S ++ +++ +LR LFPGYF Sbjct: 21 VQRTALPGVIDRIINTLDDPECFAHIGDEPIHFST-----SVGDMIEKLRNILFPGYFSN 75 Query: 69 SNIVLESMRYHLAANLDSIYRILAEQVRRGGCFACADYATDCQNCESHSQETAMEFMRAL 128 + ++ YH+ + +Y IL+ QV C Y C CE E A + + Sbjct: 76 EKVDSVNLTYHMGQEITRLYDILSRQVIHVLRHDCLRYDRVCSECERRGNEAAFTVIEQI 135 Query: 129 PRIRQLLATDVKAAYEGDPAAKSPGETIFCYPSIYAMIHHRIAHELYRLDVPVIPRIISE 188 P +R+ L+ DV+AAY+GDPAAKS E IF YP +YA+ HRIA L++LD+P +PRI+SE Sbjct: 136 PVLRKKLSADVRAAYDGDPAAKSHDEIIFSYPGLYAITVHRIARILHQLDIPQLPRIMSE 195 Query: 189 MAHSRTGIDIHPGATVGEEFFIDHGTGVVIGETCIIGRGCRLYQGVTLGALSFPKDGGGA 248 +AHS TGIDIHPGAT+GE F IDHGTGVVIGET +IG R+YQ VT+GALS P+D G Sbjct: 196 LAHSLTGIDIHPGATIGERFVIDHGTGVVIGETSVIGDNVRIYQNVTIGALSLPRDAGEK 255 Query: 249 LIKGIPRHPILQDGVTVYAGATILGRVT-IGAGAIVGGNVWVTHDVAPGAKVVQQK 303 L + RHP ++D V VY+GAT+LG T IGA ++VGGNVW+TH + K+ ++ Sbjct: 256 L-RWAKRHPTIEDDVIVYSGATVLGGDTVIGARSVVGGNVWLTHSIPADTKIFMEE 310 Lambda K H 0.320 0.137 0.410 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: 362 Number of extensions: 22 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: 323 Length of database: 327 Length adjustment: 28 Effective length of query: 295 Effective length of database: 299 Effective search space: 88205 Effective search space used: 88205 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: 48 (23.1 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