Align acetyl-CoA:acetyl-CoA C-acetyltransferase / acetyl-CoA:propanoyl-CoA 2-C-acetyltransferase (EC 2.3.1.9; EC 2.3.1.16) (characterized)
to candidate GFF2716 PS417_13855 acetyl-CoA acetyltransferase
Query= reanno::pseudo3_N2E3:AO353_25685 (397 letters) >FitnessBrowser__WCS417:GFF2716 Length = 394 Score = 686 bits (1769), Expect = 0.0 Identities = 346/392 (88%), Positives = 370/392 (94%) Query: 6 DPIVIVSAVRTPMGGFQGELKSLSAPQLGAAAIRAAVERAGVAADAVEEVLFGCVLSAGL 65 DPIVIVSAVRTPMGGFQG+LK L+APQLG+AAIRAAVERAG+A DAV+EVLFGCVL AGL Sbjct: 3 DPIVIVSAVRTPMGGFQGDLKGLTAPQLGSAAIRAAVERAGIATDAVDEVLFGCVLPAGL 62 Query: 66 GQAPARQAALGAGLDKSTRCTTLNKMCGSGMEAAILAHDMLLAGSADVVVAGGMESMSNA 125 GQAPARQAALGAGLDK+TRCTTLNKMCGSGMEAAILAHD LLAGS DVV+AGGMESMSNA Sbjct: 63 GQAPARQAALGAGLDKATRCTTLNKMCGSGMEAAILAHDSLLAGSVDVVIAGGMESMSNA 122 Query: 126 PYLLDRARSGYRMGHGKVLDHMFLDGLEDAYDKGRLMGTFAEDCAEANGFTREAQDEFAI 185 PYLLDRARSGYRMGH KVLDHMFLDGLEDAYDKGRLMGTFAEDCA NGFTREAQD FAI Sbjct: 123 PYLLDRARSGYRMGHSKVLDHMFLDGLEDAYDKGRLMGTFAEDCALHNGFTREAQDAFAI 182 Query: 186 ASTTRAQQAIKDGSFNAEIVPLQVIVGKEQKLITDDEQPPKAKLDKIASLKPAFRDGGTV 245 AS TRAQ+AI G+F AEIVP+QV VGKEQK I DEQPPKAKLDKI+SLK AFRDGGTV Sbjct: 183 ASLTRAQEAISHGNFAAEIVPVQVTVGKEQKTILHDEQPPKAKLDKISSLKAAFRDGGTV 242 Query: 246 TAANSSSISDGAAALLLMRRSEAEKRGLKPLAVIHGHAAFADTPGLFPVAPVGAIKKLLK 305 TAAN+SSISDGAAALLLMR+SEA+KRGLKPLAVIHGHAAFAD PGLFPVAPVGAI+KL+ Sbjct: 243 TAANASSISDGAAALLLMRQSEAQKRGLKPLAVIHGHAAFADEPGLFPVAPVGAIRKLMT 302 Query: 306 KTGWSLDEVELFEVNEAFAVVSLVTMTKLEIPHSKVNVHGGACALGHPIGASGARILVTL 365 KTGW++ EV+LFE+NEAFAVVSLVTM+KL+IPH+KVN+HGGACALGHPIGASGARILVTL Sbjct: 303 KTGWNVGEVDLFEINEAFAVVSLVTMSKLDIPHAKVNIHGGACALGHPIGASGARILVTL 362 Query: 366 LSALRQKGLKRGVAAICIGGGEATAMAVECLY 397 LSALRQ GLKRGVAAICIGGGEATAMAVECLY Sbjct: 363 LSALRQNGLKRGVAAICIGGGEATAMAVECLY 394 Lambda K H 0.318 0.133 0.378 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: 593 Number of extensions: 10 Number of successful extensions: 1 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: 397 Length of database: 394 Length adjustment: 31 Effective length of query: 366 Effective length of database: 363 Effective search space: 132858 Effective search space used: 132858 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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