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 WP_043745132.1 AMB_RS18210 acetyl-CoA C-acyltransferase
Query= reanno::pseudo3_N2E3:AO353_25685 (397 letters) >lcl|NCBI__GCF_000009985.1:WP_043745132.1 AMB_RS18210 acetyl-CoA C-acyltransferase Length = 394 Score = 553 bits (1425), Expect = e-162 Identities = 280/392 (71%), Positives = 329/392 (83%) Query: 3 MSHDPIVIVSAVRTPMGGFQGELKSLSAPQLGAAAIRAAVERAGVAADAVEEVLFGCVLS 62 M+ DPIVIV A RTPMGGFQG+ SL+APQLGAAAIRAAVER+G+A D V+EV GCVL Sbjct: 1 MTTDPIVIVGAARTPMGGFQGDFASLAAPQLGAAAIRAAVERSGLAPDQVDEVFMGCVLP 60 Query: 63 AGLGQAPARQAALGAGLDKSTRCTTLNKMCGSGMEAAILAHDMLLAGSADVVVAGGMESM 122 AG+GQAPARQA+LGAGL +S CTT++K+CGSGM+AA+LAHD+L+AG+A V+VAGGMESM Sbjct: 61 AGVGQAPARQASLGAGLPRSAGCTTISKVCGSGMKAAMLAHDLLVAGTAKVMVAGGMESM 120 Query: 123 SNAPYLLDRARSGYRMGHGKVLDHMFLDGLEDAYDKGRLMGTFAEDCAEANGFTREAQDE 182 SNAPYLLD+AR GYR+GHGKVLDHMFLDGLEDAYD+GRLMGTFAE+CA + FTREAQD Sbjct: 121 SNAPYLLDKARGGYRLGHGKVLDHMFLDGLEDAYDRGRLMGTFAEECAGSYKFTREAQDG 180 Query: 183 FAIASTTRAQQAIKDGSFNAEIVPLQVIVGKEQKLITDDEQPPKAKLDKIASLKPAFRDG 242 FA+AS +RA++AI DG F AEI P+ V K + LIT DEQP KA DKI +LKPAF Sbjct: 181 FALASLSRAKKAIADGLFAAEITPVAVAGRKGETLITIDEQPGKALPDKIPTLKPAFAKD 240 Query: 243 GTVTAANSSSISDGAAALLLMRRSEAEKRGLKPLAVIHGHAAFADTPGLFPVAPVGAIKK 302 GTVTAANSSSISDGAAAL++MRRSEAEKRGLKPLA + GH FA P LF APVGAIK Sbjct: 241 GTVTAANSSSISDGAAALVMMRRSEAEKRGLKPLATVLGHTNFAQEPALFTTAPVGAIKT 300 Query: 303 LLKKTGWSLDEVELFEVNEAFAVVSLVTMTKLEIPHSKVNVHGGACALGHPIGASGARIL 362 LL K G +++L+E+NEAFAVV++ M L++ H +VNVHGGACALGHPIGASGARI+ Sbjct: 301 LLDKVGCKAGDIDLWEINEAFAVVTMAAMHDLKLEHERVNVHGGACALGHPIGASGARII 360 Query: 363 VTLLSALRQKGLKRGVAAICIGGGEATAMAVE 394 VTLLSAL+ G+KRGVA++CIGGGEATA+ VE Sbjct: 361 VTLLSALKTYGMKRGVASLCIGGGEATALMVE 392 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: 548 Number of extensions: 6 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