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 H281DRAFT_06132 H281DRAFT_06132 acetyl-CoA C-acetyltransferase
Query= reanno::pseudo3_N2E3:AO353_25685 (397 letters) >lcl|FitnessBrowser__Burk376:H281DRAFT_06132 H281DRAFT_06132 acetyl-CoA C-acetyltransferase Length = 395 Score = 528 bits (1361), Expect = e-155 Identities = 268/393 (68%), Positives = 322/393 (81%), Gaps = 1/393 (0%) Query: 3 MSHDPIVIVSAVRTPMGGFQGELKSLSAPQLGAAAIRAAVERAGVAADAVEEVLFGCVLS 62 M++DPIVIVSA RTPMGGFQGEL L+AP LGA AI+AA+ERAGV+ V+E+ GCVLS Sbjct: 1 MNNDPIVIVSAARTPMGGFQGELNLLTAPALGAVAIKAALERAGVSGSQVDELTLGCVLS 60 Query: 63 AGLGQAPARQAALGAGLDKSTRCTTLNKMCGSGMEAAILAHDMLLAGSADVVVAGGMESM 122 AGLGQAPARQAA+ AGL S C+T++K+CGSGM+A ++AHD L AGSA V+VAGGMESM Sbjct: 61 AGLGQAPARQAAIAAGLPLSVHCSTVSKVCGSGMKAVMVAHDALAAGSASVIVAGGMESM 120 Query: 123 SNAPYLLDRARSGYRMGHGKVLDHMFLDGLEDAY-DKGRLMGTFAEDCAEANGFTREAQD 181 SNAPYLL +AR+G RMGH LDHMF DGLEDAY D+GRLMGTFAEDCAE FTR QD Sbjct: 121 SNAPYLLPKARAGLRMGHAAALDHMFFDGLEDAYFDRGRLMGTFAEDCAERFCFTRGDQD 180 Query: 182 EFAIASTTRAQQAIKDGSFNAEIVPLQVIVGKEQKLITDDEQPPKAKLDKIASLKPAFRD 241 +AIAST +AQQAI+ G+F+ EI P+ V +K + DEQPPKA+LDKI SLK AF+ Sbjct: 181 SYAIASTVKAQQAIESGAFDWEIAPVTVTSKVGEKTVDTDEQPPKARLDKIQSLKAAFKK 240 Query: 242 GGTVTAANSSSISDGAAALLLMRRSEAEKRGLKPLAVIHGHAAFADTPGLFPVAPVGAIK 301 GTVTAANSSSISDGAAAL+LMR S AE++GL+PLAV+ GH+ +AD P LF AP+GAI+ Sbjct: 241 DGTVTAANSSSISDGAAALVLMRLSTAERQGLQPLAVVVGHSTYADEPRLFTTAPIGAIR 300 Query: 302 KLLKKTGWSLDEVELFEVNEAFAVVSLVTMTKLEIPHSKVNVHGGACALGHPIGASGARI 361 KLL +T WS+ +V+L+E+NEAFAVVS+ +L I +VN+HGGACALGHPIGASGARI Sbjct: 301 KLLDRTEWSIGDVDLWEINEAFAVVSMACTKELGIAPERVNIHGGACALGHPIGASGARI 360 Query: 362 LVTLLSALRQKGLKRGVAAICIGGGEATAMAVE 394 LVTLL ALRQ G KRG+A++CIGGGEATA+A+E Sbjct: 361 LVTLLGALRQTGGKRGIASLCIGGGEATAVAIE 393 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: 492 Number of extensions: 10 Number of successful extensions: 2 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: 395 Length adjustment: 31 Effective length of query: 366 Effective length of database: 364 Effective search space: 133224 Effective search space used: 133224 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