Align acetyl-CoA C-acetyltransferase (EC 2.3.1.9) (characterized)
to candidate GFF4143 PS417_21220 acetyl-CoA acetyltransferase
Query= BRENDA::Q0KAI3 (392 letters) >FitnessBrowser__WCS417:GFF4143 Length = 401 Score = 287 bits (735), Expect = 3e-82 Identities = 168/412 (40%), Positives = 244/412 (59%), Gaps = 31/412 (7%) Query: 1 MQQAVIVDAIRSPMGRSKPGSAFTELHATELLAQVIKGLVERNKLDPGLVDDVITGCVTQ 60 M QA+I DAIR+P G+ K A + L+A ++ L R+ LD VDD++ GCVT Sbjct: 1 MTQALIFDAIRTPRGKGKADGALHSVKPVNLVAGLLTALARRSDLDTHQVDDIVLGCVTP 60 Query: 61 AGEQSAGPGRVAWLAAGFPDHVPATTIDRKCGSSQQAVHFAAQGIMAGAYDIVIACGIES 120 G+Q A + A L A + V I+R C S +AV+ A + +G D+V+ G+ES Sbjct: 61 IGDQGADIAKTAALVADWDISVAGVQINRFCASGLEAVNVGAMKVRSGFEDLVVVGGVES 120 Query: 121 MSRVPMGSARIGQNPYGP--SMEARYAPGLVSQGVAAELVAAKYELSRHDMDSYSARSHE 178 MSRVPMGS G P +M + + P QG+ A+L+A +R D+D+++ S + Sbjct: 121 MSRVPMGSDG-GAWVLDPQTNMHSHFTP----QGIGADLIATLEGFTRDDVDAFALHSQQ 175 Query: 179 LAATARESGAFRREILGISTPNGLV--EQDETIRPGTSVEKLGTLQASFRNDELSARFPQ 236 AA AR G+F + ++ + NG+V + DE IR +++E LG L+ SF Q Sbjct: 176 KAARARADGSFNKSLIAVQDQNGIVLLDHDEFIRGDSTLEGLGKLKPSFE------MMGQ 229 Query: 237 IGWNVTA----------------GNASQISDGASAMLLMSESMAQRLGLKPRARFVAFDV 280 +G++ TA GN+S I DGA+ ML+ SE+ + LGL+PRAR VA V Sbjct: 230 MGFDATALRVYSHVERIHHVHTPGNSSGIVDGAALMLIGSEAKGRELGLQPRARIVATAV 289 Query: 281 CGDDPVMMLTAPIPASQRAIKKSGLKLDQIDHYEINEAFACVPLAWQRALGADPARLNPR 340 DP +MLT P PA+++A+ K+GL+++ ID +E+NEAFA V L + + +G D AR+N Sbjct: 290 TSTDPTIMLTGPAPATRKALAKAGLRIEDIDLFEVNEAFASVVLKFIKDMGIDAARVNVN 349 Query: 341 GGAIALGHPLGASGVRLMTTMLHALEDSGQRYGLQSMCEAGGMANATIIERL 392 GG+IA+GHPLGA+G ++ T+L LE QRYGL ++C GGM ATIIERL Sbjct: 350 GGSIAMGHPLGATGCAILGTLLDELEVRQQRYGLATLCVGGGMGIATIIERL 401 Lambda K H 0.318 0.132 0.384 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: 421 Number of extensions: 21 Number of successful extensions: 3 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: 392 Length of database: 401 Length adjustment: 31 Effective length of query: 361 Effective length of database: 370 Effective search space: 133570 Effective search space used: 133570 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 Apr 09 2024. 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:
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