Align acetyl-CoA C-acetyltransferase (EC 2.3.1.9) (characterized)
to candidate WP_059150365.1 V474_RS04935 acetyl-CoA C-acyltransferase
Query= BRENDA::Q0KAI3 (392 letters) >NCBI__GCF_001046635.1:WP_059150365.1 Length = 417 Score = 246 bits (628), Expect = 9e-70 Identities = 155/419 (36%), Positives = 228/419 (54%), Gaps = 29/419 (6%) Query: 1 MQQAVIVDAIRSPMGRSKPGS-AFTELHATELLAQVIKGLVERNKLDPGLVDDVITGCVT 59 M +A I+DA+R+P G K G A +++H L A V+ L +RN +D VDDVI G Sbjct: 1 MTEAYIIDAVRTPRGLGKMGKGALSQMHPEHLSASVLAALKDRNAIDTAEVDDVIWGVSA 60 Query: 60 QAGEQSAGPGRVAWLAAGFPDHVPATTIDRKCGSSQQAVHFAAQGIMAGAYDIVIACGIE 119 G+Q+ GR+A L AG+ T++R CGSS + AA I +G D+++A G++ Sbjct: 61 ALGQQAGDIGRMAALDAGYDVKAGGVTLNRFCGSSITSTSLAAAMIKSGMADLMVAGGMD 120 Query: 120 SMSRVPM--------GSARIGQNPYGPSMEARYAPGLVSQGVAAELVAAKYELSRHDMDS 171 +S M G G P ++A++ +QGVAA+ +AA +R ++++ Sbjct: 121 MLSYAGMYGMKMREAGLGSAGMGAGNPRLQAKHPQS--NQGVAADAIAAMEGFTRAELEA 178 Query: 172 YSARSHELAATARESGAFRREILGISTPNG--LVEQDETIRPGTSVEKLGTLQASFRN-- 227 S AA A G F R + + G +++ +E RP T+ E L L +F Sbjct: 179 LGVESQRRAALAIAEGRFDRSTITVKDDEGNVILDHEEYPRPETTAESLAQLTPAFEMFY 238 Query: 228 ------------DELSARFPQIGWNVT--AGNASQISDGASAMLLMSESMAQRLGLKPRA 273 ++ +P++ G +S + DGASA+LL S A+ GL PRA Sbjct: 239 DMPSAPGGKTYVQLINQVYPELEIKPIHHVGISSGVVDGASAILLASRDYAKSHGLTPRA 298 Query: 274 RFVAFDVCGDDPVMMLTAPIPASQRAIKKSGLKLDQIDHYEINEAFACVPLAWQRALGAD 333 R VA GD P +ML P+PA+++ + K+GL + ID +E+NEAFA V + R L D Sbjct: 299 RIVAMAETGDCPTLMLNGPVPAARKVLAKAGLTVADIDVFEVNEAFAVVVEKFIRDLDLD 358 Query: 334 PARLNPRGGAIALGHPLGASGVRLMTTMLHALEDSGQRYGLQSMCEAGGMANATIIERL 392 AR+NP GG++ALGHP+GA+G L+ T L LE +G RYGL +MC AGGMA A IIER+ Sbjct: 359 RARVNPNGGSMALGHPIGATGAMLIGTALDELERTGGRYGLITMCAAGGMAPAIIIERV 417 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: 399 Number of extensions: 21 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: 392 Length of database: 417 Length adjustment: 31 Effective length of query: 361 Effective length of database: 386 Effective search space: 139346 Effective search space used: 139346 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 24 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:
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