Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; Beta-ketothiolase; EC 2.3.1.9 (characterized)
to candidate Dsui_0325 Dsui_0325 acetyl-CoA acetyltransferase
Query= SwissProt::P07097 (392 letters) >FitnessBrowser__PS:Dsui_0325 Length = 432 Score = 237 bits (605), Expect = 4e-67 Identities = 158/427 (37%), Positives = 229/427 (53%), Gaps = 43/427 (10%) Query: 4 PSIVIASARTAVGSFNGAFANTPAHELGATVISAVLERAGVAAGEVNEVILGQVLPAGEG 63 P V+ ART A +L A+L R A +++EV+LG P+ + Sbjct: 9 PVYVVDGARTPFLKAKNGPGPFSAADLAVQAGRALLARQPFAPEDLDEVVLGCASPSPDE 68 Query: 64 QNPARQAAMKAGVPQEATAWGMNQLCGSGLRAVALGMQQIATGDASIIVAGGMESMSMAP 123 N R AA++ G + T W + + C SG++A+ M I +G + +++AGG++++S AP Sbjct: 69 VNIGRVAALRLGCGNKVTGWTVMRNCASGMQALDSAMANIQSGRSELVLAGGVDALSRAP 128 Query: 124 HCAH------LAG-------GVKMGDFKMIDTMI--------KDGLTDAFYGYHMGTTAE 162 + AG G K G F + + GLTD G MG TAE Sbjct: 129 LLYNDAMVLWFAGMMQMKTLGQKAGHFLKLRPSVLLNPVIGLMKGLTDPVVGLLMGQTAE 188 Query: 163 NVAKQWQLSRDEQDAFAVASQNKAEAAQKDGRFKDEIVPFIVKGRKGDITVDADEYIRHG 222 N+A ++ +SR+E DAF+V S + A + F EIVP + G G + + D+ +R Sbjct: 189 NLAWRFGISREEMDAFSVRSHQRVMAGRAKQAF-GEIVPLV--GNDGTVYAE-DDGVRVD 244 Query: 223 ATLDSMAKLRPAFDKE-GTVTAGNASGLNDGAAAALLMSEAEASRRGIQPLGRIVSWATV 281 A++D M KL+P FDK+ G VT N+S + DG A LL SE+ R ++PLGRIV Sbjct: 245 ASMDGMKKLKPFFDKKYGRVTPANSSQITDGGAWLLLASESAVKRWKLEPLGRIVDAQWA 304 Query: 282 GVDPKVMGTGPIPASRKALERAGWKIGDLDLVEANEAFAAQACAVNK----------DLG 331 G+DP MG GP+ A L+R G + D+DL+E NEAFAAQ K +LG Sbjct: 305 GLDPSQMGLGPVHAVTPILQRHGLGLNDVDLMEINEAFAAQVLGCLKAWEDDAYCREELG 364 Query: 332 -------WDPSIVNVNGGAIAIGHPIGASGARILNTLLFEMKRRGARKGLATLCIGGGMG 384 D +NV+GGA+A GHP+GASGARI+ LL +K RG ++G+A++CIGGG G Sbjct: 365 LPGALGSLDQDKLNVDGGAVAQGHPVGASGARIVLHLLHALKARGGKRGVASICIGGGQG 424 Query: 385 VAMCIES 391 AM +E+ Sbjct: 425 GAMLVET 431 Lambda K H 0.317 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: 450 Number of extensions: 26 Number of successful extensions: 5 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: 432 Length adjustment: 31 Effective length of query: 361 Effective length of database: 401 Effective search space: 144761 Effective search space used: 144761 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