Align Beta-ketothiolase BktB; Acetyl-CoA acetyltransferase; Acetyl-CoA acyltransferase; EC 2.3.1.16; EC 2.3.1.9 (characterized)
to candidate Ac3H11_178 3-ketoacyl-CoA thiolase (EC 2.3.1.16) @ Acetyl-CoA acetyltransferase (EC 2.3.1.9)
Query= SwissProt::Q0KBP1 (394 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_178 Length = 394 Score = 608 bits (1567), Expect = e-178 Identities = 305/394 (77%), Positives = 338/394 (85%) Query: 1 MTREVVVVSGVRTAIGTFGGSLKDVAPAELGALVVREALARAQVSGDDVGHVVFGNVIQT 60 MTREVVVVS VRTAIGTFGGSLKD+AP +LGALVV+E+LARA V G DVGHVVFG+V+ T Sbjct: 1 MTREVVVVSAVRTAIGTFGGSLKDIAPTDLGALVVKESLARASVEGKDVGHVVFGHVVNT 60 Query: 61 EPRDMYLGRVAAVNGGVTINAPALTVNRLCGSGLQAIVSAAQTILLGDTDVAIGGGAESM 120 EP+DMYL RVAA+NGG PA VNRLCGSGLQAIVSAAQ I LGD DV IG GAE M Sbjct: 61 EPKDMYLSRVAAINGGCAEGTPAFNVNRLCGSGLQAIVSAAQAIQLGDADVTIGAGAEVM 120 Query: 121 SRAPYLAPAARWGARMGDAGLVDMMLGALHDPFHRIHMGVTAENVAKEYDISRAQQDEAA 180 SRAP+ + RWGARMGD +VDMM+GALHDPFH IHMGVTAEN+A ++ ISR QD+ A Sbjct: 121 SRAPFASLNMRWGARMGDTKMVDMMIGALHDPFHTIHMGVTAENIAAKWGISREDQDKLA 180 Query: 181 LESHRRASAAIKAGYFKDQIVPVVSKGRKGDVTFDTDEHVRHDATIDDMTKLRPVFVKEN 240 +ESH RA A AGYFKDQIVPV K +KGDV + TDEH R AT+DD KL+PVFVKEN Sbjct: 181 VESHNRAERATAAGYFKDQIVPVTLKSKKGDVQYATDEHFRPGATLDDFAKLKPVFVKEN 240 Query: 241 GTVTAGNASGLNDAAAAVVMMERAEAERRGLKPLARLVSYGHAGVDPKAMGIGPVPATKI 300 GTVTAGNASG+NDAAAAVV+M+ A A+ RG KPLARLV+Y HAGVDPK MGIGPVPAT++ Sbjct: 241 GTVTAGNASGINDAAAAVVLMDAAAAKARGAKPLARLVAYAHAGVDPKYMGIGPVPATQL 300 Query: 301 ALERAGLQVSDLDVIEANEAFAAQACAVTKALGLDPAKVNPNGSGISLGHPIGATGALIT 360 AL++AGL V+DLDVIEANEAFAAQACAVTK LGLDPAKVNPNGSGISLGHPIGATGALIT Sbjct: 301 ALKKAGLTVADLDVIEANEAFAAQACAVTKDLGLDPAKVNPNGSGISLGHPIGATGALIT 360 Query: 361 VKALHELNRVQGRYALVTMCIGGGQGIAAIFERI 394 VKA+HEL RVQGRYALVTMCIGGGQGIAAIFER+ Sbjct: 361 VKAIHELQRVQGRYALVTMCIGGGQGIAAIFERL 394 Lambda K H 0.318 0.134 0.381 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: 569 Number of extensions: 7 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: 394 Length of database: 394 Length adjustment: 31 Effective length of query: 363 Effective length of database: 363 Effective search space: 131769 Effective search space used: 131769 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)
Align candidate Ac3H11_178 (3-ketoacyl-CoA thiolase (EC 2.3.1.16) @ Acetyl-CoA acetyltransferase (EC 2.3.1.9))
to HMM TIGR01930 (acetyl-CoA C-acyltransferase (EC 2.3.1.16))
# hmmsearch :: search profile(s) against a sequence database # HMMER 3.3.1 (Jul 2020); http://hmmer.org/ # Copyright (C) 2020 Howard Hughes Medical Institute. # Freely distributed under the BSD open source license. # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # query HMM file: ../tmp/path.carbon/TIGR01930.hmm # target sequence database: /tmp/gapView.4131.genome.faa # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Query: TIGR01930 [M=385] Accession: TIGR01930 Description: AcCoA-C-Actrans: acetyl-CoA C-acyltransferase Scores for complete sequences (score includes all domains): --- full sequence --- --- best 1 domain --- -#dom- E-value score bias E-value score bias exp N Sequence Description ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 9e-141 455.2 8.5 1e-140 455.0 8.5 1.0 1 lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_178 3-ketoacyl-CoA thiolase (EC 2.3. Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_178 3-ketoacyl-CoA thiolase (EC 2.3.1.16) @ Acetyl-CoA acetyltransferase # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 455.0 8.5 1e-140 1e-140 1 385 [] 7 392 .. 7 392 .. 0.99 Alignments for each domain: == domain 1 score: 455.0 bits; conditional E-value: 1e-140 TIGR01930 1 ivdavRtpigklggslkelsaedLlaavikelleragldpekidevilGnvlqageq.aniaR 62 +v+avRt+ig++ggslk++ + dL+a v+ke l+ra ++ +++ +v++G+v+++ + + + R lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_178 7 VVSAVRTAIGTFGGSLKDIAPTDLGALVVKESLARASVEGKDVGHVVFGHVVNTEPKdMYLSR 69 79***************************************************99998***** PP TIGR01930 63 eaalaaglpesvpaltvnrvCaSglqAvalaaqkikaGeadvvvaGGvEsmSrvpillkaslr 125 aa++ g+ e +pa++vnr+C+SglqA+ +aaq+i+ G+adv + +G+E mSr+p+ + + lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_178 70 VAAINGGCAEGTPAFNVNRLCGSGLQAIVSAAQAIQLGDADVTIGAGAEVMSRAPFASLNM-- 130 *******************************************************998886.. PP TIGR01930 126 reslklgkakledqllkdl..vktklsmgetAenlakkygisReeqDeyalrShqkaakAiee 186 r+++++g++k+ d+++ l + + ++mg+tAen+a+k+gisRe+qD++a++Sh++a++A+++ lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_178 131 RWGARMGDTKMVDMMIGALhdPFHTIHMGVTAENIAAKWGISREDQDKLAVESHNRAERATAA 193 8************9999989999**************************************** PP TIGR01930 187 gkfkdeivpvevkgk..kkvvskDegirpnttlekLakLkpafkekkgstvtAgNssqlnDGA 247 g+fkd+ivpv++k k ++++++De+ rp+ tl++ akLkp+f +++g tvtAgN+s++nD+A lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_178 194 GYFKDQIVPVTLKSKkgDVQYATDEHFRPGATLDDFAKLKPVFVKENG-TVTAGNASGINDAA 255 *************99999999***************************.6************* PP TIGR01930 248 aalllmseevakelgltplarivsaavagvdpeemglgpvpAiekaLkkaglsisdidlvEin 310 aa++lm ++ak+ g +plar+v++a+agvdp++mg+gpvpA++ aLkkagl++ d+d++E n lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_178 256 AAVVLMDAAAAKARGAKPLARLVAYAHAGVDPKYMGIGPVPATQLALKKAGLTVADLDVIEAN 318 *************************************************************** PP TIGR01930 311 EAFAaqvlavekelgsldlekvNvnGGAiAlGHPlGasGarivltllkeLkergkkyGlatlC 373 EAFAaq+ av+k+lg ld++kvN nG+ i+lGHP+Ga+Ga i+++ ++eL++ +++y+l+t+C lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_178 319 EAFAAQACAVTKDLG-LDPAKVNPNGSGISLGHPIGATGALITVKAIHELQRVQGRYALVTMC 380 ***************.99********************************************* PP TIGR01930 374 vggGqGaAvile 385 +ggGqG+A+i+e lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_178 381 IGGGQGIAAIFE 392 **********97 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (385 nodes) Target sequences: 1 (394 residues searched) Passed MSV filter: 1 (1); expected 0.0 (0.02) Passed bias filter: 1 (1); expected 0.0 (0.02) Passed Vit filter: 1 (1); expected 0.0 (0.001) Passed Fwd filter: 1 (1); expected 0.0 (1e-05) Initial search space (Z): 1 [actual number of targets] Domain search space (domZ): 1 [number of targets reported over threshold] # CPU time: 0.02u 0.01s 00:00:00.03 Elapsed: 00:00:00.01 # Mc/sec: 9.49 // [ok]
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