Align 3-ketoacyl-CoA thiolase; Acetyl-CoA acyltransferase; Beta-ketothiolase; EC 2.3.1.16 (characterized)
to candidate Ac3H11_1916 3-ketoacyl-CoA thiolase (EC 2.3.1.16) @ Acetyl-CoA acetyltransferase (EC 2.3.1.9)
Query= SwissProt::O32177 (391 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_1916 Length = 399 Score = 341 bits (874), Expect = 2e-98 Identities = 184/393 (46%), Positives = 257/393 (65%), Gaps = 5/393 (1%) Query: 1 MKEAVIVSGARTPVGKAKKGSLATVRPDDLGAICVKETLKRAGGYEGN-IDDLIIGCATP 59 +++A IV+ RTP+G++ +G RPDDL +K + + + I+D IIGC+ P Sbjct: 6 VQDAYIVAATRTPIGRSGRGYFKNTRPDDLLVAAIKSAMLQVPTLDPKAIEDAIIGCSFP 65 Query: 60 EAEQGLNMARNIGALAGLPYTVPAITVNRYCSSGLQSIAYAAEKIMLGAYDTAIAGGAES 119 E EQG+NMAR LA + V +TVNR+C+SG+ ++ AA++I +G D IAGGAES Sbjct: 66 EGEQGMNMARIAVGLA-FNHPVGGVTVNRFCASGITALQMAADRIRVGEADVLIAGGAES 124 Query: 120 MSQVPMMGHVTRPNLALAEKAPEYYMS--MGHTAEQVAKKYGVSREDQDAFAVRSHQNAA 177 MS VPM G+ N + + + ++ MG TAE+VA+++ +SRE QDAFA+ SH A Sbjct: 125 MSLVPMGGNKPSFNAEVFARDEDVGIAYGMGLTAEKVAQQWKISREAQDAFALESHLRAI 184 Query: 178 KALAEGKFKDEIVPVEVTVTEIG-EDHKPMEKQFVFSQDEGVRPQTTADILSTLRPAFSV 236 KA G+F DEI P EV + +EK+ S DEG RP T+ + L+ L+P F+ Sbjct: 185 KAQKAGEFTDEITPFEVVERSPNLATGEVVEKRRTVSLDEGPRPDTSLEGLAKLKPVFAA 244 Query: 237 DGTVTAGNSSQTSDGAAAVMLMDREKADALGLAPLVKFRSFAVGGVPPEVMGIGPVEAIP 296 G+VTAGNSSQTSDGA A+++ + GL PL +F S+A GVPPE+MGIGP+EAIP Sbjct: 245 RGSVTAGNSSQTSDGAGALIVASEKAVKQFGLTPLARFVSYAARGVPPEIMGIGPIEAIP 304 Query: 297 RALKLAGLQLQDIGLFELNEAFASQAIQVIRELGIDEEKVNVNGGAIALGHPLGCTGTKL 356 AL+ AGL+ DIG +ELNEAFA+Q++ VI LG++ VN GGAIALGHPLG TG Sbjct: 305 AALRYAGLKSDDIGWYELNEAFAAQSLAVINTLGLNPANVNPMGGAIALGHPLGATGAIR 364 Query: 357 TLSLIHEMKRRNEQFGVVTMCIGGGMGAAGVFE 389 +++H ++R ++G+VTMC+G G GAAG+ E Sbjct: 365 AATVVHALRRHKLKYGMVTMCVGTGQGAAGIIE 397 Lambda K H 0.316 0.133 0.377 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: 426 Number of extensions: 19 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: 391 Length of database: 399 Length adjustment: 31 Effective length of query: 360 Effective length of database: 368 Effective search space: 132480 Effective search space used: 132480 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 (21.6 bits) S2: 50 (23.9 bits)
Align candidate Ac3H11_1916 (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.30428.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 ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 3.5e-139 449.9 1.5 3.9e-139 449.8 1.5 1.0 1 lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_1916 3-ketoacyl-CoA thiolase (EC 2.3. Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_1916 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 ! 449.8 1.5 3.9e-139 3.9e-139 1 385 [] 11 397 .. 11 397 .. 0.96 Alignments for each domain: == domain 1 score: 449.8 bits; conditional E-value: 3.9e-139 TIGR01930 1 ivdavRtpig.klggslkelsaedLlaavikellera.gldpekidevilGnvlqageq.an 59 iv+a+Rtpig + +g +k+++++dLl+a+ik+++ ++ ldp++i+++i+G+++++geq +n lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_1916 11 IVAATRTPIGrSGRGYFKNTRPDDLLVAAIKSAMLQVpTLDPKAIEDAIIGCSFPEGEQgMN 72 8*********9889***********************9*********************999 PP TIGR01930 60 iaReaalaaglpesvpaltvnrvCaSglqAvalaaqkikaGeadvvvaGGvEsmSrvpillk 121 +aR a+ +++ v ++tvnr+CaSg++A+++aa++i++Geadv++aGG+EsmS vp++ + lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_1916 73 MARI-AVGLAFNHPVGGVTVNRFCASGITALQMAADRIRVGEADVLIAGGAESMSLVPMGGN 133 9996.678889************************************************999 PP TIGR01930 122 aslrreslklgk.akledqllkdlvktklsmgetAenlakkygisReeqDeyalrShqkaak 182 + s++ + a++ed v ++ mg tAe++a++++isRe qD++al+Sh +a k lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_1916 134 KP----SFNAEVfARDED------VGIAYGMGLTAEKVAQQWKISREAQDAFALESHLRAIK 185 86....344433044444......5578********************************** PP TIGR01930 183 Aieegkfkdeivpvevkgk............kkvvskDegirpnttlekLakLkpafkekkg 232 A+++g+f dei+p+ev ++ ++vs Deg+rp+t+le LakLkp+f+ g lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_1916 186 AQKAGEFTDEITPFEVVERspnlatgevvekRRTVSLDEGPRPDTSLEGLAKLKPVFAA-RG 246 ****************9999*********99999***********************96.8* PP TIGR01930 233 stvtAgNssqlnDGAaalllmseevakelgltplarivsaavagvdpeemglgpvpAiekaL 294 s vtAgNssq++DGA+al+++se+++k++gltplar+vs+a gv+pe+mg+gp++Ai++aL lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_1916 247 S-VTAGNSSQTSDGAGALIVASEKAVKQFGLTPLARFVSYAARGVPPEIMGIGPIEAIPAAL 307 7.************************************************************ PP TIGR01930 295 kkaglsisdidlvEinEAFAaqvlavekelgsldlekvNvnGGAiAlGHPlGasGarivltl 356 + agl+ +di ++E+nEAFAaq lav++ lg l++++vN GGAiAlGHPlGa+Ga+ +t+ lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_1916 308 RYAGLKSDDIGWYELNEAFAAQSLAVINTLG-LNPANVNPMGGAIALGHPLGATGAIRAATV 368 *******************************.88**************************** PP TIGR01930 357 lkeLkergkkyGlatlCvggGqGaAvile 385 +++L++++ kyG++t+Cvg+GqGaA i+e lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_1916 369 VHALRRHKLKYGMVTMCVGTGQGAAGIIE 397 **************************997 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (385 nodes) Target sequences: 1 (399 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: 0.01u 0.01s 00:00:00.02 Elapsed: 00:00:00.02 # Mc/sec: 6.86 // [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