Align acetyl-CoA C-acetyltransferase (EC 2.3.1.9) (characterized)
to candidate PfGW456L13_2538 3-ketoacyl-CoA thiolase (EC 2.3.1.16) @ Acetyl-CoA acetyltransferase (EC 2.3.1.9)
Query= BRENDA::Q0K368 (391 letters) >FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2538 Length = 382 Score = 377 bits (968), Expect = e-109 Identities = 205/393 (52%), Positives = 268/393 (68%), Gaps = 13/393 (3%) Query: 1 MAEAYIVAAVRTAGGRKGGKLSGWHPADLAAQVLDALVERTGADPALVEDVIMGCVSQVG 60 M EAYIV A+RT GR+ G LS H ADL A VL ALVER +DVI GCV +G Sbjct: 1 MPEAYIVDALRTPTGRRKGGLSQIHAADLGAHVLRALVERNAIPDEDYDDVIFGCVDTIG 60 Query: 61 EQAGNVARNAILASRLPESVPGTSVDRQCGSSQQALHFAAQAVMSGAMDIVIAAGVESMT 120 AG++AR + LA+ L +SVPGT++DRQCGSSQQA+HFAAQAVMSG D+VIA GV++MT Sbjct: 61 PLAGDIARTSWLAAGLSQSVPGTTIDRQCGSSQQAVHFAAQAVMSGTQDVVIAGGVQTMT 120 Query: 121 RVPMGLSSQLPAKNGFGVP--KSPGIEARYPGVQFSQFTGAEMIARKYDLSREQLDAYAL 178 ++P+ + GF P S G RY +QF A+MIA K+DLSR QL+AY+L Sbjct: 121 QIPISSAMIAAEPLGFTDPFSGSEGWVRRYGAQPPTQFRSAQMIAEKWDLSRAQLEAYSL 180 Query: 179 QSHQRAIAATKSGRFTAEILPVEVRTADGANGEMHTTDEGVRYDATLESIGSVKLIAEGG 238 +SH+RA+ A + GRF EI+P+ G +H DE R +LE + ++ + Sbjct: 181 ESHRRALQAIEQGRFNREIVPLA--------GVLH--DETPR-QTSLEKMAELEFLFGCD 229 Query: 239 RVTAASASQICDGAAGLMVVNEAGLKKLGVKPLARVHAMTVIGHDPVVMLEAPLPATEVA 298 RVTAA +SQ CD A+ +++V+EA LK+ G+ P AR+H ++V DP+ ML AP+PAT A Sbjct: 230 RVTAAVSSQTCDAASAMLIVSEAALKRYGLTPRARIHHLSVRAEDPIWMLTAPIPATAYA 289 Query: 299 LKKAGLRIGDIDLFEVNEAFAPVPLAWLKATGADPARLNVHGGAIALGHPLGGSGAKLMT 358 LK+AG+++ DID E+NEAFA V +AWLK TG + NV+GGAIALGHPLG +G +LM Sbjct: 290 LKRAGMKLEDIDRVEINEAFASVAMAWLKETGYPHEQTNVNGGAIALGHPLGATGTRLMC 349 Query: 359 TLVHALHTHGKRYGLQTMCEGGGLANVTIVERL 391 TL+H L G R+G+QTMCEGGG ANVTI+ERL Sbjct: 350 TLLHELERSGGRFGMQTMCEGGGQANVTIIERL 382 Lambda K H 0.317 0.132 0.379 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: 454 Number of extensions: 17 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: 391 Length of database: 382 Length adjustment: 30 Effective length of query: 361 Effective length of database: 352 Effective search space: 127072 Effective search space used: 127072 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