Align β-ketoadipyl-CoA thiolase (EC 2.3.1.174; EC 2.3.1.223) (characterized)
to candidate PfGW456L13_3394 3-ketoacyl-CoA thiolase (EC 2.3.1.16) @ Acetyl-CoA acetyltransferase (EC 2.3.1.9)
Query= metacyc::MONOMER-15952 (401 letters) >FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3394 Length = 391 Score = 312 bits (800), Expect = 9e-90 Identities = 184/407 (45%), Positives = 253/407 (62%), Gaps = 23/407 (5%) Query: 1 MNEALIIDAVRTPIGRYAGALASVRADDLGAIPLKALIARHPQLDWSAVDDVIYGCANQA 60 M + +I+DAVRTPIG++ G+L+ VRAD LG++ + L+ R + + VDDVI+G Q Sbjct: 1 MKDIVIVDAVRTPIGKFRGSLSGVRADHLGSLVISRLLER-VDVSPTLVDDVIFGNVTQI 59 Query: 61 GEDNRNVARMAALLAGLPVSVPGTTLNRLCGSGLDAVGSAARALRCGEAGLMLAGGVESM 120 GE + N+AR A L AG PV+V G T++R CGSG AV A A+ G A +++AGG E+M Sbjct: 60 GEQSANIARTALLGAGWPVTVAGLTIDRKCGSGEVAVHMAVGAIAAGAADIVVAGGAENM 119 Query: 121 SRAPFVMGKSEQAFGRSAEIFDTTIGWRFVNKLMQQGFGIDSMPETAENVAAQFNISRAD 180 SR P G + EI GW + Q + + S E AE +A ++ +SR Sbjct: 120 SRVPM---------GSNREIHGAAFGW-----MAAQRYELTSQGEAAERMADKWALSRDA 165 Query: 181 QDAFALRSQHKAAAAIANGRLAKEIVAVEIAQRKG-----PAKIVEHDEHPRGDTTLEQL 235 D FA S +AAAA G E + V + + + PA ++ HDE R DT+ E+L Sbjct: 166 LDDFAFASHQRAAAACDAGYFDNETIPVVVEELREKELSEPAGVLRHDETIRRDTSREKL 225 Query: 236 AKLGTPFRQG-GSVTAGNASGVNDGACALLLASSEAAQRHGLKARARVVGMATAGVEPRI 294 + L T FR G +TAGN+S ++DGA ALLL S++ A++ GLKARARVV T G +P + Sbjct: 226 STLKTSFRPDTGRITAGNSSQISDGAAALLLMSADTAKKLGLKARARVVAFTTVGSDPTL 285 Query: 295 MGIGPVPATRKVLELTGLALADMDVIELNEAFAAQGLAVLRELGLADDDERVNPNGGAIA 354 M GP+ AT+KVL GL++ D+D+ E+NEAFA+ LA ++E G+ ++N NGGAIA Sbjct: 286 MLTGPIAATQKVLAKAGLSINDIDLFEVNEAFASVPLAWMQETGV--PHSKLNVNGGAIA 343 Query: 355 LGHPLGMSGARLVTTALHELEERQGRYALCTMCIGVGQGIALIIERI 401 LGHPLG SGARL+TT L+ELE R GRY L +C G G A IIER+ Sbjct: 344 LGHPLGASGARLMTTMLNELERRGGRYGLQAICCAGGMGTATIIERL 390 Lambda K H 0.319 0.134 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: 441 Number of extensions: 21 Number of successful extensions: 6 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: 401 Length of database: 391 Length adjustment: 31 Effective length of query: 370 Effective length of database: 360 Effective search space: 133200 Effective search space used: 133200 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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