Align acetyl-CoA C-acetyltransferase (EC 2.3.1.9) (characterized)
to candidate PfGW456L13_3394 3-ketoacyl-CoA thiolase (EC 2.3.1.16) @ Acetyl-CoA acetyltransferase (EC 2.3.1.9)
Query= BRENDA::Q0KAI3 (392 letters) >FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3394 Length = 391 Score = 358 bits (919), Expect = e-103 Identities = 211/403 (52%), Positives = 262/403 (65%), Gaps = 24/403 (5%) Query: 1 MQQAVIVDAIRSPMGRSKPGSAFTELHATELLAQVIKGLVERNKLDPGLVDDVITGCVTQ 60 M+ VIVDA+R+P+G+ + + + + A L + VI L+ER + P LVDDVI G VTQ Sbjct: 1 MKDIVIVDAVRTPIGKFR--GSLSGVRADHLGSLVISRLLERVDVSPTLVDDVIFGNVTQ 58 Query: 61 AGEQSAGPGRVAWLAAGFPDHVPATTIDRKCGSSQQAVHFAAQGIMAGAYDIVIACGIES 120 GEQSA R A L AG+P V TIDRKCGS + AVH A I AGA DIV+A G E+ Sbjct: 59 IGEQSANIARTALLGAGWPVTVAGLTIDRKCGSGEVAVHMAVGAIAAGAADIVVAGGAEN 118 Query: 121 MSRVPMGSAR-IGQNPYGPSMEARYAPGLVSQGVAAELVAAKYELSRHDMDSYSARSHEL 179 MSRVPMGS R I +G RY L SQG AAE +A K+ LSR +D ++ SH+ Sbjct: 119 MSRVPMGSNREIHGAAFGWMAAQRYE--LTSQGEAAERMADKWALSRDALDDFAFASHQR 176 Query: 180 AATARESGAFRREILGI----------STPNGLVEQDETIRPGTSVEKLGTLQASFRNDE 229 AA A ++G F E + + S P G++ DETIR TS EKL TL+ SFR D Sbjct: 177 AAAACDAGYFDNETIPVVVEELREKELSEPAGVLRHDETIRRDTSREKLSTLKTSFRPDT 236 Query: 230 LSARFPQIGWNVTAGNASQISDGASAMLLMSESMAQRLGLKPRARFVAFDVCGDDPVMML 289 +TAGN+SQISDGA+A+LLMS A++LGLK RAR VAF G DP +ML Sbjct: 237 ---------GRITAGNSSQISDGAAALLLMSADTAKKLGLKARARVVAFTTVGSDPTLML 287 Query: 290 TAPIPASQRAIKKSGLKLDQIDHYEINEAFACVPLAWQRALGADPARLNPRGGAIALGHP 349 T PI A+Q+ + K+GL ++ ID +E+NEAFA VPLAW + G ++LN GGAIALGHP Sbjct: 288 TGPIAATQKVLAKAGLSINDIDLFEVNEAFASVPLAWMQETGVPHSKLNVNGGAIALGHP 347 Query: 350 LGASGVRLMTTMLHALEDSGQRYGLQSMCEAGGMANATIIERL 392 LGASG RLMTTML+ LE G RYGLQ++C AGGM ATIIERL Sbjct: 348 LGASGARLMTTMLNELERRGGRYGLQAICCAGGMGTATIIERL 390 Lambda K H 0.318 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: 411 Number of extensions: 12 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: 391 Length adjustment: 31 Effective length of query: 361 Effective length of database: 360 Effective search space: 129960 Effective search space used: 129960 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