Align 3-oxopimeloyl-CoA:CoA acetyltransferase (characterized)
to candidate WP_011384976.1 AMB_RS13060 acetyl-CoA C-acyltransferase
Query= metacyc::MONOMER-20679 (395 letters) >lcl|NCBI__GCF_000009985.1:WP_011384976.1 AMB_RS13060 acetyl-CoA C-acyltransferase Length = 398 Score = 233 bits (595), Expect = 6e-66 Identities = 158/410 (38%), Positives = 220/410 (53%), Gaps = 28/410 (6%) Query: 1 MTEAVIVSTARTPIGKAYRGALNATEGATLLGHAIEHAVKRAGIDPKEVEDVVMGAAMQQ 60 M +A I R+PIG+ + G L L I V R+ P++VEDV++G Q Sbjct: 1 MLDAYIYDGLRSPIGR-HGGGLAPVRSDDLAAEVIRALVARSSFKPEDVEDVILGCTNQA 59 Query: 61 GATGGNIARKALLRAGLPVTTAGTTIDRQCASGLQAIALAARSVLFDGVEIAVGGGGESI 120 G N+AR A L AGLPV AG T++R CASGL A+ AARSV ++ + GG ES+ Sbjct: 60 GEDSRNVARHAALLAGLPVEVAGQTVNRLCASGLAAVLDAARSVTCGEGDLYLAGGVESM 119 Query: 121 S-----LVQNDKM---------NTFHAVDPALEAIKGDVYMAMLDTAETVAKRYGISRER 166 + L + D T A + +K +M +TA+ +A G+SRE Sbjct: 120 TRAPFVLAKGDSAWSRDARIFDTTIGARFANPKVVKSFGGHSMPETADNIAHDLGLSREA 179 Query: 167 QDEYSLESQRRTAAAQQGGKFNDEIAPISTKMGVVDKATGAVSFKDITLSQDEGPRPETT 226 D ++ SQ + A A+ G + EI PI T A D +++DE PRP+T Sbjct: 180 SDAFAAASQAKYAKAKAEGFYEGEIHPI----------TIAGRKGDTIVAEDEHPRPQTD 229 Query: 227 AEGLAGLKAVRGEGFTITAGNASQLSDGASATVIMSDKTAAAKGLKPLGIFRGMVSYGCE 286 L LK + EG +TAGNAS ++DGA+A I S G+ P+ + G Sbjct: 230 LAALTKLKPLF-EGGVVTAGNASGINDGAAALFIGSRAAGEKAGIAPIARIVAGAAAGVP 288 Query: 287 PDEMGIGPVFAVPRLLKRHGLSVDDIGLWELNEAFAVQVLYCRDKLGI--DPEKLNVNGG 344 P MG+GPV A+ + L R LS+ D+ L E+NEAFAVQVL C +LG+ D +LN NGG Sbjct: 289 PRVMGLGPVPAITKALARAKLSLKDLDLIEINEAFAVQVLGCVTQLGVAADDSRLNPNGG 348 Query: 345 AISVGHPYGMSGARLAGHALIEGRRRKAKYAVVTMCVGGGMGSAGLFEIV 394 AI++GHP G SGARLA A + +R ++AVV++C+G G G A + E V Sbjct: 349 AIAIGHPLGCSGARLALTAARQLQRTGGRHAVVSLCIGVGHGLAAVIERV 398 Lambda K H 0.316 0.134 0.378 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: 24 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: 395 Length of database: 398 Length adjustment: 31 Effective length of query: 364 Effective length of database: 367 Effective search space: 133588 Effective search space used: 133588 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)
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