Align acyl CoA carboxylase biotin carboxylase subunit (EC 2.1.3.15; EC 6.4.1.3; EC 6.3.4.14) (characterized)
to candidate PP_0558 PP_0558 acetyl-CoA carboxylase - biotin carboxylase subunit
Query= metacyc::MONOMER-13597 (509 letters) >FitnessBrowser__Putida:PP_0558 Length = 451 Score = 376 bits (965), Expect = e-108 Identities = 200/445 (44%), Positives = 289/445 (64%), Gaps = 6/445 (1%) Query: 6 RVLVANRGEIATRVLKAIKEMGMTAIAVYSEADKYAVHTKYADEAYYIGKAPALDSYLNI 65 +VL+ANRGEIA R+L+A KE+G+ +AV+S AD+ +H ADE+ IG A + DSYL+I Sbjct: 7 KVLIANRGEIALRILRACKELGIKTVAVHSTADRELMHLGLADESVCIGPASSKDSYLHI 66 Query: 66 EHIIDAAEKAHVDAIHPGYGFLSENAEFAEAVEKAGITFIGPSSEVMRKIKDKLDGKRLA 125 II AAE AIHPGYGFL+ENA+FAE VEK+G FIGP ++ +R + DK+ K Sbjct: 67 PAIIAAAEVTGATAIHPGYGFLAENADFAEQVEKSGFAFIGPKADTIRLMGDKVSAKDAM 126 Query: 126 NMAGVPTAPGSDGPVTSIDE-ALKLAEKIGYPIMVKAASGGGGVGITRVDNQDQLMDVWE 184 +GVPT PGSDGP+ +E AL +A +GYP+++KAA GGGG G+ V ++ L+ + Sbjct: 127 IKSGVPTVPGSDGPLPEDEEVALAIARDVGYPVIIKAAGGGGGRGMRVVHKEEDLISSAK 186 Query: 185 RNKRLAYQAFGKADLFIEKYAVNPRHIEFQLIGDKYGNYVVAWERECTIQRRNQKLIEEA 244 + A AFG +++EK+ NPRH+E Q++ D GN + +R+C++QRR+QK++EEA Sbjct: 187 LTRTEAGAAFGNPMVYLEKFLTNPRHVEVQVLSDGQGNAIHLGDRDCSLQRRHQKVLEEA 246 Query: 245 PSPALKMEERESMFEPIIKFGKLINYFTLGTFETAFSDVSRDFYFLELNKRLQVEHPTTE 304 P+P + + R+ +F+ + I Y GTFE + + FYF+E+N R+QVEHP +E Sbjct: 247 PAPGIDEKARQEVFKRCVDACIEIGYRGAGTFEFLYE--NGRFYFIEMNTRVQVEHPVSE 304 Query: 305 LIFRIDLVKLQIKLAAGEHLPFSQEDLNKRVRGTAIEYRINAEDALNNFTGSSGFVTYYR 364 ++ ID+VK + +AAG L F QED+ +RG ++E RINAED F S G V ++ Sbjct: 305 MVTGIDIVKEMLSIAAGNKLSFRQEDV--VIRGHSLECRINAEDP-KKFIPSPGKVKHFH 361 Query: 365 EPTGPGVRVDSGIESGSYVPPYYDSLVSKLIVYGESREYAIQAGIRALADYKIGGIKTTI 424 P G GVRVDS + SG VPP YDSL+ KLI YG+ R+ A+ AL + + GIKT I Sbjct: 362 APGGNGVRVDSHLYSGYSVPPNYDSLIGKLITYGKDRDEAMARMRNALDEIVVDGIKTNI 421 Query: 425 ELYKWIMQDPDFQEGKFSTSYISQK 449 L++ +++D F +G + Y+ K Sbjct: 422 PLHRDLVRDEGFCKGGVNIHYLEHK 446 Lambda K H 0.317 0.135 0.385 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: 534 Number of extensions: 18 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: 509 Length of database: 451 Length adjustment: 34 Effective length of query: 475 Effective length of database: 417 Effective search space: 198075 Effective search space used: 198075 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: 51 (24.3 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