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 CCNA_01905 CCNA_01905 urea carboxylase
Query= metacyc::MONOMER-13597 (509 letters) >FitnessBrowser__Caulo:CCNA_01905 Length = 1207 Score = 323 bits (829), Expect = 2e-92 Identities = 176/441 (39%), Positives = 268/441 (60%), Gaps = 7/441 (1%) Query: 4 FSRVLVANRGEIATRVLKAIKEMGMTAIAVYSEADKYAVHTKYADEAYYIGKAPALDSYL 63 F +VL+ANRG IA R+++ ++ MG+ ++AV+S+AD ++H ADEA +G APA +SYL Sbjct: 2 FDKVLIANRGAIACRIIRTLRAMGVKSVAVFSDADAGSLHVSMADEAVRLGPAPAAESYL 61 Query: 64 NIEHIIDAAEKAHVDAIHPGYGFLSENAEFAEAVEKAGITFIGPSSEVMRKIKDKLDGKR 123 + ++ AA+ AIHPGYGFLSE+A FA+A E AG+TFIGPS++ +R K + Sbjct: 62 RADLVLAAAQATGAQAIHPGYGFLSESAAFAQACEDAGVTFIGPSADNIRAFGLKHTARD 121 Query: 124 LANMAGVPTAPGSDGPVTSIDEALKLAEKIGYPIMVKAASGGGGVGITRVDNQDQLMDVW 183 LA GVP APG+D +T AL A++IG+P+++KA +GGGG+G+ ++ + + + + Sbjct: 122 LAQAHGVPLAPGTD-LLTDPAAALAAAQRIGFPVILKATAGGGGIGMRVCESAEAVEEAF 180 Query: 184 ERNKRLAYQAFGKADLFIEKYAVNPRHIEFQLIGDKYGNYVVAWERECTIQRRNQKLIEE 243 +RLA F +F+E+Y RHIE Q+ GD G ER+C++QRRNQK++EE Sbjct: 181 AAVRRLATGNFSDGGVFLERYVHKARHIEVQVFGDGAGRVAALGERDCSLQRRNQKVVEE 240 Query: 244 APSPALKMEERESMFEPIIKFGKLINYFTLGTFETAFSDVSRDFYFLELNKRLQVEHPTT 303 P+P L R ++ + ++ K NY + GT E + DF+FLE+N RLQVEH T Sbjct: 241 TPAPGLPAATRTALLDAAVRLAKAANYRSAGTVEFLYDADRDDFFFLEVNTRLQVEHGVT 300 Query: 304 ELIFRIDLVKLQIKLAAGEHLPFSQEDLNKRV-RGTAIEYRINAEDALNNFTGSSGFVTY 362 E + +DLV+ ++ AAG+ FS D RG AI+ R+ AED ++ S+G +T Sbjct: 301 EQVTGVDLVEWMVRGAAGD---FSFLDTPPPAPRGAAIQVRLYAEDPAQDYRPSAGVLTE 357 Query: 363 YREPTGPGVRVDSGIESGSYVPPYYDSLVSKLIVYGESREYAIQAGIRALADYKIGGIKT 422 P GVR D + G+ V +YD +++KLIV E R A+ A AL ++ GI+T Sbjct: 358 VAFP--EGVRADGWVVDGTEVSAFYDPMLAKLIVIAEHRPAAVAALQAALDATRLAGIET 415 Query: 423 TIELYKWIMQDPDFQEGKFST 443 ++ + + + F G+ ST Sbjct: 416 NLDWLRTVTRSQPFVSGEVST 436 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: 1366 Number of extensions: 62 Number of successful extensions: 4 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: 1207 Length adjustment: 41 Effective length of query: 468 Effective length of database: 1166 Effective search space: 545688 Effective search space used: 545688 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: 55 (25.8 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