Align Propionyl-CoA carboxylase biotin-containing subunit (EC 6.4.1.3) (characterized)
to candidate CCNA_01905 CCNA_01905 urea carboxylase
Query= reanno::Dino:3607308 (681 letters) >FitnessBrowser__Caulo:CCNA_01905 Length = 1207 Score = 403 bits (1035), Expect = e-116 Identities = 223/459 (48%), Positives = 296/459 (64%), Gaps = 24/459 (5%) Query: 1 MFKKILIANRGEIACRVIKTARKMGIQTVAIYSDADRNALHVRMADEAVHIGPSPANQSY 60 MF K+LIANRG IACR+I+T R MG+++VA++SDAD +LHV MADEAV +GP+PA +SY Sbjct: 1 MFDKVLIANRGAIACRIIRTLRAMGVKSVAVFSDADAGSLHVSMADEAVRLGPAPAAESY 60 Query: 61 IVIDKVMDAIRQTGAEAVHPGYGFLSENKLFAEALEKEGVAFIGPPANAIEAMGDKITSK 120 + D V+ A + TGA+A+HPGYGFLSE+ FA+A E GV FIGP A+ I A G K T++ Sbjct: 61 LRADLVLAAAQATGAQAIHPGYGFLSESAAFAQACEDAGVTFIGPSADNIRAFGLKHTAR 120 Query: 121 KIAQEANVSTVPGYMGLIADADEAVKISGEIGYPVMIKASAGGGGKGMRIAWNDAEAREG 180 +AQ V PG L+ D A+ + IG+PV++KA+AGGGG GMR+ + E Sbjct: 121 DLAQAHGVPLAPG-TDLLTDPAAALAAAQRIGFPVILKATAGGGGIGMRVCESAEAVEEA 179 Query: 181 FQSSKNEAANSFGDDRIFIEKFVTQPRHIEIQVLADTHGNCIYLGERECSIQRRNQKVVE 240 F + + A +F D +F+E++V + RHIE+QV D G LGER+CS+QRRNQKVVE Sbjct: 180 FAAVRRLATGNFSDGGVFLERYVHKARHIEVQVFGDGAGRVAALGERDCSLQRRNQKVVE 239 Query: 241 EAPSPFLDEATRKAMGEQSCALAQAVGYASAGTVEFIVDGDR-NFYFLEMNTRLQVEHPV 299 E P+P L ATR A+ + + LA+A Y SAGTVEF+ D DR +F+FLE+NTRLQVEH V Sbjct: 240 ETPAPGLPAATRTALLDAAVRLAKAANYRSAGTVEFLYDADRDDFFFLEVNTRLQVEHGV 299 Query: 300 TELITGVDLVEQMIRVAAGEKLPMTQDDVTLTGWAIENRLYAEDPYRNFLPSIGRLTRYR 359 TE +TGVDLVE M+R AAG+ + G AI+ RLYAEDP +++ PS G LT Sbjct: 300 TEQVTGVDLVEWMVRGAAGDFSFLDTPPPAPRGAAIQVRLYAEDPAQDYRPSAGVLT--- 356 Query: 360 PPVEVAAGPLEANGKWHGDAPSGPTAVRNDTGVYEGGEISMYYDPMIAKLCTWGPDRPAA 419 EVA P VR D V +G E+S +YDPM+AKL RPAA Sbjct: 357 ---EVAF----------------PEGVRADGWVVDGTEVSAFYDPMLAKLIVIAEHRPAA 397 Query: 420 IEAMRNALDGFEVEGIGHNLPFVAAVMDHPVFIKGEMTT 458 + A++ ALD + GI NL ++ V F+ GE++T Sbjct: 398 VAALQAALDATRLAGIETNLDWLRTVTRSQPFVSGEVST 436 Lambda K H 0.318 0.134 0.392 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: 2084 Number of extensions: 102 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: 681 Length of database: 1207 Length adjustment: 43 Effective length of query: 638 Effective length of database: 1164 Effective search space: 742632 Effective search space used: 742632 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: 56 (26.2 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