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_02250 CCNA_02250 methylcrotonyl-CoA carboxylase biotin-containing subunit
Query= metacyc::MONOMER-13597 (509 letters) >FitnessBrowser__Caulo:CCNA_02250 Length = 654 Score = 350 bits (899), Expect = e-101 Identities = 196/474 (41%), Positives = 280/474 (59%), Gaps = 9/474 (1%) Query: 5 SRVLVANRGEIATRVLKAIKEMGMTAIAVYSEADKYAVHTKYADEAYYIGKAPALDSYLN 64 S VL+ANRGEIA R+++ +E+G+ IAVYSEAD A AD A IG APA +SYL+ Sbjct: 3 SSVLIANRGEIARRIIRTARELGVRTIAVYSEADANAPFVMEADAAILIGPAPAKESYLD 62 Query: 65 IEHIIDAAEKAHVDAIHPGYGFLSENAEFAEAVEKAGITFIGPSSEVMRKIKDKLDGKRL 124 I+ AA + +AIHPGYGFLSENAEFA++V AG+ +IGP +R + K K + Sbjct: 63 PRKILAAARQMGAEAIHPGYGFLSENAEFAQSVIDAGLVWIGPPPSAIRAMGLKDAAKAV 122 Query: 125 ANMAGVPTAPGSDGPVTSIDEALKLAEKIGYPIMVKAASGGGGVGITRVDNQDQLMDVWE 184 AGVPT PG G S++ A KIGYP+++KA +GGGG G+ +V+ + Sbjct: 123 MIKAGVPTTPGYLGEDQSVERLTVEAAKIGYPVLIKAVAGGGGKGMRKVERAEDFEAALG 182 Query: 185 RNKRLAYQAFGKADLFIEKYAVNPRHIEFQLIGDKYGNYVVAWERECTIQRRNQKLIEEA 244 +R A AFG + +EKY PRHIE Q+ GD +GN V +ER+C++QRR+QK+IEEA Sbjct: 183 SCRREASAAFGDDRVLLEKYVTRPRHIEVQVFGDSHGNVVHLFERDCSLQRRHQKVIEEA 242 Query: 245 PSPALKMEERESMFEPIIKFGKLINYFTLGTFETAFSDVSRD-----FYFLELNKRLQVE 299 P+P + RE++ +K + +NY GT E +D S +F+E+N RLQVE Sbjct: 243 PAPGMDEATREAVCAAAVKAAQAVNYVGAGTVE-FIADASEGLRADRIWFMEMNTRLQVE 301 Query: 300 HPTTELIFRIDLVKLQIKLAAGEHLPFSQEDLNKRVRGTAIEYRINAEDALNNFTGSSGF 359 HP TE++ DLV+ Q+++A+GE LP Q+++ + G A+E R+ AE+ F S+G Sbjct: 302 HPVTEMVTGQDLVEWQLRVASGEPLPLEQDEIT--LDGWAMEARLYAENPATGFLPSTGK 359 Query: 360 VTYYREPTGPGVRVDSGIESGSYVPPYYDSLVSKLIVYGESREYAIQAGIRALADYKIGG 419 + ++R P G VRVDS +E G V P+YD +++KLI +G RE A Q A A ++ Sbjct: 360 LKHFRLPEG-DVRVDSAVEEGGEVTPFYDPMIAKLIAHGADREDAAQRLAEACALVEVWP 418 Query: 420 IKTTIELYKWIMQDPDFQEGKFSTSYISQKTDQFVKYLREQEEIKAAIAAEIQS 473 +KT PDF +G T +I + D+ + E AAI + S Sbjct: 419 VKTNAAFLAKCASHPDFVDGAVDTGFIEARLDELTERAFSDEPAMAAIGWRLDS 472 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: 797 Number of extensions: 37 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: 654 Length adjustment: 36 Effective length of query: 473 Effective length of database: 618 Effective search space: 292314 Effective search space used: 292314 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: 53 (25.0 bits)
This GapMind analysis is from Apr 09 2024. 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:
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