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 WP_027457248.1 K420_RS0105835 acetyl-CoA carboxylase biotin carboxylase subunit
Query= metacyc::MONOMER-13597 (509 letters) >NCBI__GCF_000519045.1:WP_027457248.1 Length = 452 Score = 389 bits (1000), Expect = e-113 Identities = 213/463 (46%), Positives = 298/463 (64%), Gaps = 13/463 (2%) Query: 4 FSRVLVANRGEIATRVLKAIKEMGMTAIAVYSEADKYAVHTKYADEAYYIGKAPALDSYL 63 F +VL+ANRGEIA RV +A +E+G+ + V+SEAD+ A + K ADE+ IG A + SYL Sbjct: 2 FEKVLIANRGEIALRVQRACRELGIKTVVVHSEADREAKYVKLADESVCIGPAASAQSYL 61 Query: 64 NIEHIIDAAEKAHVDAIHPGYGFLSENAEFAEAVEKAGITFIGPSSEVMRKIKDKLDGKR 123 NI II AAE AIHPGYGFLSENA+FAE VE +G FIGP +E +R + DK+ K Sbjct: 62 NIPAIISAAEVTDAQAIHPGYGFLSENADFAERVETSGFVFIGPKAETIRLMGDKVSAKD 121 Query: 124 LANMAGVPTAPGSDGPV-TSIDEALKLAEKIGYPIMVKAASGGGGVGITRVDNQDQLMDV 182 AGVP PGSDG + E +K+A +GYP+++KAA GGGG G+ V + L++ Sbjct: 122 AMKAAGVPCVPGSDGALPEDPKEIVKIARAVGYPVIIKAAGGGGGRGMRVVHTEAALVNA 181 Query: 183 WERNKRLAYQAFGKADLFIEKYAVNPRHIEFQLIGDKYGNYVVAWERECTIQRRNQKLIE 242 ++ A Q FG +++EK+ NPRH+E Q++ D+Y N + ER+C++QRR+QK+IE Sbjct: 182 VAMTRQEAGQFFGNPAVYMEKFLENPRHVEIQVLADEYKNAIYLGERDCSMQRRHQKVIE 241 Query: 243 EAPSPALKMEERESMFEPIIKFGKLINYFTLGTFETAFSDVSRDFYFLELNKRLQVEHPT 302 EAP+P + + E + + I Y GTFE + + +FYF+E+N R+QVEHP Sbjct: 242 EAPAPHIPARLISRIGERCAEACRKIGYRGAGTFEFLYE--NGEFYFIEMNTRVQVEHPV 299 Query: 303 TELIFRIDLVKLQIKLAAGEHLPFSQEDLNKRVRGTAIEYRINAEDALNNFTGSSGFVTY 362 +E+I +D+V+ QI++AAGE L + Q+D+ RG AIE RINAED F S G + + Sbjct: 300 SEMITGVDIVQEQIRVAAGEKLRYKQKDI--VFRGHAIECRINAEDPF-TFVPSPGNIEF 356 Query: 363 YREPTGPGVRVDSGIESGSYVPPYYDSLVSKLIVYGESREYAIQAGIRALADYKIGGIKT 422 Y P GPG+RVDS I G VPP+YDS+V+K+I YG++RE AI+ AL++ I GIKT Sbjct: 357 YHPPGGPGIRVDSHIYQGYRVPPHYDSMVAKVISYGDTREQAIRRMRIALSEMSIQGIKT 416 Query: 423 TIELYKWIMQDPDFQEGKFSTSYISQKTDQFVKYLREQEEIKA 465 I L++ +MQD F EG S Y+ K L ++ E+KA Sbjct: 417 NIPLHQELMQDARFIEGGTSIHYLEHK-------LADKSEVKA 452 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: 554 Number of extensions: 17 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: 452 Length adjustment: 34 Effective length of query: 475 Effective length of database: 418 Effective search space: 198550 Effective search space used: 198550 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 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