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_015799645.1 BMI_RS05560 acetyl/propionyl/methylcrotonyl-CoA carboxylase subunit alpha
Query= metacyc::MONOMER-13597 (509 letters) >NCBI__GCF_000022745.1:WP_015799645.1 Length = 667 Score = 398 bits (1023), Expect = e-115 Identities = 215/475 (45%), Positives = 307/475 (64%), Gaps = 12/475 (2%) Query: 6 RVLVANRGEIATRVLKAIKEMGMTAIAVYSEADKYAVHTKYADEAYYIGKAPALDSYLNI 65 ++L+ANRGEIA RV+K+ K+MG+ +AVYS+AD+ A+H K ADEA +IG AP+ SY+ I Sbjct: 4 KILIANRGEIACRVIKSAKKMGIATVAVYSDADRNALHVKMADEAVHIGPAPSNQSYIVI 63 Query: 66 EHIIDAAEKAHVDAIHPGYGFLSENAEFAEAVEKAGITFIGPSSEVMRKIKDKLDGKRLA 125 + I+ A ++ DA+HPGYGFLSEN FAEA++ A +TFIGP + + DK+ K+LA Sbjct: 64 DKILAAIKETGADAVHPGYGFLSENPRFAEALKAANVTFIGPPVNAIDAMGDKITSKKLA 123 Query: 126 NMAGVPTAPGSDGPVTSIDEALKLAEKIGYPIMVKAASGGGGVGITRVDNQDQLMDVWER 185 AGV T PG G + DEA+++A IGYP+M+KA++GGGG G+ N ++ + ++ Sbjct: 124 AEAGVSTVPGHMGLIEDADEAVRIAGSIGYPVMIKASAGGGGKGMRIAWNDEEAREGFQL 183 Query: 186 NKRLAYQAFGKADLFIEKYAVNPRHIEFQLIGDKYGNYVVAWERECTIQRRNQKLIEEAP 245 ++ A +FG +FIEK+ PRHIE Q++GD++GN V EREC+IQRRNQK+IEEAP Sbjct: 184 SRNEAKSSFGDDRIFIEKFVTQPRHIEIQVLGDQHGNVVYLGERECSIQRRNQKVIEEAP 243 Query: 246 SPALKMEERESMFEPIIKFGKLINYFTLGTFETAFSDVSRDFYFLELNKRLQVEHPTTEL 305 SP L R++M E + K + Y++ GT E D +R+FYFLE+N RLQVEHP TEL Sbjct: 244 SPFLDEATRKAMGEQAVALAKAVGYYSAGTVE-FIVDGNRNFYFLEMNTRLQVEHPVTEL 302 Query: 306 IFRIDLVKLQIKLAAGEHLPFSQEDLNKRVRGTAIEYRINAEDALNNFTGSSGFVTYY-- 363 I IDLV+ I++A+GE L F+Q D+ ++ G AIE R+ AED NF S G +T Y Sbjct: 303 ITGIDLVEEMIRVASGEKLRFAQADV--KLNGWAIESRLYAEDPYRNFLPSIGRLTRYRP 360 Query: 364 ----REPTGPGVRVDSGIESGSYVPPYYDSLVSKLIVYGESREYAIQAGIRALADYKIGG 419 R P G +R D+G+ G + YYD +++KL +G R AI A AL +++ G Sbjct: 361 PVEGRNPDGTVIRNDTGVFEGGEISMYYDPMIAKLCTWGPDRISAIDAMGHALDAFEVEG 420 Query: 420 IKTTIELYKWIMQDPDFQEGKFSTSYISQK-TDQF--VKYLREQEEIKAAIAAEI 471 I + +M P F+EG +T++I+++ D F VK + AA+AAEI Sbjct: 421 IGHNLPFLSAVMDHPRFREGALTTAFIAEEYPDGFSGVKCSEDDARTLAAVAAEI 475 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: 757 Number of extensions: 38 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 509 Length of database: 667 Length adjustment: 36 Effective length of query: 473 Effective length of database: 631 Effective search space: 298463 Effective search space used: 298463 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 Sep 24 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:
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