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_028989551.1 G579_RS0106615 acetyl-CoA carboxylase biotin carboxylase subunit
Query= metacyc::MONOMER-13597 (509 letters) >NCBI__GCF_000423825.1:WP_028989551.1 Length = 471 Score = 404 bits (1037), Expect = e-117 Identities = 213/471 (45%), Positives = 306/471 (64%), Gaps = 4/471 (0%) Query: 4 FSRVLVANRGEIATRVLKAIKEMGMTAIAVYSEADKYAVHTKYADEAYYIGKAPALDSYL 63 F ++L+ANRGEIATR+ +A E+G+ ++A+Y+E D+YA+H K ADEAY +G P L YL Sbjct: 2 FKKILIANRGEIATRISRACSELGIKSVAIYAEPDRYALHVKKADEAYSLGPDPLL-GYL 60 Query: 64 NIEHIIDAAEKAHVDAIHPGYGFLSENAEFAEAVEKAGITFIGPSSEVMRKIKDKLDGKR 123 N +++ A +A DA+HPGYGFLSEN + AE + GITFIGP +E +R + DK ++ Sbjct: 61 NPHRVVNLAVEAGCDALHPGYGFLSENPKLAEICARRGITFIGPDAETIRIMGDKTLARQ 120 Query: 124 LANMAGVPTAPGSDGPVTSIDEALKLAEKIGYPIMVKAASGGGGVGITRVDNQDQLMDVW 183 AG+P PG+ + S+DEA+ +A +IGYP+M+KA+ GGGG GI R +++ +L + + Sbjct: 121 AMIDAGIPVIPGTQSSLGSVDEAIAVAGEIGYPVMLKASGGGGGRGIRRCNDEAELRNSY 180 Query: 184 ERNKRLAYQAFGKADLFIEKYAVNPRHIEFQLIGDKYGNYVVAWERECTIQRRNQKLIEE 243 R A +AFG+++LF+EKY PRHIE Q++GD +GN + +ER+C+IQRR+QKLIE Sbjct: 181 ARVISEAEKAFGRSELFLEKYIDRPRHIEVQVLGDAFGNVIHLFERDCSIQRRHQKLIEI 240 Query: 244 APSPALKMEERESMFEPIIKFGKLINYFTLGTFETAFSDVSRDFYFLELNKRLQVEHPTT 303 APSP L +R + E ++ + +NY GT E R FYF+E+N RLQVEH T Sbjct: 241 APSPQLDESQRTYIGELAVRAARAVNYRNAGTVEFLLDPEGR-FYFMEMNTRLQVEHTVT 299 Query: 304 ELIFRIDLVKLQIKLAAGEHLPFSQEDLNKRVRGTAIEYRINAEDALNNFTGSSGFVTYY 363 E I ID+V+ Q ++AAG L SQ D++ RG AI++RINAED NNF S G +T Y Sbjct: 300 EQITGIDVVQEQTRIAAGLPLSVSQADVSH--RGYAIQFRINAEDPQNNFLPSFGRITRY 357 Query: 364 REPTGPGVRVDSGIESGSYVPPYYDSLVSKLIVYGESREYAIQAGIRALADYKIGGIKTT 423 P GPGVR D+ I +G +PPYYDSL +KL V+ + A++ RAL D + G+K+T Sbjct: 358 YSPGGPGVRTDAAIYTGYEIPPYYDSLCAKLTVWALDWDQAVRRARRALNDMGLYGVKST 417 Query: 424 IELYKWIMQDPDFQEGKFSTSYISQKTDQFVKYLREQEEIKAAIAAEIQSR 474 I Y I+ PDF + + T+++ + + R + E A IA I +R Sbjct: 418 IPYYLEILNHPDFVQHRLDTTFVERHPELTRYASRRRPEWAAIIAVAIATR 468 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: 620 Number of extensions: 29 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: 471 Length adjustment: 34 Effective length of query: 475 Effective length of database: 437 Effective search space: 207575 Effective search space used: 207575 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: 52 (24.6 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