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_091518618.1 BM253_RS02595 acetyl-CoA carboxylase biotin carboxylase subunit
Query= metacyc::MONOMER-13597 (509 letters) >NCBI__GCF_900115115.1:WP_091518618.1 Length = 481 Score = 421 bits (1081), Expect = e-122 Identities = 221/466 (47%), Positives = 308/466 (66%), Gaps = 5/466 (1%) Query: 6 RVLVANRGEIATRVLKAIKEMGMTAIAVYSEADKYAVHTKYADEAYYIGKAPALDSYLNI 65 ++LVANRGEIA RV+K K+MG+ +AVYS AD+ + H K+ADEA IG+AP+ SYL Sbjct: 3 KILVANRGEIALRVMKTAKKMGIKTVAVYSVADRQSPHVKFADEAVCIGEAPSNQSYLLG 62 Query: 66 EHIIDAAEKAHVDAIHPGYGFLSENAEFAEAVEKAGITFIGPSSEVMRKIKDKLDGKRLA 125 + II+ ++ VD IHPGYGFLSEN++FAE EK GITFIGP S + + DKL K Sbjct: 63 DKIIEVCKELGVDGIHPGYGFLSENSKFAELAEKNGITFIGPKSHAIEVMGDKLAAKDTV 122 Query: 126 NMAGVPTAPGSDGPVTSIDEALKLAEKIGYPIMVKAASGGGGVGITRVDNQDQLMDVWER 185 +P PG D +T IDEA K+A+++G+PI++KA++GGGG G+ V+ ++ +R Sbjct: 123 KAYDIPMVPGLDHAITDIDEAKKVAKEVGFPILIKASAGGGGKGMRVVEKEEDFESQMQR 182 Query: 186 NKRLAYQAFGKADLFIEKYAVNPRHIEFQLIGDKYGNYVVAWERECTIQRRNQKLIEEAP 245 A AFG +FIEKY +PRHIE Q++ D +GN V +EREC++QRR+QK++EEAP Sbjct: 183 AISEATSAFGDGSVFIEKYVGSPRHIEIQVMADTHGNVVYLFERECSVQRRHQKVVEEAP 242 Query: 246 SPALKMEERESMFEPIIKFGKLINYFTLGTFETAFSDVSRDFYFLELNKRLQVEHPTTEL 305 S L E R++M E +K K +Y GT E D +++FYFLE+N RLQVEHP TEL Sbjct: 243 SAVLTPEIRQAMGEAAVKVAKSCDYVGAGTVEFLL-DENKNFYFLEMNTRLQVEHPVTEL 301 Query: 306 IFRIDLVKLQIKLAAGEHLPFSQEDLNKRVRGTAIEYRINAEDALNNFTGSSGFVTYYRE 365 I IDLV++QI++A GE LP QEDL +++G A+E R+ AED LN+F S G ++ Y Sbjct: 302 ITGIDLVEMQIRVARGEVLPIKQEDL--KIKGHALELRVYAEDPLNDFLPSVGNLSTYIL 359 Query: 366 PTGPGVRVDSGIESGSYVPPYYDSLVSKLIVYGESREYAIQAGIRALADYKIGGIKTTIE 425 P G GVRVD+G E G VP YYD ++SKLI YG+ R AI+ ++A+ DYKI G+ TT+ Sbjct: 360 PEGEGVRVDNGFEQGMDVPIYYDPMLSKLITYGKDRNEAIELMLKAIQDYKIEGVSTTLP 419 Query: 426 LYKWIMQDPDFQEGKFSTSYISQKTDQFVKYLREQEEIKAAIAAEI 471 ++ + F G F T+++ K ++E + +A +AA I Sbjct: 420 FGTFVFKHDAFVSGDFDTNFV--KKFYSADIIKESQAKEAEVAALI 463 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: 584 Number of extensions: 20 Number of successful extensions: 3 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: 481 Length adjustment: 34 Effective length of query: 475 Effective length of database: 447 Effective search space: 212325 Effective search space used: 212325 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 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