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_094506529.1 CEV31_RS05800 acetyl/propionyl/methylcrotonyl-CoA carboxylase subunit alpha
Query= metacyc::MONOMER-13597 (509 letters) >NCBI__GCF_002252445.1:WP_094506529.1 Length = 655 Score = 345 bits (884), Expect = 4e-99 Identities = 197/488 (40%), Positives = 285/488 (58%), Gaps = 15/488 (3%) Query: 4 FSRVLVANRGEIATRVLKAIKEMGMTAIAVYSEADKYAVHTKYADEAYYIGKAPALDSYL 63 F ++L+ANRGEIA R+++ +G+ +A+YS+ADK +H + ADEA +G A + SYL Sbjct: 2 FQKILIANRGEIACRIIRTAHRLGIATVAIYSDADKNTLHVEMADEAVRVGPAQSAQSYL 61 Query: 64 NIEHIIDAAEKAHVDAIHPGYGFLSENAEFAEAVEKAGITFIGPSSEVMRKIKDKLDGKR 123 NIE II AA +AIHPGYGFLSEN F EAVEKA + FIGPS++ +R + K K Sbjct: 62 NIEAIIKAAHDTGAEAIHPGYGFLSENPAFVEAVEKAELVFIGPSAKAIRAMGLKDAAKS 121 Query: 124 LANMAGVPTAPGSDGPVTSIDEALKLAEKIGYPIMVKAASGGGGVGITRVDNQDQLMDVW 183 L A VP PG G A+ I YP+++KA +GGGG G+ RVD+ Sbjct: 122 LMERAAVPVVPGYHGDNQDNAFLKSQADAITYPVLIKARAGGGGKGMRRVDDPAHFSAAL 181 Query: 184 ERNKRLAYQAFGKADLFIEKYAVNPRHIEFQLIGDKYGNYVVAWERECTIQRRNQKLIEE 243 E +R A +FG + IEKY PRHIE Q+ GD +GN V +ER+C++QRR+QK+IEE Sbjct: 182 ESARREAEASFGDGAVLIEKYMTKPRHIEVQIFGDNFGNAVHLFERDCSLQRRHQKVIEE 241 Query: 244 APSPALKMEERESMFEPIIKFGKLINYFTLGTFETAFSDVSRD-----FYFLELNKRLQV 298 AP+P + E R +M E +K I Y GT E +DVS F+F+E+N RLQV Sbjct: 242 APAPGMTPEMRTAMGEAAVKAALAIGYSGAGTVE-FIADVSEGLRPDRFFFMEMNTRLQV 300 Query: 299 EHPTTELIFRIDLVKLQIKLAAGEHLPFSQEDLNKRVRGTAIEYRINAEDALNNFTGSSG 358 EHP TE I +DLV+ Q+++A+GE LP Q++L + G A E R+ AED +F ++G Sbjct: 301 EHPVTEAITCLDLVEWQLRVASGEPLPKRQDEL--AINGWAFEARLYAEDPARDFMPATG 358 Query: 359 FVTYYREPTGPGVRVDSGIESGSYVPPYYDSLVSKLIVYGESREYAIQAGIRALADYKIG 418 + + P RVDSG+ SG + P+YD +++K+I +G +R+ A+ AL I Sbjct: 359 RLALFAPP--ENARVDSGVRSGDTITPFYDPMIAKIITHGATRDEALSRLDAALNKTCIA 416 Query: 419 GIKTTIELYKWIMQDPDFQEGKFSTSYISQKTDQFVKYLREQEEIKAAIAAEIQSRGLLR 478 G+ T + + + F++G T I+++T V R+++ + A A + + G L Sbjct: 417 GLVTNRQFLTALCKLEAFRKGDVDTGLIARET---VVLFRDEKPSEVAFA--LATLGALD 471 Query: 479 TSSTDNKG 486 KG Sbjct: 472 LLDAPQKG 479 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: 724 Number of extensions: 34 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: 655 Length adjustment: 36 Effective length of query: 473 Effective length of database: 619 Effective search space: 292787 Effective search space used: 292787 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