Align Propionyl-CoA carboxylase, biotin carboxylase and biotin-carboxyl carrier subunit; PCC; EC 6.4.1.3; EC 6.3.4.14 (characterized)
to candidate WP_017867313.1 LACPOB_RS0102790 acetyl-CoA carboxylase biotin carboxylase subunit
Query= SwissProt::I3R7G3 (601 letters) >NCBI__GCF_000349725.1:WP_017867313.1 Length = 459 Score = 422 bits (1085), Expect = e-122 Identities = 215/449 (47%), Positives = 302/449 (67%), Gaps = 2/449 (0%) Query: 1 MFSKVLVANRGEIAVRVMRACEELGVRTVAVYSEADKHGGHVRYADEAYNIGPARAADSY 60 MFSKVLVANRGEIAVR++R+ +ELG+++VA+YS D+ HV+ ADEA +G AR DSY Sbjct: 1 MFSKVLVANRGEIAVRIIRSLKELGIQSVAIYSTEDRESLHVQLADEAVCVGTARPQDSY 60 Query: 61 LDHESVIEAARKADADAIHPGYGFLAENAEFARKVEDSEFTWVGPSADAMERLGEKTKAR 120 L+ ++++ AA A AIHPG+GFL+EN+ F ED T++GP ++ ++ +G K AR Sbjct: 61 LNMKNILAAAVGTGAQAIHPGFGFLSENSRFVEMCEDCGITFIGPRSETIDLMGNKANAR 120 Query: 121 SLMQDADVPVVPGTTEPADSAEDVKAVADDYGYPVAIKAEGGGGGRGLKVVHSEDEVDGQ 180 MQ + VPV+PG+ A + K VA + G+P+ +KA GGGG+G++ V D + Sbjct: 121 EQMQKSGVPVIPGSEGFLQDATEAKKVAKEVGFPILLKAAAGGGGKGIRRVDDIDSLTAS 180 Query: 181 FETAKREGEAYFDNASVYVEKYLEAPRHIEVQILADEHGNVRHLGERDCSLQRRHQKVIE 240 FE A RE ++ F + +Y+EK ++ +HIEVQI D+ GN + ERDCS+QR QK+IE Sbjct: 181 FEEASREAKSAFGDGRMYLEKIMDNVKHIEVQIFCDQQGNSVYFPERDCSVQRGKQKMIE 240 Query: 241 EAPSPALSEDLRERIGEAARRGVRAAEYTNAGTVEFLVED-GEFYFMEVNTRIQVEHTVT 299 E+P +S + R+ +GE A R + +Y N GT+EFL++ FYFME+NTRIQVEHTVT Sbjct: 241 ESPCSLISPEQRQHLGEIALRAANSIDYLNTGTIEFLMDQKHNFYFMEMNTRIQVEHTVT 300 Query: 300 EEVTGLDVVKWQLRVAAGEELDFSQDDVEIEGHSMEFRINAEAPEKEFAPATGTLS-TYD 358 E VTG+D+VK Q++VAAGE L F Q+D+ +EG ++E RINAE P K F P+TG + Y Sbjct: 301 EMVTGIDLVKAQVKVAAGESLPFKQEDIHLEGVAIECRINAEDPSKNFFPSTGEVKYLYV 360 Query: 359 PPGGIGIRMDDAVRQGDEIGGDYDSMIAKLIVTGSDREEVLVRAERALNEFDIEGLRTVI 418 P G +G+RMD A+ G I YDSMIAKLI G DR E + + +R L+E I G+ T Sbjct: 361 PVGNLGMRMDTALYAGCNISPFYDSMIAKLIGLGHDRNEAIEKVKRLLDEMVISGITTNQ 420 Query: 419 PFHRLMLTDEAFREGSHTTKYLDEVLDPE 447 F+ +L DE F++G+ TT Y++ V PE Sbjct: 421 KFYLSLLKDEEFKKGTITTDYVERVFLPE 449 Lambda K H 0.312 0.132 0.371 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: 570 Number of extensions: 18 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: 601 Length of database: 459 Length adjustment: 35 Effective length of query: 566 Effective length of database: 424 Effective search space: 239984 Effective search space used: 239984 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (21.8 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