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_035133360.1 Q763_RS08915 acetyl-CoA carboxylase biotin carboxylase subunit
Query= SwissProt::I3R7G3 (601 letters) >NCBI__GCF_000769915.1:WP_035133360.1 Length = 449 Score = 427 bits (1098), Expect = e-124 Identities = 212/442 (47%), Positives = 309/442 (69%), Gaps = 3/442 (0%) Query: 1 MFSKVLVANRGEIAVRVMRACEELGVRTVAVYSEADKHGGHVRYADEAYNIGPARAADSY 60 MF K+L+ANRGEIA+RV+R C E+G++TVAVYS AD HV++ADEA IGPA + SY Sbjct: 1 MFKKILIANRGEIALRVIRTCREMGIKTVAVYSTADAESLHVKFADEAVCIGPAPSNLSY 60 Query: 61 LDHESVIEAARKADADAIHPGYGFLAENAEFARKVEDSEFTWVGPSADAMERLGEKTKAR 120 L ++I AA +ADAIHPGYGFL+ENA+F++ ++ ++G S + +E++G+K A+ Sbjct: 61 LKMSNIIAAAEITNADAIHPGYGFLSENAKFSKICQEHGIKFIGASPEMIEKMGDKATAK 120 Query: 121 SLMQDADVPVVPGTTEPADSAEDVKAVADDYGYPVAIKAEGGGGGRGLKVVHSEDEVDGQ 180 + M+ A VP VPG+ +S E +A ++GYPV +KA GGGG+G++ V +++ Sbjct: 121 ATMKAAGVPCVPGSDGLLESFEQADMLAKEFGYPVMLKATAGGGGKGMRAVWKAEDLLKA 180 Query: 181 FETAKREGEAYFDNASVYVEKYLEAPRHIEVQILADEHGNVRHLGERDCSLQRRHQKVIE 240 +E+A++E A F N +Y+EK +E PRHIE+Q++ D +G HL ERDCS+QRRHQK+ E Sbjct: 181 WESARQEAGAAFGNDGMYMEKLIEEPRHIEIQVVGDSYGKACHLSERDCSVQRRHQKLTE 240 Query: 241 EAPSPALSEDLRERIGEAARRGVRAAEYTNAGTVEFLVE-DGEFYFMEVNTRIQVEHTVT 299 E PSP ++++LR+ +G+AA + +Y AGTVEFLV+ FYFME+NTRIQVEH +T Sbjct: 241 ETPSPFMTDELRQAMGDAAVKAAEFIKYEGAGTVEFLVDKHRNFYFMEMNTRIQVEHPIT 300 Query: 300 EEVTGLDVVKWQLRVAAGEELDFSQDDVEIEGHSMEFRINAEAPEKEFAPATGTLSTYDP 359 E+V D+++ Q+ VAAG + S + + HS+E RINAE P +F P+ G ++T Sbjct: 301 EQVIDYDLIREQILVAAG--VPISGKNYLPQLHSIECRINAEDPYNDFRPSPGKITTLHM 358 Query: 360 PGGIGIRMDDAVRQGDEIGGDYDSMIAKLIVTGSDREEVLVRAERALNEFDIEGLRTVIP 419 PGG G+R+D V G I +YDSMIAKLI T REE + + +RAL+EF IEG++T IP Sbjct: 359 PGGHGVRLDTHVYSGYTIPPNYDSMIAKLITTAQTREEAINKMKRALDEFVIEGIKTTIP 418 Query: 420 FHRLMLTDEAFREGSHTTKYLD 441 FHR ++ ++A+ EG +TTK+++ Sbjct: 419 FHRQLMDEQAYVEGDYTTKFME 440 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: 629 Number of extensions: 19 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: 449 Length adjustment: 35 Effective length of query: 566 Effective length of database: 414 Effective search space: 234324 Effective search space used: 234324 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