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_028990341.1 G579_RS0111780 acetyl-CoA carboxylase biotin carboxylase subunit
Query= SwissProt::I3R7G3 (601 letters) >NCBI__GCF_000423825.1:WP_028990341.1 Length = 448 Score = 456 bits (1172), Expect = e-132 Identities = 227/447 (50%), Positives = 311/447 (69%), Gaps = 4/447 (0%) Query: 1 MFSKVLVANRGEIAVRVMRACEELGVRTVAVYSEADKHGGHVRYADEAYNIGPARAADSY 60 MF K+++ANRGEIA+R+ RAC ELG++TVAV+SE D+ HV+ A+E+ IGP + SY Sbjct: 1 MFDKIVIANRGEIALRIQRACRELGIKTVAVHSEPDRDLTHVKLANESVCIGPGPSDQSY 60 Query: 61 LDHESVIEAARKADADAIHPGYGFLAENAEFARKVEDSEFTWVGPSADAMERLGEKTKAR 120 L+ +VI AA DA+AIHPGYGFL+ENA+FA +VE S F ++GP + + +G+K A+ Sbjct: 61 LNIPAVISAAEVTDAEAIHPGYGFLSENADFAERVEKSGFVFIGPRPETIRLMGDKVAAK 120 Query: 121 SLMQDADVPVVPGTTEPADSAED-VKAVADDYGYPVAIKAEGGGGGRGLKVVHSEDEVDG 179 + M+ A VP VPG+ ED ++ +A + GYPV IKA GGGGGRG++VVH+E + Sbjct: 121 AAMKAAGVPCVPGSDGALPEDEDEIRRLAREIGYPVIIKAAGGGGGRGMRVVHTEANLLS 180 Query: 180 QFETAKREGEAYFDNASVYVEKYLEAPRHIEVQILADEHGNVRHLGERDCSLQRRHQKVI 239 + E F N+ VY+EK+LE PRHIE Q+LAD HGNV HLGERDCS+QRRHQKVI Sbjct: 181 SVNLTRAEAAKAFGNSMVYMEKFLETPRHIEFQVLADAHGNVIHLGERDCSVQRRHQKVI 240 Query: 240 EEAPSPALSEDLRERIGEAARRGVRAAEYTNAGTVEFLVE--DGEFYFMEVNTRIQVEHT 297 EEAP+P +SE +R+++GE + + Y AGT EFL++ DG+FYF+E+NTR+QVEH Sbjct: 241 EEAPAPGISEKVRKQMGEVVVKACKRIHYRGAGTFEFLMDTRDGKFYFIEMNTRVQVEHP 300 Query: 298 VTEEVTGLDVVKWQLRVAAGEELDFSQDDVEIEGHSMEFRINAEAPEKEFAPATGTLSTY 357 VTE +TG+D+VK Q+R+AAG L Q+DV +GH++E RINAE PE+ F P+ G ++ Y Sbjct: 301 VTELITGIDIVKEQIRIAAGLPLSVRQEDVRFQGHAIECRINAEDPER-FVPSPGRITGY 359 Query: 358 DPPGGIGIRMDDAVRQGDEIGGDYDSMIAKLIVTGSDREEVLVRAERALNEFDIEGLRTV 417 PGG GIR+D + G + YDSMI KLI G DR+E L R AL EF ++G++T Sbjct: 360 HVPGGPGIRVDSHIYAGYTVPPYYDSMIGKLIAHGKDRDEALARMRSALTEFVVDGIKTT 419 Query: 418 IPFHRLMLTDEAFREGSHTTKYLDEVL 444 IP HR +L + + +G YL+ +L Sbjct: 420 IPLHRRILHEATYIQGGVNIHYLEGLL 446 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: 648 Number of extensions: 27 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: 601 Length of database: 448 Length adjustment: 35 Effective length of query: 566 Effective length of database: 413 Effective search space: 233758 Effective search space used: 233758 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 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