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_041763610.1 BPHY_RS13340 acetyl-CoA carboxylase biotin carboxylase subunit
Query= SwissProt::I3R7G3 (601 letters) >NCBI__GCF_000020045.1:WP_041763610.1 Length = 455 Score = 448 bits (1152), Expect = e-130 Identities = 235/456 (51%), Positives = 308/456 (67%), Gaps = 5/456 (1%) Query: 1 MFSKVLVANRGEIAVRVMRACEELGVRTVAVYSEADKHGGHVRYADEAYNIGPARAADSY 60 MF K+L+ANRGEIA+R+ RAC ELGV+TV VYSEADK +V+ ADEA IGPA + SY Sbjct: 1 MFEKILIANRGEIALRIQRACRELGVKTVVVYSEADKEAKYVKLADEAVCIGPAPSNLSY 60 Query: 61 LDHESVIEAARKADADAIHPGYGFLAENAEFARKVEDSEFTWVGPSADAMERLGEKTKAR 120 L+ ++I AA DA+AIHPGYGFL+ENA+FA +VE S F ++GP D + +G+K A+ Sbjct: 61 LNMPALISAAEVTDAEAIHPGYGFLSENADFAERVEQSGFVFIGPRPDTIRMMGDKVTAK 120 Query: 121 SLMQDADVPVVPGTTE--PADSAEDVKAVADDYGYPVAIKAEGGGGGRGLKVVHSEDEVD 178 M VP VPG+ P D E VK +A GYPV IKA GGGGGRG++VVH+E + Sbjct: 121 QTMIKTGVPCVPGSEGALPEDPKEIVK-IARSIGYPVIIKAAGGGGGRGMRVVHTEAALV 179 Query: 179 GQFETAKREGEAYFDNASVYVEKYLEAPRHIEVQILADEHGNVRHLGERDCSLQRRHQKV 238 + E F N VY+EKYLE PRHIE+Q+LAD N LGERDCS+QRRHQKV Sbjct: 180 NAVNMTREEAGRAFGNPQVYMEKYLENPRHIEIQVLADSFKNALWLGERDCSMQRRHQKV 239 Query: 239 IEEAPSPALSEDLRERIGEAARRGVRAAEYTNAGTVEFLVEDGEFYFMEVNTRIQVEHTV 298 IEEAP+P ++ L ERIG+ + Y AGT EFL E+GEFYF+E+NTR+QVEH V Sbjct: 240 IEEAPAPGIARRLIERIGDRCADACKKMGYLGAGTFEFLYENGEFYFIEMNTRVQVEHPV 299 Query: 299 TEEVTGLDVVKWQLRVAAGEELDFSQDDVEIEGHSMEFRINAEAPEKEFAPATGTLSTYD 358 TE +TG+D+V+ Q+R+AAGE+L Q D++ GH++E RINAE P K F P+ G L+++ Sbjct: 300 TELITGIDIVQEQIRIAAGEKLAMRQRDIQFRGHAIECRINAEDPFK-FTPSPGRLTSWH 358 Query: 359 PPGGIGIRMDDAVRQGDEIGGDYDSMIAKLIVTGSDREEVLVRAERALNEFDIEGLRTVI 418 PGG GIR+D G + +YDSMI KLI G+ RE+ + R AL+E +EG++T I Sbjct: 359 MPGGPGIRVDSHAYNGYFVPPNYDSMIGKLIAYGATREQAIKRMRIALSEMVVEGIQTNI 418 Query: 419 PFHRLMLTDEAFREGSHTTKYLDEVLDPERIEAAVE 454 P HR ++ D F EG + YL+ L +++AA E Sbjct: 419 PLHRELMLDAKFVEGGTSIHYLENRL-AAKLQAAPE 453 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: 632 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: 455 Length adjustment: 35 Effective length of query: 566 Effective length of database: 420 Effective search space: 237720 Effective search space used: 237720 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