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 5210939 Shew_3365 acetyl-CoA carboxylase, biotin carboxylase (RefSeq)
Query= SwissProt::I3R7G3 (601 letters) >FitnessBrowser__PV4:5210939 Length = 450 Score = 434 bits (1115), Expect = e-126 Identities = 222/448 (49%), Positives = 300/448 (66%), Gaps = 2/448 (0%) Query: 2 FSKVLVANRGEIAVRVMRACEELGVRTVAVYSEADKHGGHVRYADEAYNIGPARAADSYL 61 F KVLVANRGEIA+R++RAC +LG++TVA+YS ADK GH+R AD+ IGPA A +SYL Sbjct: 4 FDKVLVANRGEIALRIIRACRQLGIKTVALYSSADKDSGHLRLADQQICIGPAPAKESYL 63 Query: 62 DHESVIEAARKADADAIHPGYGFLAENAEFARKVEDSEFTWVGPSADAMERLGEKTKARS 121 + +++ AA A DAIHPGYGFLAENA+FA++V DS F ++GP AD + +G+K A + Sbjct: 64 NIAAILGAADLARVDAIHPGYGFLAENADFAQQVTDSGFHFIGPKADTIRLMGDKVSAIA 123 Query: 122 LMQDADVPVVPGTTEP-ADSAEDVKAVADDYGYPVAIKAEGGGGGRGLKVVHSEDEVDGQ 180 M+ A VP VPG+ D+ +A GYP+ IKA GGGG+G++VV E ++ G Sbjct: 124 AMKAAGVPTVPGSDGLLGDNEAQSLEIAAQIGYPLIIKATAGGGGKGMRVVEDEAQLLGA 183 Query: 181 FETAKREGEAYFDNASVYVEKYLEAPRHIEVQILADEHGNVRHLGERDCSLQRRHQKVIE 240 ++E EA F N VY+EKYL PRHIEVQ+L D G+ LGERDCSLQR QKVIE Sbjct: 184 IALTRQEAEAAFGNGGVYLEKYLTRPRHIEVQVLCDHQGHCISLGERDCSLQRAQQKVIE 243 Query: 241 EAPSPALSEDLRERIGEAARRGVRAAEYTNAGTVEFLVEDGEFYFMEVNTRIQVEHTVTE 300 AP+P L+ + R++I E+ R +A Y AGT+EFL +DGEFYFME+NTRIQVEHT++E Sbjct: 244 SAPAPGLTPEQRQQISESCIRACQAIGYRGAGTLEFLYQDGEFYFMEMNTRIQVEHTISE 303 Query: 301 EVTGLDVVKWQLRVAAGEELDFSQDDVEIEGHSMEFRINAEAPEKEFAPATGTLSTYDPP 360 VTG+D++ QLRVA GE L + ++ +GH++E RINAE P FAP+ G + P Sbjct: 304 MVTGVDLLVLQLRVAQGEPLALQESLIQPKGHAIECRINAEDP-ASFAPSPGRIDRLVVP 362 Query: 361 GGIGIRMDDAVRQGDEIGGDYDSMIAKLIVTGSDREEVLVRAERALNEFDIEGLRTVIPF 420 GG+G+R + + G + YD+MIAKLI G DR + + R AL+E I G++T +P Sbjct: 363 GGLGVRWESHLSPGAHVPPQYDAMIAKLIAWGDDRAQAIARMRTALDELTITGIKTNVPL 422 Query: 421 HRLMLTDEAFREGSHTTKYLDEVLDPER 448 R +L D ++G + YL+E P R Sbjct: 423 LRALLADPQVQQGETSIHYLEETFLPRR 450 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: 25 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: 450 Length adjustment: 35 Effective length of query: 566 Effective length of database: 415 Effective search space: 234890 Effective search space used: 234890 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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