Align methylcrotonoyl-CoA carboxylase (EC 6.4.1.4) (characterized)
to candidate GFF1244 PGA1_c12600 biotin carboxylase AccA
Query= BRENDA::Q42523 (734 letters) >lcl|FitnessBrowser__Phaeo:GFF1244 PGA1_c12600 biotin carboxylase AccA Length = 450 Score = 425 bits (1093), Expect = e-123 Identities = 218/443 (49%), Positives = 289/443 (65%), Gaps = 4/443 (0%) Query: 39 EKILVANRGEIACRIMRTAKRLGIQTVAVYSDADRDSLHVKSADEAVRIGPPSARLSYLS 98 +KIL+ANRGEIA R++R + +GIQ+VAV+S AD D++HV+ ADE+V IGPPS SYLS Sbjct: 3 DKILIANRGEIALRVIRACREMGIQSVAVHSTADADAMHVRMADESVCIGPPSGTHSYLS 62 Query: 99 GVTIMEAAARTGAQAIHPGYGFLSESSDFAQLCEDSGLTFIGPPASAIRDMGDKSASKRI 158 I+ A TGAQAIHPGYGFLSE+++F Q+ ED GLTFIGP A IR MGDK +K Sbjct: 63 IPAIISACEITGAQAIHPGYGFLSENANFVQIVEDHGLTFIGPTAEHIRVMGDKITAKDT 122 Query: 159 MGAAGVPLVPGYHGHEQDIDHMKSEAEKIGYPIIIKPTHGGGGKGMRIVQSGKDFADSFL 218 M GVP VPG G D++ K E IGYP+IIK T GGGG+GM++ ++ D +F+ Sbjct: 123 MKDLGVPCVPGSDGGVPDLETAKKIGEDIGYPVIIKATAGGGGRGMKVAKTAADMEQAFM 182 Query: 219 GAQREAAASFGVNTILLEKYITRPRHIEVQIFGDKHGNVLHLYERDCSVQRRHQKIIEEA 278 A+ E A+FG + + +EKY+T PRHIE+Q+FGD G +HL ERDCS+QRRHQK+ EEA Sbjct: 183 TARAEGKAAFGNDEVYIEKYLTTPRHIEIQVFGDGKGKAVHLGERDCSLQRRHQKVFEEA 242 Query: 279 PAPNISEKFRANLGQAAVSAARAVGYYNAGTVEFIVDTESDQFYFMEMNTRLQVEHPVTE 338 P P I+ + RA +G+ A + Y AGT+EF+ E +FYF+EMNTRLQVEHPVTE Sbjct: 243 PGPCITPEERARIGKTCAEAVAKINYIGAGTIEFLY--EKGEFYFIEMNTRLQVEHPVTE 300 Query: 339 MIVGQDLVEWQIRVANGEPLPLSQSEVPMSGHAFEARIYAENVPKGFLPATGVLNHYRPV 398 I G DLV QIRVA G P+ SQ ++ ++GH+ E RI AE +P F P G + Y Sbjct: 301 SIFGVDLVREQIRVAEGLPMSFSQDDLEINGHSIEVRINAEKLP-NFSPCPGRITQYHAP 359 Query: 399 AVSPSVRVETGVEQGDTVSMHYDPMIAKLVVWGGNRGEALVKLKDCLSNFQVAGVPTNIN 458 VR+++ + G ++ +YD +I KL+V G +R EAL +L L V GV T + Sbjct: 360 G-GLGVRMDSALYDGYSIPPYYDSLIGKLIVHGRDRPEALARLSRALGELIVDGVDTTVP 418 Query: 459 FLQKLASHKEFAVGNVETHFIEH 481 L K+ G H++EH Sbjct: 419 LFHALLEEKDIRTGEYNIHWLEH 441 Lambda K H 0.316 0.132 0.386 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: 863 Number of extensions: 35 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: 734 Length of database: 450 Length adjustment: 36 Effective length of query: 698 Effective length of database: 414 Effective search space: 288972 Effective search space used: 288972 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 53 (25.0 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 preprint 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