Align D-gluconate dehydrogenase cytochrome c subunit (EC 1.1.99.3) (characterized)
to candidate H281DRAFT_04220 H281DRAFT_04220 Cytochrome c, mono- and diheme variants
Query= metacyc::MONOMER-12746 (434 letters) >FitnessBrowser__Burk376:H281DRAFT_04220 Length = 432 Score = 342 bits (876), Expect = 2e-98 Identities = 196/438 (44%), Positives = 261/438 (59%), Gaps = 40/438 (9%) Query: 4 LVIATLALL------------GSAAANAAEADQQALVQQGEYLARAGDCVACHTAKDGKP 51 +V+AT AL+ GSA A A ADQ ALV++GEYLARAGDC+ACHT + GK Sbjct: 13 VVVATAALVPVLWSGGDNLHNGSAVA-ATPADQAALVKKGEYLARAGDCIACHTVRGGKQ 71 Query: 52 FAGGLPMETPIGVIYSTNITPD-KTGIGDYSFEDFDKAVRHGVAKGGSTLYPAMPFPSYA 110 FAGGLPM TP G +++ NITPD + GIG ++ +DF +A+ G +K GS LYP PF SY Sbjct: 72 FAGGLPMATPFGTMFTPNITPDDQYGIGKWTQDDFYRAMHTGRSKDGSLLYPGFPFTSYT 131 Query: 111 RVSDADMQALYAYFMKGVAPVARDNQDSDIPWPLSMRWPLSIWRWMFAPSVETPAPAAGS 170 +V+ AD A+YAY ++ V PV ++ ++ +P + R L WR +F E A Sbjct: 132 KVTRADSDAIYAY-LRSVTPVNVASRPHELKFPFNQRNMLIGWRTLFFREGEYKA----- 185 Query: 171 DPVIS----RGAYLVEGLGHCGACHTPRALTMQEKALSASGG----SDFLSGSAPLEGWI 222 DP S RGAYL+EGLGHCG CHT +++A GG + F G PL+ W Sbjct: 186 DPTKSVEWNRGAYLIEGLGHCGMCHT---------SINAMGGPVSSAAFAGGLIPLQNWY 236 Query: 223 AKSLRGDHKDGLGSWSEEQLVQFLKTGRSDRSAVFGGMSDVVVHSMQYMTDADLTAIARY 282 A SL + + GLG W + + LKTG S+R AVFG M++VV +S+QYMTDAD+ A+A Y Sbjct: 237 APSLTSNKEAGLGDWETKDIADLLKTGVSNRGAVFGPMAEVVHNSLQYMTDADINAMATY 296 Query: 283 LKSLPANDPKDQPHQYDKQVAQALWNGDDSKPGAAVYIDNCAACHRTDGHGYTRVFPALA 342 LK++P +P Q + + G+ K G +Y DNCA CH +G G FP LA Sbjct: 297 LKTIPQKSEAPEPLQLE---TSEKFGGELLKQGQKIYADNCAKCHADNGLGQPPAFPPLA 353 Query: 343 GNPVLQSADATSLIHIVLKGGTLPATHSAPSTFTMPAFAWRLSDQEVADVVNFIRSSWGN 402 N +Q A + I +VL GG P+T + P + MP FA LS+QEVA VV +IR SWGN Sbjct: 354 NNQSIQMPSAVNPIRMVLNGGYPPSTDANPHPYGMPPFAQSLSNQEVAAVVTYIRMSWGN 413 Query: 403 QASAVKPGDVAALRNGDL 420 +AV P V+ LR+ L Sbjct: 414 HGTAVSPQQVSDLRSAPL 431 Lambda K H 0.316 0.131 0.404 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: 619 Number of extensions: 47 Number of successful extensions: 9 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: 434 Length of database: 432 Length adjustment: 32 Effective length of query: 402 Effective length of database: 400 Effective search space: 160800 Effective search space used: 160800 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: 51 (24.3 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