Align D-gluconate dehydrogenase cytochrome c subunit (EC 1.1.99.3) (characterized)
to candidate HSERO_RS16735 HSERO_RS16735 alcohol dehydrogenase
Query= metacyc::MONOMER-12746 (434 letters) >FitnessBrowser__HerbieS:HSERO_RS16735 Length = 444 Score = 488 bits (1257), Expect = e-142 Identities = 251/417 (60%), Positives = 306/417 (73%), Gaps = 8/417 (1%) Query: 3 ALVIATLALLGSAAANAA--EADQQALVQQGEYLARAGDCVACHTAKDGKPFAGGLPMET 60 A V++ AL +A +N A ADQQ LVQ+GEYLA+AGDCVACHTAK GKPFAGGL + T Sbjct: 14 AAVMSLSALTAAAQSNPAAPSADQQ-LVQRGEYLAKAGDCVACHTAKGGKPFAGGLAIAT 72 Query: 61 PIGVIYSTNITPDK-TGIGDYSFEDFDKAVRHGVAKGGSTLYPAMPFPSYARVSDADMQA 119 PIG +YS+NITPDK GIG+YS EDFD+A+RHG+ K G++LYPAMP+PSYA+V AD++A Sbjct: 73 PIGTVYSSNITPDKENGIGNYSEEDFDRALRHGIRKDGASLYPAMPYPSYAKVKPADVKA 132 Query: 120 LYAYFMKGVAPVARDNQDSDIPWPLSMRWPLSIWRWMFAPSVETPAPAAGSDPVISRGAY 179 LYAYFM GV N+ DI WPLSMRWPLSIWR +FAP+V P S V RG Y Sbjct: 133 LYAYFMHGVQADPAPNRGVDITWPLSMRWPLSIWRKVFAPAVAVDGPEDNSPLV--RGQY 190 Query: 180 LVEGLGHCGACHTPRALTMQEKALSASGGSDFLSGSAPLEGWIAKSLRGDHKDGLGSWSE 239 LVEGLGHCGACHTPR + MQEKALS + S FLSG ++G++A +LRGD +DGLG+WSE Sbjct: 191 LVEGLGHCGACHTPRGVGMQEKALS-NDSSQFLSGGV-IDGYLANNLRGDGRDGLGNWSE 248 Query: 240 EQLVQFLKTGRSDRSAVFGGMSDVVVHSMQYMTDADLTAIARYLKSLPANDPKDQPHQYD 299 +V FLKTGR+ SA FGGM+DVV +S QYMT+ DL+A+A+YLKSL YD Sbjct: 249 ADIVAFLKTGRNSHSAAFGGMADVVANSTQYMTEEDLSAMAKYLKSLKPVKDGTPALAYD 308 Query: 300 KQVAQALWNGDDSKPGAAVYIDNCAACHRTDGHGYTRVFPALAGNPVLQSADATSLIHIV 359 + QAL G D PGA +++NCAACHR+ G GY FP+LA +P + + + SLI IV Sbjct: 309 DKTHQALRKGSDQSPGAMAFLNNCAACHRSSGKGYDETFPSLALSPTVNAENPASLIRIV 368 Query: 360 LKGGTLPATHSAPSTFTMPAFAWRLSDQEVADVVNFIRSSWGNQASAVKPGDVAALR 416 L+G +P TH AP+ F MPAF RLSDQEVA+VV FIRSSWGNQAS+V DVA +R Sbjct: 369 LEGAEMPWTHKAPTQFAMPAFGSRLSDQEVAEVVTFIRSSWGNQASSVSASDVAKVR 425 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: 679 Number of extensions: 45 Number of successful extensions: 7 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: 444 Length adjustment: 32 Effective length of query: 402 Effective length of database: 412 Effective search space: 165624 Effective search space used: 165624 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