Align D-gluconate dehydrogenase cytochrome c subunit (EC 1.1.99.3) (characterized)
to candidate AO353_10800 AO353_10800 alcohol dehydrogenase
Query= metacyc::MONOMER-12746 (434 letters) >FitnessBrowser__pseudo3_N2E3:AO353_10800 Length = 435 Score = 746 bits (1927), Expect = 0.0 Identities = 362/433 (83%), Positives = 390/433 (90%) Query: 1 MKALVIATLALLGSAAANAAEADQQALVQQGEYLARAGDCVACHTAKDGKPFAGGLPMET 60 MK LVIATLALLGS + +AAE QAL++QGEYLARAGDCVACHTAK GKPFAGGLPMET Sbjct: 1 MKNLVIATLALLGSCSISAAEDASQALIKQGEYLARAGDCVACHTAKGGKPFAGGLPMET 60 Query: 61 PIGVIYSTNITPDKTGIGDYSFEDFDKAVRHGVAKGGSTLYPAMPFPSYARVSDADMQAL 120 PIG IYSTNITPDKTG+GDYSF+DFDKAVRHGVAK GSTLYPAMP+PSYARVSDADM+AL Sbjct: 61 PIGTIYSTNITPDKTGLGDYSFDDFDKAVRHGVAKNGSTLYPAMPYPSYARVSDADMKAL 120 Query: 121 YAYFMKGVAPVARDNQDSDIPWPLSMRWPLSIWRWMFAPSVETPAPAAGSDPVISRGAYL 180 YAYFMKGVAPV ++N+ SDIPWPLSMRWPL+ WRWMFAPSV PA G + ISRGAYL Sbjct: 121 YAYFMKGVAPVTQENKGSDIPWPLSMRWPLTGWRWMFAPSVVAYQPADGKEAAISRGAYL 180 Query: 181 VEGLGHCGACHTPRALTMQEKALSASGGSDFLSGSAPLEGWIAKSLRGDHKDGLGSWSEE 240 VEGLGHCGACHTPRALTMQEKALSA+ GS FLSGSAPLEGWIAKSLRGDHKDGLGSWSEE Sbjct: 181 VEGLGHCGACHTPRALTMQEKALSANEGSAFLSGSAPLEGWIAKSLRGDHKDGLGSWSEE 240 Query: 241 QLVQFLKTGRSDRSAVFGGMSDVVVHSMQYMTDADLTAIARYLKSLPANDPKDQPHQYDK 300 QLVQFLKTGRSDRSAVFGGMSDVV HSMQYM+D DLTAIARYLKSLPANDP DQPH YD Sbjct: 241 QLVQFLKTGRSDRSAVFGGMSDVVEHSMQYMSDDDLTAIARYLKSLPANDPNDQPHPYDP 300 Query: 301 QVAQALWNGDDSKPGAAVYIDNCAACHRTDGHGYTRVFPALAGNPVLQSADATSLIHIVL 360 QVAQALW GDDSKPGA+VYIDNCAACHRTDGHGYTRVFPALAGNPVLQS D SLI+IVL Sbjct: 301 QVAQALWKGDDSKPGASVYIDNCAACHRTDGHGYTRVFPALAGNPVLQSDDPVSLINIVL 360 Query: 361 KGGTLPATHSAPSTFTMPAFAWRLSDQEVADVVNFIRSSWGNQASAVKPGDVAALRNGDL 420 KG TLPATH+APSTFTMPAFAWRLSDQEVADVVNFIR+SWGN+ + +KP DVA +R ++ Sbjct: 361 KGATLPATHTAPSTFTMPAFAWRLSDQEVADVVNFIRTSWGNKGAQIKPADVADVRKDEV 420 Query: 421 QSTSNDDLGQVTS 433 +S D G++TS Sbjct: 421 KSMPADKSGKLTS 433 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: 798 Number of extensions: 34 Number of successful extensions: 2 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: 435 Length adjustment: 32 Effective length of query: 402 Effective length of database: 403 Effective search space: 162006 Effective search space used: 162006 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