Align Alcohol dehydrogenase (quinone), cytochrome c subunit; ADH; Alcohol dehydrogenase (quinone), subunit II; Cytochrome c-553; Cytochrome c553; Ethanol:Q2 reductase; G3-ADH subunit II; Quinohemoprotein-cytochrome c complex; Ubiquinol oxidase; EC 1.1.5.5 (characterized)
to candidate GFF2557 PS417_13035 aldehyde dehydrogenase
Query= SwissProt::P0A388 (468 letters) >lcl|FitnessBrowser__WCS417:GFF2557 PS417_13035 aldehyde dehydrogenase Length = 1175 Score = 221 bits (563), Expect = 1e-61 Identities = 139/388 (35%), Positives = 205/388 (52%), Gaps = 32/388 (8%) Query: 31 ALVQKGAYVARLGDCVACHTALHGQSYAGGLEIKSPIGTIYSTNITPDPTYGIGRYTFAE 90 A +++G +A +GDC CHTA G + AGGL +++P GT+YS+NITPD GIG +++ Sbjct: 795 ATLERGRLLAAVGDCAVCHTAPGGATNAGGLAMQTPFGTLYSSNITPDVKTGIGAWSYPA 854 Query: 91 FDEAVRHGIRKDGSTLYPAMPYPSFSRMTKEDMQALYAYFMHGVKPVAQPDKQPDISWPL 150 F+ A+R GI +DG LYPA PY +F + + DMQALYAY M V PV+Q + +P Sbjct: 855 FERAMRDGIGRDGRNLYPAFPYTAFRNINEADMQALYAYLMSQV-PVSQAPTPNAMRFPF 913 Query: 151 SMRWPLGIWRMMFSPSPKDFTPAPGTDPEIARGDYLVTGPGHCGACHTPRGFAMQEKALD 210 ++R + W + + + +P P + RG+YLV G GHC ACH+PR EK Sbjct: 914 NIRPLMAGWNAL-NLRRGEISPQPERSEQWNRGNYLVNGLGHCAACHSPRNLMGAEK--- 969 Query: 211 AAGGPDFLSGGAPIDNWVAPSLRNDPVVGLGR----WSEDDIYTFLKSGRID-HSAVFGG 265 GG FL+GG +D W AP+L GL + W+ED ++T+L +G D H G Sbjct: 970 --GGKSFLAGGT-VDGWEAPALN-----GLSKASTPWTEDQLFTYLSTGYSDAHGVAAGP 1021 Query: 266 MGDVVAWSTQYFTDDDLHAIAKYLKSLPPVPPSQGNYTYDPSTANMLASGNTASVPGADT 325 MG VV+ D+ A+A YL SL +G+ + A + + N + G Sbjct: 1022 MGPVVS-ELSKLPKADIRAMAVYLASL------KGDAA---AEAPAVTAANVPNPDGRRV 1071 Query: 326 YVKECAICHRND-GGGVARMFPPLAGNPVVVTENPTSLVNVIAHGGVLPPSNWAPSAVAM 384 + C CH + G + + P A N V ++ P +L+ VI G P + M Sbjct: 1072 FEGACKACHADGLGPKLFGVSPSFATNTNVHSDQPDNLIKVILQGISKPATQ---DLGYM 1128 Query: 385 PGYSKSLSAQQIADVVNFIRTSWGNKAP 412 PG+ SLS Q+AD+ ++R + AP Sbjct: 1129 PGFKDSLSNSQVADLAAYLRAQFAPNAP 1156 Lambda K H 0.317 0.134 0.425 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: 1569 Number of extensions: 91 Number of successful extensions: 6 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: 468 Length of database: 1175 Length adjustment: 40 Effective length of query: 428 Effective length of database: 1135 Effective search space: 485780 Effective search space used: 485780 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: 55 (25.8 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