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 PP_3948 PP_3948 nicotinate dehydrogenase subunit B
Query= SwissProt::P0A388 (468 letters) >FitnessBrowser__Putida:PP_3948 Length = 1187 Score = 224 bits (572), Expect = 9e-63 Identities = 145/390 (37%), Positives = 202/390 (51%), Gaps = 31/390 (7%) Query: 30 SALVQKGAYVARLGDCVACHTALHGQSYAGGLEIKSPIGTIYSTNITPDPTYGIGRYTFA 89 +A++++G VA GDC CHT G++ AGGL + +P GT+YSTNITPDP GIGR++FA Sbjct: 803 AAMLERGRQVAAAGDCAVCHTVSGGKANAGGLAMDTPFGTLYSTNITPDPETGIGRWSFA 862 Query: 90 EFDEAVRHGIRKDGSTLYPAMPYPSFSRMTKEDMQALYAYFMHGVKPVAQPDKQPDISWP 149 F+ A+R GI +DG LYPA PY SF + DMQALYAY M PV Q + +P Sbjct: 863 AFERAMREGISRDGRHLYPAFPYTSFRNINDADMQALYAYLM-SQTPVRQEAPANQMRFP 921 Query: 150 LSMRWPLGIWRMMFSPSPKDFTPAPGTDPEIARGDYLVTGPGHCGACHTPRGFAMQEKAL 209 + R + W F ++ P P + RG YLV G GHC ACH+PR EK Sbjct: 922 FNQRPLMAGWNARFL-QRGEYQPDPQRSAQWNRGAYLVDGLGHCTACHSPRNLMGAEK-- 978 Query: 210 DAAGGPDFLSGGAPIDNWVAPSLRNDPVVGLGR----WSEDDIYTFLKSGRID-HSAVFG 264 GG +L+GG +D W AP+L LG+ WSED+++ +L +G + H G Sbjct: 979 ---GGSSYLAGGM-VDGWEAPALN-----ALGKSSTPWSEDELFNYLSTGFSEKHGVAAG 1029 Query: 265 GMGDVVAWSTQYFTDDDLHAIAKYLKSLPPVPPSQGNYTYDPSTANMLASGNTASVPGAD 324 MG VV+ D+ AIA YL SL P + ++ S GA Sbjct: 1030 PMGPVVS-ELATLPKSDVRAIAHYLSSLEGEPQALAANAAPQVDTHVSLSNGERVFKGA- 1087 Query: 325 TYVKECAICHRNDGGG--VARMFPPLAGNPVVVTENPTSLVNVIAHGGVLPPSNWAPSAV 382 C CH +DG G + + P +A N V ++ P +L+ V+ HG P + Sbjct: 1088 -----CLGCH-SDGLGPKLFGVSPSMAVNSNVHSDLPDNLLRVVLHGIPTPATR---DLG 1138 Query: 383 AMPGYSKSLSAQQIADVVNFIRTSWGNKAP 412 MPG+ SLS +Q+AD+ ++R + P Sbjct: 1139 YMPGFKDSLSDRQVADLAAYLRHRFAADKP 1168 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: 1527 Number of extensions: 84 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: 468 Length of database: 1187 Length adjustment: 40 Effective length of query: 428 Effective length of database: 1147 Effective search space: 490916 Effective search space used: 490916 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