Align alcohol dehydrogenase (cytochrome c) (EC 1.1.2.8) (characterized)
to candidate HSERO_RS16735 HSERO_RS16735 alcohol dehydrogenase
Query= BRENDA::D2SZY5 (472 letters) >FitnessBrowser__HerbieS:HSERO_RS16735 Length = 444 Score = 442 bits (1137), Expect = e-128 Identities = 227/428 (53%), Positives = 296/428 (69%), Gaps = 10/428 (2%) Query: 2 MINRLKAALGAVAVGLLAGTSLAH----AQNADEDLIKKGEYVARLGDCVACHTSLNGQK 57 MI A A + L A T+ A A +AD+ L+++GEY+A+ GDCVACHT+ G+ Sbjct: 4 MIKHYFIAACAAVMSLSALTAAAQSNPAAPSADQQLVQRGEYLAKAGDCVACHTAKGGKP 63 Query: 58 YAGGLSIKTPIGTIYSTNITPDPTYGIGTYTFKEFDEAVRHGVRKDGATLYPAMPYPSFA 117 +AGGL+I TPIGT+YS+NITPD GIG Y+ ++FD A+RHG+RKDGA+LYPAMPYPS+A Sbjct: 64 FAGGLAIATPIGTVYSSNITPDKENGIGNYSEEDFDRALRHGIRKDGASLYPAMPYPSYA 123 Query: 118 RMTQDDMKALYAYFMHGVQPIAQKNHPTDISWPMSMRWPLSIWRSVFAPAPKDFTPAPGT 177 ++ D+KALYAYFMHGVQ N DI+WP+SMRWPLSIWR VFAPA P Sbjct: 124 KVKPADVKALYAYFMHGVQADPAPNRGVDITWPLSMRWPLSIWRKVFAPAVA--VDGPED 181 Query: 178 DAEIARGEYLVTGPGHCGACHTPRGFGMQEKALDASGGPDFLGGGGVIDNWIAPSLRNDP 237 ++ + RG+YLV G GHCGACHTPRG GMQEKAL ++ FL GGVID ++A +LR D Sbjct: 182 NSPLVRGQYLVEGLGHCGACHTPRGVGMQEKAL-SNDSSQFL-SGGVIDGYLANNLRGDG 239 Query: 238 VLGLGRWSDEDLFLFLKSGRTDHSAAFGGMADVVGWSTQYYTDADLHAMVKYIKSLPPVP 297 GLG WS+ D+ FLK+GR HSAAFGGMADVV STQY T+ DL AM KY+KSL PV Sbjct: 240 RDGLGNWSEADIVAFLKTGRNSHSAAFGGMADVVANSTQYMTEEDLSAMAKYLKSLKPVK 299 Query: 298 PARGDYSYDASTAQMLDSNNFSGNAGAKTYVEQCAICHRNDGGGVARMFPPLAGNPVVVS 357 +YD T Q L + + GA ++ CA CHR+ G G FP LA +P V + Sbjct: 300 DGTPALAYDDKTHQALRKGS-DQSPGAMAFLNNCAACHRSSGKGYDETFPSLALSPTVNA 358 Query: 358 DNPTSVAHIVVDGGVLPPTNWAPSAVAMPDYKNILSDQQIADVVNFIRSAWGNRAPANTT 417 +NP S+ IV++G +P T+ AP+ AMP + + LSDQ++A+VV FIRS+WGN+A ++ + Sbjct: 359 ENPASLIRIVLEGAEMPWTHKAPTQFAMPAFGSRLSDQEVAEVVTFIRSSWGNQA-SSVS 417 Query: 418 AADIQKLR 425 A+D+ K+R Sbjct: 418 ASDVAKVR 425 Lambda K H 0.318 0.135 0.430 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: 701 Number of extensions: 36 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: 472 Length of database: 444 Length adjustment: 33 Effective length of query: 439 Effective length of database: 411 Effective search space: 180429 Effective search space used: 180429 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 (21.7 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