Align alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate WP_012050692.1 SWIT_RS22820 GMC family oxidoreductase N-terminal domain-containing protein
Query= BRENDA::Q76HN6 (526 letters) >NCBI__GCF_000016765.1:WP_012050692.1 Length = 550 Score = 387 bits (994), Expect = e-112 Identities = 220/525 (41%), Positives = 297/525 (56%), Gaps = 4/525 (0%) Query: 3 FDYLIVGAGSAGCVLANRLSADPSVTVCLLEAGPEDRSPLIHTPLGLAAILPTRHVNWAF 62 FDY+I GAG+AGC+LANRLSADP+ V LLEAG +D H P+G + +W F Sbjct: 21 FDYVIAGAGTAGCLLANRLSADPAKRVLLLEAGGKDSWIWFHIPVGYLFAIGNPRADWMF 80 Query: 63 KTTPQPGLGGRVGYQPRGKVLGGSSSINGMIYIRGHQDDFNDWQALGNEGWGFDDVLPYF 122 +T + GLGGR PRGKV+GG SSIN M+Y+RG D++ W+ LG GWG+DDVLPYF Sbjct: 81 ETVEEAGLGGRRLAYPRGKVIGGCSSINAMVYMRGQAADYDGWRQLGLAGWGWDDVLPYF 140 Query: 123 RKSEMHHGGSSEYHGGDGELYVS-PANRHAASEAFVESALRAGHSYNPDFNGATQEGAGY 181 + E H + E+HG GE V P R +A E+ G + DFN G+ Y Sbjct: 141 LRHEDHAVATGEHHGRGGEWRVEHPRIRWDILDAIREAGAAVGIAPIEDFNRGDNAGSSY 200 Query: 182 YDVTIRDGRRWSTATAFLKPVRHRSNLTVLTHTHVESIVLLGKQATGVQALIKGSRVHLR 241 + V R GRR S A AFLKPV R NL + T ++ I+ G++A G+ G R R Sbjct: 201 FHVNQRGGRRVSAAGAFLKPVLRRPNLRLETGVEIDRILFDGRRAAGLSFRRGGERWTAR 260 Query: 242 ARKEVILSAGAFGSPHLLMLSGIGSAAELEPQGIAPRHELPGVGQNLQDHADVVLCYKSN 301 A EVIL+ GA G+P LL LSGIG A L+ GI P H LPGVG NLQDH + +K Sbjct: 261 AEGEVILATGAVGTPKLLQLSGIGDAERLKALGIEPVHHLPGVGANLQDHLQIRPIFKVE 320 Query: 302 DTSLLGFSLSGGVKMGKAMFDYARHRNGPVASNCAEAGAFLKTDPGLERPDIQLHSVIGT 361 L + ++ +YA R GP+ ++ G F ++ P++Q H + Sbjct: 321 GVRTLNTDYANLLRRAAMGIEYALFRAGPLTMAPSQLGMFARSSDIHATPNLQFHFQPLS 380 Query: 362 VDDHNRKLHWGHGFSCHVCVLRPKSIGSVGLASPDPRKAPRIDPNFLAHDDDVATLLKGY 421 +D LH F+ VC LRP S G + LAS DP PRI P +L+ ++D ++ Sbjct: 381 LDSWGSGLHRFGAFTASVCNLRPTSRGRIDLASADPAAPPRIAPGYLSTEEDRRVAIESL 440 Query: 422 RITRDIIAQTPMASFGLRDMY-SAGLHNDEQLIELLRKRTDTIYHPIGTCKMG--QDEMA 478 R+TR I+AQ P+A + + +DE L+ + TI+HP+GT MG D A Sbjct: 441 RLTRRIVAQAPLARYRPEEFRPGPAADSDEALLIAAEELGTTIFHPVGTAAMGADHDRGA 500 Query: 479 VVDSQLRVHGIEGLRVVDASIMPTLVGGNTNAAAIMIAERAAEWI 523 V+D +LRV G++GLRVVDAS MP + GNT++ +MIAE+ A I Sbjct: 501 VLDERLRVRGLDGLRVVDASAMPRIPSGNTSSPTLMIAEKGAAMI 545 Lambda K H 0.319 0.137 0.419 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: 808 Number of extensions: 41 Number of successful extensions: 4 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: 526 Length of database: 550 Length adjustment: 35 Effective length of query: 491 Effective length of database: 515 Effective search space: 252865 Effective search space used: 252865 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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:
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