Align alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate WP_012067082.1 SMED_RS14400 GMC family oxidoreductase N-terminal domain-containing protein
Query= BRENDA::Q76HN6 (526 letters) >NCBI__GCF_000017145.1:WP_012067082.1 Length = 531 Score = 439 bits (1129), Expect = e-127 Identities = 245/526 (46%), Positives = 313/526 (59%), Gaps = 8/526 (1%) Query: 3 FDYLIVGAGSAGCVLANRLSADPSVTVCLLEAGPEDRSPLIHTPLGLAAILPTRHVNWAF 62 FDY+IVGAGSAGCVLANRLS +P V LLEAG D IH P+G + +W F Sbjct: 4 FDYIIVGAGSAGCVLANRLSENPDRRVLLLEAGGSDNYHWIHIPVGYLYCINNPRTDWCF 63 Query: 63 KTTPQPGLGGRVGYQPRGKVLGGSSSINGMIYIRGHQDDFNDWQALGNEGWGFDDVLPYF 122 T + GL GR PRGKVLGG SSINGMIY+RG D++ W+ LG GW ++DVLP F Sbjct: 64 TTAAEEGLNGRSLGYPRGKVLGGCSSINGMIYMRGQARDYDLWRQLGCAGWSWNDVLPLF 123 Query: 123 RKSEMHHGGSSEYHGGDGELYVSPAN-RHAASEAFVESALRAGHSYNPDFNGATQEGAGY 181 RK E HH G+ E HG GE V A R A +AF ++A AG DFN T EG+GY Sbjct: 124 RKCEDHHRGADEMHGAGGEWRVEKARVRWAVLDAFQKAATEAGIPETDDFNRGTNEGSGY 183 Query: 182 YDVTIRDGRRWSTATAFLKPVRHRSNLTVLTHTHVESIVLLGKQATGVQALIKGSRVHLR 241 +DV R G RW+TA AFL+P R NLT+LT HV +VL ++ +GV+ G + Sbjct: 184 FDVNQRSGIRWNTAKAFLRPAMRRRNLTILTKAHVRRLVLNDRRVSGVEFQHDGVTKSVL 243 Query: 242 ARKEVILSAGAFGSPHLLMLSGIGSAAELEPQGIAPRHELPGVGQNLQDHADVVLCYKSN 301 AR+EV+LSAGA GSPH+L LSGIG L GI RHELP VG+NLQDH + L YK Sbjct: 244 ARREVVLSAGAIGSPHILELSGIGRPDVLRENGIEVRHELPAVGENLQDHLQLRLAYKVT 303 Query: 302 DTSLL---GFSLSGGVKMGKAMFDYARHRNGPVASNCAEAGAFLKTDPGLERPDIQLHSV 358 L SL G +G +Y R+GP+A ++ G F ++ P E PD+Q H Sbjct: 304 GVPTLNEKATSLFGKAAIG---LEYLVRRSGPMAMAPSQLGIFTRSGPEKETPDLQYHVQ 360 Query: 359 IGTVDDHNRKLHWGHGFSCHVCVLRPKSIGSVGLASPDPRKAPRIDPNFLAHDDDVATLL 418 T++ +H + VC LRP+S GSV L SPD AP I P +L+ + D + Sbjct: 361 PVTLEKFGEPVHPFPAITASVCNLRPESRGSVHLKSPDFAAAPNIRPRYLSAEADREVAV 420 Query: 419 KGYRITRDIIAQTPMASF-GLRDMYSAGLHNDEQLIELLRKRTDTIYHPIGTCKMGQDEM 477 K R+TR I++Q A + + DE L + TI+HP+GTC+MG D+ Sbjct: 421 KAIRLTRRIVSQPAFARYKPVEFKPGPSYETDEDLKRAAGEIGTTIFHPVGTCRMGGDQA 480 Query: 478 AVVDSQLRVHGIEGLRVVDASIMPTLVGGNTNAAAIMIAERAAEWI 523 +VVD +LR+ G+ GLR+ DASIMPT+ GNTN+ IMIAE+AAE I Sbjct: 481 SVVDPELRLRGLAGLRIADASIMPTITSGNTNSPTIMIAEKAAEMI 526 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: 760 Number of extensions: 30 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: 531 Length adjustment: 35 Effective length of query: 491 Effective length of database: 496 Effective search space: 243536 Effective search space used: 243536 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