Align Dihydrolipoyl dehydrogenase; Dihydrolipoamide dehydrogenase; EC 1.8.1.4 (characterized)
to candidate SM_b21143 SM_b21143 mercuric reductase
Query= SwissProt::P85207 (461 letters) >FitnessBrowser__Smeli:SM_b21143 Length = 473 Score = 238 bits (606), Expect = 4e-67 Identities = 141/446 (31%), Positives = 231/446 (51%), Gaps = 8/446 (1%) Query: 2 KTYDLIVIGTGPGGYPAAIRGAQLGLKVLAVEAAEVGGVCLNVGCIPTKALLHAAETVHH 61 K +D ++IG G G A R + +G V +E GG C+N GC+PTKA++ +A +H Sbjct: 19 KHFDAVIIGAGQAGPSLAGRLSGVGKTVALIERKLFGGTCVNTGCMPTKAMVASAYAIHT 78 Query: 62 LKGAEGFGLKAKP-ELDLKKLGAWRDGVVKKLTGGVAGLLKGNK-VELLRGFARFKGPRE 119 + +G+ P +D ++ A ++ V GV LKG K + G ARF+GPRE Sbjct: 79 ARRGAEYGMTTGPVSVDFGRVMARKEKVRLDARSGVEKWLKGMKNCTVFEGHARFEGPRE 138 Query: 120 IEVNGETYGAQSFIIATGSEPMPLKGFPFGEDVWDSTRALRVEEG-IPKRLLVIGGGAVG 178 + + E + + G + P DV T + ++ +P+ L+V+GG +G Sbjct: 139 VRIGDELISGERIFVNVGGRAA-VADLPGVNDVPYLTNSSIMDLAELPEHLVVVGGSYIG 197 Query: 179 LELGQIYHRLGSEVTLIEYMPEILPAGDRETAALLRKALEKEGLKVRTGTKAVGYEKKQD 238 LE Q++ R GS+VT+IE ++ D E + +R+ LE EG+++RT + + + D Sbjct: 198 LEFAQMFRRFGSDVTVIEKGARLIGREDPEVSDAIREILENEGVRIRTNAECIRFSNHAD 257 Query: 239 GLHVLLEAAQGGSQEEIVVDKILVAVGRRPRTEGLGLEKAGVKVDERGFIQVNARMETSA 298 + V ++ G + E+ +L+A GR P T+ LGL+KAGVK DERG+I+V+ + T+ Sbjct: 258 SVAVGVDCTSG--EPEVSGSHVLLATGRHPNTDDLGLDKAGVKTDERGYIEVDDSLRTNV 315 Query: 299 PGVYAIGDVARPPLLAHKAMKEGLVAAENAAGKNA--LFDFQVPSVVYTGPEWAGVGLTE 356 P ++A+GD H + + + A N + + D +Y P G+TE Sbjct: 316 PHIFAMGDCNGRGAFTHTSYNDFEIVAANLIDNDPRRVSDRIQTYALYIDPPLGRAGMTE 375 Query: 357 EEARKAGYNVKVGKFPFSASGRALTLGGAEGLIKVVGDAETDLLLGVFVVGPQAGELIAE 416 EARK G+ + VG P + GRA+ G +G +KV+ DAETD +LG ++G E + Sbjct: 376 TEARKKGHKLLVGTRPMTRVGRAVEKGETQGFMKVIVDAETDEILGASILGTGGDEAVQS 435 Query: 417 ATLALEMGATVSDLGLTIHPHPTLSE 442 + + + +H HPT+SE Sbjct: 436 ILDVMYAKKPYTMIARAVHIHPTVSE 461 Lambda K H 0.316 0.138 0.395 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: 583 Number of extensions: 35 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: 461 Length of database: 473 Length adjustment: 33 Effective length of query: 428 Effective length of database: 440 Effective search space: 188320 Effective search space used: 188320 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: 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