Align dihydrolipoyl dehydrogenase; EC 1.8.1.4 (characterized)
to candidate 5211244 Shew_3660 glutathione reductase (RefSeq)
Query= CharProtDB::CH_004665 (470 letters) >FitnessBrowser__PV4:5211244 Length = 451 Score = 211 bits (536), Expect = 5e-59 Identities = 143/454 (31%), Positives = 235/454 (51%), Gaps = 26/454 (5%) Query: 11 DTLVIGAGPGGYVAAIRAAQLGQKVTVVEKATLGGVCLNVGCIPSKALINAGHRYENAKH 70 D + +GAG GG +A RAA G KV ++E LGG C+NVGC+P K + G + A H Sbjct: 6 DYICLGAGSGGIASANRAAMRGAKVLLIEAKALGGTCVNVGCVPKKVMWY-GAQVAEAMH 64 Query: 71 --SDDMGITAENVTVDFTKVQEWKASVVNKLTGGVAGLLKGNKVDVVKGEAYFVDSNSVR 128 + D G D++K+ E + + + ++ G L N V +V+G FVD+N++ Sbjct: 65 LYAKDYGFDVSVNKFDWSKLVESREAYIERIHGAYDRGLDSNGVTLVRGYGQFVDNNTIE 124 Query: 129 VMDENSAQTYTFKNAIIATGSRPIELPNFKYSERVLNSTGALALKEIPKKLVVIGGGYIG 188 V E+ Y+ + +IATG P +PN +E ++S G AL E PK++ V+G GYI Sbjct: 125 VNGEH----YSADHILIATGGTPT-IPNIPGAEYGIDSDGFFALNEQPKRVAVVGAGYIA 179 Query: 189 TELGTAYANFGTELVILEGGDEILPGFEKQMSSLVTRRLKKKGNVEIHTNAMAKGVEERP 248 EL G+E + L F+ +S + + G +HT+++ + V + Sbjct: 180 VELAGVLHALGSETHLFVRKHAPLRSFDPMLSEALMESMATDGP-SLHTHSIPESVTKNA 238 Query: 249 DGVTVTFEVKGEEKTVDADYVLITVGRRPNTDELGLEQVGIEMTDRGIVKTDKQCRTNVP 308 DG ++T +++ E + + D ++ +GRRP+TD++GLE +++ D+G V D Q T Sbjct: 239 DG-SLTLKLENGE-SYEIDTLIWAIGRRPSTDKIGLENTDVKLNDKGYVVVDAQQNTTAK 296 Query: 309 NIYAIGDIIEG----PPLAHKASYEGKIAAEAIAG--EPAEIDYLGIPAVVFSEPELASV 362 IY +GDIIEG P+A KA G++ +E + A++DY +P VVFS P + ++ Sbjct: 297 GIYCVGDIIEGGIELTPVAVKA---GRLLSEHLFNGMTDAKMDYSLVPTVVFSHPAIGTM 353 Query: 363 GYTE----AQAKEEGLDIVAAKFPFAANGRALSLNETDGFMKLITRKEDGLVIGAQIAGA 418 G TE AQ EE + + + F + A++ + MKL+ ++ V+G G Sbjct: 354 GLTEPEAIAQYGEENVKVYNS--GFTSMYTAVTAHRQACKMKLVCAGKEEKVVGIHGIGY 411 Query: 419 SASDMISELSLAIEGGMTAEDIAMTIHAHPTLGE 452 +++ +AI+ G T D + HPT E Sbjct: 412 GMDEILQGFGVAIKMGATKADFDAVVAIHPTGAE 445 Lambda K H 0.314 0.134 0.372 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: 528 Number of extensions: 27 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: 470 Length of database: 451 Length adjustment: 33 Effective length of query: 437 Effective length of database: 418 Effective search space: 182666 Effective search space used: 182666 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (21.9 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