Align Dihydrolipoyl dehydrogenase; Dihydrolipoamide dehydrogenase; EC 1.8.1.4 (characterized)
to candidate PP_3819 PP_3819 glutathione reductase (NADPH)
Query= SwissProt::P85207 (461 letters) >FitnessBrowser__Putida:PP_3819 Length = 451 Score = 257 bits (657), Expect = 5e-73 Identities = 167/443 (37%), Positives = 242/443 (54%), Gaps = 10/443 (2%) Query: 4 YDLIVIGTGPGGYPAAIRGAQLGLKVLAVEAAEVGGVCLNVGCIPTKALLHAAETVHHLK 63 +DL VIG G GG AA A G KV E+ +GG C+NVGC+P K L++ A L+ Sbjct: 5 FDLFVIGAGSGGVRAARFAAGFGAKVAVAESRYLGGTCVNVGCVPKKLLVYGAHVADELE 64 Query: 64 GAEGFGLKAKP-ELDLKKLGAWRDGVVKKLTGGVAGLLKGNKVELLRGFARFKGPREIEV 122 A GFG + D L A ++ +++L G LL + V LL+G AR G E+EV Sbjct: 65 QAAGFGWTLEEGHFDWGTLIANKNREIERLNGIYRNLLVNSGVTLLQGHARLTGANEVEV 124 Query: 123 NGETYGAQSFIIATGSEPMPLKGFPFGEDVWDSTRALRVEEGIPKRLLVIGGGAVGLELG 182 +G+ Y A+ +IATG P + P E S A +++ +P+R+LV+GGG + +E Sbjct: 125 DGQRYTAEHILIATGGWPQ-VPDIPGKELAITSNEAFYLKD-LPRRVLVVGGGYIAVEFA 182 Query: 183 QIYHRLGSEVTLIEYMPEILPAGDRETAALLRKALEKEGLKVRTGTKAVGYEKKQDGLHV 242 I+ LG++ TL+ L D L++ LEK GL ++ +K +DG Sbjct: 183 GIFQGLGADTTLLYRGDLFLRGFDGSVRTHLKQELEKRGLDLQFNADIQRIDKLEDGR-- 240 Query: 243 LLEAAQGGSQEEIVVDKILVAVGRRPRTEGLGLEKAGVKVDERGFIQVNARMETSAPGVY 302 L + G E+V D + A GRRP + LGLE GV++DERG+I+V+ + +T+AP + Sbjct: 241 LKATLKDG--RELVADCVFYATGRRPMLDNLGLENTGVELDERGYIRVDEQYQTTAPSIL 298 Query: 303 AIGDVARPPLLAHKAMKEGLVAAENAAGKNAL--FDFQ-VPSVVYTGPEWAGVGLTEEEA 359 AIGDV L A+ EG+ A D+Q +P+ V++ P VGLTEE+A Sbjct: 299 AIGDVIGRVQLTPVALAEGMAVARRLFKPEQYRPVDYQNIPTAVFSQPPIGTVGLTEEQA 358 Query: 360 RKAGYNVKVGKFPFSASGRALTLGGAEGLIKVVGDAETDLLLGVFVVGPQAGELIAEATL 419 +AG+ V+V + F A LT + L+K+V DAETD +LG +VGP AGE+I + Sbjct: 359 LEAGHKVQVFESRFRAMKLTLTDIQEKTLMKLVVDAETDKVLGCHMVGPDAGEIIQGLGI 418 Query: 420 ALEMGATVSDLGLTIHPHPTLSE 442 AL+ GAT TI HPT +E Sbjct: 419 ALKAGATKQQFDETIGVHPTAAE 441 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: 552 Number of extensions: 29 Number of successful extensions: 5 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: 451 Length adjustment: 33 Effective length of query: 428 Effective length of database: 418 Effective search space: 178904 Effective search space used: 178904 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