Align dihydrolipoyl dehydrogenase; EC 1.8.1.4 (characterized)
to candidate 7026925 Shewana3_4054 glutathione reductase (RefSeq)
Query= CharProtDB::CH_015561 (478 letters) >FitnessBrowser__ANA3:7026925 Length = 451 Score = 188 bits (477), Expect = 4e-52 Identities = 136/465 (29%), Positives = 226/465 (48%), Gaps = 29/465 (6%) Query: 1 MTQKFDVVVIGAGPGGYVAAIKAAQLGLKTACIEKYTDAEGKLALGGTCLNVGCIPSKAL 60 M Q FD + +GAG GG +A +AA G K IE +GGTC+NVGC+P K + Sbjct: 1 MAQHFDYICLGAGSGGIASANRAAMRGAKVLLIEAKH-------VGGTCVNVGCVPKKVM 53 Query: 61 LDSSWKYKEAKESFNVH----GISTGEVKMDVAAMVGRKAGIVKNLTGGVATLFKANGVT 116 W E+ N++ G K D +V + + + F N VT Sbjct: 54 ----WYGAHIAEAMNLYAKDYGFDVSVNKFDWNTLVNSREAYIGRIHEAYGRGFTNNKVT 109 Query: 117 SIQGHGKLLAGKKVEVTKADGTTEVIEAENVILASGSRPIDIPPAPVDQNVIVDSTGALE 176 + G+G+ + G +EV T A+++++A+G P IP P + I DS G Sbjct: 110 LLNGYGRFVNGNTIEVNGEHYT-----ADHILIATGGAPT-IPNIPGAEYGI-DSDGFFA 162 Query: 177 FQAVPKRLGVIGAGVIGLELGSVWARLGAEVTVLEALDTFLMAADTAVSKEAQKTLTKQG 236 + PKR+ V+GAG I +E+ V LG+E + L D + + +G Sbjct: 163 LREQPKRVAVVGAGYIAVEVAGVLHALGSETHLFVRKHAPLRNFDPMLIDALVDAMKTEG 222 Query: 237 LDIKLGARVTGSKVNGNEVEVTYTNAEGEQKITFDKLIVAVGRRPVTTDLLAADSGVTID 296 + + V S V + +T N E + +T D LI A+GR P T ++ ++ V +D Sbjct: 223 PTLHTNS-VPQSVVKNADDSLTL-NLENGESVTVDCLIWAIGRSPATGNIGLENTDVQLD 280 Query: 297 ERGYIFVDDYCATSVPGVYAIGDVVR-GMMLAHKASEEGIMVVERIKG--HKAQMNYDLI 353 +GY+ D T+ G+Y +GD++ G+ L A + G ++ ER+ A+M+Y I Sbjct: 281 SKGYVITDAQQNTTHKGIYCVGDIMAGGVELTPVAVKAGRLLSERLFNGMSDAKMDYSQI 340 Query: 354 PSVIYTHPEIAWVGKTEQALKAEGVEVNVGTFP--FAASGRAMAANDTGGFVKVIADAKT 411 P+V+++HP I +G TE +A+ + NV + F + A+ ++ +K++ K Sbjct: 341 PTVVFSHPPIGTMGLTEPEARAQYGDDNVKVYTSGFTSMYTAVTSHRQACKMKLVCAGKE 400 Query: 412 DRVLGVHVIGPSAAELVQQGAIAMEFGTSAEDLGMMVFSHPTLSE 456 ++V+G+H IG E++Q +AM+ G + D +V HPT +E Sbjct: 401 EKVVGIHGIGFGMDEILQGFGVAMKMGATKADFDAVVAIHPTGAE 445 Lambda K H 0.316 0.133 0.374 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: 7 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: 478 Length of database: 451 Length adjustment: 33 Effective length of query: 445 Effective length of database: 418 Effective search space: 186010 Effective search space used: 186010 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