Align Dihydrolipoyl dehydrogenase; Dihydrolipoamide dehydrogenase; E3 component of pyruvate complex; EC 1.8.1.4 (characterized)
to candidate WP_012405489.1 BPHY_RS31340 FAD-dependent oxidoreductase
Query= SwissProt::P11959 (470 letters) >NCBI__GCF_000020045.1:WP_012405489.1 Length = 466 Score = 232 bits (592), Expect = 2e-65 Identities = 140/445 (31%), Positives = 236/445 (53%), Gaps = 5/445 (1%) Query: 11 ETLVVGAGPGGYVAAIRAAQLGQKVTIVEKGNLGGVCLNVGCIPSKALISASHRYEQAKH 70 +TL++G+G GG + A + GQ+V +VE+ +GG C V C+PSK I ++ A+H Sbjct: 8 DTLILGSGQGGKLLAWHLGRSGQRVAVVERQWVGGSCPAVACLPSKNEIWSARVAHLARH 67 Query: 71 SEEMGIKAENVTIDFAKVQEWKASVVKKLTGGVEGLLKGNKVEIVKGEAYFVDANTVRV- 129 + + G V ID AKV+E K +V++ + + E+V G FV TV V Sbjct: 68 AADFGATTGPVAIDMAKVRERKRGMVEREAAFHVQAYESSGAELVMGVGRFVGPKTVEVQ 127 Query: 130 VNGDSAQTYTFKNAIIATGSRPI--ELPNFKFSNRILDSTGALNLGEVPKSLVVIGGGYI 187 +N +T + + ++ G+ ++P + + L GAL+L P L+V+GGGYI Sbjct: 128 LNDGGTRTLSGRQVVVNVGTHAAIPDVPGLRAAEP-LTHIGALDLDRAPSHLIVLGGGYI 186 Query: 188 GIELGTAYANFGTKVTILEGAGEILSGFEKQMAAIIKKRLKKKGVEVVTNALAKGAEERE 247 G+E+ AY FG+ VTI+E + +++ + + A + + L+ +G++VV +A E R Sbjct: 187 GVEMAQAYVRFGSHVTIIERSTRLMAREDADVGAEMLRILRAEGIDVVLDARTVSVEGRS 246 Query: 248 DG-VTVTYEANGETKTIDADYVLVTVGRRPNTDELGLEQIGIKMTNRGLIEVDQQCRTSV 306 V V +T+D +LV GR PNT +GLE GI++ RG I V+ + +TS Sbjct: 247 GTQVRVVVRTPSGDRTLDGSDILVAAGRVPNTASIGLEHAGIQLDERGYIRVNDRLQTSA 306 Query: 307 PNIFAIGDIVPGPALAHKASYEGKVAAEAIAGHPSAVDYVAIPAVVFSDPECASVGYFEQ 366 P+++AIG++ P H + + ++ + +AG IP +F+DP A VG E Sbjct: 307 PDVWAIGEVAGSPQFTHVSVDDFRIVRDNLAGGNRGTGDRLIPYTLFTDPPLARVGLSES 366 Query: 367 QAKDEGIDVIAAKFPFAANGRALALNDTDGFLKLVVRKEDGVIIGAQIIGPNASDMIAEL 426 A+ +GI V A P R A ++T GF+K++V D I+G +IG A +++A + Sbjct: 367 DAQRQGIAVRVATLPMNNVLRTEATDETQGFMKVLVSANDDRILGFTMIGSEAGEVMAAM 426 Query: 427 GLAIEAGMTAEDIALTIHAHPTLGE 451 A+ A + + + + +H T+ E Sbjct: 427 QTAMLADLPYQKLRDAVISHLTVAE 451 Lambda K H 0.316 0.135 0.376 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: 461 Number of extensions: 24 Number of successful extensions: 3 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: 466 Length adjustment: 33 Effective length of query: 437 Effective length of database: 433 Effective search space: 189221 Effective search space used: 189221 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 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