Align D-2-hydroxyglutarate--pyruvate transhydrogenase DLD2; D-2HG--pyruvate transhydrogenase DLD2; Actin-interacting protein 2; D-lactate dehydrogenase [cytochrome] 2, mitochondrial; D-lactate ferricytochrome C oxidoreductase; D-LCR; EC 1.1.99.40; EC 1.1.2.4 (characterized)
to candidate WP_038067571.1 DL1_RS14145 FAD-binding oxidoreductase
Query= SwissProt::P46681 (530 letters) >NCBI__GCF_000715505.1:WP_038067571.1 Length = 467 Score = 246 bits (628), Expect = 1e-69 Identities = 144/437 (32%), Positives = 236/437 (54%), Gaps = 19/437 (4%) Query: 97 KYKGQSKLVLRPKSVEKVSLILNYCNDEKIAVVPQGGNTGLVGGSVPIFDE--LILSLAN 154 +Y G L++RP+S ++V+ I+ C+ +++A+VP GG TGLVGG + ++LSL Sbjct: 36 RYHGLGGLLVRPRSTQEVAAIVALCHADRVAIVPYGGGTGLVGGQILESGPPPVLLSLEA 95 Query: 155 LNKIRDFDPVSGILKCDAGVILENANNYVMEQNYMFPLDLGAKGSCHVGGVVATNAGGLR 214 L +R +L+ +AG L++A++ + +FPL + ++GS +GGV+ATNAGG+ Sbjct: 96 LRSVRAV--TRHVLEIEAGASLQDAHDAADAEGRLFPLTIASQGSAQIGGVLATNAGGVN 153 Query: 215 LLRYGSLHGSVLGLEVVMPNGQIVNSMHSMRKDNTGYDLKQLFIGSEGTIGIITGVSILT 274 +LRYG+ LG+E V+ +G +++ + +RKDNTGYDLK L IGSEG++GIIT ++ Sbjct: 154 VLRYGNARELCLGVEAVLADGTVISGLKHLRKDNTGYDLKDLLIGSEGSLGIITAATLRL 213 Query: 275 VPKPKAFNVSYLSVESFEDVQKVFVRARQELSEILSAFEFMDAKSQVLAKSQLKDAAFPL 334 P+P + + V + A + +SAFE + + + + P Sbjct: 214 HPRPATQGTAMMVVRDPAAALSLLELAEARMPGCISAFELISGQGLGFLRDVGPEVHQPF 273 Query: 335 EDEHPFYILIETSGSNKDHDDSKLETFLENVMEEGIVTDGVVAQDETELQNLWKWREMIP 394 + + +L E + + L E E +V DGV+A + + +W RE +P Sbjct: 274 AEPPEWMVLTEIGLPDGIAPEEALTDLFEAAGE--LVQDGVIASSQGQRNQMWTLRESLP 331 Query: 395 EASQANGGVYKYDVSLPLKDLYSLVEATNARLSEAELVGDSPKPVVGAIGYGHVGDGNLH 454 EA++ G + +D+SLPL L ++ AR++ +GD + +GHVGDGNLH Sbjct: 332 EANKRIGSISSHDISLPLPKLAEFIDTARARIA---ALGD-----MRINCFGHVGDGNLH 383 Query: 455 LNV-----AVREYNKNIEKTLEPFVYEFVSSKHGSVSAEHGLGFQKKNYIGYSKSPEEVK 509 NV R + + K + VY+ V + GS+SAEHG+G K + + P ++ Sbjct: 384 FNVFPAKGRERSEYEALRKDVAALVYDLVDTFGGSISAEHGIGRLKVADLVHYGDPGKLA 443 Query: 510 MMKDLKVHYDPNGILNP 526 M+ +K DP GILNP Sbjct: 444 AMRAIKAALDPEGILNP 460 Lambda K H 0.316 0.135 0.385 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: 564 Number of extensions: 22 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: 530 Length of database: 467 Length adjustment: 34 Effective length of query: 496 Effective length of database: 433 Effective search space: 214768 Effective search space used: 214768 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: 52 (24.6 bits)
This GapMind analysis is from Sep 24 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:
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