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_108401568.1 B9Z44_RS02025 FAD-binding oxidoreductase
Query= SwissProt::P46681 (530 letters) >NCBI__GCF_003063475.1:WP_108401568.1 Length = 474 Score = 304 bits (779), Expect = 4e-87 Identities = 172/476 (36%), Positives = 266/476 (55%), Gaps = 19/476 (3%) Query: 64 DDLNYFKSILSEQEILRASESEDLSFYNEDWMRKYKGQSKLVLRPKSVEKVSLILNYCND 123 D L + + +L E +L DLS Y +DW ++ +G++ V+RP ++V+ ++ C Sbjct: 8 DLLTHLRELLGEAHVLTEG---DLSAYEQDWRKRTRGKALAVVRPSKTQEVAEVVKACAK 64 Query: 124 EKIAVVPQGGNTGLVGGSVP--IFDELILSLANLNKIRDFDPVSGILKCDAGVILENANN 181 +++VPQGGNTGLV G +P +++LSL +N +R D + L +AG +L+N Sbjct: 65 AGVSIVPQGGNTGLVVGGIPDDTGTQVLLSLQRMNAVRAVDTDNLTLTVEAGCVLQNLQQ 124 Query: 182 YVMEQNYMFPLDLGAKGSCHVGGVVATNAGGLRLLRYGSLHGSVLGLEVVMPNGQIVNSM 241 + ++FPL LGA+GSC +GG +ATNAGG ++LRYG+ LGLEVV G++++S+ Sbjct: 125 AAEQAGFLFPLSLGAEGSCTIGGNLATNAGGTQVLRYGNARELCLGLEVVTAQGEVMHSL 184 Query: 242 HSMRKDNTGYDLKQLFIGSEGTIGIITGVSILTVPKPKAFNVSYLSVESFEDVQKVFVRA 301 +RKDNTGYDL+ L IGSEGT+GIIT ++ P P ++ +V S K+ A Sbjct: 185 SGLRKDNTGYDLRNLMIGSEGTLGIITAATMKLYPMPAVSLTAWAAVPSVACAVKLLGLA 244 Query: 302 RQELSEILSAFEFMDAKSQVLAKSQLKDAAFPLEDEHPFYILIETSGSNKD-HDDSKLET 360 Q L L+ FE M + L PL + P+ +L+E S S + H + E Sbjct: 245 HQHLGAGLTGFEMMGQFALHLVDKHYPHLRVPLWQDTPYCVLLENSDSESEAHARERFEH 304 Query: 361 FLENVMEEGIVTDGVVAQDETELQNLWKWREMIPEASQANGGVYKYDVSLPLKDLYSLVE 420 L E+G V+D VVA+ ++ +NLW RE I A G K+D+S+P+ + + VE Sbjct: 305 LLGLAFEDGCVSDAVVAESLSQARNLWHIRESITLAQAEEGLNIKHDISVPISSIPNFVE 364 Query: 421 ATNARLSEAELVGDSPKPVVGAIGYGHVGDGNLHLNVAVRE------YNKNIEKTLEPFV 474 AT+A L P + + +GH+GDGNLH NV E + ++ E + +V Sbjct: 365 ATDALLMR-------EIPGIRLVNFGHLGDGNLHYNVQAPEHCDTKAFLRDNEDRVNTWV 417 Query: 475 YEFVSSKHGSVSAEHGLGFQKKNYIGYSKSPEEVKMMKDLKVHYDPNGILNPYKYI 530 Y+ V GS+SAEHG+G K + + K P + +M+ +K DP G+LNP + + Sbjct: 418 YQSVKRFGGSISAEHGVGSMKVDSLPDYKDPVALALMQHIKRALDPQGLLNPGRVV 473 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: 535 Number of extensions: 20 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: 474 Length adjustment: 34 Effective length of query: 496 Effective length of database: 440 Effective search space: 218240 Effective search space used: 218240 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