Align Putative D-lactate dehydrogenase C713.03, mitochondrial; EC 1.1.2.4 (characterized)
to candidate GFF2609 HP15_2553 oxidoreductase, FAD-binding protein
Query= SwissProt::Q9C1X2 (526 letters) >lcl|FitnessBrowser__Marino:GFF2609 HP15_2553 oxidoreductase, FAD-binding protein Length = 479 Score = 287 bits (734), Expect = 7e-82 Identities = 164/453 (36%), Positives = 256/453 (56%), Gaps = 18/453 (3%) Query: 77 TDPADLDAFNIDWMNKYRGKTQLALKPKTTQQVSEILKYCNQKKLAVVPQGGNTGLVGGS 136 TDPADLD + DW Y K PKTT+QV ++K+ N+ ++A+VP GG TGL G+ Sbjct: 37 TDPADLDTYGKDWTKIYPPKPLAIALPKTTEQVQALVKFANENQVALVPSGGRTGLSAGA 96 Query: 137 VPVFDEIVLNLGLMNQIHTFDEISGVITLDSGVILENADNFLAEKGYMFPLDLGAKGSCQ 196 V E+V+ MNQI F+ + +GV+ E N + G +P+D + GS Q Sbjct: 97 VAANGEVVVAFDNMNQILDFNASDRTVRCQAGVVTEQLQNCAEDNGLYYPVDFASAGSSQ 156 Query: 197 VGGCAATAAGGLRLLRYGSLHGSILGMEAVLPDGTILDNLVTLRKDNTGLDIKQLFIGSE 256 +GG +T AGG++++RYG + G++ V G ILD L K+NTG D++ LFIG+E Sbjct: 157 LGGNLSTNAGGIKVIRYGMSRDWVAGLKVVTGKGDILDLNKDLEKNNTGYDLRHLFIGAE 216 Query: 257 GYLGVITKLSVICPKRPSSTNVAFFGVPSYENVLKAFSETRSHLTEILSAFELMDNTSQT 316 G LG IT+ ++ ++P + V G+ N + + + L+A+E + + Sbjct: 217 GTLGFITEATMKLSRKPDNLTVLVLGLNDLTNTMDVLQTFQKKID--LTAYEFFSHQAMG 274 Query: 317 LVDKYSGTQRPLEDEHPFYVLVETQGSNKEHDEQKITALVEDLLEKEIISDGVLAQDESQ 376 V + Q P E E P+Y L+E + + + + + AL E +E + DGV++Q E+Q Sbjct: 275 HVLAHGQVQAPFETEAPYYALLEFESVSDQVMDDAM-ALFEQCVENGWVLDGVISQSETQ 333 Query: 377 LRVLWERREGITECLAKAGSGVYKYDVSLPLPVLYDLVNDTKKRLIEFNLLDDTPEHPVI 436 + LW+ RE I+E +A YK D+S+ +V+ L E + + T +P Sbjct: 334 AQNLWQLRERISESIAPRTP--YKNDISV-------VVSKVPGFLQEIDAV-VTEHYPDF 383 Query: 437 DVVGFGHMGDGNLHLNIAVRQ---FDKRVEKC--LEPWVYEWVSRHRGSISAEHGLGLLK 491 +++ FGH+GDGNLHLNI + + EKC + WV+E V R++GS+SAEHG+G+ K Sbjct: 384 EIIWFGHIGDGNLHLNILKPEDMANEDFFEKCQQVNKWVFEIVERYQGSVSAEHGVGMTK 443 Query: 492 KPFVGYSKSKEMIHLMKTLKNVFDPNGIMLPYK 524 KP++ Y++S+ I ++ +K VFDPNGIM P K Sbjct: 444 KPYLQYTRSEAEIAYLRGIKQVFDPNGIMNPGK 476 Lambda K H 0.319 0.138 0.405 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: 604 Number of extensions: 23 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: 526 Length of database: 479 Length adjustment: 34 Effective length of query: 492 Effective length of database: 445 Effective search space: 218940 Effective search space used: 218940 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 52 (24.6 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