Align lactate dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.110) (characterized)
to candidate WP_093427581.1 BM272_RS04575 FAD-binding protein
Query= BRENDA::H6LBS1 (466 letters) >NCBI__GCF_900112605.1:WP_093427581.1 Length = 506 Score = 236 bits (603), Expect = 1e-66 Identities = 152/459 (33%), Positives = 232/459 (50%), Gaps = 8/459 (1%) Query: 7 EASDIA-AIKELIPAERVFVGTEIGEDFSHDELGSIHSYPEVLIKVTSTEEVSKIMKYAY 65 EA+++A A++ +P V E + D L + P +++ + E+V ++ + Sbjct: 24 EAAELARALRRHLPESAVITTEEELRPWECDGLSAYRQLPMLVVIPETEEQVRAVLAACH 83 Query: 66 EHNIPVVVRGSGTGLVGACVPLFGGIMLETTLMNNILELDTENLTVTVEPGVLLMELSKF 125 +PVV RG+GT L G +PL G++L N ILE+D +N V+PGV + +S+ Sbjct: 84 ARAMPVVARGAGTSLSGGALPLERGVVLSLARFNRILEIDADNRCARVQPGVRNLAVSEA 143 Query: 126 VEENDLFYPPDPGEKSA-TIAGNISTNAGGMRAVKYGVTRDYVRGLTVVLANGEIIELGG 184 + LFY PDP + A TI GN++ NAGG+ +KYG+T V GL V+ GE +ELGG Sbjct: 144 AAPHGLFYAPDPSSQIACTIGGNVAENAGGVHCLKYGLTVHNVTGLRVLTMEGEELELGG 203 Query: 185 KIVKNSSGYSLKDLVIGSEGTLCVITKAILKLLPLPKMTLSLLIPFENISDAAGIVPKII 244 K + G L L+ GSEG L ++ +A ++L P P+ +L F+++ A V +I Sbjct: 204 K-GPDGPGLDLLALMHGSEGMLGLVMEATVRLTPKPERVQVMLAAFDDVEAAGAAVAAVI 262 Query: 245 KSKAIPTAIEFMERQTILFAEDFLGKKFPDSSSNAYILLTFDGNTKEQVEAEYETVANLC 304 + IP +E M+ I AEDF+ +P ++ A +L DG T +V E V + Sbjct: 263 AAGIIPAGLEMMDNPAIRAAEDFVHAGYPTDAA-AILLCELDG-TNREVSEEVARVRAIL 320 Query: 305 LAEGAKDVYIVDTVERKDSVWSARGAFLEAIKASTTEMDECDVVVPRNRIAEFIEFTHDL 364 GA +V DT E+ + WS R A A + D +PR + E + ++ Sbjct: 321 REAGATEVRTADTPEQAATFWSGRKAAFPATGRLAPDYYCIDGTIPRKHLGEVLLRIGEI 380 Query: 365 AKEMDVRIPSFGHAGDGNLHIYVCRDELCQADWEAKLAEAMDRMYAK-ALTFEGLVSGEH 423 ++ + + HAGDGNLH V D + D E AEA R + + G V+GEH Sbjct: 381 CRDQGLSAANVFHAGDGNLHPLVLYDANREGDLER--AEAAGRAILELCVARGGTVTGEH 438 Query: 424 GIGYAKRKYLLNDFGTEHLALMAGIKQTFDPKNLLNPKK 462 G+G K + + FG L +K FDP LLNP K Sbjct: 439 GVGVEKLDAMCSQFGAAELERFYAVKAAFDPAGLLNPGK 477 Lambda K H 0.318 0.136 0.388 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: 21 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 466 Length of database: 506 Length adjustment: 34 Effective length of query: 432 Effective length of database: 472 Effective search space: 203904 Effective search space used: 203904 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 (21.7 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