GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctD in Lysobacter daejeonensis GH1-9

Align lactate dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.110) (characterized)
to candidate WP_036136357.1 N800_RS06820 FAD-binding oxidoreductase

Query= BRENDA::H6LBS1
         (466 letters)



>NCBI__GCF_000768355.1:WP_036136357.1
          Length = 462

 Score =  201 bits (512), Expect = 3e-56
 Identities = 140/419 (33%), Positives = 212/419 (50%), Gaps = 15/419 (3%)

Query: 53  STEEVSKIMKYAYEHNIPVVVRGSGTGLVGACVPLFGGIMLETTLMNNILELDTENLTVT 112
           S E+V  I+++A E  + +V  G  TGL G  V   G ++L    MN +L  D  + T+ 
Sbjct: 48  SVEDVQGIVRWANETGVALVPSGGRTGLSGGAVAANGELVLSLERMNRVLAFDAVDRTLA 107

Query: 113 VEPGVLLMELSKFVEENDLFYPPDPGEK-SATIAGNISTNAGGMRAVKYGVTRDYVRGLT 171
           V+ GV L    +    + L YP D   + SAT+ G+I+TNAGG+R V+YG TR++V GLT
Sbjct: 108 VQAGVPLQVAQEAAASHGLAYPVDFASRGSATVGGSIATNAGGIRVVRYGNTREWVAGLT 167

Query: 172 VVLANGEIIELGGKIVKNSSGYSLKDLVIGSEGTLCVITKAILKLL--PLPKMTLSLLIP 229
           VV   G+++EL   +VKNSSGY L+ L +GSEGTL V+ +A L+L   P P   + L +P
Sbjct: 168 VVTGAGDVLELNRGLVKNSSGYDLRHLFVGSEGTLGVVVEATLRLTDPPPPTNVMLLALP 227

Query: 230 -FENISDAAGIVPKIIKSKAIPTAIEFMERQTILFAEDFLGKKFPDSSSNAYILLTFDGN 288
            FE +        + ++ +A     +   R  +       G + P + ++ Y ++T    
Sbjct: 228 SFEVLMQVFAAFRERLQLEAFEFFTDVALRHVLAH-----GAQAPFAETHPYYVVTEYAT 282

Query: 289 TKEQVEAEYETVANLCLAEG-AKDVYIVDTVERKDSVWSARGAFLEAIKASTTEMDECDV 347
             E+ EA        CL  G   D  I  +  +   +W  R    EA+  +  +  + D+
Sbjct: 283 GDEREEAAALAAFEHCLENGLVLDGVISQSDAQAAQLWRLREGITEAL--ARYKPYKNDI 340

Query: 348 VVPRNRIAEFIEFTHDLAKE--MDVRIPSFGHAGDGNLHIYVCRDELCQADWEAKLAEAM 405
            V  + +  F+  T  L  +      +  FGH GDGNLHI V + +  + D      E +
Sbjct: 341 AVRVSAMPAFLAETQALLAQEYPQFEVVWFGHIGDGNLHINVLKPDAMENDAFVAQCEQV 400

Query: 406 DRMYAKAL-TFEGLVSGEHGIGYAKRKYLLNDFGTEHLALMAGIKQTFDPKNLLNPKKV 463
            ++ A AL    G +S EHGIG  K+ YL +      +A+M GIKQ  DP  L+NP KV
Sbjct: 401 TKLLAGALQRHGGSISAEHGIGLVKKPYLSSTRSAAEVAVMKGIKQVLDPNGLMNPGKV 459


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: 441
Number of extensions: 21
Number of successful extensions: 4
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: 466
Length of database: 462
Length adjustment: 33
Effective length of query: 433
Effective length of database: 429
Effective search space:   185757
Effective search space used:   185757
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: 51 (24.3 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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