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_036138401.1 N800_RS11075 FAD-binding protein

Query= BRENDA::H6LBS1
         (466 letters)



>NCBI__GCF_000768355.1:WP_036138401.1
          Length = 462

 Score =  253 bits (647), Expect = 7e-72
 Identities = 146/420 (34%), Positives = 231/420 (55%), Gaps = 4/420 (0%)

Query: 45  PEVLIKVTSTEEVSKIMKYAYEHNIPVVVRGSGTGLVGACVPLFGGIMLETTLMNNILEL 104
           P+ +   T+ E+V  +++    H +P+V RG GT   GA VP+ GG+++    MN I+++
Sbjct: 43  PDAVALPTTREQVVALVRACRAHRVPLVARGRGTNTTGATVPISGGVVVSFERMNRIVDI 102

Query: 105 DTENLTVTVEPGVLLMELSKFVEENDLFYPPDPGEKS-ATIAGNISTNAGGMRAVKYGVT 163
              +    VEPGVL  +L   ++ + LF+PPDP     +T+ GN++ NAGG RAVKYG +
Sbjct: 103 RPGDRCAVVEPGVLNGDLQAALQPHGLFWPPDPTSAVFSTVGGNLACNAGGPRAVKYGAS 162

Query: 164 RDYVRGLTVVLANGEIIELGGKIVKNSSGYSLKDLVIGSEGTLCVITKAILKLLPLPKMT 223
           RD V  LT V   GE+IE G    K ++GY L  L++GSEGTL +I +A L+L P P   
Sbjct: 163 RDNVLALTAVTGAGELIECGTATTKGATGYDLHRLLVGSEGTLALIVEASLRLTPAPATR 222

Query: 224 LSLLIPFENISDAAGIVPKIIKSKAIPTAIEFMERQTILFAEDFLGKKFPDSSSNAYILL 283
            +L   + ++S AA  V +++     P+ +EFM+   +  A D  G   P + + A +++
Sbjct: 223 RALRAIYRDVSSAALAVARLMAQPVTPSMLEFMDAHAVRLARDVGGADLP-ADAGALLMI 281

Query: 284 TFDGNTKEQVEAEYETVANLCLAEGAKDVYIVDTVERKDSVWSARGAFLEAIKASTTEMD 343
             DG+  + +  + E +A     +G   +        +  +W+AR A   A++       
Sbjct: 282 EADGDA-DTLPHDIEALARAAEGDGLVSLDDAADEAARAKLWTARKALSPALRTLAPGKI 340

Query: 344 ECDVVVPRNRIAEFIEFTHDLAKEMDVRIPSFGHAGDGNLHIYVCRDELCQADWEAKLAE 403
             DVVVP +RI   ++    LA+E ++ I  FGHAG+GNLH+ +  D    A  + +   
Sbjct: 341 NEDVVVPVSRIPALVDGVQALAREFNLPIVCFGHAGNGNLHVNLVYDPADGAQAQ-RARG 399

Query: 404 AMDRMYAKALTFEGLVSGEHGIGYAKRKYLLNDFGTEHLALMAGIKQTFDPKNLLNPKKV 463
           AM R++  A++  G +SGEHGIG AKR ++        LA+M  +K  FDP  +LNP K+
Sbjct: 400 AMARVFTLAVSLGGTLSGEHGIGLAKRDFMPQAVTPATLAVMRQLKAVFDPDGILNPGKL 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: 440
Number of extensions: 15
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