GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctD in Bacillus horneckiae 1P01SC

Align lactate dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.110) (characterized)
to candidate WP_066199294.1 CWS20_RS05235 FAD-binding protein

Query= BRENDA::H6LBS1
         (466 letters)



>NCBI__GCF_002835735.1:WP_066199294.1
          Length = 485

 Score =  245 bits (625), Expect = 3e-69
 Identities = 134/420 (31%), Positives = 227/420 (54%), Gaps = 3/420 (0%)

Query: 45  PEVLIKVTSTEEVSKIMKYAYEHNIPVVVRGSGTGLVGACVPLFGGIMLETTLMNNILEL 104
           P+ ++   +TE+V+KI+KY ++H++P + RG+GTGL G  +PL G +++    M  +L +
Sbjct: 48  PKAVVFPENTEQVAKIVKYCHDHSLPFLARGAGTGLSGGAIPLNGEVIISMVKMKKLLSV 107

Query: 105 DTENLTVTVEPGVLLMELSKFVEENDLFYPPDPGEK-SATIAGNISTNAGGMRAVKYGVT 163
           D EN    VEPG + ++L+  + +   +Y PDP  +   TI GN++ NAGG   +KYGVT
Sbjct: 108 DLENRRAVVEPGFVNLKLTNTISDKGYYYAPDPSSQYCCTIGGNVAENAGGAHCLKYGVT 167

Query: 164 RDYVRGLTVVLANGEIIELGGKIVKNSSGYSLKDLVIGSEGTLCVITKAILKLLPLPKMT 223
            +++ GL VVL NG++IE+G   + +  GY L  L+ GSEGTL ++TK  +++L  P+  
Sbjct: 168 TNHILGLEVVLPNGDVIEIGKNGIADEPGYDLLGLITGSEGTLGIVTKITVRILKNPESK 227

Query: 224 LSLLIPFENISDAAGIVPKIIKSKAIPTAIEFMERQTILFAEDFLGKKFPDSSSNAYILL 283
            ++L  F+ + D +  V  II +  +P A+E M++  I   E             A +L+
Sbjct: 228 QTVLAYFDKVEDGSQAVSDIISAGIVPAALEMMDKTAIEGVEAAAFPVGHPKDIEALLLI 287

Query: 284 TFDGNTKEQVEAEYETVANLCLAEGAKDVYIVDTVERKDSVWSARGAFLEAIKASTTEMD 343
             DG  +  +  + E +  +C  +  ++V      + + + W+ R     A+ A + +  
Sbjct: 288 EVDG-IEAGIGEQIEQILQVCRNQNVREVRAAKDEQERAAWWANRKTGFGAMGAISPDYL 346

Query: 344 ECDVVVPRNRIAEFIEFTHDLAKEMDVRIPSFGHAGDGNLHIYVCRDELCQADWEAKLAE 403
             D V+PR+++ E +   + +++E  +RI +  HAGDGNLH  V  D     + E K  E
Sbjct: 347 VQDGVIPRSKLPEVLSKINKISEESGLRIANIFHAGDGNLHPLVLFDARIPGETE-KAME 405

Query: 404 AMDRMYAKALTFEGLVSGEHGIGYAKRKYLLNDFGTEHLALMAGIKQTFDPKNLLNPKKV 463
           A            G ++GEHG+G  KR+ +   F  E +     I+  F+P NLLN  K+
Sbjct: 406 AGSACLKVCADVGGTITGEHGVGIEKREEMRFVFKDEEIQAQTDIRDVFNPDNLLNAGKL 465


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: 512
Number of extensions: 20
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: 485
Length adjustment: 33
Effective length of query: 433
Effective length of database: 452
Effective search space:   195716
Effective search space used:   195716
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