GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glc-kinase in Shewanella loihica PV-4

Align ADP-specific glucokinase (EC 2.7.1.147) (characterized)
to candidate 5208927 Shew_1428 fructokinase (RefSeq)

Query= BRENDA::Q8R8N4
         (312 letters)



>FitnessBrowser__PV4:5208927
          Length = 296

 Score =  127 bits (319), Expect = 3e-34
 Identities = 93/317 (29%), Positives = 150/317 (47%), Gaps = 29/317 (9%)

Query: 1   MRIGVDLGGTNIAVGLVEEDGKIIATGSRPTKPERGYEAIARDIAELSFELLQRMGISVK 60
           MR+GVDLGGT I +  + E GK +     PT  E  Y+A    I  L  E    +G    
Sbjct: 2   MRMGVDLGGTKIELVALSEAGKELFRKRIPTPRE--YKATLDAIEALVNEAESTLG---- 55

Query: 61  DVKSMGIGVPGVADNEKGIVIRAVNLFWTKVPLAKEIRKYIDLPIYMENDANVAALAEAT 120
              ++G+G+PGV     G+V  A + +    PL  ++   ++  + + NDAN  A++EA 
Sbjct: 56  QKGTVGVGIPGVISPFSGLVKNANSTWINGHPLDLDLGARLEREVRVANDANCFAVSEAV 115

Query: 121 FGAGRGSKSSVTITLGTGVGSGFILDGKIYSGAHHFAPEIGHMVI------GDNGIRCNC 174
            GA  G      + +GTG G G  ++GK++ G +    E GH  +        N   C C
Sbjct: 116 DGAAAGKGLVFGVIIGTGCGGGIAINGKVHGGGNGIGGEWGHNPLPWMTPDEFNSTECFC 175

Query: 175 GKIGCFETYASATALIREGKKAAKRNPNTLILKFANGDIEGITAKNVIDAAKQYDEEALK 234
           G   C ET+ S T  +R+ K A    P+ +                +    +Q +  A  
Sbjct: 176 GNKDCIETFISGTGFVRDYKAAGGDAPSGI---------------EIARRMEQGEALATA 220

Query: 235 IFEEYVKYLAVGIVNIINLFDPEVIILGGGVANAGDFLLKPLKKEVAENILFKELPYADI 294
            FE Y+  LA  + ++IN+ DP++I+LGGGV+N  + +   L + +++ +L  E     +
Sbjct: 221 AFERYIDRLARSLAHMINMLDPDIIVLGGGVSNI-EAIYPRLPEALSKYVLGGECRTPVV 279

Query: 295 RKAELGNDAGIIGAAIL 311
           +    G  +G+ GAA L
Sbjct: 280 QNM-YGGSSGVRGAAWL 295


Lambda     K      H
   0.318    0.140    0.397 

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: 322
Number of extensions: 14
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: 312
Length of database: 296
Length adjustment: 27
Effective length of query: 285
Effective length of database: 269
Effective search space:    76665
Effective search space used:    76665
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: 48 (23.1 bits)

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

Links

Downloads

Related tools

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