GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glc-kinase in Dinoroseobacter shibae DFL-12

Align ADP-specific glucokinase (EC 2.7.1.147) (characterized)
to candidate 3608608 Dshi_2001 ROK family protein (RefSeq)

Query= BRENDA::Q8R8N4
         (312 letters)



>FitnessBrowser__Dino:3608608
          Length = 414

 Score =  148 bits (373), Expect = 3e-40
 Identities = 94/311 (30%), Positives = 149/311 (47%), Gaps = 8/311 (2%)

Query: 3   IGVDLGGTNIAVGLVEEDGKIIATGSRPTKPER-GYEAIARDIAELSFELLQRMGISVKD 61
           +G+ L      V L +  G  +AT  R ++P R   EA+  ++A L  E+L    +    
Sbjct: 99  LGLRLSDEMHTVSLSDFSGTELATAHRASQPGRYAVEALLTEMATLIDEVLAAAALPRDR 158

Query: 62  VKSMGIGVPGVADNEKGIVIRAVNLFWTKVPLAKEIRKYIDLPIYMENDANVAALAEATF 121
           V ++G+G+PG   +E G V  +  L      L   I     LP ++ENDANV  LAE  F
Sbjct: 159 VAALGVGLPGAVHHETGRVAWSPILAGQDHALQAIIEDRFGLPAHLENDANVLTLAELWF 218

Query: 122 GAGRGSKSSVTITLGTGVGSGFILDGKIYSGAHHFAPEIGHMVIGDNGIRCNCGKIGCFE 181
           GAGR  +    +T+  GVG G +L+ +++ GA     E+GH  +  +G  C CG+ GC E
Sbjct: 219 GAGRAMQDFAVVTIEQGVGMGLVLNNRLFRGAQGLGLELGHTKVQLDGALCRCGQRGCLE 278

Query: 182 TYASATALIREGKKAAKRNPNTLILKFANGDIEGITAKNVIDAAKQYDEEALKIFEEYVK 241
            Y +  AL+RE   A  R+P        +        +++ D AK  +  A  IF+   +
Sbjct: 279 AYLADYALVREASTALDRDPR-------SAQTAAAMLESLFDQAKAGNGAAKAIFQRAGR 331

Query: 242 YLAVGIVNIINLFDPEVIILGGGVANAGDFLLKPLKKEVAENILFKELPYADIRKAELGN 301
           +L++G+ N++ LFDPE+IIL G          + +  E+    L    P + +     G+
Sbjct: 332 FLSLGLANVVQLFDPELIILSGARMRYDYLYAEEVLAEMQRMTLHPATPRSRVEIHAWGD 391

Query: 302 DAGIIGAAILS 312
                GA  L+
Sbjct: 392 QVWARGATALA 402


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: 277
Number of extensions: 13
Number of successful extensions: 2
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: 414
Length adjustment: 29
Effective length of query: 283
Effective length of database: 385
Effective search space:   108955
Effective search space used:   108955
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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