GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glk in Ruegeria conchae TW15

Align Glucokinase; EC 2.7.1.2; Glucose kinase (uncharacterized)
to candidate WP_010441531.1 G7G_RS23700 ROK family protein

Query= curated2:B9JYQ5
         (340 letters)



>NCBI__GCF_000192475.1:WP_010441531.1
          Length = 618

 Score =  150 bits (379), Expect = 8e-41
 Identities = 98/313 (31%), Positives = 152/313 (48%), Gaps = 13/313 (4%)

Query: 15  LVGDIGGTNARFWILMDAHAAPKEFANIHTADFPTIDQAIQDCILDKSGFQPRSAILAVA 74
           LV DIGGTN R  ++ +      +     T     + +A+ + + D+ G QPR+ + A A
Sbjct: 299 LVADIGGTNTRLGVVTEGELT--DLRKHPTGTVSDLQEALHE-LCDEIGTQPRAVVAAGA 355

Query: 75  GPIKDDEIPLTNCPWVIRPKAMIADLGFDDVLVVNDFEAQALAAASLGRNDREPIGPLTE 134
           GP+K+  I LTN    +   A+    G     V+NDF A A + A + +ND E +     
Sbjct: 356 GPVKNGTIRLTNANLDLSEDALAKATGAHHTYVINDFTAAAWSVAEITQNDVEVLQGEAS 415

Query: 135 TSLNSRVILGPGTGLGVGGLLYTHHTWFPVPGEGGHVDIGPRSDRDWQIFPHIERIEGR- 193
             L +R+++GPGTGLGVG LLY+   +  V GEGGH+ + PR   + ++F    +I    
Sbjct: 416 PPLGTRLVVGPGTGLGVGALLYSEGHFHTVSGEGGHMGLSPRHLDEVEVFSAARQIVPEC 475

Query: 194 -------ISGEQILCGRGILHLYNAICAADG-IEPVWTDPADVTQHALKGNDPVCVETMT 245
                  I  E  L G G+  LY AI   +G +        D+ Q A  G+D   V+   
Sbjct: 476 FFSDTLAIEAEMFLSGTGLPVLYQAIGMTEGQLNVAMRSAKDILQDAQDGSDACAVKAAR 535

Query: 246 LFVTYLGRIAGDMALVFMARGGVFLSGGISQKIIPLLKSPVFRAAFEDKAPHTEMMKTIP 305
           +F  +LG + GD+A+     GGVFL GG+++K   L      R AF       ++ K + 
Sbjct: 536 MFTEHLGALMGDLAVALTPTGGVFLVGGVAEKNRWLFGQDFLR-AFNAGGRFDDLRKAMN 594

Query: 306 TFVAIHPQAALSG 318
            +V+   +  + G
Sbjct: 595 LYVSEQDEFGIVG 607


Lambda     K      H
   0.322    0.140    0.445 

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: 500
Number of extensions: 29
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: 340
Length of database: 618
Length adjustment: 33
Effective length of query: 307
Effective length of database: 585
Effective search space:   179595
Effective search space used:   179595
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 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