GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glk in Bacteroides clarus YIT 12056

Align glucokinase (EC 2.7.1.2) (characterized)
to candidate WP_087942772.1 BUB52_RS04275 ROK family protein

Query= BRENDA::Q8RDE9
         (315 letters)



>NCBI__GCF_900129655.1:WP_087942772.1
          Length = 317

 Score =  197 bits (500), Expect = 4e-55
 Identities = 106/316 (33%), Positives = 178/316 (56%), Gaps = 8/316 (2%)

Query: 1   MKKFLCGVDLGGTKISTGIVDENGNIIKSIKIPTMAEKGPDVVIERIEESIYQVLKDTGL 60
           MKK+  G+DLGGT +   ++D  G      K+P+ A+   + VI ++  +  +V+     
Sbjct: 2   MKKYAIGIDLGGTSVKYALIDNEGVFHFQGKLPSKADVSAEAVIGQLVTACKEVMASALQ 61

Query: 61  EMSNLKGIGIGSPGPLNAKKGIVIS-PPNLPHWSNVPIVEILSKRLGIEVRLENDANAAA 119
               ++GIGIG+PG ++    IV+    N+  W N+ + + +    G+ V++ NDAN   
Sbjct: 62  LGVAVEGIGIGTPGIVDETNRIVLGGAENIKGWENLNLADRIEAETGLSVQMGNDANLMG 121

Query: 120 IGEHLFGSGRGVDNFVYITVSTGIGGGVIIEGKLYSGENSNAAEIGHHTINFDGPRCNCG 179
           +GE ++G+G+G  N V++TV TGIGG V+I+GKL++G  +   E+GH  +  +G  C CG
Sbjct: 122 LGETMYGAGQGAKNVVFLTVGTGIGGAVVIDGKLFNGFANRGTELGHVPLIANGEPCACG 181

Query: 180 NYGCFEAYASGTA-IARFAREGIEKGIKTKIKELAGEGEVKAEHVFEAAKLGDEFAKELV 238
           + GC E YAS +A + RF++   E G+        GE ++  E +    K G+E A E +
Sbjct: 182 SVGCLEHYASTSALVRRFSKRAAEAGV-----SFPGE-DINGELIVRLYKEGNELATECL 235

Query: 239 EKEAFYLGVGIANIMAFYNPRKIAIGGGVSAQWDMLYEKMMETVRKKALKPNAEVCEVVK 298
           ++   +LG GIA  +  ++P++I IGGG+S   D    K+ E   + A+   A   +++ 
Sbjct: 236 DEHCDFLGHGIAGFINIFSPQRIVIGGGLSEAGDFYIRKVSEKAHRYAIADCAVNTQIMA 295

Query: 299 AQLGENIGVLGAAALL 314
           A LG   G +GAA+L+
Sbjct: 296 ASLGNKAGSIGAASLV 311


Lambda     K      H
   0.316    0.138    0.398 

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: 278
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: 315
Length of database: 317
Length adjustment: 27
Effective length of query: 288
Effective length of database: 290
Effective search space:    83520
Effective search space used:    83520
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 (21.6 bits)
S2: 48 (23.1 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