GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagK in Phyllobacterium brassicacearum STM 196

Align Glucose kinase (characterized, see rationale)
to candidate WP_106712464.1 CU102_RS17890 glucokinase

Query= uniprot:Q8P6S9
         (338 letters)



>NCBI__GCF_003010955.1:WP_106712464.1
          Length = 342

 Score =  157 bits (396), Expect = 5e-43
 Identities = 95/314 (30%), Positives = 151/314 (48%), Gaps = 6/314 (1%)

Query: 19  VAADVGGTHVRLALACESNDPRKPVTVLDYRKYRCADYPGLAEIMAAFFAELSCAPVRRG 78
           +  D+GGT+ R A+  ++    K   ++     + ADYP + E +     + +    R  
Sbjct: 16  LVGDIGGTNARFAILVDAYAEPKEFPII-----QTADYPTIDEAIQNAILDHTSIQPRSA 70

Query: 79  VIASAGYALEDGRVITANLPWVLAPEQIRQQLGMQALHLVNDFEAVAYAANYMTGNQVMQ 138
           V+A AG  +E   +   N  WV+ P Q+ + LG+  + ++NDFEA A A   +    + +
Sbjct: 71  VLAIAG-PVEGDEIDLTNCAWVVKPRQMMETLGLSDITVLNDFEAQALAVVSLEPKHLEK 129

Query: 139 LSGPAQGAPGPALVLGPGTGLGAALWIPNGGNSVVLPTEAGHAALAAASDLEVALLQELR 198
           L G      G   VLGPGTGLG A  + +  + V +P E GH  +   +  ++ L   + 
Sbjct: 130 LGGGPGDPHGSRAVLGPGTGLGVAGMVRSRNSWVPVPGEGGHVDMGPRTARDLELFPHIE 189

Query: 199 RTRTHVATEHFLSGPGLLTLYTALATLRDAPAVHATPAAVTAAALAGDDVLAHEALQTFC 258
                ++ E  L G GL  +Y A+  +   PA   TPA +TAA L+G+   A E L  F 
Sbjct: 190 HIEGRISGEQLLCGRGLQNIYRAICKVNGTPASLQTPAEITAAGLSGESAEAKETLALFV 249

Query: 259 GFMGSVVGDMMLLYGVRSGVYLAGGFLPQIADFIARSDFAARLLDKGPLRPALEQVPVRI 318
            ++G + GD  L +  R GVYLAGG + +I   +    F     DK P    L + PV I
Sbjct: 250 VYLGRLAGDFALTFMARGGVYLAGGIVQKIVAPLKDPSFRQAFEDKAPHGEILRETPVYI 309

Query: 319 VEHGQLGVIGAASW 332
           + H    + G +++
Sbjct: 310 ITHPLAALSGLSAF 323


Lambda     K      H
   0.321    0.136    0.407 

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: 260
Number of extensions: 16
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: 338
Length of database: 342
Length adjustment: 28
Effective length of query: 310
Effective length of database: 314
Effective search space:    97340
Effective search space used:    97340
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: 49 (23.5 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