GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glk in Erythrobacter marinus HWDM-33

Align Glucokinase; EC 2.7.1.2; Glucose kinase (uncharacterized)
to candidate WP_047093014.1 AAV99_RS01385 glucokinase

Query= curated2:P21908
         (324 letters)



>NCBI__GCF_001013305.1:WP_047093014.1
          Length = 326

 Score =  375 bits (964), Expect = e-109
 Identities = 182/322 (56%), Positives = 239/322 (74%), Gaps = 1/322 (0%)

Query: 2   EIVAIDIGGTHARFSIAEVSNGRVLSLGEETTFKTAEHASLQLAWERFGEKLGRPLPRAA 61
           EIV +DIGGTHARF++A  +    +S+ +  T  T +H S Q AWE +  + G  LPR  
Sbjct: 3   EIVTVDIGGTHARFALASCTADGGISMDDPVTLHTQDHVSFQTAWEDYRAQKGGTLPRHV 62

Query: 62  AIAWAGPVHGEVLKLTNNPWVLRPATLNEKLDIDTHVLINDFGAVAHAVAHMDSSYLDHI 121
           A+A AGPV G+V++ TNNPW++RPA ++EKL +D +VL+NDF AVAHAVA        H+
Sbjct: 63  AMAIAGPVGGDVIRFTNNPWIIRPALVSEKLGVDDYVLVNDFEAVAHAVARAQDDEFLHL 122

Query: 122 CGPDEALPSDGVITILGPGTGLGVAHLLRT-EGRYFVIETEGGHIDFAPLDRLEDKILAR 180
            GP+ ALP+ G +T+LGPGTGLGVAHL R  +G Y V  TEGGHIDFAPLD++ED ILAR
Sbjct: 123 TGPEGALPATGRLTVLGPGTGLGVAHLYREPDGTYRVSATEGGHIDFAPLDQIEDAILAR 182

Query: 181 LRERFRRVSIERIISGPGLGNIYEALAAIEGVPFSLLDDIKLWQMALEGKDNLAEAALDR 240
           LR+R  RVS+ER+++GP + +IY  LAA+E      L DI++W   + G+D+LA AA+DR
Sbjct: 183 LRKRHNRVSVERVVAGPAISDIYHTLAALENKSVPELADIEIWTKGMSGEDSLAAAAVDR 242

Query: 241 FCLSLGAIAGDLALAQGATSVVIGGGVGLRIASHLPESGFRQRFVSKGRFERVMSKIPVK 300
           FCLSLG++AGD+ALA GA +VVI GG+G R+ +HLP SGF +RF +KGRFE +M+ +PVK
Sbjct: 243 FCLSLGSVAGDMALAHGAKAVVIAGGLGYRLRNHLPNSGFAERFRAKGRFESLMAGLPVK 302

Query: 301 LITYPQPGLLGAAAAYANKYSE 322
           LIT+PQPGL GAAAAY  K+ E
Sbjct: 303 LITHPQPGLFGAAAAYFQKFGE 324


Lambda     K      H
   0.320    0.139    0.411 

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: 407
Number of extensions: 19
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: 324
Length of database: 326
Length adjustment: 28
Effective length of query: 296
Effective length of database: 298
Effective search space:    88208
Effective search space used:    88208
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 (21.8 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