GapMind for catabolism of small carbon sources

 

Alignments for a candidate for scrK in Tatumella morbirosei LMG 23360

Align Fructokinase-1; ZmFRK1; EC 2.7.1.4 (characterized)
to candidate WP_038021102.1 HA49_RS05790 sugar kinase

Query= SwissProt::Q6XZ79
         (323 letters)



>NCBI__GCF_000757425.2:WP_038021102.1
          Length = 317

 Score =  128 bits (321), Expect = 2e-34
 Identities = 101/323 (31%), Positives = 157/323 (48%), Gaps = 22/323 (6%)

Query: 8   VVSFGEMLIDFVPTVAGVSLAEAPAFLKA-PGGAPANVAIAVSRLGGGAAFVGKLGDDEF 66
           + + GE+L++F+        +EA  FL   P GAPA  A  V+RLG G+   G +G+D+F
Sbjct: 5   ICTMGELLVEFLSKNPNQGFSEAGEFLGPYPSGAPAIFAAQVARLGFGSTLFGCVGNDDF 64

Query: 67  GRMLAAILRDNGVDDGGVVFDSGARTALAFVTLRADGEREFMFYRNPSADMLLTADELNV 126
           GRM  A L+  GV+  G+     A T  AFV+ R   ER+F+F    SA     A  ++V
Sbjct: 65  GRMNIARLQREGVNTAGISVARQAPTGTAFVSYRTQTERDFIFNIPDSACGCFNARLIDV 124

Query: 127 ELIKRAAVFHYGSISLIAEPCRTAHLRAMEIAKEAGALLSYDPNLREALW--PSREEART 184
            L+ +   FH    SL +     A  + +EI K+    +S+DPN+R+ +   P  E+A  
Sbjct: 125 TLLSQCNHFHIMGSSLFSFRMIEAMHKVIEIVKQNNGTVSFDPNIRKEMLNIPEMEQAFD 184

Query: 185 QILSIWDQADIVKVSEVEL-EFLTGIDSVEDDVVMKLWRPTMKLLLVTLGDQGCKYY--- 240
            IL   +  DI   SE E+  F +     E  V+ +L    +  ++V  G QG  +Y   
Sbjct: 185 FIL---EYTDIFLPSESEVAHFSSRKHQSESSVIQELLNNGIAHVVVKRGPQGASHYQMT 241

Query: 241 ---ARDFHGAVPSFKVQQVDTTGAGDAFVGALLQRIVKDPSSLQDEKKLVESIKFANACG 297
                + H  V     + +D TGAGD F    +       S L     + ++++FAN  G
Sbjct: 242 AGSLNELH--VKGSGCEVIDPTGAGDCFGATFV-------SLLLAGYPIRQALEFANTSG 292

Query: 298 AITTTKKGAIPSLPTEAEVLQLI 320
           AI  + KG +  L + A++ QL+
Sbjct: 293 AIAVSNKGPMEGLSSLAQLTQLV 315


Lambda     K      H
   0.319    0.136    0.388 

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: 238
Number of extensions: 13
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: 323
Length of database: 317
Length adjustment: 28
Effective length of query: 295
Effective length of database: 289
Effective search space:    85255
Effective search space used:    85255
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