GapMind for catabolism of small carbon sources

 

Alignments for a candidate for scrK in Gallaecimonas xiamenensis 3-C-1

Align Fructokinase; D-fructose kinase; Manno(fructo)kinase; EC 2.7.1.4 (characterized)
to candidate WP_008482535.1 B3C1_RS01960 ROK family protein

Query= SwissProt::P23917
         (302 letters)



>NCBI__GCF_000299915.1:WP_008482535.1
          Length = 300

 Score =  182 bits (463), Expect = 6e-51
 Identities = 114/301 (37%), Positives = 157/301 (52%), Gaps = 9/301 (2%)

Query: 1   MRIGIDLGGTKTEVIALGDAGEQLYRHRLPTPRDDYRQTIETIATLVDMAEQATGQRGTV 60
           M  G+D+GGTK E+         L R R+ TP  DY   + TIA LV  A    G  G +
Sbjct: 1   MIYGLDVGGTKMELGCFDAQLNDLERCRVATPARDYPALLNTIAALVADARLRHGP-GPL 59

Query: 61  GMGIPGSISPYTGVVKNANSTWLNGQPFDKDLSARLQREVRLANDANCLAVSEAVDGAAA 120
           G+ +PG +    G+   AN     G+P   DL+ RL + + L ND  C A+SEA+ GA A
Sbjct: 60  GIALPGLVDGQ-GLSLCANLPGATGRPLGADLARRLGQPLTLGNDCRCFALSEALGGAGA 118

Query: 121 GAQTVFAVIIGTGCGAGVAFNGRAHIGGNGTAGEWGHNPLPWMDEDELRYREEVP---CY 177
           G + VF  ++GTG   G+  +G  + G    A E+GH PLP      L  R ++P   C 
Sbjct: 119 GYRRVFGAVLGTGAAGGLVVDGLLYQGRQDIACEYGHQPLP----ARLLLRYQLPLWTCG 174

Query: 178 CGKQGCIETFISGTGFAMDYRRLSGHALKGSEIIRLVEESDPVAELALRRYELRLAKSLA 237
           CG+QGC E ++SG G A  Y    G A   + ++ L   ++P+A+  L  Y   L    A
Sbjct: 175 CGQQGCYEAYVSGPGLARLYGHFGGQAEDAAAVLALWRRAEPLAQATLDCYLDLLGACFA 234

Query: 238 HVVNILDPDVIVLGGGMSNVDRLYQTVGQLIKQFVFGGECETPVRKAKHGDSSGVRGAAW 297
            +V   DPD+IVLGGG+S V  LYQ +   I   +FG     P+  A+ GD+SG RG A 
Sbjct: 235 GLVLAYDPDLIVLGGGLSKVPELYQLLPARIDACLFGPFQSPPLVPARFGDASGARGIAL 294

Query: 298 L 298
           L
Sbjct: 295 L 295


Lambda     K      H
   0.318    0.137    0.418 

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: 327
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: 302
Length of database: 300
Length adjustment: 27
Effective length of query: 275
Effective length of database: 273
Effective search space:    75075
Effective search space used:    75075
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 (21.7 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