GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kdgK in Echinicola vietnamensis KMM 6221, DSM 17526

Align 2-dehydro-3-deoxygluconokinase (EC 2.7.1.45) (characterized)
to candidate Echvi_3631 Echvi_3631 Sugar kinases, ribokinase family

Query= BRENDA::Q9WXS2
         (339 letters)



>FitnessBrowser__Cola:Echvi_3631
          Length = 331

 Score =  230 bits (586), Expect = 4e-65
 Identities = 132/340 (38%), Positives = 194/340 (57%), Gaps = 14/340 (4%)

Query: 2   KVVTFGEIMLRLSPPDHKRIFQTDSFDVTYGGAEANVAAFLAQMGLDAYFVTKLPNNPLG 61
           +V+T GEIM+RLS P H+R   ++ +++ YGGAEANVA  LA  G+    VT  PNN +G
Sbjct: 4   RVITLGEIMMRLSTPGHERFVSSNQYNIVYGGAEANVAISLANWGISTAHVTAFPNNDIG 63

Query: 62  DAAAGHLRKFGVKTDYIARGGNRIGIYFLEIGASQRPSKVVYDRAHSAISEAKREDFDWE 121
            AA  +LR  G+ T Y+     R+G+YF+E GA QR SK++YDR  S  +    +  DW+
Sbjct: 64  KAALQYLRYAGLDTQYVYFEEGRMGLYFVENGAMQRSSKIIYDRFDSVFANFDGDKIDWK 123

Query: 122 KILDGARWFHFSGITPPLGKELPLILEDALKVANEKGVTVSCDLNYRARLWT-KEEAQKV 180
            +  GA WFH++GITP +      I  +A+  A+E GV +S D+NYR  LW   ++   +
Sbjct: 124 AVFKGADWFHWTGITPAISASAAKICTEAVNAASELGVKISGDINYRRNLWQYGKQPLDI 183

Query: 181 MIPFMEYVDVLIANEEDIEKVLGISVEGLDLKTGKLNREAYAKIAEEVTRKYNFKTVGIT 240
           M   +   +V+IA   D E  + I  +         + EA  K A+E      +  +  T
Sbjct: 184 MPDLIAKTNVVIAGLTDFENCMDIHEQ---------DYEAACKKAQEKCPSIEY--ISTT 232

Query: 241 LRESISATVNYWSVMVFENGQPHFSNRYEI-HIVDRVGAGDSFAGALIYGSLMGFDSQKK 299
            R SISA+ N  S +++   +   S  Y++ HIVDRVG GD++   LIYG L G D Q  
Sbjct: 233 HRNSISASHNGLSGVLWNGHELLESKSYDMTHIVDRVGGGDAYMAGLIYGLLEGED-QAA 291

Query: 300 AEFAAAASCLKHTIPGDFVVLSIEEIEKLASGATSGRVER 339
            E+A AAS LKH+IPGD   ++++E+ +L  G   G++ R
Sbjct: 292 LEYAVAASVLKHSIPGDANFVTVDEVSQLVKGENVGKLLR 331


Lambda     K      H
   0.319    0.136    0.397 

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: 295
Number of extensions: 11
Number of successful extensions: 3
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: 339
Length of database: 331
Length adjustment: 28
Effective length of query: 311
Effective length of database: 303
Effective search space:    94233
Effective search space used:    94233
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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