GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glc-kinase in Dyella japonica UNC79MFTsu3.2

Align glucokinase (EC 2.7.1.1; EC 2.7.1.2; EC 2.7.1.8) (characterized)
to candidate N515DRAFT_0393 N515DRAFT_0393 glucokinase

Query= ecocyc::GLUCOKIN-MONOMER
         (321 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0393
          Length = 333

 Score =  191 bits (485), Expect = 2e-53
 Identities = 118/313 (37%), Positives = 168/313 (53%), Gaps = 8/313 (2%)

Query: 3   KYALVGDVGGTNARLALCDIA-----SGEISQAKTYSGLDYPSLEAVIRVYLEEHKVE-V 56
           K  L  DVGGT+AR+ L D A     SG ++  + Y+G D+P L  ++  +L  H    V
Sbjct: 14  KLVLAADVGGTHARIGLVDAAAPAGASGVLAYER-YAGADWPGLAEILADFLARHPGHAV 72

Query: 57  KDGCIAIACPITGDWVAMTNHTWAFSIAEMKKNLGFSHLEIINDFTAVSMAIPMLKKEHL 116
            +  IA+A  +    +   N  W   +AE+++ L    L+++NDF A++ A   L  +  
Sbjct: 73  DEAAIAVAGYVRDGELVAENLRWPVRLAELRERLRLRRLQVVNDFEALAFATQYLGADDS 132

Query: 117 IQFGGAEPVEGKPIAVYGAGTGLGVAHLVHVDKRWVSLPGEGGHVDFAPNSEEEAIILEI 176
           +    A P    P+AV G GTGLG A LV        LP EGGHV  AP SE E  +L++
Sbjct: 133 LAVIDA-PAAAGPVAVVGPGTGLGCALLVPDGNGVTVLPSEGGHVALAPGSEREMALLQL 191

Query: 177 LRAEIGHVSAERVLSGPGLVNLYRAIVKADNRLPENLKPKDITERALADSCTDCRRALSL 236
           L     +V    VLSGPGLVNLYRAI + D     + +P+ I+  AL          L  
Sbjct: 192 LSRGRDYVHTGHVLSGPGLVNLYRAIGELDGLSAVHAQPEQISAAALDGGDALALDTLHT 251

Query: 237 FCVIMGRFGGNLALNLGTFGGVFIAGGIVPRFLEFFKASGFRAAFEDKGRFKEYVHDIPV 296
           FC ++G F G+LA+     GGVF+AGGI+P+  EF   S FR  F +KG  ++++  +PV
Sbjct: 252 FCAMLGGFVGDLAVLFKASGGVFLAGGILPQLREFLPYSAFRERFFNKGVMRDFLAGVPV 311

Query: 297 YLIVHDNPGLLGS 309
            LI H   G+LG+
Sbjct: 312 RLIEHGRLGVLGA 324


Lambda     K      H
   0.322    0.141    0.426 

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: 340
Number of extensions: 21
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: 321
Length of database: 333
Length adjustment: 28
Effective length of query: 293
Effective length of database: 305
Effective search space:    89365
Effective search space used:    89365
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: 48 (23.1 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