GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glc-kinase in Erythrobacter marinus HWDM-33

Align glucokinase (EC 2.7.1.1; EC 2.7.1.2; EC 2.7.1.8) (characterized)
to candidate WP_047093014.1 AAV99_RS01385 glucokinase

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



>NCBI__GCF_001013305.1:WP_047093014.1
          Length = 326

 Score =  156 bits (395), Expect = 6e-43
 Identities = 111/326 (34%), Positives = 160/326 (49%), Gaps = 11/326 (3%)

Query: 1   MTKYALVGDVGGTNARLALCDI-ASGEISQAK--TYSGLDYPSLEAVIRVYLEEHKVEV- 56
           MT+   V D+GGT+AR AL    A G IS     T    D+ S +     Y  +    + 
Sbjct: 1   MTEIVTV-DIGGTHARFALASCTADGGISMDDPVTLHTQDHVSFQTAWEDYRAQKGGTLP 59

Query: 57  KDGCIAIACPITGDWVAMTNHTWAFSIAEMKKNLGFSHLEIINDFTAVSMAIPMLKKEHL 116
           +   +AIA P+ GD +  TN+ W    A + + LG     ++NDF AV+ A+   + +  
Sbjct: 60  RHVAMAIAGPVGGDVIRFTNNPWIIRPALVSEKLGVDDYVLVNDFEAVAHAVARAQDDEF 119

Query: 117 IQFGGAE---PVEGKPIAVYGAGTGLGVAHLVHV-DKRWVSLPGEGGHVDFAPNSEEEAI 172
           +   G E   P  G+ + V G GTGLGVAHL    D  +     EGGH+DFAP  + E  
Sbjct: 120 LHLTGPEGALPATGR-LTVLGPGTGLGVAHLYREPDGTYRVSATEGGHIDFAPLDQIEDA 178

Query: 173 ILEILRAEIGHVSAERVLSGPGLVNLYRAIVKADNRLPENLKPKDITERALADSCTDCRR 232
           IL  LR     VS ERV++GP + ++Y  +   +N+    L   +I  + ++   +    
Sbjct: 179 ILARLRKRHNRVSVERVVAGPAISDIYHTLAALENKSVPELADIEIWTKGMSGEDSLAAA 238

Query: 233 ALSLFCVIMGRFGGNLALNLGTFGGVFIAGGIVPRFLEFFKASGFRAAFEDKGRFKEYVH 292
           A+  FC+ +G   G++AL  G    V IAGG+  R       SGF   F  KGRF+  + 
Sbjct: 239 AVDRFCLSLGSVAGDMALAHGA-KAVVIAGGLGYRLRNHLPNSGFAERFRAKGRFESLMA 297

Query: 293 DIPVYLIVHDNPGLLGSGAHLRQTLG 318
            +PV LI H  PGL G+ A   Q  G
Sbjct: 298 GLPVKLITHPQPGLFGAAAAYFQKFG 323


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: 333
Number of extensions: 26
Number of successful extensions: 5
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: 326
Length adjustment: 28
Effective length of query: 293
Effective length of database: 298
Effective search space:    87314
Effective search space used:    87314
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 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