GapMind for catabolism of small carbon sources

 

Alignments for a candidate for araUsh in Dyella japonica UNC79MFTsu3.2

Align Periplasmic binding protein/LacI transcriptional regulator (characterized, see rationale)
to candidate N515DRAFT_2412 N515DRAFT_2412 simple sugar transport system substrate-binding protein

Query= uniprot:A0KWY4
         (313 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2412
          Length = 319

 Score =  301 bits (770), Expect = 2e-86
 Identities = 162/291 (55%), Positives = 206/291 (70%), Gaps = 5/291 (1%)

Query: 24  TVGFSQVGSESGWRTSFSEAVKAEAKQRGIDLKFADAQQKQENQIKAVRSFIAQGVDAII 83
           TVGFSQVG+ES WRT+ + +VK+     G DLKF+DAQQKQENQIKA+RSFIAQ VD I 
Sbjct: 30  TVGFSQVGAESEWRTANTASVKSALVAPGFDLKFSDAQQKQENQIKALRSFIAQRVDVIA 89

Query: 84  IAPVVETGWKPVLKEAKRAKIPVVIVDRNIKVDDDSLFLTRIASDFSEEGRKIGQWLMDK 143
            +PVVE+GW+PVL+EAK A IPVV+ DR +KV D SL+ + I SDF EEGRK G+WL+  
Sbjct: 90  FSPVVESGWEPVLREAKAAGIPVVLTDRAVKVSDASLYASLIGSDFIEEGRKAGRWLLQD 149

Query: 144 TQGN---CDIAELQGTVGATAAIDRAAGFNQVIANYPNAKIVRSQTGEFTRAKGKEVMEG 200
           + G      + ELQGTVG+  AIDR  GF++VI   P  K+VRSQ+G+FTRAKGKEVME 
Sbjct: 150 STGKPGPIRVVELQGTVGSAPAIDRMKGFHEVIDTDPRFKLVRSQSGDFTRAKGKEVMEA 209

Query: 201 FLKAQNGQPLCAVWSHNDEMALGAVQAIKEAGLKPGKDILIVSVDGVPDYFKAMADGDVN 260
           FLKA+ G  +  +++HND+MA+GA+QAI+EAGL PGKDI IVS+DGV   F+AM  G +N
Sbjct: 210 FLKAEGGH-IDVLFAHNDDMAIGAIQAIEEAGLTPGKDIRIVSIDGVRGAFEAMKAGKLN 268

Query: 261 ATVELSPYLGGPAFDAIDAYLKGNKDQAKLISTTGDVFTQETAAAEYEKRR 311
           AT+E +P  G      I     G     +++   G VFTQ+ AAA    R+
Sbjct: 269 ATIECNPLFGAQLAQLIRDVHAGKPVPKRIVVEEG-VFTQDQAAAALPGRK 318


Lambda     K      H
   0.316    0.131    0.376 

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: 304
Number of extensions: 6
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: 313
Length of database: 319
Length adjustment: 27
Effective length of query: 286
Effective length of database: 292
Effective search space:    83512
Effective search space used:    83512
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 (21.6 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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