GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK in Sinorhizobium meliloti 1021

Align Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale)
to candidate SM_b21605 SM_b21605 sugar uptake ABC transporter ATP-binding protein

Query= uniprot:A8LLL2
         (373 letters)



>FitnessBrowser__Smeli:SM_b21605
          Length = 362

 Score =  338 bits (867), Expect = 1e-97
 Identities = 186/357 (52%), Positives = 244/357 (68%), Gaps = 4/357 (1%)

Query: 1   MADLKLTGVEKAYGDVKVLSNINLDIQQGELIVFVGPSGCGKSTLLRMIAGLEKITGGTL 60
           M+ +KLTGV K++G VKV+  ++++I QGE  VFVGPSGCGKSTLLRMIAGLE+ TGG +
Sbjct: 1   MSGIKLTGVSKSFGAVKVIHGVDIEIGQGEFAVFVGPSGCGKSTLLRMIAGLEETTGGEI 60

Query: 61  EIDGTVVNDVPPAQRGIAMVFQSYALYPHMTVRENMSFALKIAKKSQAEIDAAVEAAAEK 120
            ID   V    P++RG+AMVFQSYALYPH++V +NM+F+L IA++ +AEI+  V+AAAE 
Sbjct: 61  RIDAEDVTHKEPSKRGVAMVFQSYALYPHLSVFDNMAFSLSIARRPKAEIEQKVKAAAEI 120

Query: 121 LQLGQYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRLEIAQLK 180
           L+L  YLD  P  LSGGQRQRVAIGR+IVR+P+V+LFDEPLSNLDA LRV  R+EIA+L 
Sbjct: 121 LRLSDYLDSKPSQLSGGQRQRVAIGRAIVREPRVFLFDEPLSNLDAELRVKMRMEIARLH 180

Query: 181 EAMPESTMVYVTHDQVEAMTLATRIVVLAGGGIAQVGSPLELYEKPENEFVAQFIGSPKM 240
             +  +TMVYVTHDQVEAMTLA RIVVL  G + Q G+PLELY  P+N FVA FIGSP M
Sbjct: 181 RQI-GATMVYVTHDQVEAMTLADRIVVLKAGVVQQTGAPLELYRNPDNMFVAGFIGSPGM 239

Query: 241 NLLPGKII-GTGAQTTVEMTDGGRAVSDYPS-DDSLMGAAVNVGVRPEDMVEAAPGGDYV 298
           N L  +++ G+G + T+E+ D      + P+     +G  + VGVRPE +      G   
Sbjct: 240 NFLKARVVPGSGDRLTIELHDAPGVPFEIPARTGPAVGEEIFVGVRPEHITLGEREGGVG 299

Query: 299 FEGKVAITEALGEVTLLYFEAPSGEDPTIGKLQGIHKDLKGQVTRLTAEPAKVHVFK 355
            +      E LG    L+    +GE+ TI + +G  +    Q  RLT  P ++  F+
Sbjct: 300 LDVTAEFIEELGGTGYLHALTVTGEEMTI-ECRGEERPQPKQAVRLTLAPEEMFAFE 355


Lambda     K      H
   0.316    0.135    0.379 

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: 436
Number of extensions: 22
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: 373
Length of database: 362
Length adjustment: 30
Effective length of query: 343
Effective length of database: 332
Effective search space:   113876
Effective search space used:   113876
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: 49 (23.5 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