GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK' in Brucella inopinata BO1

Align Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale)
to candidate WP_008507759.1 BIBO1_RS12775 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= uniprot:A8LLL2
         (373 letters)



>NCBI__GCF_000182725.1:WP_008507759.1
          Length = 363

 Score =  311 bits (796), Expect = 2e-89
 Identities = 182/360 (50%), Positives = 231/360 (64%), Gaps = 13/360 (3%)

Query: 1   MADLKLTGVEKAYGDVKVLSNINLDIQQGELIVFVGPSGCGKSTLLRMIAGLEKITGGTL 60
           MA L +  + K YG ++V+  INL+I   E +  VGPSGCGKST LRMIAGLE I+GGTL
Sbjct: 1   MAQLSIKNLVKRYGSIEVVHGINLEIADKEFVALVGPSGCGKSTTLRMIAGLESISGGTL 60

Query: 61  EIDGTVVNDVPPAQRGIAMVFQSYALYPHMTVRENMSFALKIAKKSQAEIDAAVEAAAEK 120
           EI G VVND+PP  R I+MVFQSYALYPHM+VRENM F+LKIAK+ QAEID  V  AA  
Sbjct: 61  EIGGKVVNDLPPRDRNISMVFQSYALYPHMSVRENMGFSLKIAKQPQAEIDRRVNEAAAV 120

Query: 121 LQLGQYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRLEIAQLK 180
           L L   +DR P  LSGGQRQRVA+GR+IVR+P+V+LFDEPLSNLDA LR   R EI +L 
Sbjct: 121 LGLEALMDRRPAQLSGGQRQRVAMGRAIVRNPEVFLFDEPLSNLDAKLRTQMRTEIKKL- 179

Query: 181 EAMPESTMVYVTHDQVEAMTLATRIVVLAGGGIAQVGSPLELYEKPENEFVAQFIGSPKM 240
            A  +ST+VYVTHDQVEAMTLA RIV++  G I Q G+P E++++P  +FVA FIGSP M
Sbjct: 180 HAKVQSTVVYVTHDQVEAMTLADRIVIMRDGHIEQAGTPDEVFKRPATQFVAGFIGSPPM 239

Query: 241 NLLPGKIIGTGAQTTVEMTDGGRAVSDYPSDDSL-MGAAVNVGVRPEDMVEAAPG---GD 296
           N+    + G      +   +G R          +  GA V  G+RP+D+     G   GD
Sbjct: 240 NMAEATVKG----NELLFANGDRLPLPARFKARVGEGAKVTFGLRPDDIFPKGHGLSTGD 295

Query: 297 YVFEG--KVAITEALGEVTLLYFEAPSGEDPTIGKLQGIHKDLKGQVTRLTAEPAKVHVF 354
            V E   +V ITE LG  TL++ E    E   + ++        G+   +  + A+ H+F
Sbjct: 296 GVHEKELRVVITEPLGNETLVFAEFAGRE--WVARMLNPRPMQPGESIAMQFDLAQAHLF 353


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: 370
Number of extensions: 24
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: 363
Length adjustment: 30
Effective length of query: 343
Effective length of database: 333
Effective search space:   114219
Effective search space used:   114219
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 24 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