GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK in Pseudomonas litoralis 2SM5

Align ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized)
to candidate WP_090274680.1 BLU11_RS14815 polyamine ABC transporter ATP-binding protein

Query= reanno::Smeli:SMc03065
         (362 letters)



>NCBI__GCF_900105005.1:WP_090274680.1
          Length = 378

 Score =  209 bits (533), Expect = 7e-59
 Identities = 121/318 (38%), Positives = 177/318 (55%), Gaps = 9/318 (2%)

Query: 6   LKDIRKSYGAVDVIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITGGDMFIDGE 65
           ++ + K +     +  + L I  GE    +G SG GKSTLLR++AG E  + G + +DG+
Sbjct: 23  IERVSKQFDDALAVDDVTLTINRGEIFALLGGSGSGKSTLLRILAGFETPSEGRVLLDGQ 82

Query: 66  RVNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGAADMLQLTP 125
            +  +PP KR I M+FQSYAL+PHMTV  N+AFG++  + S  EI  RV     ++ +  
Sbjct: 83  NITALPPHKRPINMMFQSYALFPHMTVEQNIAFGLKQDKLSNTEISERVAEMLKLVHMAK 142

Query: 126 YLDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIAKLSERMSD 185
           Y  R P  LSGGQRQRVA+ R++ + PK+ L DEP+  LD  LR   ++E+ ++ ER+  
Sbjct: 143 YAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRSQMQLELVEIIERVG- 201

Query: 186 TTMIYVTHDQVEAMTLADRIVVLSAGHIEQVGAPLELYERPANLFVARFIGSPAMNVIPA 245
            T I VTHDQ EAMT+A RI ++  G I QVG P+++YE P N  VA F+GS  +N+   
Sbjct: 202 VTCIMVTHDQEEAMTMAQRIAIMDQGWIVQVGTPMDIYESPVNRHVAEFVGS--VNIFEG 259

Query: 246 TITATGQQTAVSLAG--GKSVTLDVPTNASENGKTASFGVRPEDLRVT----EADDFLFE 299
            I A      +       + + L          K+A + +RPE + VT    E       
Sbjct: 260 EIVADMDDHVIIECPQLDRQIYLGHGVTTRAEDKSAIYALRPEKVFVTTEQPEQPYNWAH 319

Query: 300 GTVSIVEALGEVTLLYIE 317
           G V  +  LG  ++ YI+
Sbjct: 320 GEVHDIAYLGGHSVYYIK 337


Lambda     K      H
   0.320    0.137    0.387 

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: 345
Number of extensions: 12
Number of successful extensions: 2
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: 362
Length of database: 378
Length adjustment: 30
Effective length of query: 332
Effective length of database: 348
Effective search space:   115536
Effective search space used:   115536
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 (21.8 bits)
S2: 49 (23.5 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