GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuG in Pseudomonas fluorescens FW300-N2E3

Align ABC transporter for D-Trehalose, permease component 2 (characterized)
to candidate AO353_03845 AO353_03845 ABC transporter permease

Query= reanno::Smeli:SM_b20327
         (276 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_03845
          Length = 282

 Score = 91.3 bits (225), Expect = 2e-23
 Identities = 71/223 (31%), Positives = 109/223 (48%), Gaps = 17/223 (7%)

Query: 14  LVAVIILVAVFPFYYAILTSLKSGTALFRIDYWPTDISLANYAGIFSHGTFV-------- 65
           L  VI+ +AV P    I+ S    + L   D+ P+  SL  Y   +   TFV        
Sbjct: 23  LSGVILFLAVLPILTMIVMSFSGSSNL---DFPPSSYSLQWYKAAWH--TFVSPDASDVL 77

Query: 66  ---RNLGNSLLVATLVVAISLLLAVTAAYALARVRFRGRGLLLLTILSVSMFPQIAVLAG 122
              + +  SL+V+ + +  + L+AV AAYAL R+ FRG+ + L  +    +FP + +   
Sbjct: 78  SLGKAMSTSLMVSFMAMIFATLVAVPAAYALTRLEFRGKAMALQLMSLPLVFPMVVLGLA 137

Query: 123 LFELIRFVGIFNTPLALIFSYMIFTLPFTVWVLTTFMRDLPIEIEEAAIVDGASPWVVIT 182
           L  +   +    T   L+ +++I  LPF V   T  M  +  E+EEAA + GASP   I 
Sbjct: 138 LLLVFDSLPFQMTVSRLVIAHVILALPFVVKNCTAAMLSIGSEVEEAAQMLGASPTRAIV 197

Query: 183 RVFMPLMWPALVTTGLLAFIAAWNEFLFALTFTSSNTQRTVPV 225
            V +PLM   ++   LLAFI ++NEF     F  +    TVP+
Sbjct: 198 DVVVPLMKSGILAGMLLAFIVSFNEFTVTY-FLYTIDVMTVPI 239



 Score = 22.7 bits (47), Expect = 0.009
 Identities = 13/54 (24%), Positives = 25/54 (46%), Gaps = 2/54 (3%)

Query: 119 VLAGLFELIRFVGIFNTPLALIFSYMIFTLPFTVWVLTTFMRDLPIEIEEAAIV 172
           +LAG+  L+ F+  FN      F Y I  +   +W+ +  +  L   +   A++
Sbjct: 208 ILAGM--LLAFIVSFNEFTVTYFLYTIDVMTVPIWMFSRTVSSLDPTVFSFAVL 259


Lambda     K      H
   0.332    0.143    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: 184
Number of extensions: 13
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 276
Length of database: 282
Length adjustment: 26
Effective length of query: 250
Effective length of database: 256
Effective search space:    64000
Effective search space used:    64000
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.9 bits)
S2: 47 (22.7 bits)

This GapMind analysis is from Sep 17 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