GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Pseudomonas fluorescens FW300-N2C3

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate AO356_00960 AO356_00960 ABC transporter permease

Query= uniprot:B2T9V8
         (351 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_00960
          Length = 325

 Score =  115 bits (288), Expect = 2e-30
 Identities = 91/302 (30%), Positives = 149/302 (49%), Gaps = 10/302 (3%)

Query: 41  LALLPALALLIVIGAFISPSFLTKANLISVLGASAALALVVLAESLIVLTGKFDLSLEST 100
           L L  AL  ++ + + +S  FL+     ++      L ++ +  + I++ G  DLS+ S 
Sbjct: 21  LGLAGALLAMVALFSTLSSHFLSYDTFSTLANQIPDLMVLAVGMTFILIIGGIDLSVGSV 80

Query: 101 VGIAPAVGAMLVMPAASAGFGMQ-WPAAAGLLAIVVVGAVIGFINGFLVVRLRLNAFIVT 159
           + +A +  ++ V+     G+G   WP+A   L  + V A+ G + G + V  R+ +FIV+
Sbjct: 81  LALAASTVSVAVL-----GWGWSVWPSA---LLGMAVAALAGTVTGSITVAWRIPSFIVS 132

Query: 160 LAMLIVLRGMLVGATKGGTLFDMPTSFFALATTIVLGLPLSVWLAAAAFAIAAFMLRYHR 219
           L +L + RG+    T   T + +  SF  L+  I  G+  S  +A     IA  +L    
Sbjct: 133 LGVLEMARGLAYQMTGSRTAY-IGDSFAWLSNPIAFGISPSFIIALLVIFIAQAVLTRTV 191

Query: 220 LGRALYAIGGNPEAARAAGIRVERITWGVFVLGSILASVGGLIVTGYVGAINANQGNGMI 279
            GR L  IG N EA R AGI  +     VF L  +LA V  L     + A + N G+G+ 
Sbjct: 192 FGRYLIGIGTNEEAVRLAGINPKPYKILVFSLMGLLAGVAALFQISRLEAADPNAGSGLE 251

Query: 280 FTVFAAAVIGGISLDGGKGTMFGALTGVLLLGVVQNLLTLAQVPSFWIQAIYGAIILGSL 339
             V AA VIGG SL GG+G++     GVL++ V+   L          + I GA+I+ ++
Sbjct: 252 LQVIAAVVIGGTSLMGGRGSVISTFFGVLIISVLAAGLAQIGATEPTKRIITGAVIVVAV 311

Query: 340 MV 341
           ++
Sbjct: 312 VL 313


Lambda     K      H
   0.326    0.140    0.397 

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: 261
Number of extensions: 20
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: 351
Length of database: 325
Length adjustment: 28
Effective length of query: 323
Effective length of database: 297
Effective search space:    95931
Effective search space used:    95931
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (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.

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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