GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rbsC in Pseudomonas fluorescens FW300-N2E2

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family (characterized, see rationale)
to candidate Pf6N2E2_1457 Xylose ABC transporter, permease protein XylH

Query= uniprot:A0A1N7UNQ5
         (325 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1457
          Length = 378

 Score =  120 bits (301), Expect = 5e-32
 Identities = 99/347 (28%), Positives = 160/347 (46%), Gaps = 66/347 (19%)

Query: 41  FLSYDTFSTLANQIPDLMVLAVGMTFILIIGGIDLSVGSVLALAASAVSVA--------- 91
           F++    S L  Q+    +LA GM  ++I G IDLSVGS+L L     ++          
Sbjct: 35  FVTPRNLSNLLRQMSITGILACGMVLVIISGEIDLSVGSLLGLLGGLAAILDVVYHIPLL 94

Query: 92  -----------ILGWG------WSVLPAAVLGMG-CAALAGT---ITGSITVAWRIPSFI 130
                      ++G G      +  +P+ ++G+G   A  G    +TG  T+A   P  +
Sbjct: 95  ANLSLVALCGLVIGLGNGYMTAYLRIPSFIVGLGGMLAFRGVLLGVTGGTTIAPVSPELV 154

Query: 131 ------------VSLGVLEMARGV----------------AYQMTGS--RTAYIGD---S 157
                         LG+L  A  +                A+ +     R   IG     
Sbjct: 155 YVGQGYLPHTVGTGLGILLFALTLFLTWKQRRNRALHGLAAHSLVRDVLRVVVIGAVLAG 214

Query: 158 FAWLSNPIAFGISPSFIIALLVIIAAQLVLTRTVFGRYLIGIGTNEEAVRLAGINPKPYK 217
           F +  N    GI    ++ L+++     V ++TVFGR +  +G+N EA RL+GIN +  K
Sbjct: 215 FVYTLNSYD-GIPVPVLLLLILLGVFSYVTSQTVFGRRVYSVGSNMEATRLSGINVQAVK 273

Query: 218 ILVFSLMGLLAGVAALFQISRLEAADPNAGSGLELQVIAAVVIGGTSLMGGRGSVISTFF 277
           + +F +MG++  +A +   +RL A  P+AG+  EL  IAA  IGGTS+ GG G+V     
Sbjct: 274 LWIFGIMGVMCALAGVVNTARLAAGSPSAGNMGELDAIAACFIGGTSMRGGSGTVYGALL 333

Query: 278 GVLIISVLAAGLAQIGATEPTKRIITGAVIVIAVVLDTYRSQRASRR 324
           G L+I+ L  G++ +      + I+ G+++V+AV +D   S R  RR
Sbjct: 334 GALVITSLDNGMSMLDVDSYWQMIVKGSILVLAVWVDV--STRTGRR 378


Lambda     K      H
   0.324    0.139    0.399 

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: 364
Number of extensions: 26
Number of successful extensions: 4
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: 325
Length of database: 378
Length adjustment: 29
Effective length of query: 296
Effective length of database: 349
Effective search space:   103304
Effective search space used:   103304
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 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