GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rbsC in Phaeobacter inhibens BS107

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family (characterized, see rationale)
to candidate GFF2275 PGA1_c23070 putative ribose transport system permease protein

Query= uniprot:A0A1N7UNQ5
         (325 letters)



>FitnessBrowser__Phaeo:GFF2275
          Length = 333

 Score =  157 bits (397), Expect = 3e-43
 Identities = 99/288 (34%), Positives = 152/288 (52%), Gaps = 7/288 (2%)

Query: 34  FSVLSDHFLSYDTFSTLANQIPDLMVLAVGMTFILIIGGIDLSVGSVLALAA-----SAV 88
           FSV    F+  D    L  Q   + ++A+GMT +++ G IDLSVG++ A+ A     S  
Sbjct: 33  FSVSDKAFMDTDNMLLLLKQSAPIGIIAMGMTIVMVNGNIDLSVGAIYAICAIILLDSMT 92

Query: 89  SVAILGWGWSVLPAA-VLGMGCAALAGTITGSITVAWRIPSFIVSLGVLEMARGVAYQMT 147
                G G  V+P A  L +    + G I G I     + +FIV+LG +   RG+ +   
Sbjct: 93  WTMFAGLGNWVIPVAWCLALLTGVVLGAINGLIVWKTGVDAFIVTLGSMLGYRGLVFMYN 152

Query: 148 GSR-TAYIGDSFAWLSNPIAFGISPSFIIALLVIIAAQLVLTRTVFGRYLIGIGTNEEAV 206
           G + T+++  +    +     G+  +    L+V +A   ++ RTV GR    IG N EA 
Sbjct: 153 GEQPTSHLNWTLVDFAEAQFLGLHTATWFLLVVTVAIWFLMNRTVHGRNAYAIGNNREAA 212

Query: 207 RLAGINPKPYKILVFSLMGLLAGVAALFQISRLEAADPNAGSGLELQVIAAVVIGGTSLM 266
             AGI   P+ ++ F ++G LA ++A+   S   + +PN G   EL VI AVV+GGT L 
Sbjct: 213 VNAGIRVGPHMMINFMIIGFLAALSAVVFYSESGSVNPNDGQLYELWVITAVVLGGTKLT 272

Query: 267 GGRGSVISTFFGVLIISVLAAGLAQIGATEPTKRIITGAVIVIAVVLD 314
           GG GS++STF GV+ I +L  GLA IGA   T  ++ G +++  + LD
Sbjct: 273 GGAGSIVSTFGGVIAIQLLRKGLAHIGADTSTVNLVIGLILIAVLFLD 320


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: 248
Number of extensions: 12
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: 325
Length of database: 333
Length adjustment: 28
Effective length of query: 297
Effective length of database: 305
Effective search space:    90585
Effective search space used:    90585
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.

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