GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rbsC in Phaeobacter inhibens BS107

Align Ribose import permease protein RbsC (characterized)
to candidate GFF2762 PGA1_c28050 putative sugar transport system, permease protein

Query= SwissProt::P0AGI1
         (321 letters)



>FitnessBrowser__Phaeo:GFF2762
          Length = 353

 Score =  171 bits (433), Expect = 2e-47
 Identities = 110/309 (35%), Positives = 167/309 (54%), Gaps = 17/309 (5%)

Query: 22  SLIALLVLIAIVST----LSPNFFTINNLFNILQQTSVNAIMAVGMTLVILTSGIDLSVG 77
           SL+ L+VL+  V      L   FF+   L  ILQQ  +  I+A   +LVILT+GIDLSVG
Sbjct: 41  SLVPLIVLVLSVIVFGLLLGSKFFSPFALTLILQQVGIVGIVACAQSLVILTAGIDLSVG 100

Query: 78  SLLALTGAVAASIV---GIEVNALVAVAAALALGAAIGAVTGVIVAKGRVQAFIATLVMM 134
           +++ L+  V        G+     VAVA  L  G   G + G +VA+ ++  FI TL M 
Sbjct: 101 AIMVLSSVVMGQFTFRYGLPPE--VAVACGLICGTICGFINGWLVARMKLPPFIVTLGMW 158

Query: 135 LLLRGVTMVYTNGSPVNTG-FTENADLFGWFGIGRPLGVPTPVWIMGIVFLAAW-----Y 188
            ++     +Y+    + +      A L   FG    + +   V+  G++F+        Y
Sbjct: 159 QIVLASNFLYSANETIRSQTIAAEAPLLQLFG--EKIKIGGAVFTYGVIFMVILVVLLAY 216

Query: 189 MLHHTRLGRYIYALGGNEAATRLSGINVNKIKIIVYSLCGLLASLAGIIEVARLSSAQPT 248
           +L HT  GR++YA+G +  A  LSG+ V ++ I VY L GL+ + AG   + R+ S  PT
Sbjct: 217 VLRHTAWGRHVYAVGDDPEAAELSGVKVTRVLISVYMLSGLICAFAGWAMIGRIGSVSPT 276

Query: 249 AGTGYELDAIAAVVLGGTSLAGGKGRIVGTLIGALILGFLNNGLNLLGVSSYYQMIVKAV 308
           +G    +++I AVV+GG SL GG+G I+GT  GALI+G    GL LLG  + +  ++  +
Sbjct: 277 SGQLANIESITAVVIGGISLFGGRGSILGTFFGALIVGVFTLGLRLLGADAQWTYLLIGL 336

Query: 309 VILLAVLVD 317
           +I+ AV VD
Sbjct: 337 LIIAAVAVD 345


Lambda     K      H
   0.324    0.139    0.393 

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: 262
Number of extensions: 16
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: 321
Length of database: 353
Length adjustment: 28
Effective length of query: 293
Effective length of database: 325
Effective search space:    95225
Effective search space used:    95225
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