GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rbsC in Caulobacter crescentus NA1000

Align Ribose import permease protein RbsC (characterized)
to candidate CCNA_00904 CCNA_00904 inositol ABC transport system, permease protein IatP

Query= SwissProt::P0AGI1
         (321 letters)



>FitnessBrowser__Caulo:CCNA_00904
          Length = 332

 Score =  236 bits (603), Expect = 4e-67
 Identities = 136/314 (43%), Positives = 192/314 (61%), Gaps = 9/314 (2%)

Query: 10  RYFTKAWLMEQKSLIALLVLIAIVSTLSPNFFTINNLFNILQQTSVNAIMAVGMTLVILT 69
           R+   A+  + ++++ LL+L+A+    +  F T  N  NIL + S+  I+AVGMT VIL 
Sbjct: 16  RFDLLAFARKHRTILFLLLLVAVFGAANERFLTARNALNILSEVSIYGIIAVGMTFVILI 75

Query: 70  SGIDLSVGSLLALTGAVAASIVGIEVNA-----LVAVAAALALGAAIGAVTGVIVAKGRV 124
            GID++VGSLLA     AA +V   V       L+A+  +  +G A G V G  V    V
Sbjct: 76  GGIDVAVGSLLAFASIAAAYVVTAVVGDGPATWLIALLVSTLIGLAGGYVQGKAVTWLHV 135

Query: 125 QAFIATLVMMLLLRGVTMVYTNGSPVNTGFTENADLFGWFGIGRPLGVPTPVWIMGIVFL 184
            AFI TL  M + RG T++  +G P++ GF    D + W+G G  L +P PV I  +V  
Sbjct: 136 PAFIVTLGGMTVWRGATLLLNDGGPIS-GFN---DAYRWWGSGEILFLPVPVVIFALVAA 191

Query: 185 AAWYMLHHTRLGRYIYALGGNEAATRLSGINVNKIKIIVYSLCGLLASLAGIIEVARLSS 244
           A    L +TR GR +YA+GGN  A RLSG+NV+ I   VY++ G LA L+G +  ARL S
Sbjct: 192 AGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGLSGFLLSARLGS 251

Query: 245 AQPTAGTGYELDAIAAVVLGGTSLAGGKGRIVGTLIGALILGFLNNGLNLLGVSSYYQMI 304
           A+  AGTGYEL  IA+VV+GG SL GG G + GT++GAL++G L+NGL +L V+SY Q +
Sbjct: 252 AEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLVMLHVTSYVQQV 311

Query: 305 VKAVVILLAVLVDN 318
           V  ++I+ AV  D+
Sbjct: 312 VIGLIIVAAVAFDH 325


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: 290
Number of extensions: 15
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: 321
Length of database: 332
Length adjustment: 28
Effective length of query: 293
Effective length of database: 304
Effective search space:    89072
Effective search space used:    89072
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: 48 (23.1 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