GapMind for catabolism of small carbon sources

 

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

Align RhaP, component of Rhamnose porter (Richardson et al., 2004) (Transport activity is dependent on rhamnokinase (RhaK; AAQ92412) activity (Richardson and Oresnik, 2007) This could be an example of group translocation!) (characterized)
to candidate AO356_23210 AO356_23210 ABC transporter

Query= TCDB::Q7BSH3
         (333 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_23210
          Length = 340

 Score =  157 bits (396), Expect = 5e-43
 Identities = 93/281 (33%), Positives = 153/281 (54%), Gaps = 17/281 (6%)

Query: 44  SILIILALAQMTVILTKSIDLSVAANLAFTGMAIAMM-------NAAHP---DLPLVVLI 93
           SI+ +LA+    VI+T  IDLS  + LA + M  A +        A  P   DLP+ + +
Sbjct: 64  SIIGLLAIGVTQVIITTGIDLSSGSVLALSAMIAASLAQTSDFARAVFPSLTDLPVWIPV 123

Query: 94  LMAVVIGACLGAINGFLVWALEIPPIVVTLGTLTIYRGMAFVLSGGAWVNAHQMTPIFLS 153
           +  + +G   GAING ++    IPP + TLG +   RG+A   + G  V+    +   + 
Sbjct: 124 VAGLGVGLLAGAINGSIIAITGIPPFIATLGMMVSARGLARYYTEGQPVSMLSDSYTAIG 183

Query: 154 VPRTPVLGLPVLSWVGIIIVILMYVLLRYTQFGRSAYATGGNPTAAVYAGIDTGWTKFLA 213
               PV+       + +++ ++ ++ LRYT++G+  YA GGN  AA  +GI+      + 
Sbjct: 184 HGAMPVI-------IFLVVAVIFHIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLVIV 236

Query: 214 FVLSGALAGLASYLWVSRYAVAYVDIANGFELDSVAACVIGGISIAGGVGSVAGTVLGAL 273
           + ++G LAGLA  +  +R A     +   +ELD++AA VIGG S+AGGVG + GTV+GAL
Sbjct: 237 YSIAGLLAGLAGVVASARAATGQAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGAL 296

Query: 274 FLGVIKNALPVIGISPFTQMAISGTVIILAVAFNARRERNR 314
            LGV+ +    +G+  + Q  I G +I++AV  +  R + +
Sbjct: 297 ILGVMASGFTFVGVDAYIQDIIKGLIIVVAVVIDQYRNKRK 337


Lambda     K      H
   0.328    0.141    0.413 

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: 289
Number of extensions: 17
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: 333
Length of database: 340
Length adjustment: 28
Effective length of query: 305
Effective length of database: 312
Effective search space:    95160
Effective search space used:    95160
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 (21.8 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