GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rhaP in Azospirillum brasilense Sp245

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 AZOBR_RS27940 AZOBR_RS27940 ABC transporter permease

Query= TCDB::Q7BSH3
         (333 letters)



>FitnessBrowser__azobra:AZOBR_RS27940
          Length = 329

 Score =  144 bits (363), Expect = 3e-39
 Identities = 102/303 (33%), Positives = 164/303 (54%), Gaps = 14/303 (4%)

Query: 13  FLIIVVMIVVFSTRAADFATPGNLAGIFNDTSILIILALAQMTVILTKSIDLSVAANLAF 72
           FL +  +IV+ +     F +PGN+  +   T+ + I+A+    VI    IDLSV +  AF
Sbjct: 20  FLALAALIVLGTIVNPVFLSPGNIGNVLTRTAFIGIIAVGATFVITAGGIDLSVGSLAAF 79

Query: 73  -TGMAIAMMNA----AHPDLPLVVL-ILMAVVIGACLGAINGFLVWALEIPPIVVTLGTL 126
            +G+ I +MNA        LP++++ +L+A+ +G   G +NG LV    +   +VTLGT+
Sbjct: 80  ASGVMIVVMNALVGSMGAGLPVILIGVLVALGLGLVAGLVNGLLVTKGRMEAFIVTLGTM 139

Query: 127 TIYRGM-AFVLSGGAWVNAHQMTPIFLSVPRTPVLGL--PVLSWVGIIIVILMYVLLRY- 182
            I+R +  ++  GG      ++  I+  V    V G+  P+L++    +V L+  L+ Y 
Sbjct: 140 GIFRSLVTYIADGGTLSLNSEIRTIYRPVYYGGVFGISYPILAFA---VVALIGALIMYR 196

Query: 183 TQFGRSAYATGGNPTAAVYAGIDTGWTKFLAFVLSGALAGLASYLWVSRYAVAYVDIANG 242
           T+FGR   A G +   A Y+ I+    K LAFVL G    +A  ++V R   A       
Sbjct: 197 TRFGRYCAAIGSSEDVARYSAINVDRVKLLAFVLQGICVAIAVVIYVPRLGSASATTGLL 256

Query: 243 FELDSVAACVIGGISIAGGVGSVAGTVLGALFLGVIKNALPVIG-ISPFTQMAISGTVII 301
           +EL+++AA +IGG  + GG G + GTV+GA+ L +I N L + G IS +    I G +II
Sbjct: 257 WELEAIAAVIIGGTMLKGGYGRIWGTVVGAVMLTLIDNILNLTGAISVYLNGTIQGVIII 316

Query: 302 LAV 304
           +AV
Sbjct: 317 VAV 319


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: 283
Number of extensions: 17
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: 333
Length of database: 329
Length adjustment: 28
Effective length of query: 305
Effective length of database: 301
Effective search space:    91805
Effective search space used:    91805
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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