GapMind for catabolism of small carbon sources

 

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

Align Ribose ABC transport system, permease protein RbsC (characterized, see rationale)
to candidate AO356_23210 AO356_23210 ABC transporter

Query= uniprot:A0A0C4Y7K0
         (337 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_23210
          Length = 340

 Score =  212 bits (540), Expect = 1e-59
 Identities = 140/331 (42%), Positives = 194/331 (58%), Gaps = 33/331 (9%)

Query: 26  TQERLRALGMLPVLVLLCIGFSVLTENFAGW-----------QNLSIIAQQASINMVLAA 74
           T+ R R    L + ++L IG  ++ E F GW           Q L ++  Q SI  +LA 
Sbjct: 14  TRSRRRLPTELSIFLVL-IGIGLVFEMF-GWIMRDQSFLMNSQRLVLMILQVSIIGLLAI 71

Query: 75  GMTFVILTGGIDLSVGSILSISAVVAMLVS--------LMPQLGMLSV----PAALLCGL 122
           G+T VI+T GIDLS GS+L++SA++A  ++        + P L  L V     A L  GL
Sbjct: 72  GVTQVIITTGIDLSSGSVLALSAMIAASLAQTSDFARAVFPSLTDLPVWIPVVAGLGVGL 131

Query: 123 LFGIVNGALVAFMKLPPFIVTLGTLTAVRGLARLVGNDSTIYNPDIGFAFIGNGEVLGVP 182
           L G +NG+++A   +PPFI TLG + + RGLAR       +      +  IG+G      
Sbjct: 132 LAGAINGSIIAITGIPPFIATLGMMVSARGLARYYTEGQPVSMLSDSYTAIGHGA----- 186

Query: 183 WLVIIAFAVVAVSWFV-LRRTVLGLQIYAVGGNAEAARLSGIKVWVVLLFVYAVSGLLAG 241
            + +I F VVAV + + LR T  G   YA+GGN +AAR SGI V   L+ VY+++GLLAG
Sbjct: 187 -MPVIIFLVVAVIFHIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLVIVYSIAGLLAG 245

Query: 242 LGGVMSSARLYAANGLQLGQSYELDAIAAVILGGTSFVGGTGSIVGTLVGALIIAVLSNG 301
           L GV++SAR  A     +G SYELDAIAA ++GGTS  GG G I GT++GALI+ V+++G
Sbjct: 246 LAGVVASARA-ATGQAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGALILGVMASG 304

Query: 302 LVLLGVSDIWQYIIKGLVIIGAVALDSYRRK 332
              +GV    Q IIKGL+I+ AV +D YR K
Sbjct: 305 FTFVGVDAYIQDIIKGLIIVVAVVIDQYRNK 335


Lambda     K      H
   0.325    0.141    0.409 

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: 350
Number of extensions: 20
Number of successful extensions: 4
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: 337
Length of database: 340
Length adjustment: 28
Effective length of query: 309
Effective length of database: 312
Effective search space:    96408
Effective search space used:    96408
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.

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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