GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11895 in Cupriavidus basilensis 4G11

Align Inositol transport system permease protein (characterized)
to candidate RR42_RS03365 RR42_RS03365 ribose ABC transporter permease

Query= reanno::WCS417:GFF2333
         (340 letters)



>FitnessBrowser__Cup4G11:RR42_RS03365
          Length = 333

 Score =  211 bits (537), Expect = 2e-59
 Identities = 141/331 (42%), Positives = 195/331 (58%), Gaps = 33/331 (9%)

Query: 14  TKSRRRLPTELSIFLVL-IGIGLVFELF-GWIVRDQSFLMNSQRLVLMILQVSIIGLLAI 71
           T+ R R    L + ++L IG  ++ E F GW           Q L ++  Q SI  +LA 
Sbjct: 22  TQERLRALGMLPVLVLLCIGFSVLTENFAGW-----------QNLSIIAQQASINMVLAA 70

Query: 72  GVTQVIITTGIDLSSGSVLALSAMIAASLAQTSDFSRAVFPSLTDLPVWIPVAMGLGVGL 131
           G+T VI+T GIDLS GS+L++SA++A  ++        + P L  L V  P A  L  GL
Sbjct: 71  GMTFVILTGGIDLSVGSILSISAVVAMLVS--------LMPQLGMLSV--PAA--LLCGL 118

Query: 132 LAGAINGSIIAVTGIPPFIATLGMMVSARGLARYYTEGQPVSMLSDSYTAIGHGA----- 186
           L G +NG+++A   +PPFI TLG + + RGLAR       +      +  IG+G      
Sbjct: 119 LFGIVNGALVAFMKLPPFIVTLGTLTAVRGLARLVGNDSTIYNPDIGFAFIGNGEVLGVP 178

Query: 187 -MPVIIFLVVAVIFHIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLIIVYSIAGLLAG 245
            + +I F VVAV + + LR T  G   YA+GGN +AAR SGI V   L+ VY+++GLLAG
Sbjct: 179 WLVIIAFAVVAVSWFV-LRRTVLGLQIYAVGGNAEAARLSGIKVWVVLLFVYAVSGLLAG 237

Query: 246 LAGVVASARA-ATGQAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGALILGVMASG 304
           L GV++SAR  A     +G SYELDAIAA ++GGTS  GG G I GT++GALI+ V+++G
Sbjct: 238 LGGVMSSARLYAANGLQLGQSYELDAIAAVILGGTSFVGGTGSIVGTLVGALIIAVLSNG 297

Query: 305 FTFVGVDAYIQDIIKGLIIVVAVVIDQYRNK 335
              +GV    Q IIKGL+I+ AV +D YR K
Sbjct: 298 LVLLGVSDIWQYIIKGLVIIGAVALDSYRRK 328


Lambda     K      H
   0.325    0.140    0.394 

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: 291
Number of extensions: 16
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: 340
Length of database: 333
Length adjustment: 28
Effective length of query: 312
Effective length of database: 305
Effective search space:    95160
Effective search space used:    95160
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