GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS03645 in Acidovorax sp. GW101-3H11

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate Ac3H11_2880 Ribose ABC transport system, permease protein RbsC (TC 3.A.1.2.1)

Query= uniprot:D8IZC8
         (344 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2880
          Length = 350

 Score =  172 bits (436), Expect = 1e-47
 Identities = 114/326 (34%), Positives = 174/326 (53%), Gaps = 20/326 (6%)

Query: 17  ARRSSSTTAQW-LLHRLGMLPVLVVLYLLFYGLTLYLSGDGTSNFASAENTMNILRQVAI 75
           A  ++  +A W  LH LG  PV+ ++ L   G  L       SNFA+ +N MN+L + A 
Sbjct: 25  AAAATGASAWWGKLHGLG--PVIGLVLLCIAGTLL------NSNFATYDNVMNVLTRTAF 76

Query: 76  NLVLAAGMTFVILTAGIDLSVGSVLAVSAVLGMQVSLGAAPGWAIPMF---------IFS 126
             ++A GM FVI++ GIDLSVGS+ A+ A   +      AP    PM          +  
Sbjct: 77  IGIIAVGMCFVIISGGIDLSVGSMAALIAGSVILFMNAMAPVLGSPMAAVVVGMLLAVVL 136

Query: 127 GLVMGMVNGAMVALLNINAFVVTLGTMTAFRG-AAYLLADGTTVLNNDIPS-FEWIGNGD 184
           G V G+V+G ++    I  F+VTLGT+  FR    Y    G   L ND+   +  +   +
Sbjct: 137 GAVFGLVHGLLITKGRIEPFIVTLGTLGIFRAYLTYFSNGGAITLENDLSDIYSPVYYAN 196

Query: 185 FLHVPWLIWVAVAVVLLSWVILRKTVLGMHIYAIGGNLQAARLTGIRVGLVLLFVYSISG 244
            L VP  +W+ + V ++  VIL +T  G ++ AIG N Q A+   + V  + +  Y + G
Sbjct: 197 LLGVPIPVWIFLLVAIVGGVILNRTAYGRYVQAIGSNEQVAQYAAVDVHKIKILTYMLLG 256

Query: 245 LFSGLAGAMSASRLYGANGNWGSGYELDAIAAVVLGGTSLMGGVGSIWGTVVGALIIGVM 304
           +  G+A  +   RL  A+   G  +EL+AIAAV++GGT L GG GSI GTVVGA+++ V+
Sbjct: 257 VCVGIATLLYVPRLGSASPTTGLLWELEAIAAVIVGGTVLKGGAGSITGTVVGAILLSVI 316

Query: 305 NNGLTILGLSSFWQYVAKGAVIVLAV 330
           +N L +  + S +   A    +++AV
Sbjct: 317 SNILNLTSIISVYLNAAVQGFVIIAV 342


Lambda     K      H
   0.324    0.138    0.417 

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: 363
Number of extensions: 29
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: 344
Length of database: 350
Length adjustment: 29
Effective length of query: 315
Effective length of database: 321
Effective search space:   101115
Effective search space used:   101115
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