GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcC in Dinoroseobacter shibae DFL-12

Align Ribose ABC transport system, permease protein RbsC (characterized, see rationale)
to candidate 3609043 Dshi_2432 Monosaccharide-transporting ATPase (RefSeq)

Query= uniprot:A0A0C4Y7K0
         (337 letters)



>FitnessBrowser__Dino:3609043
          Length = 327

 Score =  174 bits (442), Expect = 2e-48
 Identities = 113/316 (35%), Positives = 179/316 (56%), Gaps = 11/316 (3%)

Query: 24  LTTQERLRALGMLPVLVLLCIGFSVLTENFAGWQNLSIIAQQASINMVLAAGMTFVILTG 83
           + ++E L    +L +L L+   F      F    NL+ +    S  ++LA G   VILT 
Sbjct: 6   IASRETLLIAAILLLLALIASRFPA----FIAPSNLAHVFNDTSPLILLAIGQMIVILTR 61

Query: 84  GIDLSVGSILSISAVVAMLVSLM-PQLGMLSVPA-ALLCGLLFGIVNGALVAFMKLPPFI 141
            IDLSV + L+++ +V  +V++  P L ++ + A A+  G L G+ NG LV  +++PP +
Sbjct: 62  CIDLSVAANLALTGMVVSMVNVAAPGLPIVVILAIAIGLGTLLGMFNGLLVWKLQIPPIV 121

Query: 142 VTLGTLTAVRGLARLVGNDSTIYNPDIGFAF--IGNGEVLGVPWLVIIAFAVVAVSWFVL 199
           VTLGT+T  RG+  L+ +   + + ++  AF      E+LG+P L  IA   V +   V+
Sbjct: 122 VTLGTMTIFRGIIFLISDGKWVNSHEMSPAFKAFPRAELLGLPVLSWIAILAVILFTIVM 181

Query: 200 RRTVLGLQIYAVGGNAEAARLSGIKVWVVLLFVYAVSGLLAGLGGVMSSARLYAANGLQL 259
            RT LG   YA GGN  AA  +GI V     + + +SG LAGL G +  +R +A + + +
Sbjct: 182 TRTTLGRAFYAAGGNPHAATYAGIDVGKTQFWAFTISGALAGLTGYLWVSR-FAVSYVDI 240

Query: 260 GQSYELDAIAAVILGGTSFVGGTGSIVGTLVGALIIAVLSNGLVLLGVSDIWQYIIKGLV 319
              +ELD +AA ++GG S +GG G++ G L+GAL + ++ N L ++ +S  WQ  I G  
Sbjct: 241 AGGFELDVVAACVIGGVSIMGGVGTVGGALLGALFLGIIKNALPVVDISPFWQLAISGGA 300

Query: 320 IIGAVALDSY--RRKG 333
           II AVAL++   R+KG
Sbjct: 301 IIIAVALNAQANRKKG 316


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: 337
Number of extensions: 19
Number of successful extensions: 5
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: 327
Length adjustment: 28
Effective length of query: 309
Effective length of database: 299
Effective search space:    92391
Effective search space used:    92391
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.

Links

Downloads

Related tools

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