GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcC in Pseudomonas fluorescens GW456-L13

Align Ribose ABC transport system, permease protein RbsC (characterized, see rationale)
to candidate PfGW456L13_2122 L-arabinose transport system permease protein (TC 3.A.1.2.2)

Query= uniprot:A0A0C4Y7K0
         (337 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2122
          Length = 323

 Score =  175 bits (444), Expect = 1e-48
 Identities = 97/298 (32%), Positives = 165/298 (55%), Gaps = 1/298 (0%)

Query: 35  MLPVLVLLCIGFSVLTENFAGWQNLSIIAQQASINMVLAAGMTFVILTGGIDLSVGSILS 94
           ML   V + +  ++L +NF    N+  +    S   + A  M + + +G  DLSVGS+++
Sbjct: 27  MLLAAVGIFVACTLLIDNFLSPLNMRGLGLAISTTGIAACTMLYCLASGHFDLSVGSVIA 86

Query: 95  ISAVVAMLVSLMPQLGMLSVPAALLCGLLFGIVNGALVAFMKLPPFIVTLGTLTAVRGLA 154
            + VVA +V        L V AAL+ GL+ G++NG ++A +++   I TL T+  VRGLA
Sbjct: 87  CAGVVAAVVMRDTNSVFLGVCAALVMGLIVGLINGIVIAKLRVNALITTLATMQIVRGLA 146

Query: 155 RLVGNDSTIYNPDIGFAFIGNGEVLGVPWLVIIAFAVVAVSWFVLRRTVLGLQIYAVGGN 214
            +  N   +      F   GNG++ GVP  ++I         ++L  T  G    A+GGN
Sbjct: 147 YIFANGKAVGVSQESFFVFGNGQMFGVPVPILITIVCFLFFGWLLNYTTYGRNTMAIGGN 206

Query: 215 AEAARLSGIKVWVVLLFVYAVSGLLAGLGGVMSSARLYAANGLQLGQSYELDAIAAVILG 274
            EAA L+G+ V    + ++AV G++  L GV+ ++R+ +   + +GQ +EL  I+A +LG
Sbjct: 207 QEAALLAGVNVDRTKIIIFAVHGVIGALAGVILASRMTSGQPM-IGQGFELTVISACVLG 265

Query: 275 GTSFVGGTGSIVGTLVGALIIAVLSNGLVLLGVSDIWQYIIKGLVIIGAVALDSYRRK 332
           G S  GG G I   + G LI+A++ N + L  +   +QY+I+G +++ AV +D  +++
Sbjct: 266 GVSLSGGIGMIRHVIAGVLILAIIENAMNLKNIDTFYQYVIRGSILLLAVVIDRLKQR 323


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: 297
Number of extensions: 23
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: 337
Length of database: 323
Length adjustment: 28
Effective length of query: 309
Effective length of database: 295
Effective search space:    91155
Effective search space used:    91155
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