GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS16925 in Pseudomonas fluorescens FW300-N2E2

Align Arabinose ABC transporter permease (characterized, see rationale)
to candidate Pf6N2E2_992 Ribose ABC transport system, permease protein RbsC (TC 3.A.1.2.1)

Query= uniprot:A0A161GM94
         (322 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_992
          Length = 342

 Score =  140 bits (354), Expect = 3e-38
 Identities = 95/294 (32%), Positives = 152/294 (51%), Gaps = 21/294 (7%)

Query: 39  LMIDNFLSPLNMRGLGLAISTTGIAACTMLYCLASGH-FDLSVGSVIACAGVVAAVVMRD 97
           L +DNFL+P N+  +  ++S  GIAA  M +   SG+ F LS+ +  A + +V A     
Sbjct: 56  LSVDNFLTPANLNAIMYSVSAIGIAAVGMAFITLSGNLFMLSMAATAALSTIVFA----- 110

Query: 98  TNSVFLGISAAL----VMGLIVGLINGIVIAKLRVNALITTLATMQIVRGL-AYIFANGK 152
            +++  G+  AL    V+G+ +G I G+V+   RVN +I T+A   IV G+ +Y+     
Sbjct: 111 -STLHFGLPVALLSVSVLGIAIGSIQGVVVGTARVNPIIATIAVASIVMGVGSYVSGGMT 169

Query: 153 AVGVSQESFFVFGNGQMFGVPVPILITIVCFLFFGWLLNY----TTYGRNTMAIGGNQEA 208
            VG    S+   G    F   VP  + I  FL F    NY    T +GR    IG N   
Sbjct: 170 VVGKGDASWLGIGK---FASLVPNQLVI--FLAFSLAANYWVERTRFGRELRLIGLNPVT 224

Query: 209 ALLAGVNVDRTKIIIFAVHGVIGALAGVILASRMTSGQPMIGQGFELTVISACVLGGVSL 268
           A  +G+ V RT +I F + G   ALAG + AS+   G   +  G +   I+A ++ G+S+
Sbjct: 225 AAYSGIRVPRTLVIAFVIAGFSAALAGGLFASQAGQGNLKLAAGLDFDAIAAVLVAGISI 284

Query: 269 SGGIGMIRHVIAGVLILAIIENAMNLKNIDTFYQYVIRGSILLLAVVIDRLKQR 322
            GG G I   + G + LA+I N + +  +    Q +++G++++LAV++  L  R
Sbjct: 285 RGGQGKIIDAVYGAIFLALIGNLLLVHGLSFEIQLMVKGAVVVLAVILAALIAR 338


Lambda     K      H
   0.330    0.144    0.420 

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: 266
Number of extensions: 11
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: 322
Length of database: 342
Length adjustment: 28
Effective length of query: 294
Effective length of database: 314
Effective search space:    92316
Effective search space used:    92316
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 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