GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21106 in Pseudomonas fluorescens FW300-N2C3

Align ABC transporter for L-Fucose, ATPase component (characterized)
to candidate AO356_28585 AO356_28585 ABC transporter

Query= reanno::Smeli:SM_b21106
         (365 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_28585
          Length = 379

 Score =  305 bits (780), Expect = 2e-87
 Identities = 169/356 (47%), Positives = 228/356 (64%), Gaps = 15/356 (4%)

Query: 6   LKKLVKRYGALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGAIEIGGR 65
           L  + K+ G   ++  + LE+   EF+  VGPSGCGKST LR+IAGL+ + GG + I GR
Sbjct: 6   LDNVNKQLGGARILRDVSLEISAGEFVVFVGPSGCGKSTLLRLIAGLDSICGGDLLIDGR 65

Query: 66  KVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAAILDLAH 125
           +VNDL PR R + MVFQSYALYPHM+V +N+ F LK+A      ++ RV + A IL L  
Sbjct: 66  RVNDLEPRERGVGMVFQSYALYPHMSVYDNISFGLKLAKTEKTSLRERVLKTAQILQLDK 125

Query: 126 LLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKLHARMQA 185
           LL+R+P +LSGGQRQRVAMGRA+ R+PD+ LFDEPLSNLDA LR Q+R EI +LH R+ +
Sbjct: 126 LLQRKPRELSGGQRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLHGRLGS 185

Query: 186 TMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPMNMEEAV 245
           TMIYVTHDQVEAMTL+D+IV++  G IEQVG+P +++ RPA++FVAGF+GSP MN   A 
Sbjct: 186 TMIYVTHDQVEAMTLADKIVVLNGGRIEQVGSPRELYERPASRFVAGFLGSPRMNFLAAF 245

Query: 246 L-TDGKLAFASGATLPLP--PRFRSLVREGQKVTFGLRPDDVYPSGHGLHAGDADAVHEI 302
           L T G+ +      L +   P   S +    +++ G+RP+ +      L A    A    
Sbjct: 246 LHTPGETSQVESLVLGMTSLPFDSSGLAANTQLSLGIRPEHI-----ALKAAQGTA---- 296

Query: 303 ELPVTITEPLGNETLVFTQFNGRD--WVSRMLNPRPLRPGEAVPMSFDLARAHLFD 356
            + V+  E LG+ET V     G+D   V R       R G+ V +  D+   H+FD
Sbjct: 297 GIAVSGVEYLGSETYVHLD-TGQDDPMVCRCEVNAGWRVGDRVELQLDIDNLHVFD 351


Lambda     K      H
   0.320    0.137    0.397 

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: 384
Number of extensions: 13
Number of successful extensions: 1
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: 365
Length of database: 379
Length adjustment: 30
Effective length of query: 335
Effective length of database: 349
Effective search space:   116915
Effective search space used:   116915
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (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.

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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