GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21106 in Burkholderia phytofirmans PsJN

Align ABC transporter for L-Fucose, ATPase component (characterized)
to candidate BPHYT_RS05040 BPHYT_RS05040 sugar ABC transporter ATPase

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



>FitnessBrowser__BFirm:BPHYT_RS05040
          Length = 371

 Score =  319 bits (817), Expect = 9e-92
 Identities = 180/378 (47%), Positives = 245/378 (64%), Gaps = 21/378 (5%)

Query: 1   MAPVTLKKLVKRY-GALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGA 59
           MA ++++ + K Y   + V+ G++++++D +F+ LVG SGCGKST L MIAGLE V+ G 
Sbjct: 1   MASLSIRDVYKTYPNGVPVLKGVNIDIEDGQFLILVGGSGCGKSTLLNMIAGLETVTKGE 60

Query: 60  IEIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAA 119
           I+I G+ VN+L P+ R+I+MVFQSYALYP MTV EN+ F L I   P  E    V   + 
Sbjct: 61  IQIDGKTVNNLSPKDRDIAMVFQSYALYPSMTVRENISFGLNIRKVPKNEQTQIVDRVSN 120

Query: 120 ILDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKL 179
            L + HLL+R+P QLSGGQRQRVAMGRA+ R P +FLFDEPLSNLDAKLR ++R+EIK L
Sbjct: 121 TLQITHLLDRKPGQLSGGQRQRVAMGRALARDPVMFLFDEPLSNLDAKLRIEMRSEIKLL 180

Query: 180 HARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPM 239
           H R+  T++YVTHDQ+EAMTL DRI +M+DG ++Q G P++++  P+  FVAGFIG+PPM
Sbjct: 181 HQRLGTTIVYVTHDQIEAMTLGDRIAVMKDGIVQQFGAPQEIYDSPSNLFVAGFIGAPPM 240

Query: 240 NMEEAVLTDGKLAFA-------SGATLPLP---PRFRSLVREGQKVTFGLRPDDVYPSGH 289
           N  +  L +     A       +   L LP    + RS V  G++V  GLRP+ +     
Sbjct: 241 NFIQGKLVEQGAGVALELDTGVARTALNLPFDSAKVRSHV--GREVILGLRPERI-TDAR 297

Query: 290 GLHAGDADAVHEIELPVTITEPLGNETLVFTQFNGRDWVSRM---LNPRPLRPGEAVPMS 346
           G H GD   +  IE+ V + EP G +TLVF Q NG+  VSR+    NP+PL       + 
Sbjct: 298 GAH-GDNAKLQPIEVKVDVIEPTGPDTLVFAQVNGKRIVSRVHPASNPQPL---ANTTLL 353

Query: 347 FDLARAHLFDGETGRALA 364
           FD ++A LFD      +A
Sbjct: 354 FDTSKAVLFDPSNEERIA 371


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: 396
Number of extensions: 19
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: 365
Length of database: 371
Length adjustment: 30
Effective length of query: 335
Effective length of database: 341
Effective search space:   114235
Effective search space used:   114235
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