GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21106 in Phaeobacter inhibens BS107

Align ABC transporter for L-Fucose, ATPase component (characterized)
to candidate GFF262 PGA1_c02740 sn-glycerol-3-phosphate import ATP-binding protein UgbC

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



>FitnessBrowser__Phaeo:GFF262
          Length = 348

 Score =  323 bits (828), Expect = 4e-93
 Identities = 177/363 (48%), Positives = 238/363 (65%), Gaps = 19/363 (5%)

Query: 1   MAPVTLKKLVKRY-GALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGA 59
           MA VTL  + K Y   +E V     +++D EF+ LVGPSGCGKST LRMIAGLE+++ G 
Sbjct: 1   MAQVTLNSVRKVYPNGVEAVTSSSFKIEDGEFVVLVGPSGCGKSTLLRMIAGLEDITEGT 60

Query: 60  IEIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAA 119
           +EIG R VN++ P  R+I+MVFQ+YALYPHMTV +N+ + LK    P  EIK +VAEAA 
Sbjct: 61  LEIGDRVVNNVDPADRDIAMVFQNYALYPHMTVRKNIAYGLKNRKTPEAEIKQKVAEAAK 120

Query: 120 ILDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKL 179
           +L+L   L+R+PSQLSGGQRQRVAMGRAIVR P +FLFDEPLSNLDAKLR Q+R EIK L
Sbjct: 121 MLNLEEYLDRKPSQLSGGQRQRVAMGRAIVRDPALFLFDEPLSNLDAKLRNQMRIEIKAL 180

Query: 180 HARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPM 239
             R+  T IYVTHDQVEAMT++DRI+++  G IEQ+GTP +++  PA+ FVA F+G+PPM
Sbjct: 181 QRRLGVTSIYVTHDQVEAMTMADRIIVLNGGRIEQIGTPSEIYHNPASVFVASFMGAPPM 240

Query: 240 NMEEAVLTDGKLAFASGATLPLPPRFRSLVREGQ-KVTFGLRPDDVYPSGHGLHAGDADA 298
           N+ +A + +G++    G ++       +L    Q  V  G+RP+DV     G        
Sbjct: 241 NLLDATIANGQVTLPDGVSM------GALDTSAQGAVKLGIRPEDVQLVAEG-------- 286

Query: 299 VHEIELPVTITEPLGNETLVFTQFNGRDWVSRMLNPRPLRPGEAVPMSFDLARAHLFDGE 358
              + + V + E LG   L+  +  G+ +   +L   P+ PG    +S D A   LFD E
Sbjct: 287 --GLAIDVELIEELGAHRLLHGKLGGQPFTIHVLKDIPVDPG-THQISVDPAAICLFDAE 343

Query: 359 TGR 361
           +G+
Sbjct: 344 SGQ 346


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: 355
Number of extensions: 9
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: 348
Length adjustment: 29
Effective length of query: 336
Effective length of database: 319
Effective search space:   107184
Effective search space used:   107184
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