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 GFF1645 PGA1_c16680 sugar ABC transporter, ATP-binding protein

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



>FitnessBrowser__Phaeo:GFF1645
          Length = 355

 Score =  327 bits (838), Expect = 3e-94
 Identities = 182/359 (50%), Positives = 238/359 (66%), Gaps = 17/359 (4%)

Query: 1   MAPVTLKKLVKRYGALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGAI 60
           MA + L+ + KRYGA+EV+  I+L+++D EFI LVGPSGCGKST LRMIAGLE ++ G  
Sbjct: 1   MARIELRDVAKRYGAVEVLRDINLDIQDGEFIVLVGPSGCGKSTLLRMIAGLEPITSGDF 60

Query: 61  EIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAAI 120
           EI G+++ND+ PR R+I+MVFQSYALYPHM VA NMGFS++I   PAEE ++RVA AA  
Sbjct: 61  EIDGQRMNDVRPRDRDIAMVFQSYALYPHMDVARNMGFSMEIRKDPAEERRSRVARAAET 120

Query: 121 LDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKLH 180
           L L+ L++R P  LSGGQRQRVAMGRAI+R P  FLFDEPLSNLDA LR ++R EI +LH
Sbjct: 121 LGLSSLVDRLPKALSGGQRQRVAMGRAIIRDPRAFLFDEPLSNLDAALRVEMRLEIARLH 180

Query: 181 ARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPMN 240
            ++ ATMIYVTHDQVEA+TL+DRIV++  G I+QVG+P +++ RPA KFVA FIGSP MN
Sbjct: 181 KQLGATMIYVTHDQVEALTLADRIVVLNGGDIQQVGSPLELYERPANKFVAQFIGSPTMN 240

Query: 241 MEEAVLTDGKLAFASGATLPLPPRFRSLVREGQKVTFGLRPD--DVYPSGHGLHAGDADA 298
           +         +   +G  L L      +      V  G+RP+  DV   G G     AD 
Sbjct: 241 ILPVSGAASGVMATNGMMLTLD----HMHDTAAAVELGIRPEHLDVVEPGEGHLIAVADV 296

Query: 299 VHEIELPVTITEPLGNETLVFTQFNG-RDWVSRMLNPRPLRPGEAVPMSFDLARAHLFD 356
           V          E LG++T ++ + +G    + R     P+R GE + +      AH+FD
Sbjct: 297 V----------ERLGSDTNIYAKVDGLGPLMVRKHGNVPVRSGERLGLRVQAQNAHIFD 345


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: 363
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: 355
Length adjustment: 29
Effective length of query: 336
Effective length of database: 326
Effective search space:   109536
Effective search space used:   109536
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