GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08240 in Azospirillum brasilense Sp245

Align Leucine/isoleucine/valine ABC transporter,permease component (characterized, see rationale)
to candidate AZOBR_RS32410 AZOBR_RS32410 branched-chain amino acid ABC transporter permease

Query= uniprot:G8ALI9
         (505 letters)



>FitnessBrowser__azobra:AZOBR_RS32410
          Length = 355

 Score =  221 bits (562), Expect = 4e-62
 Identities = 135/353 (38%), Positives = 188/353 (53%), Gaps = 40/353 (11%)

Query: 156 VVVALAFPFTPLA-----DRQLLDIGILLLTYIMLGWGLNIVVGLAGLLDLGYVAFYAVG 210
           +++A+AF   P A        L  I I  + +++L   LN V G AGLL +G+ AFY +G
Sbjct: 33  LLLAVAFGAVPAAIVGTGSSYLAQIAITTMIFVILSASLNHVTGTAGLLSIGHAAFYGIG 92

Query: 211 AYSYALLAHYFGFSFWVCLPLAGFLAAMSGVLLGFPVLRLRGDYFAIVTLGFGEIIRIIL 270
           AY+ ALL+   G  F V LP AG +AA+ G L+  P +RL   YFA+ TLG GE+I ++L
Sbjct: 93  AYAAALLSTKLGLPFIVTLPAAGLIAALFGFLVALPTMRLVSIYFAVATLGIGEMIYVVL 152

Query: 271 INWYQFTGGPNGISGIPRPSFFGIADFTRTPAEGTAAFHEMFGLEFSPLHRIIFLYYLIL 330
           +NW   T GP GI GIP    FG    T                       ++  Y  + 
Sbjct: 153 LNWVDVTRGPMGIRGIPPIELFGWQADT-----------------------LLTRYLAVA 189

Query: 331 VLALVVNLFTMRVRKLPLGRAWEALREDDIACASLGINRTNMKLAAFAIAAMFGGFAGSF 390
           V+A+       R+     G A  ALREDD    S+GIN   +K+ +F +A  F G AG+ 
Sbjct: 190 VIAVACVWVLHRLTHSYYGNALRALREDDQCADSMGINVERLKIESFVVATFFAGIAGAL 249

Query: 391 FATRQGFISPESFTFIESAIILAIVVLGGMGSQIGVVVAAFLVIGLPEAFRELADYRMLA 450
            A    +I+P++F F+ES +ILA+VV+GG+GS  G VV A  +I LPEA R++ DYRM+A
Sbjct: 250 LAHTSAYIAPDNFRFMESILILAMVVVGGLGSLPGAVVGALFMIVLPEALRDIGDYRMIA 309

Query: 451 FGMGMVLIMLWRPRGLLAHRDPTILLHGRPKGGAGGPAAGSAAAGGQGIAGGS 503
            G  M L +L  P+G+LA            +G A G    S + G   IAGG+
Sbjct: 310 VGATMFLSILLLPKGMLA------------EGTALGFVRRSFSRGWATIAGGT 350


Lambda     K      H
   0.329    0.144    0.438 

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: 449
Number of extensions: 25
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 505
Length of database: 355
Length adjustment: 32
Effective length of query: 473
Effective length of database: 323
Effective search space:   152779
Effective search space used:   152779
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: 50 (23.9 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