GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01112 in Pseudomonas simiae WCS417

Align deoxynucleoside transporter, permease component 2 (characterized)
to candidate GFF3462 PS417_17725 ribose ABC transporter permease

Query= reanno::Burk376:H281DRAFT_01112
         (364 letters)



>FitnessBrowser__WCS417:GFF3462
          Length = 330

 Score =  150 bits (380), Expect = 4e-41
 Identities = 104/310 (33%), Positives = 155/310 (50%), Gaps = 13/310 (4%)

Query: 45  RLARNPEWFTVALIVVTCLIVGAINPRFFQFATLFDLLHSATTMSLFALGTLVVLASGGI 104
           RL R+P ++    +VV  L++   +  F   + L ++    +  ++ A+G   V+ +GGI
Sbjct: 25  RLVRSPAFYPFVGLVVVTLVMILASDTFLTASNLSNIARQVSINAIIAVGMTCVILTGGI 84

Query: 105 DVSFTAIAALTMYGITKAVFAWWPDAPFALILVTGALGGVVLGMVNGLLVHRLKAPSLIV 164
           D+S   + AL+       + A  P     L +  G L GV  G+ NGL V  L  P +IV
Sbjct: 85  DLSVGPVMALSGTLTAGLMVAGLPPG---LAIGAGMLIGVAFGIGNGLFVAYLHMPPIIV 141

Query: 165 TIGTQYLYRGLLLTFIGTTFFMNIPHSMDRFGRIPLFFYHTADGLRAVLPVSVLALVAAA 224
           T+ T  + RGL L +        +P     FGR  LF           + V +L ++   
Sbjct: 142 TLATMGIARGLGLMYTDGYPISGLPDWFAFFGRESLFG----------IQVPILIMLLTY 191

Query: 225 VVTWWLLNRTMMGRAVYAMGGSLAIAERLGYNLRAIHLFVFGYTGMLAGIAGILHVSNNR 284
           +V + LL  T +GR +YA+GG+       G       L V+G +G+ A IAG++  S   
Sbjct: 192 LVAYVLLQHTRIGRYIYAIGGNEEAVRLSGVRAARFKLLVYGISGLTAAIAGLVLTSRLM 251

Query: 285 LANPFDLVGSELDVIAAVILGGARITGGTGTVVGTLLGVVLVTLIKSVLILVGVPSTWQK 344
              P   V  ELD IAAV+LGGA I GG G +VGTLLG +L+ ++ + L ++GV    Q 
Sbjct: 252 SGQPNAGVSFELDAIAAVVLGGASIAGGRGVIVGTLLGAMLLGVLNNGLNMLGVSPYVQS 311

Query: 345 VIIGAFILLA 354
           VI G  ILLA
Sbjct: 312 VIKGGIILLA 321


Lambda     K      H
   0.328    0.141    0.426 

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: 285
Number of extensions: 13
Number of successful extensions: 3
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: 364
Length of database: 330
Length adjustment: 29
Effective length of query: 335
Effective length of database: 301
Effective search space:   100835
Effective search space used:   100835
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 (21.7 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