GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Pseudomonas fluorescens GW456-L13

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate PfGW456L13_2122 L-arabinose transport system permease protein (TC 3.A.1.2.2)

Query= uniprot:B2T9V8
         (351 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2122
          Length = 323

 Score =  152 bits (385), Expect = 9e-42
 Identities = 93/299 (31%), Positives = 157/299 (52%), Gaps = 15/299 (5%)

Query: 47  LALLIVIGAFISPSFLTKANL-ISVLGASAALALVVLAESLIVLTGKFDLSLESTVGIAP 105
           +A  ++I  F+SP  +    L IS  G +A   L  LA      +G FDLS+ S +  A 
Sbjct: 36  VACTLLIDNFLSPLNMRGLGLAISTTGIAACTMLYCLA------SGHFDLSVGSVIACAG 89

Query: 106 AVGAMLVMPAASAGFGMQWPAAAGLLAIVVVGAVIGFINGFLVVRLRLNAFIVTLAMLIV 165
            V A+++    S   G+         A +V+G ++G ING ++ +LR+NA I TLA + +
Sbjct: 90  VVAAVVMRDTNSVFLGV--------CAALVMGLIVGLINGIVIAKLRVNALITTLATMQI 141

Query: 166 LRGMLVGATKGGTLFDMPTSFFALATTIVLGLPLSVWLAAAAFAIAAFMLRYHRLGRALY 225
           +RG+      G  +     SFF      + G+P+ + +    F    ++L Y   GR   
Sbjct: 142 VRGLAYIFANGKAVGVSQESFFVFGNGQMFGVPVPILITIVCFLFFGWLLNYTTYGRNTM 201

Query: 226 AIGGNPEAARAAGIRVERITWGVFVLGSILASVGGLIVTGYVGAINANQGNGMIFTVFAA 285
           AIGGN EAA  AG+ V+R    +F +  ++ ++ G+I+   + +     G G   TV +A
Sbjct: 202 AIGGNQEAALLAGVNVDRTKIIIFAVHGVIGALAGVILASRMTSGQPMIGQGFELTVISA 261

Query: 286 AVIGGISLDGGKGTMFGALTGVLLLGVVQNLLTLAQVPSFWIQAIYGAIILGSLMVARL 344
            V+GG+SL GG G +   + GVL+L +++N + L  + +F+   I G+I+L ++++ RL
Sbjct: 262 CVLGGVSLSGGIGMIRHVIAGVLILAIIENAMNLKNIDTFYQYVIRGSILLLAVVIDRL 320


Lambda     K      H
   0.326    0.140    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: 242
Number of extensions: 7
Number of successful extensions: 2
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: 351
Length of database: 323
Length adjustment: 28
Effective length of query: 323
Effective length of database: 295
Effective search space:    95285
Effective search space used:    95285
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 (21.6 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