GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK in Pseudomonas fluorescens FW300-N2E2

Align ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized)
to candidate Pf6N2E2_1649 Maltose/maltodextrin transport ATP-binding protein MalK (EC 3.6.3.19)

Query= reanno::Smeli:SMc03065
         (362 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1649
          Length = 384

 Score =  335 bits (860), Expect = 9e-97
 Identities = 184/362 (50%), Positives = 240/362 (66%), Gaps = 8/362 (2%)

Query: 4   LLLKDIRKSYGAVDVIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITGGDMFID 63
           L L ++ K  G   ++  + L+I  GEFVVFVGPSGCGKSTLLR+IAGL+ I  GD+ ID
Sbjct: 4   LKLDNVNKQLGGARILRDVSLEISAGEFVVFVGPSGCGKSTLLRLIAGLDSICDGDLLID 63

Query: 64  GERVNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGAADMLQL 123
           G RVND+ P +RG+ MVFQSYALYPHM+VYDN++FG+++A+  K  +  RV   A +LQL
Sbjct: 64  GRRVNDLEPRERGVGMVFQSYALYPHMSVYDNISFGLKLAKTEKASLRERVLKTAQILQL 123

Query: 124 TPYLDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIAKLSERM 183
              L R P+ LSGGQRQRVA+GRA+ R P + LFDEPLSNLDA+LRV  R EIA+L  R+
Sbjct: 124 DKLLQRKPRELSGGQRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLHGRL 183

Query: 184 SDTTMIYVTHDQVEAMTLADRIVVLSAGHIEQVGAPLELYERPANLFVARFIGSPAMNVI 243
             +TMIYVTHDQVEAMTLAD+IVVL+ G IEQVG+P ELYE PA+ FVA F+GSP MN +
Sbjct: 184 G-STMIYVTHDQVEAMTLADKIVVLNGGRIEQVGSPRELYEHPASRFVAGFLGSPKMNFL 242

Query: 244 PATITATGQQTAVS--LAGGKSVTLDVPTNASENGKTASFGVRPEDLRVTEADDFLFEGT 301
           PA + + G+ + +   L G   +  D    A   G   + G+RPE + +  A      G 
Sbjct: 243 PARLHSPGETSQIDSPLLGMTPLPFDSAHLAV--GSPLTLGIRPEHMSLKAAQGSAGVGV 300

Query: 302 VSI--VEALGEVTLLYIEGLVENEPIIAKMPGIARVGRGDKVRFTADKAKLHLFDTNGQS 359
           V +  VE LG  T +++E   E+EP+I +    A    GD+V        +HLFD +G +
Sbjct: 301 VGVVGVEYLGSETYVHLES-GEDEPLICRCEVNAGWRVGDRVELQLAFGSVHLFDADGTA 359

Query: 360 YR 361
            R
Sbjct: 360 LR 361


Lambda     K      H
   0.320    0.137    0.387 

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: 382
Number of extensions: 18
Number of successful extensions: 5
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: 362
Length of database: 384
Length adjustment: 30
Effective length of query: 332
Effective length of database: 354
Effective search space:   117528
Effective search space used:   117528
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: 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