GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PA5503 in Pseudomonas fluorescens GW456-L13

Align Methionine import ATP-binding protein MetN 2, component of L-Histidine uptake porter, MetIQN (characterized)
to candidate PfGW456L13_453 Methionine ABC transporter ATP-binding protein

Query= TCDB::Q9HT70
         (335 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_453
          Length = 373

 Score =  277 bits (709), Expect = 3e-79
 Identities = 156/323 (48%), Positives = 205/323 (63%), Gaps = 6/323 (1%)

Query: 2   IEFHDVHKTYRVAGREIPALQPTRLNIQAGQIFGLIGHSGAGKSTLLRLINRLEEPSGGR 61
           + F  + KTY      + AL    L IQ G++FG+IG SGAGKS+L+R INRLE+PS GR
Sbjct: 31  VRFIGLGKTYNGQQGPVAALHGIDLAIQRGEVFGIIGRSGAGKSSLIRTINRLEQPSSGR 90

Query: 62  ILVEGEDVTALDAEGLRRFRQRVGMIFQHFNLLSSKTVADNIAMPLRLAGGFSRAEVDAR 121
           +L++  D+   D + L   R+R+GMIFQHFNL+S+KTV  N+ +PL++AG   + + + +
Sbjct: 91  VLIDQVDIGEFDEDRLVALRRRIGMIFQHFNLMSAKTVWQNVELPLKVAG-VPKEQRERK 149

Query: 122 VSELLARVGLSDHARKYPAQLSGGQKQRVGIARALACRPSILLCDEATSALDPQTTASVL 181
           V ELL  VGL    + YPAQLSGGQKQRVGIARAL   P ILLCDEATSALDP+TT S+L
Sbjct: 150 VRELLELVGLQAKHKAYPAQLSGGQKQRVGIARALVHDPQILLCDEATSALDPETTQSIL 209

Query: 182 QLLAEINRELKLTIVLITHEMDVIRRVCDQVAVMDGGAIVEQGDVADVFLHPQHPTTRRF 241
            LL EIN+ L LTIVLITHEM VIR +CD+V V++ G IVEQG V +VF +PQH  ++  
Sbjct: 210 GLLREINQRLGLTIVLITHEMAVIREICDRVVVLEHGRIVEQGPVWEVFGNPQHEVSKTL 269

Query: 242 VFEAERVDEDERH-----DDFAHVPGLILRLTFRGEATYAPLLGTVARQTGVDYSILSGR 296
           +   +     E          A    ++LRL F G     P L  +    G    +L G 
Sbjct: 270 LAPLQHALPQELQSRLLAQSSACDAAVVLRLQFTGSQRDEPDLAALFSALGGRVRLLQGG 329

Query: 297 IDRIKDTPYGQLTLALVGGDLEA 319
           ++RI+    GQL LA+ G  L+A
Sbjct: 330 VERIQGHALGQLLLAVTGSSLDA 352


Lambda     K      H
   0.322    0.138    0.393 

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: 359
Number of extensions: 16
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: 335
Length of database: 373
Length adjustment: 29
Effective length of query: 306
Effective length of database: 344
Effective search space:   105264
Effective search space used:   105264
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 (21.9 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