GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc02869 in Pseudomonas fluorescens FW300-N1B4

Align N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized)
to candidate Pf1N1B4_3974 ABC transporter, ATP-binding protein

Query= reanno::Smeli:SMc02869
         (352 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3974
          Length = 341

 Score =  242 bits (618), Expect = 9e-69
 Identities = 127/305 (41%), Positives = 192/305 (62%), Gaps = 11/305 (3%)

Query: 20  LQLKTIRKAFGSHEVLKGIDLDVKDGEFVIFVGPSGCGKSTLLRTIAGLEDATSGSVQID 79
           +QL+ + K +G  + +   +L V+ GEFV  +GPSGCGK+T L+ IAG  + +SG + +D
Sbjct: 4   VQLENLGKRYGEIDAVVATNLSVEKGEFVSLLGPSGCGKTTTLQMIAGFVEVSSGRIVLD 63

Query: 80  GVEVGHVAPAKRGIAMVFQSYALYPHLTVKDNMGLGLKQAGVPKAEIEEKVAKAAGMLSL 139
           G ++ H  PA RG+ +VFQSYAL+PH+TV+DN+  GL+   VP  E++++V +   ++ L
Sbjct: 64  GRDITHAKPASRGLGVVFQSYALFPHMTVRDNVAFGLRMRKVPNDELQQRVDRVLKLVRL 123

Query: 140 EPYLARRPAELSGGQRQRVAIGRAIVREPKLFLFDEPLSNLDAALRVNTRLEIARLHRSL 199
             +  R P ELSGGQRQRVA+ RA+V EP + L DEPLSNLDA LR   + EI R+ R +
Sbjct: 124 NQHAERYPRELSGGQRQRVALARALVIEPPVLLLDEPLSNLDANLREEMQFEIRRIQREV 183

Query: 200 KATMIYVTHDQVEAMTLADKIVVLNAGRIEQVGSPMELYNRPANLFVAGFIGSPQM---- 255
             T + VTHDQ EA++++D++VV+ AGRI Q+ +P  LY  P   F++GF+G   +    
Sbjct: 184 GITTLMVTHDQSEALSISDRVVVMQAGRITQIDAPYTLYEHPRTEFISGFVGKANLLPGE 243

Query: 256 ----NFIEAAKLGDGEAKTIGIRPEHIGLSRES-GDWKGKVIHVEHLGADTIIYIESETV 310
                 ++     +GE  T+ +RPE I L     G  +GK++    LG+   +Y  S ++
Sbjct: 244 RDSAGVVQVCNRDNGEL-TLSLRPEKIDLRDVGLGRLQGKIVSRFFLGSQW-LYGVSTSL 301

Query: 311 GLLTV 315
           G L+V
Sbjct: 302 GELSV 306


Lambda     K      H
   0.320    0.137    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: 296
Number of extensions: 12
Number of successful extensions: 1
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: 352
Length of database: 341
Length adjustment: 29
Effective length of query: 323
Effective length of database: 312
Effective search space:   100776
Effective search space used:   100776
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: 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