GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Pseudomonas simiae WCS417

Align Trehalose/maltose import ATP-binding protein MalK; EC 7.5.2.1 (characterized)
to candidate GFF5296 PS417_27115 transporter

Query= SwissProt::Q9YGA6
         (372 letters)



>FitnessBrowser__WCS417:GFF5296
          Length = 380

 Score =  241 bits (614), Expect = 3e-68
 Identities = 145/352 (41%), Positives = 210/352 (59%), Gaps = 27/352 (7%)

Query: 4   VRLVDVWKVFGEVTAVREMSLEVKDGEFMILLGPSGCGKTTTLRMIAGLEEPSRGQIYIG 63
           V++  V K F E  AV ++SLE+K GE   LLG SG GK+T LRM+AG E P+ G+IY+ 
Sbjct: 23  VKIDRVTKKFDETIAVDDVSLEIKKGEIFALLGGSGSGKSTLLRMLAGFERPTEGRIYLD 82

Query: 64  DKLVADPEKGIFVPPKDRDIAMVFQSYALYPHMTVYDNIAFPLKLRKVPRQEIDQRVREV 123
            + + D      +PP +R I M+FQSYAL+PHMTV  NIAF L+  K+P+ EID RV E+
Sbjct: 83  GEDITD------MPPYERPINMMFQSYALFPHMTVAQNIAFGLQQDKIPKAEIDARVAEM 136

Query: 124 AELLGLTELLNRKPRELSGGQRQRVALGRAIVRKPQVFLMDEPLSNLDAKLRVRMRAELK 183
            +L+ +++   RKP +LSGGQRQRVAL R++ ++P++ L+DEP+  LD KLR +M+ EL 
Sbjct: 137 LKLVQMSQYAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRSQMQLELV 196

Query: 184 KLQRQLGVTTIYVTHDQVEAMTMGDRIAVMNRGVLQQVGSPDEVYDKPANTFVAGFIGSP 243
           ++  ++GVT + VTHDQ EAMTM +RIA+M+ G + Q+GSP ++Y+ P +  V  FIG+ 
Sbjct: 197 EIIERVGVTCVMVTHDQEEAMTMAERIAIMHLGWIAQIGSPIDIYETPTSRLVCEFIGN- 255

Query: 244 PMNFLDAIVTEDGFVDFGEFRLKLLPDQFEVLGELGYVG---------REVIFGIRPEDL 294
            +N  D  V +D     G   LK  PD    L    YVG         + V + IRPE L
Sbjct: 256 -VNIFDTQVVDDA---EGHAVLK-CPD----LDRDIYVGYGIATSVEDKSVTYAIRPEKL 306

Query: 295 YDAMFAQVRVPGENLVRAVVEIVENLGSERIVHLRVGGVTFVGSFRSESRVR 346
              +  ++     N     V  +  LG   + ++ +     V SF + +  R
Sbjct: 307 --LVTTEMPTCEHNWSSGKVHDIAYLGGHSVFYVELPSGKLVQSFVANAERR 356


Lambda     K      H
   0.323    0.142    0.406 

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: 349
Number of extensions: 10
Number of successful extensions: 2
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: 372
Length of database: 380
Length adjustment: 30
Effective length of query: 342
Effective length of database: 350
Effective search space:   119700
Effective search space used:   119700
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 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