GapMind for catabolism of small carbon sources

 

Alignments for a candidate for musK in Synechococcus elongatus PCC 7942

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate Synpcc7942_0960 Synpcc7942_0960 ATPase

Query= BRENDA::Q8NMV1
         (376 letters)



>FitnessBrowser__SynE:Synpcc7942_0960
          Length = 417

 Score =  310 bits (793), Expect = 6e-89
 Identities = 180/364 (49%), Positives = 230/364 (63%), Gaps = 51/364 (14%)

Query: 1   MATVTFKDASLSYPG-AKEP------TVKKFNLEIADGEFLVLVGPSGCGKSTTLRMLAG 53
           +A V F++    +P  A+ P       +   NLEIADGEF+V+VGPSGCGKST LR+LAG
Sbjct: 23  VAGVVFEEIEKRFPEQARSPQKGEVVVLNGINLEIADGEFMVVVGPSGCGKSTLLRLLAG 82

Query: 54  LENVTDGAIFIGDKDVTHVAPRDRDIAMVFQNYALYPHMTVGENMGFALKIAG------- 106
           LE  + G I +GD+ V  +  + RDIAMVFQ+YALYPH++V +N+ F L+  G       
Sbjct: 83  LETPSRGLIKVGDRRVDRLPAKARDIAMVFQSYALYPHLSVYDNLAFGLRRQGDRPWWQQ 142

Query: 107 -----------------KSQDEINKRVDEAAATLGLTEFLERKPKALSGGQRQRVAMGRA 149
                            + +  I +RV E A  L L   L+R+PK LSGGQ+QRVA+GRA
Sbjct: 143 QLALATRSLPKSLQYEPEQEARIKRRVREVATMLQLDTLLDRQPKQLSGGQKQRVALGRA 202

Query: 150 IVRNPQVFLMDEPLSNLDAKLRVQTRTQIAALQRKLGVTTVYVTHDQTEALTMGDRIAVL 209
           I RNPQVFLMDEPLSNLDAKLR +TR QI +LQR+LGVTT+YVTHDQTEA+TMGDRIAVL
Sbjct: 203 IARNPQVFLMDEPLSNLDAKLRAETRAQIVSLQRQLGVTTLYVTHDQTEAMTMGDRIAVL 262

Query: 210 KDGYLQQVGAPRELYDRPANVFVAGFIGSPAMNLGTFSVKDGDATSGHARIKLSPETLAA 269
             G+LQQV +P E+YDRPAN FVA FIGSP MNL   +V+        A ++L+ E    
Sbjct: 263 NRGHLQQVASPLEIYDRPANRFVAQFIGSPPMNLIPVTVR--------APLQLTTENFRC 314

Query: 270 MTPE---------DNGRITIGFRPEALEIIPEGESTDLSIPIKLDFVEELGSDSFLYGKL 320
             PE         D   + +G RPE LE+   G +   ++ I +  VE LGSD+F+ G+L
Sbjct: 315 TLPEAWEPVLRLYDGQTVELGIRPEHLEV---GAAASKNLLITVTGVEALGSDTFIAGEL 371

Query: 321 VGEG 324
              G
Sbjct: 372 KESG 375


Lambda     K      H
   0.316    0.135    0.380 

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: 424
Number of extensions: 14
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: 376
Length of database: 417
Length adjustment: 31
Effective length of query: 345
Effective length of database: 386
Effective search space:   133170
Effective search space used:   133170
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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