GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK' in Synechococcus elongatus PCC 7942

Align Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale)
to candidate Synpcc7942_0960 Synpcc7942_0960 ATPase

Query= uniprot:A8LLL2
         (373 letters)



>FitnessBrowser__SynE:Synpcc7942_0960
          Length = 417

 Score =  249 bits (636), Expect = 1e-70
 Identities = 159/366 (43%), Positives = 210/366 (57%), Gaps = 29/366 (7%)

Query: 14  GDVKVLSNINLDIQQGELIVFVGPSGCGKSTLLRMIAGLEKITGGTLEIDGTVVNDVPPA 73
           G+V VL+ INL+I  GE +V VGPSGCGKSTLLR++AGLE  + G +++    V+ +P  
Sbjct: 45  GEVVVLNGINLEIADGEFMVVVGPSGCGKSTLLRLLAGLETPSRGLIKVGDRRVDRLPAK 104

Query: 74  QRGIAMVFQSYALYPHMTVRENMSFALK-------------IAKKS-----------QAE 109
            R IAMVFQSYALYPH++V +N++F L+             +A +S           +A 
Sbjct: 105 ARDIAMVFQSYALYPHLSVYDNLAFGLRRQGDRPWWQQQLALATRSLPKSLQYEPEQEAR 164

Query: 110 IDAAVEAAAEKLQLGQYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALR 169
           I   V   A  LQL   LDR PK LSGGQ+QRVA+GR+I R+P+V+L DEPLSNLDA LR
Sbjct: 165 IKRRVREVATMLQLDTLLDRQPKQLSGGQKQRVALGRAIARNPQVFLMDEPLSNLDAKLR 224

Query: 170 VATRLEIAQLKEAMPESTMVYVTHDQVEAMTLATRIVVLAGGGIAQVGSPLELYEKPENE 229
             TR +I  L+  +  +T+ YVTHDQ EAMT+  RI VL  G + QV SPLE+Y++P N 
Sbjct: 225 AETRAQIVSLQRQLGVTTL-YVTHDQTEAMTMGDRIAVLNRGHLQQVASPLEIYDRPANR 283

Query: 230 FVAQFIGSPKMNLLPGKIIGTGAQTTVEMTDGGRAVSDYPSDDSLMGAAVNVGVRPEDM- 288
           FVAQFIGSP MNL+P   +    Q T E        +  P      G  V +G+RPE + 
Sbjct: 284 FVAQFIGSPPMNLIP-VTVRAPLQLTTENFRCTLPEAWEPVLRLYDGQTVELGIRPEHLE 342

Query: 289 VEAAPGGDYVFEGKVAITEALGEVTLLYFEAPSGEDPTIGKLQGIHKDLKGQVTRLTAEP 348
           V AA   + +    V   EALG  T +  E          +L        G    LT +P
Sbjct: 343 VGAAASKNLLI--TVTGVEALGSDTFIAGELKESGIAVQARLAPQQCWQMGDRLWLTFKP 400

Query: 349 AKVHVF 354
            ++H+F
Sbjct: 401 DQIHLF 406


Lambda     K      H
   0.316    0.135    0.379 

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: 423
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: 373
Length of database: 417
Length adjustment: 31
Effective length of query: 342
Effective length of database: 386
Effective search space:   132012
Effective search space used:   132012
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