GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc02869 in Synechococcus elongatus PCC 7942

Align N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized)
to candidate Synpcc7942_0960 Synpcc7942_0960 ATPase

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



>FitnessBrowser__SynE:Synpcc7942_0960
          Length = 417

 Score =  270 bits (691), Expect = 4e-77
 Identities = 163/371 (43%), Positives = 216/371 (58%), Gaps = 51/371 (13%)

Query: 30  GSHEVLKGIDLDVKDGEFVIFVGPSGCGKSTLLRTIAGLEDATSGSVQIDGVEVGHVAPA 89
           G   VL GI+L++ DGEF++ VGPSGCGKSTLLR +AGLE  + G +++    V  +   
Sbjct: 45  GEVVVLNGINLEIADGEFMVVVGPSGCGKSTLLRLLAGLETPSRGLIKVGDRRVDRLPAK 104

Query: 90  KRGIAMVFQSYALYPHLTVKDNMGLGLKQAG---------------VPK---------AE 125
            R IAMVFQSYALYPHL+V DN+  GL++ G               +PK         A 
Sbjct: 105 ARDIAMVFQSYALYPHLSVYDNLAFGLRRQGDRPWWQQQLALATRSLPKSLQYEPEQEAR 164

Query: 126 IEEKVAKAAGMLSLEPYLARRPAELSGGQRQRVAIGRAIVREPKLFLFDEPLSNLDAALR 185
           I+ +V + A ML L+  L R+P +LSGGQ+QRVA+GRAI R P++FL DEPLSNLDA LR
Sbjct: 165 IKRRVREVATMLQLDTLLDRQPKQLSGGQKQRVALGRAIARNPQVFLMDEPLSNLDAKLR 224

Query: 186 VNTRLEIARLHRSLKATMIYVTHDQVEAMTLADKIVVLNAGRIEQVGSPMELYNRPANLF 245
             TR +I  L R L  T +YVTHDQ EAMT+ D+I VLN G ++QV SP+E+Y+RPAN F
Sbjct: 225 AETRAQIVSLQRQLGVTTLYVTHDQTEAMTMGDRIAVLNRGHLQQVASPLEIYDRPANRF 284

Query: 246 VAGFIGSPQMNFIEAA------------------------KLGDGEAKTIGIRPEHIGL- 280
           VA FIGSP MN I                           +L DG+   +GIRPEH+ + 
Sbjct: 285 VAQFIGSPPMNLIPVTVRAPLQLTTENFRCTLPEAWEPVLRLYDGQTVELGIRPEHLEVG 344

Query: 281 SRESGDWKGKVIHVEHLGADTIIYIESETVGL-LTVRLFGEHRYATDDIVHATPVIGSMH 339
           +  S +    V  VE LG+DT I  E +  G+ +  RL  +  +   D +  T     +H
Sbjct: 345 AAASKNLLITVTGVEALGSDTFIAGELKESGIAVQARLAPQQCWQMGDRLWLTFKPDQIH 404

Query: 340 RFDAD-GRVIK 349
            FD + G+ I+
Sbjct: 405 LFDLETGKAIR 415


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: 357
Number of extensions: 11
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: 352
Length of database: 417
Length adjustment: 30
Effective length of query: 322
Effective length of database: 387
Effective search space:   124614
Effective search space used:   124614
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: 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