GapMind for catabolism of small carbon sources

 

Alignments for a candidate for msiK in Actinomyces timonensis 7400942

Align MsiK protein, component of The cellobiose/cellotriose (and possibly higher cellooligosaccharides), CebEFGMsiK [MsiK functions to energize several ABC transporters including those for maltose/maltotriose and trehalose] (characterized)
to candidate WP_017177725.1 A1QA_RS0104460 ABC transporter ATP-binding protein

Query= TCDB::P96483
         (377 letters)



>NCBI__GCF_000295095.1:WP_017177725.1
          Length = 372

 Score =  164 bits (415), Expect = 4e-45
 Identities = 125/358 (34%), Positives = 176/358 (49%), Gaps = 35/358 (9%)

Query: 4   VTFDKATRIYPGSDKP----AVDQLDIAIEDGEFLVLVGPSGCGKSTSLRMLAGLEDVNG 59
           +T D    +YPG        AVD +D+ I  G  + L+G SG GKS+ LR +AGLE V  
Sbjct: 5   LTIDGLRVVYPGGRGAGPVVAVDGVDLEIPAGRIVALLGASGSGKSSLLRAVAGLEPVAA 64

Query: 60  GAIRIGDRDVTHLPPKDRDIAMVFQNYALYPHMTVADNMGFALKIAGVPKAEIRQKVEEA 119
           G+IR   RDV   P   R   ++FQ   L+P   V  N+ + L   G+P+AE  ++V E 
Sbjct: 65  GSIRWDGRDVVGTPVHRRGFGLMFQEGQLFPFRDVGGNVAYGL--TGLPRAERARRVAEM 122

Query: 120 AKILDLTQYLDRKPKALSGGQRQRVAMGRAIVREPQVFLMDEPLSNLDAKLRVSTRTQIA 179
            +++ L  Y  R    LSGGQ QRVA+ RA+   P++ L+DEPLS LD  LR      + 
Sbjct: 123 LELVGLPGYGPRPITTLSGGQAQRVALARALAPRPRLLLLDEPLSALDRALREQLAVDLR 182

Query: 180 SLQRRLGITTVYVTHDQVEAMTMGDRVAVLKDGLLQQVDSPRNMYDKPANLFVAGFIG-S 238
           ++    G T +YVTHDQ EAMT+ D V V++ G L ++ +P  ++  P +  VA F+G  
Sbjct: 183 AILAEQGTTALYVTHDQDEAMTVADEVGVMEAGRLARLAAPAELWADPGSASVAAFLGFG 242

Query: 239 PAMNLVEVP------ITDG--------GVKFGNSVVPVNREALSA------ADKGDRTVT 278
           P +   +        + DG        G   G + + +   ALS       A +GD    
Sbjct: 243 PILTREQTEALGWAVLLDGGRPGAREAGSGGGGAALALAPGALSVVGLAGEAPRGDDAGA 302

Query: 279 VG--VRPEHFDVV----ELGGAVAASLSKDSADAPAGLAVSVNVVEELGADGYVYGTA 330
            G  + PE    V       G V A +S D  D  A +A  VN VE  G  G +  TA
Sbjct: 303 PGTAMLPEVSGTVLARRVRRGRVEADVSLDFPDGDAVVATGVNGVE--GPAGEIGTTA 358


Lambda     K      H
   0.317    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: 371
Number of extensions: 23
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: 377
Length of database: 372
Length adjustment: 30
Effective length of query: 347
Effective length of database: 342
Effective search space:   118674
Effective search space used:   118674
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 24 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