GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK' in Halomonas desiderata SP1

Align Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale)
to candidate WP_086510097.1 BZY95_RS11680 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= uniprot:A8LLL2
         (373 letters)



>NCBI__GCF_002151265.1:WP_086510097.1
          Length = 368

 Score =  330 bits (845), Expect = 5e-95
 Identities = 184/359 (51%), Positives = 236/359 (65%), Gaps = 6/359 (1%)

Query: 1   MADLKLTGVEKAYGDVKVLSNINLDIQQGELIVFVGPSGCGKSTLLRMIAGLEKITGGTL 60
           MA + L  + K +G   ++ +++L I +GE +VFVGPSGCGKSTLLR+IAGLE IT G L
Sbjct: 1   MASVTLDKINKVFGSTHIIKDVDLAIGEGEFVVFVGPSGCGKSTLLRLIAGLESITDGEL 60

Query: 61  EIDGTVVNDVPPAQRGIAMVFQSYALYPHMTVRENMSFALKIAKKSQAEIDAAVEAAAEK 120
            I   VVN++PP +RG+ MVFQSYALYPHMTV ENM+F LK+AK ++  +   V A A  
Sbjct: 61  SIGDQVVNELPPRERGVGMVFQSYALYPHMTVYENMAFGLKLAKTAKETVHERVMATARI 120

Query: 121 LQLGQYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRLEIAQLK 180
           LQL + L+R PKALSGGQRQRVA+GR++ R+P++ LFDEPLSNLDA+LRV  R EIA+L 
Sbjct: 121 LQLEELLERKPKALSGGQRQRVAMGRAMAREPRILLFDEPLSNLDASLRVQMRNEIARLH 180

Query: 181 EAMPESTMVYVTHDQVEAMTLATRIVVLAGGGIAQVGSPLELYEKPENEFVAQFIGSPKM 240
           + +  STMVYVTHDQVEAMTLA +IVVL GG + QVGSP ELY++P  +FVA FIGSP M
Sbjct: 181 KRL-GSTMVYVTHDQVEAMTLADKIVVLDGGRVEQVGSPQELYQRPATKFVAGFIGSPTM 239

Query: 241 NLLPGKIIGTGAQTTVEMTDGGRAVSDYPSDDS--LMGAAVNVGVRPEDMVEAAPGGDYV 298
           N LP +++G  A T   +   G      P D S    GAA+ +G+RPE +  +   G   
Sbjct: 240 NFLPARLLGADA-TGCRIGATGLTELALPQDASGHAQGAALTLGIRPEHLRLSEAQGSEG 298

Query: 299 FEGKVAITEALGEVTLLYFEAPSGEDPTIGKLQGIHKDLKGQVTRLTAEPAKVHVFKDG 357
           FE  +   E LG    +Y E   GE   I + +       GQ   L  +P  VH+F  G
Sbjct: 299 FE--IVNVEYLGNEVYVYLEPKEGETLLIQRGEAPTTWRVGQRVTLAPDPEHVHLFDAG 355


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: 413
Number of extensions: 22
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: 368
Length adjustment: 30
Effective length of query: 343
Effective length of database: 338
Effective search space:   115934
Effective search space used:   115934
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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