GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK in Pseudovibrio axinellae Ad2

Align ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized)
to candidate WP_068010540.1 PsAD2_RS21550 ABC transporter ATP-binding protein

Query= reanno::Smeli:SMc03065
         (362 letters)



>NCBI__GCF_001623255.1:WP_068010540.1
          Length = 370

 Score =  290 bits (741), Expect = 6e-83
 Identities = 169/366 (46%), Positives = 221/366 (60%), Gaps = 16/366 (4%)

Query: 1   MTGLLLKDIRKSYGAVDVIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITGGDM 60
           M  + ++   KS+G+  V+  I LD+K+GEF+V +G SGCGKSTLL +IAGLE +  G +
Sbjct: 1   MATISIEHASKSFGSTKVLKDISLDVKDGEFLVLLGASGCGKSTLLNIIAGLEPMADGTI 60

Query: 61  FIDGERVNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGAADM 120
            +DGE VNDV P  R IAMVFQSYALYP+MTV  N+AFG+ + + SK E    VR  A  
Sbjct: 61  RLDGEVVNDVHPKNRDIAMVFQSYALYPNMTVERNIAFGLEMRKISKAERKATVREVAST 120

Query: 121 LQLTPYLDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIAKLS 180
           LQ+   L R P  LSGGQRQRVA+GRA+ R PK+FLFDEPLSNLDA LR   R EI KL 
Sbjct: 121 LQIEHLLSRKPSQLSGGQRQRVAMGRALVRRPKIFLFDEPLSNLDAKLRGEMRTEIKKLH 180

Query: 181 ERMSDTTMIYVTHDQVEAMTLADRIVVLSAGHIEQVGAPLELYERPANLFVARFIGSPAM 240
           + +   TM+YVTHDQ+EAMTLADRI ++  G I+Q+G P E+Y +PAN++VA F+G+P M
Sbjct: 181 QTLK-ATMVYVTHDQIEAMTLADRIAIMKDGEIQQIGTPQEIYSKPANMYVAGFVGAPPM 239

Query: 241 NVIPATITATGQQTAVSLAG---GKSVTLDVP------TNASENGKTASFGVRPE---DL 288
           N +   +    +Q    L     G+ V   +P        A EN K    G+RPE   D 
Sbjct: 240 NFVEVDLVKREEQLGAILPAVLKGEPVDHFLPLPNSKHLEARENTKVI-LGLRPEIITDS 298

Query: 289 RVTEADDFLFEGTVSIVEALGEVTLLYIEGLVENEPIIAKMPGIARVGRGDKVRFTADKA 348
             T +     E  V  +E  G  TL  I   +   P  A++  +     G+ +RFT D  
Sbjct: 299 TSTHSSAPEIECDVEFLEPTGADTLCIIR--LNGHPAKARVSPLFACPPGESMRFTLDTH 356

Query: 349 KLHLFD 354
           +  LFD
Sbjct: 357 RACLFD 362


Lambda     K      H
   0.320    0.137    0.387 

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: 355
Number of extensions: 16
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: 362
Length of database: 370
Length adjustment: 30
Effective length of query: 332
Effective length of database: 340
Effective search space:   112880
Effective search space used:   112880
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: 49 (23.5 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