GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Pseudovibrio axinellae Ad2

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate WP_068006708.1 PsAD2_RS13385 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::Dino:3607124
         (338 letters)



>NCBI__GCF_001623255.1:WP_068006708.1
          Length = 375

 Score =  332 bits (852), Expect = 7e-96
 Identities = 176/359 (49%), Positives = 238/359 (66%), Gaps = 23/359 (6%)

Query: 1   MAGIKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRI 60
           MA + +  I K +G+T+ +  ++L I+D E +VFVGPSGCGKSTLLR +AGLE +S G +
Sbjct: 1   MADVTLKGIVKDFGSTRIIHGVDLQIKDRELIVFVGPSGCGKSTLLRLIAGLEDISDGEM 60

Query: 61  EIGGRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAARV 120
            I G  V    P +R +AMVFQSYALYPHM+V ENM FG++++       K+++ EAAR+
Sbjct: 61  FIDGELVNQCSPKERRIAMVFQSYALYPHMSVYENMAFGLQLSKHSKKDIKDKVMEAARI 120

Query: 121 LQLEDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEGLH 180
           L+L   L+R+P QLSGGQRQRVAIGRAIV+NP VFLFDEPLSNLDA LRVQMR+E+  LH
Sbjct: 121 LELTPLLERQPKQLSGGQRQRVAIGRAIVRNPKVFLFDEPLSNLDASLRVQMRIEIAKLH 180

Query: 181 KQLGATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPAMN 240
           + + ATM+YVTHDQVEAMT+AD+IVVLN GRIEQVGSP++LYH+P ++FVA FIGSP MN
Sbjct: 181 QDMDATMVYVTHDQVEAMTLADRIVVLNAGRIEQVGSPLELYHRPRNKFVAGFIGSPKMN 240

Query: 241 -VFSSDVGLQDISLDASAAFVGCRPEHIEIVPDG--------------------DGHIAA 279
            + ++ V + +  ++ S A  G  P  +++VPDG                     G ++ 
Sbjct: 241 FIEATVVSVAESGVEVSVA--GSEPVKVDVVPDGLSVGERIEYGIRPEHLGAGTTGDLSG 298

Query: 280 TVHVKERLGGESLLYLGLKGGGQIVARVGGDDETKVGAAVSLRFSRHRLHQFDEAGRAI 338
            + V E LG    L++ L  G  I  +  GD + + G +  ++F R     F   G A+
Sbjct: 299 KIEVIEELGESHFLHMRLSNGALITVQGRGDAQVRAGESCLVKFDREHAQVFRGDGFAV 357


Lambda     K      H
   0.320    0.139    0.396 

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: 398
Number of extensions: 17
Number of successful extensions: 1
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: 338
Length of database: 375
Length adjustment: 29
Effective length of query: 309
Effective length of database: 346
Effective search space:   106914
Effective search space used:   106914
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