GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Lactobacillus shenzhenensis LY-73

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate WP_022529099.1 L248_RS05360 ABC transporter ATP-binding protein

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



>NCBI__GCF_000469325.1:WP_022529099.1
          Length = 376

 Score =  255 bits (652), Expect = 1e-72
 Identities = 147/325 (45%), Positives = 197/325 (60%), Gaps = 22/325 (6%)

Query: 4   IKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRIEIG 63
           IK+D + K +G T  L  I+  I++GEF V VGPSG GKSTLLR +AGL   SSG +   
Sbjct: 3   IKLDHLTKQFGDTAVLDGISAQIQEGEFFVLVGPSGSGKSTLLRIIAGLIPASSGSVFFD 62

Query: 64  GRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAARVLQL 123
            ++VT + P DR L MVFQ+YAL P M+V +N+ FG+     +     +R+ +A  ++ L
Sbjct: 63  SQNVTDLPPKDRHLTMVFQNYALLPFMSVADNIRFGLHNLDLDATEEAKRVNDALDMVHL 122

Query: 124 EDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEGLHKQL 183
            +  DRKP +LSGGQ+QRVA+ RAI    S+ L DEPLSNLDA+LR +MR EL  LHK+L
Sbjct: 123 TELRDRKPKELSGGQQQRVALARAIATKASLVLMDEPLSNLDAQLRTEMRQELVQLHKEL 182

Query: 184 GATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPAMNVFS 243
           G T++YVTHDQVEAMTM ++I+VLN   I+QVG+P+DLY+ P ++FVA FIGSP MN+F 
Sbjct: 183 GMTLLYVTHDQVEAMTMGERIMVLNDHHIQQVGTPLDLYNHPANKFVATFIGSPKMNMFD 242

Query: 244 SDVGLQD--------------------ISLDASAAFVGCRPEHIEIVPDGD-GHIAATVH 282
           + V   +                      L A A  +G RPE I +      G     V 
Sbjct: 243 ATVDALEHFATLELTDANQHSVRLPLPYDLAAGAYQLGIRPEKITLSRSASAGSFPVRVM 302

Query: 283 VKERLGGESLLYLGLKGGGQIVARV 307
               LG ES + L +  G + +A V
Sbjct: 303 AVANLGRESSVSL-VNNGHEFIASV 326


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: 316
Number of extensions: 9
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: 376
Length adjustment: 29
Effective length of query: 309
Effective length of database: 347
Effective search space:   107223
Effective search space used:   107223
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