GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Lactobacillus shenzhenensis LY-73

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale)
to candidate WP_022530416.1 L248_RS11545 sugar ABC transporter permease YjfF

Query= uniprot:A0A1N7UKA9
         (325 letters)



>NCBI__GCF_000469325.1:WP_022530416.1
          Length = 345

 Score =  146 bits (368), Expect = 8e-40
 Identities = 91/306 (29%), Positives = 162/306 (52%), Gaps = 12/306 (3%)

Query: 30  VFILLCVVMAFSSEYFMTWRNWMDILRQTSINGILAVGMTYVILTKGIDLSVGSILAFAG 89
           +F +L +  +     F++ R  +++L   +   +LA G+ + ILT GIDLS+G+++A   
Sbjct: 18  IFAILFIAGSVMYPNFLSLRVLLNLLINNAYMIVLAGGVCFTILTGGIDLSIGAVVAMTS 77

Query: 90  LCSAMVATQGYGLLAAVSAGMFAGAMLGVVNGFMVANLSIPPFVATLGMLSIARGMTFIL 149
           + +A +   G      ++  +  G + G V G ++    + P++ TL  +  ARG  +++
Sbjct: 78  MIAASLLRSGMNAYLVIAICLLTGVVFGTVQGLLIQYFGLHPWIVTLAGMFFARGACYLI 137

Query: 150 N-DGSPITD-----LPDAYLALGIGKIGPIGVPIIIFAVVALIFWMVLRYTTYGRYVYAV 203
           + +  PI +     +    L LG G+   I + +I+  V   +   + ++T +GR  YA+
Sbjct: 138 SVEAIPIKNQAFYNISQFKLYLGPGRF--ISLNVIVALVFLALCLYLAKFTKFGRTTYAL 195

Query: 204 GGNEKSARTSGIGVRKVMFSVYVVSGLLAGLAGVVLSARTTSALPQAGVSYELDAIAAVV 263
           GGN +SA   G+ V +    VY  SG  A L+G++ +  T S         E+DAIAA V
Sbjct: 196 GGNRQSALLMGLPVARTKILVYTFSGFSATLSGLMFTLYTLSGYGLNANGAEMDAIAACV 255

Query: 264 IGGTSLSGGTGSIVGTLFGALLIGVINNGLNLLG-VSSYYQQVAKGLIIVFAVLID---V 319
           IGG SL GG GS+ G   G L+ GVI   ++  G +SS++ ++  G +++F +++    V
Sbjct: 256 IGGVSLYGGIGSLFGPFIGVLVAGVIRTMVDFQGTLSSWWTKIFVGTLMLFCIVLQAVIV 315

Query: 320 WRKKKR 325
            R+K R
Sbjct: 316 EREKAR 321


Lambda     K      H
   0.326    0.141    0.412 

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: 246
Number of extensions: 12
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: 325
Length of database: 345
Length adjustment: 28
Effective length of query: 297
Effective length of database: 317
Effective search space:    94149
Effective search space used:    94149
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (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