GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Collimonas arenae Ter10

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_061532690.1 CAter10_RS05915 ABC transporter permease

Query= uniprot:A0A1N7UKA9
         (325 letters)



>NCBI__GCF_001584165.1:WP_061532690.1
          Length = 348

 Score =  228 bits (581), Expect = 2e-64
 Identities = 120/303 (39%), Positives = 193/303 (63%), Gaps = 9/303 (2%)

Query: 32  ILLCVVMAFSSEYFMTWRNWMDILRQTSINGILAVGMTYVILTKGIDLSVGSILAFAGLC 91
           + L V  + +S  F+   N + IL+ T++NG+LA+  T+VI+T GIDLSVG+++ F  + 
Sbjct: 46  LALLVFFSLASPNFLEIDNLVSILQSTAVNGVLAIACTFVIITAGIDLSVGTLMTFCAVM 105

Query: 92  SAMVATQ-GYGLLAAVSAGMFAGAMLGVVNGFMVANLSIPPFVATLGMLSIARGMTFILN 150
           + +  T  G  +   ++A +  GA+ G V+G ++A L IPPF+ATLGM+ + +G++ +++
Sbjct: 106 AGVFLTYWGLPIYVGIAAAILFGALCGWVSGVLIAKLKIPPFIATLGMMMLLKGLSLVIS 165

Query: 151 DGSPI--TDLPDAYLALGIGKIG------PIGVPIIIFAVVALIFWMVLRYTTYGRYVYA 202
              PI   D P          IG      PI   ++I  +VA+   + L  + +GRY +A
Sbjct: 166 GTKPIYFNDTPGFSSISQDSLIGTLIPALPIPNAVLILFLVAIAAGIALNKSIFGRYTFA 225

Query: 203 VGGNEKSARTSGIGVRKVMFSVYVVSGLLAGLAGVVLSARTTSALPQAGVSYELDAIAAV 262
           +G NE++ R SG+ V     +VY VSG + G+AG+++++R  SA P  G  YELDAIAAV
Sbjct: 226 LGSNEEALRLSGVNVDFWKVTVYSVSGAICGIAGLLIASRLNSAQPALGQGYELDAIAAV 285

Query: 263 VIGGTSLSGGTGSIVGTLFGALLIGVINNGLNLLGVSSYYQQVAKGLIIVFAVLIDVWRK 322
           VIGGTSLSGGTG+I+GT+ GA ++ V+ NGL ++ V+  +Q V  G+II+ AV +D+ R+
Sbjct: 286 VIGGTSLSGGTGTILGTIIGAFIMSVLINGLRMMSVAQEWQTVVTGVIIILAVYMDILRR 345

Query: 323 KKR 325
           +++
Sbjct: 346 RRQ 348


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: 254
Number of extensions: 13
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: 325
Length of database: 348
Length adjustment: 28
Effective length of query: 297
Effective length of database: 320
Effective search space:    95040
Effective search space used:    95040
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.

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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