GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Escherichia coli BW25113

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate 16645 b2546 predicted sugar transporter subunit: membrane component of ABC superfamily (NCBI)

Query= uniprot:B2T9V8
         (351 letters)



>FitnessBrowser__Keio:16645
          Length = 332

 Score =  164 bits (414), Expect = 4e-45
 Identities = 100/325 (30%), Positives = 178/325 (54%), Gaps = 13/325 (4%)

Query: 19  SQLALPASRGKRARSELAR-LRELALLPALALLIVIGAFISPSFLTKANLISVLGASAAL 77
           S L LP  +    +  ++R + E+ LL  +A+L ++ +  +P F++  N ++VL  +A +
Sbjct: 4   SSLPLPQGKSVSLKQFVSRHINEIGLLVVIAILYLVFSLNAPGFISLNNQMNVLRDAATI 63

Query: 78  ALVVLAESLIVLTGKFDLSLESTVGIAPAVGAMLVMPAASAGFGMQW--PAAAGLLAIVV 135
            +   A +LI+++G+ D+S          VG M+   +    F +Q+  P A   L +++
Sbjct: 64  GIAAWAMTLIIISGEIDVS----------VGPMVAFVSVCLAFLLQFEVPLAVACLLVLL 113

Query: 136 VGAVIGFINGFLVVRLRLNAFIVTLAMLIVLRGMLVGATKGGTLFDMPTSFFALATTIVL 195
           +GA++G + G L     + +F+ TL +   LRGM +  T    +               L
Sbjct: 114 LGALMGTLAGVLRGVFNVPSFVATLGLWSALRGMGLFMTNALPVPIDENEVLDWLGGQFL 173

Query: 196 GLPLSVWLAAAAFAIAAFMLRYHRLGRALYAIGGNPEAARAAGIRVERITWGVFVLGSIL 255
           G+P+S  +    FA+  F+ R    GR+++A+GGN  AA+  GI V R+   +F L  +L
Sbjct: 174 GVPVSALIMIVLFALFVFISRKTAFGRSVFAVGGNATAAQLCGINVRRVRILIFTLSGLL 233

Query: 256 ASVGGLIVTGYVGAINANQGNGMIFTVFAAAVIGGISLDGGKGTMFGALTGVLLLGVVQN 315
           A+V G+++   +G+ NA   NG+ F V AA V+GG +L GG+G++FG L GVL++ ++ N
Sbjct: 234 AAVTGILLAARLGSGNAGAANGLEFDVIAAVVVGGTALSGGRGSLFGTLLGVLVITLIGN 293

Query: 316 LLTLAQVPSFWIQAIYGAIILGSLM 340
            L L  + SF+ Q + G II+ +++
Sbjct: 294 GLVLLGINSFFQQVVRGVIIVVAVL 318


Lambda     K      H
   0.326    0.140    0.397 

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: 265
Number of extensions: 14
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: 351
Length of database: 332
Length adjustment: 29
Effective length of query: 322
Effective length of database: 303
Effective search space:    97566
Effective search space used:    97566
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 17 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