GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Escherichia coli BW25113

Align ABC transporter for D-Sorbitol, ATPase component (characterized)
to candidate 14980 b0855 ATP-binding component of putrescine transport system (VIMSS)

Query= reanno::BFirm:BPHYT_RS16095
         (369 letters)



>FitnessBrowser__Keio:14980
          Length = 377

 Score =  229 bits (583), Expect = 1e-64
 Identities = 134/338 (39%), Positives = 193/338 (57%), Gaps = 10/338 (2%)

Query: 6   LRNIRKAYDENEVMRDINLDIADGEFVVFVGPSGCGKSTLMRMIAGLEDISGGDLTIDGM 65
           +RN+ K+YD    + D++L I  GE    +G SGCGKSTL+RM+AG E  S G + +DG+
Sbjct: 22  IRNLTKSYDGQHAVDDVSLTIYKGEIFALLGASGCGKSTLLRMLAGFEQPSAGQIMLDGV 81

Query: 66  RVNDVAPAKRGIAMVFQSYALYPHMTLYDNMAFGLKLAGTKKPEIDAAVRNAAKILHIDH 125
            ++ V P  R I M+FQSYAL+PHMT+  N+AFGLK     K EI + V     ++H+  
Sbjct: 82  DLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEIASRVNEMLGLVHMQE 141

Query: 126 LLDRKPKQLSGGQRQRVAIGRAITRKPKVFLFDEPLSNLDAALRVKMRLEFARLHDELKT 185
              RKP QLSGGQRQRVA+ R++ ++PK+ L DEP+  LD  LR +M+LE   + + +  
Sbjct: 142 FAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRDRMQLEVVDILERVGV 201

Query: 186 TMIYVTHDQVEAMTLADKIVVLSAGNLEQVGSPTMLYHAPANRFVAGFIGSPKMNFMEGV 245
           T + VTHDQ EAMT+A +I +++ G   Q+G P  +Y  P  R+ A FIGS  +N  EGV
Sbjct: 202 TCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYSAEFIGS--VNVFEGV 259

Query: 246 VQSVTHDGVTVRYETGETQRVAVE-PAAVKQGDKVTVGIRPEHLHVGMAEDGISARTMAV 304
           ++    DG+ V    G    + V+  A+V     V V +RPE + +   E   +    AV
Sbjct: 260 LKERQEDGL-VLDSPGLVHPLKVDADASVVDNVPVHVALRPEKIML-CEEPPANGCNFAV 317

Query: 305 ESLGDAAYL-----YAESSVAPDGLIARIPPLERHTKG 337
             +   AYL     Y     +   + A++    RH KG
Sbjct: 318 GEVIHIAYLGDLSVYHVRLKSGQMISAQLQNAHRHRKG 355


Lambda     K      H
   0.320    0.135    0.384 

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: 347
Number of extensions: 11
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: 369
Length of database: 377
Length adjustment: 30
Effective length of query: 339
Effective length of database: 347
Effective search space:   117633
Effective search space used:   117633
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: 50 (23.9 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