GapMind for catabolism of small carbon sources

 

Aligments for a candidate for gntEIID in Escherichia coli BW25113

Align PTS system, IID component, component of The gluconate PTS uptake system. IIAGnt and IIBGnt form a high affinity 2:2 heterotetrameric complex (characterized)
to candidate 15937 b1819 mannose-specific enzyme IID component of PTS (NCBI)

Query= TCDB::Q82ZC6
         (290 letters)



>lcl|FitnessBrowser__Keio:15937 b1819 mannose-specific enzyme IID
           component of PTS (NCBI)
          Length = 283

 Score =  125 bits (313), Expect = 1e-33
 Identities = 89/266 (33%), Positives = 135/266 (50%), Gaps = 15/266 (5%)

Query: 8   VVPKTTNLAPEEITNKDVTKAYLRWHFANEIPHSFERYLAPSLLYAMMPLLKKLY-KDDE 66
           +V  T     +++T  D+   +LR +       +FER  A    ++M+P +++LY +++E
Sbjct: 1   MVDTTQTTTEKKLTQSDIRGVFLRSNLFQG-SWNFERMQALGFCFSMVPAIRRLYPENNE 59

Query: 67  QLKAAYMRQLLFFNTQLSWGGGVITGLMASMEQERAKEEHEGREIMMQDDLMYNTKAGLM 126
             K A  R L FFNTQ  +    I G+  ++E++RA     G EI   D  +   K GLM
Sbjct: 60  ARKQAIRRHLEFFNTQ-PFVAAPILGVTLALEEQRAN----GAEI--DDGAINGIKVGLM 112

Query: 127 GALAGIGDAIDSGTVQYIFIAIAVPWAQQGSALGAIFPFVAFALYQVLLGVFFARQSFKM 186
           G LAG+GD I  GTV+ +F A+    A  GS LG +  F+ F L ++    +     +  
Sbjct: 113 GPLAGVGDPIFWGTVRPVFAALGAGIAMSGSLLGPLLFFILFNLVRLATRYYGVAYGYSK 172

Query: 187 GRNATGLMQSAGIQKAIEMLSVLGLFMMGILAGNYVKVSSTLQFK----LSGREFV--VQ 240
           G +    M    +QK  E  S+LGLF+MG L   +  V+  L        +G+E V  VQ
Sbjct: 173 GIDIVKDMGGGFLQKLTEGASILGLFVMGALVNKWTHVNIPLVVSRITDQTGKEHVTTVQ 232

Query: 241 DILDQIVPGLLPLAVVMGVYWFYTKK 266
            ILDQ++PGL+PL +     W   KK
Sbjct: 233 TILDQLMPGLVPLLLTFACMWLLRKK 258


Lambda     K      H
   0.324    0.138    0.402 

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: 228
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: 290
Length of database: 283
Length adjustment: 26
Effective length of query: 264
Effective length of database: 257
Effective search space:    67848
Effective search space used:    67848
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (22.0 bits)
S2: 47 (22.7 bits)

This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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