GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cebG in Pseudomonas fluorescens GW456-L13

Align CBP protein aka CebG, component of The cellobiose/cellotriose (and possibly higher cellooligosaccharides), CebEFGMsiK [MsiK functions to energize several ABC transporters including those for maltose/maltotriose and trehalose] (characterized)
to candidate PfGW456L13_1896 Glucose ABC transport system, inner membrane component 2

Query= TCDB::Q9X9R5
         (276 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1896
          Length = 281

 Score = 89.7 bits (221), Expect = 6e-23
 Identities = 78/278 (28%), Positives = 125/278 (44%), Gaps = 29/278 (10%)

Query: 14  YVVLTVFALVSLAPLVWTAIAASRTNHRLAETPPPLWFGGNLFKNLEAAWEQAGLGTAML 73
           Y  L + A V L PLV   + + ++   +          GNL      +W     G   +
Sbjct: 18  YATLLLAAAVYLIPLVVMLLTSFKSPEDIRT--------GNLL-----SWPTVIDGIGWI 64

Query: 74  NSVIVAG-------TITVSTVLFST----LAGFAFAKLRFRFSGLLLLLTIGTMMIPPQL 122
            +  V G        ITV  VL ST    + G+  +  RFR S L   L +    +P Q 
Sbjct: 65  KAWDVVGGYFWNSVKITVPAVLISTFIGAMNGYVLSMWRFRGSQLFFGLLLFGCFLPFQT 124

Query: 123 AVVPLYLWMSDLGWSNQLHTVILPSLV--TAFGTFFMRQYLVQALPTELIEAARVDGASS 180
            ++P    +   G +N    ++L  +V   AF T F R Y V ++P  L++AAR+DGA  
Sbjct: 125 VLLPASFTLGKFGLANTTTGLVLVHVVYGLAFTTLFFRNYYV-SIPDALVKAARLDGAGF 183

Query: 181 LRIVWHVVFPAARPAMAVLGLLTFVFAWNDFLWPII--ALNQQNPTVQVGPELARHRVLP 238
             I   ++ P + P + V  +  F   WNDFL+ ++  + + Q  TV +   +       
Sbjct: 184 FTIFLKILLPMSIPIVMVCLIWQFTQIWNDFLFGVVFASGDAQPITVALNNLVNTSTGAK 243

Query: 239 DQAVIMAGALLGTLPLLVAFLLFGKQIVGGIMQGAIKG 276
           +  V MA A++  LP L+ ++  GK  + G+  GA+KG
Sbjct: 244 EYNVDMAAAMIAGLPTLLVYIFAGKYFLRGLTSGAVKG 281


Lambda     K      H
   0.327    0.140    0.434 

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: 227
Number of extensions: 11
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: 276
Length of database: 281
Length adjustment: 25
Effective length of query: 251
Effective length of database: 256
Effective search space:    64256
Effective search space used:    64256
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 (21.7 bits)
S2: 47 (22.7 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