GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rhaS in Burkholderia phytofirmans PsJN

Align RhaS, component of Rhamnose porter (Richardson et al., 2004) (Transport activity is dependent on rhamnokinase (RhaK; AAQ92412) activity (Richardson and Oresnik, 2007) This could be an example of group translocation!) (characterized)
to candidate BPHYT_RS28200 BPHYT_RS28200 sugar ABC transporter substrate-binding protein

Query= TCDB::Q7BSH5
         (331 letters)



>FitnessBrowser__BFirm:BPHYT_RS28200
          Length = 335

 Score =  253 bits (647), Expect = 4e-72
 Identities = 143/327 (43%), Positives = 201/327 (61%), Gaps = 6/327 (1%)

Query: 6   TLALGVAL-AVAMMAGTASAKD-IKIGLVVKSLGNGFFDAANKGAQEAAKELGGVEVIYT 63
           T AL VAL A++  A  A  K  +KI  V K + N +   A+ G   A KE  GV     
Sbjct: 10  TAALCVALLAISCAASAADLKSGLKIAFVPKQINNPYEVIADDGGMTAIKEFKGVGKA-V 68

Query: 64  GPTSTTAEGQIEVINSLIAQGVDAIAVSANDPDALVPALKKATQRGIKVISWDSGVAPEG 123
           GP+   A  Q++ IN+LI Q  DAI ++AND +A+VP LKKA  +GIKV+++DS  APEG
Sbjct: 69  GPSDAGASSQVQYINTLITQRQDAIVIAANDANAVVPYLKKAMSQGIKVVTFDSDTAPEG 128

Query: 124 RILQLNPSSNELIGKMCLTLAKDHLEGGKGDFAILSATTTSTNQNIWIDQMKKQLK--DF 181
           R L +N ++ E IG+  + L    L GG+G+FA+LSAT  +TNQN WI  M+++LK  ++
Sbjct: 129 RQLFVNQANAEGIGRGQVQLVSK-LMGGEGEFAVLSATPNATNQNTWIKWMQEELKKPEY 187

Query: 182 PGLNLVTTVYGDDLSDKSYREAEGLLKSNPNVKVIVAPTTVGVLAASKVVEDKGLVGKVY 241
             + LV   YG+D   KS+ E +GLL++ PN+K IVAPTTVG+ AA++ +      GKV 
Sbjct: 188 SKIKLVKIAYGNDDDQKSFTETQGLLQAYPNLKAIVAPTTVGIAAAARYISTSSSKGKVA 247

Query: 242 VTGLGLPSEMAGAIKSGATKEFAIWNPIDLGYSATQIAYRLVKGETDGKPGSEINAGRMG 301
           VTGLG P++M   +K+G  K F +W+P  LGY A   A  L  G   GK G   +AG++G
Sbjct: 248 VTGLGTPNQMRAFVKNGTVKAFQLWDPGQLGYLAAYAAAALASGTISGKEGESFDAGKLG 307

Query: 302 KIKVGDNGEAAMADPFVYNASNIDQFS 328
           K  +G  GE  +  P  +++SNID F+
Sbjct: 308 KRTIGPQGEIILGPPTTFDSSNIDNFN 334


Lambda     K      H
   0.313    0.131    0.365 

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: 318
Number of extensions: 17
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: 331
Length of database: 335
Length adjustment: 28
Effective length of query: 303
Effective length of database: 307
Effective search space:    93021
Effective search space used:    93021
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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