GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rhaP in Dinoroseobacter shibae DFL-12

Align RhaP, 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 3607107 Dshi_0529 Monosaccharide-transporting ATPase (RefSeq)

Query= TCDB::Q7BSH3
         (333 letters)



>FitnessBrowser__Dino:3607107
          Length = 333

 Score =  157 bits (397), Expect = 4e-43
 Identities = 99/317 (31%), Positives = 166/317 (52%), Gaps = 13/317 (4%)

Query: 7   KRETLLFLIIVVMIVVFSTRAADFATPGNLAGIFNDTSILIILALAQMTVILTKSIDLSV 66
           + ETL+  +I++   V +     F T   ++ +   + ++ ILA+  M V+++  ID+S 
Sbjct: 12  RNETLVAGVIMLFCFVATVSDPRFLTITTVSDLLRASIVIGILAVGAMLVLVSGGIDVSF 71

Query: 67  AANLAFTGMAIAMMNAA-HPDLPLVVLILMAVVIGACLGAINGFLVWALEIPPIVVTLGT 125
            A   F   +  +++    P++P  V+ +++VV GA LGAINGF +  L +P ++VTLGT
Sbjct: 72  TAIAVFAMYSSTVLSLTIWPEIPWPVIFVISVVFGAALGAINGFFIAFLGLPTLIVTLGT 131

Query: 126 LTIYRGMAFVLSGGAWVNAHQMTPIFLSVPRTPV----------LGLPVLSWVGIIIVIL 175
           L+I+RG      G   ++   + P      R  +            +P  +   + +++L
Sbjct: 132 LSIFRGFLLTFIGSQRIS--DLPPSMRDFSRGVIARGTTEAGNFYSIPWAALALLFVIVL 189

Query: 176 MYVLLRYTQFGRSAYATGGNPTAAVYAGIDTGWTKFLAFVLSGALAGLASYLWVSRYAVA 235
            + +L+ T  GRS YA GG+  +A   GI+  WT+F  +V  GALAGLA  +  S   +A
Sbjct: 190 TWFILKKTMLGRSIYAIGGSVESARRIGINVKWTQFFVYVYVGALAGLAGIIHGSVGRMA 249

Query: 236 YVDIANGFELDSVAACVIGGISIAGGVGSVAGTVLGALFLGVIKNALPVIGISPFTQMAI 295
                 G EL  +AA V+GG  + GG G++ GT+LG   + +++N+L VIGI    Q   
Sbjct: 250 DPFSLVGLELSVIAAVVLGGARLIGGYGTLTGTMLGVALIVIVQNSLIVIGIPTTWQSVT 309

Query: 296 SGTVIILAVAFNARRER 312
            G +I+L     A R +
Sbjct: 310 IGILILLGTGVPAYRAK 326


Lambda     K      H
   0.328    0.141    0.413 

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: 309
Number of extensions: 14
Number of successful extensions: 4
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: 333
Length of database: 333
Length adjustment: 28
Effective length of query: 305
Effective length of database: 305
Effective search space:    93025
Effective search space used:    93025
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 (21.8 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