GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0030 in Pseudomonas putida KT2440

Align TM0030, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized)
to candidate PP_4455 PP_4455 glutathione ABC transporter permease subunit

Query= TCDB::Q9WXN7
         (338 letters)



>FitnessBrowser__Putida:PP_4455
          Length = 313

 Score =  171 bits (432), Expect = 3e-47
 Identities = 102/330 (30%), Positives = 170/330 (51%), Gaps = 19/330 (5%)

Query: 6   MFKYLLRRFIFLLVTYIVATTIVFILPRAIPGNPLSQILSGLSRVAQANPEAIRAAERTL 65
           M ++ ++R +  + T +   T VF+L R +PG+P + IL       QA+ E++ A    +
Sbjct: 1   MIQFAIKRLMLAIPTLLAMLTAVFVLVRLVPGDPAAVILGD-----QASAESLAA----M 51

Query: 66  MEEFGLGKPWYVQYFEFITKALRGDLGTSITFYPRKVIDLIIPVIPWTLILLLPATIVAW 125
            E+ GL +P  +QY  F+   L G+ G S+T   R V+  +  V+PWTL L   + ++  
Sbjct: 52  REQLGLNQPIAMQYIHFLGDMLSGNFGVSMTS-GRTVLQEVSLVLPWTLQLTFASVLIGL 110

Query: 126 ILGNSLGALAAYKRNTWIDKGVLTTSLIVSQIPYYWLGMIFIFLFGVKLGWLPVQGAYSQ 185
           + G  LG  AA +RN W D      SL     P +   M+ + +F +   W PV G+   
Sbjct: 111 VFGLPLGVWAALRRNAWPDYVGRILSLTGLSFPAFVSAMLMLLVFAIHFRWFPVIGSLVD 170

Query: 186 GTIPNLSWSFFVDVLKHYIMPFASIVVSAMGGWAIGMRLMVIYELGSDYAMFSEYLGMKD 245
           G         F+  L    +P  ++ +          R  +I  LG DY   ++  G++ 
Sbjct: 171 GG--------FLSQLHALTLPALNLGLIMTAYVMRVTRSSMISVLGEDYIRTAKAKGVRP 222

Query: 246 KR-IFKYVFRNSLLPQITGLALSLGGVLGGALITEIVFNYPGTGYLLFRALTTLDYPLIQ 304
            R + ++  RN+L+P +T + L  G ++G +++TEIVFN PG G L+  AL T DY L+Q
Sbjct: 223 MRLVLRHGLRNALIPIVTVVGLYFGTLIGNSVLTEIVFNRPGLGKLILGALNTRDYTLLQ 282

Query: 305 GIFVILIASIYLANFIVDFLYALIDPRIRL 334
           G+ V+    + + N I D +Y L+DPR+++
Sbjct: 283 GLMVVFALCVIVVNIITDIVYGLVDPRVKI 312


Lambda     K      H
   0.329    0.146    0.449 

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: 288
Number of extensions: 20
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: 338
Length of database: 313
Length adjustment: 28
Effective length of query: 310
Effective length of database: 285
Effective search space:    88350
Effective search space used:    88350
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: 48 (23.1 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