GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0030 in Dinoroseobacter shibae DFL-12

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 3609627 Dshi_3010 binding-protein-dependent transport systems inner membrane component (RefSeq)

Query= TCDB::Q9WXN7
         (338 letters)



>FitnessBrowser__Dino:3609627
          Length = 339

 Score =  232 bits (591), Expect = 1e-65
 Identities = 123/333 (36%), Positives = 199/333 (59%), Gaps = 6/333 (1%)

Query: 9   YLLRRFIFLLVTYIVATTIVFILPRAIPGNPLSQILSGLSRV--AQANPEAIRAAERTLM 66
           YL+ R I  ++T  +A T+++++PR  P +P   +LS ++    A A+ EAI A  R   
Sbjct: 8   YLINRTITFVLTVFIAATLIWLIPRFSPVDPAEIMLSRMAAGGGAVADSEAILAQLRA-- 65

Query: 67  EEFGLGKPWYVQYFEFITKALRGDLGTSITFYPRKVIDLIIPVIPWTLILLLPATIVAWI 126
            +FGL  P  VQY +++   L  +LG S   +P  V  LI   +PWTL L++ + ++ ++
Sbjct: 66  -DFGLNDPLIVQYLKYMGNLLTFNLGISTASFPTPVSVLIAQALPWTLGLMILSVVITFV 124

Query: 127 LGNSLGALAAYKRNTWIDKGVLTTSLIVSQIPYYWLGMIFIFLFGVKLGWLPVQGAYSQG 186
           +GN+LGA   ++R   I K V+ T +I + IP    G++ +++F + L WLP+ G+Y   
Sbjct: 125 IGNALGAFMVWERTPKIWKVVIPTFMIFTSIPPILSGLLLMYIFSITLRWLPLTGSYGLT 184

Query: 187 TIPNLSWSFFVDVLKHYIMPFASIVVSAMGGWAIGMRLMVIYELGSDYAMFSEYLGMKDK 246
             P   W+F   V++H  +P  SI+V   G W +GMR ++I   G DY   ++  G+K +
Sbjct: 185 VEPGWDWAFISSVIEHGTLPALSIIVVTFGFWTLGMRGLMISVQGEDYVNLAKAKGLKPR 244

Query: 247 RI-FKYVFRNSLLPQITGLALSLGGVLGGALITEIVFNYPGTGYLLFRALTTLDYPLIQG 305
            + +KY+ RN++LPQIT  AL +G ++ G ++ E +F Y G G LL+ A+   D+ +IQG
Sbjct: 245 YVLYKYMVRNAILPQITAFALKIGLLVSGQILVERIFGYNGMGKLLYDAILDQDFAVIQG 304

Query: 306 IFVILIASIYLANFIVDFLYALIDPRIRLGQEA 338
           +  I+I    L+ F+VD +Y LIDPRIRL +EA
Sbjct: 305 VSYIIILMTALSVFLVDLIYPLIDPRIRLSEEA 337


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: 371
Number of extensions: 21
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: 338
Length of database: 339
Length adjustment: 28
Effective length of query: 310
Effective length of database: 311
Effective search space:    96410
Effective search space used:    96410
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