GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0030 in Dechlorosoma suillum PS

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 Dsui_0412 Dsui_0412 ABC-type dipeptide/oligopeptide/nickel transport system, permease component

Query= TCDB::Q9WXN7
         (338 letters)



>FitnessBrowser__PS:Dsui_0412
          Length = 317

 Score =  188 bits (477), Expect = 2e-52
 Identities = 111/327 (33%), Positives = 177/327 (54%), Gaps = 13/327 (3%)

Query: 6   MFKYLLRRFIFLLVTYIVATTIVFILPRAIPGNPLSQILSGLSRVAQANPEAIRAAERTL 65
           MF Y+L+R I+ +   +  T + F+L    PG+PL+ I       A A  E I+A    L
Sbjct: 1   MFAYILKRLIYAIPIALSVTVVSFVLVYLAPGDPLNAIAP-----ADAPEEVIQA----L 51

Query: 66  MEEFGLGKPWYVQYFEFITKALRGDLGTSITFYPRKVIDLIIPVIPWTLILLLPATIVAW 125
              +GL KP  VQY  ++ +A++GDLG SI    R+V   ++  +  TL+L   A  +  
Sbjct: 52  KSAYGLDKPVPVQYGLWLMRAVQGDLGLSIAS-GREVTAEVLSAVSNTLLLAGMAAAIGV 110

Query: 126 ILGNSLGALAAYKRNTWIDKGVLTTSLIVSQIPYYWLGMIFIFLFGVKLGWLPVQGAYSQ 185
           +LG  LGALA Y+  TWIDK     S++   IP+YWLG++   LF + L W P  GA   
Sbjct: 111 VLGCILGALAGYRHGTWIDKAATALSVVGVSIPHYWLGLVLTILFSIWLPWFPAMGAGPG 170

Query: 186 GTIPNLSWSFFVDVLKHYIMPFASIVVSAMGGWAIGMRLMVIYELGSDYAMFSEYLGMKD 245
           G+     W + ++ L++ ++P  ++ V  MG     +R +V   LG ++       G+  
Sbjct: 171 GSG---EWLWDLEHLRYLVLPALTLSVIPMGIITRTVRALVADMLGQEFVTALRARGLSG 227

Query: 246 KRIFKYVFRNSLLPQITGLALSLGGVLGGALITEIVFNYPGTGYLLFRALTTLDYPLIQG 305
             +F++V +N+    +    L +G ++GG+++ E VF +PGTG+LL  A+   D PL+QG
Sbjct: 228 GAVFRHVAKNTAPTVLAVAGLQIGYLMGGSILVETVFAWPGTGFLLNTAIFQRDIPLLQG 287

Query: 306 IFVILIASIYLANFIVDFLYALIDPRI 332
             ++L     + N +VD L  LIDPR+
Sbjct: 288 TILVLCMFFVVLNLLVDILQPLIDPRM 314


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: 328
Number of extensions: 18
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: 317
Length adjustment: 28
Effective length of query: 310
Effective length of database: 289
Effective search space:    89590
Effective search space used:    89590
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