GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0030 in Escherichia coli BW25113

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 14956 b0831 predicted peptide transporter subunit: membrane component of ABC superfamily (NCBI)

Query= TCDB::Q9WXN7
         (338 letters)



>FitnessBrowser__Keio:14956
          Length = 306

 Score =  167 bits (422), Expect = 4e-46
 Identities = 104/329 (31%), Positives = 167/329 (50%), Gaps = 26/329 (7%)

Query: 6   MFKYLLRRFIFLLVTYIVATTIVFILPRAIPGNPLSQILSGLSRVAQANPEAIRAAERTL 65
           M  Y+++R + L+ T  + + +VF+    +PG+P   I         A PEA       +
Sbjct: 1   MLNYVIKRLLGLIPTLFIVSVLVFLFVHMLPGDPARLI---------AGPEADAQVIELV 51

Query: 66  MEEFGLGKPWYVQYFEFITKALRGDLGTSITFYPRKVIDLIIPVIPWTLILLLPATIVAW 125
            ++ GL +P Y Q++ +I+ A++GD G S+    R V D I      TL L + + + A 
Sbjct: 52  RQQLGLDQPLYHQFWHYISNAVQGDFGLSMVSR-RPVADEIASRFMPTLWLTITSMVWAV 110

Query: 126 ILGNSLGALAAYKRNTWIDKGVLTTSLIVSQIPYYWLGMIFIFLFGVKLGWLPVQGAYSQ 185
           I G + G +AA  RN W D+  +T ++     P + LGM+ I +F V+LGWLP  GA   
Sbjct: 111 IFGMAAGIIAAVWRNRWPDRLSMTIAVSGISFPAFALGMLLIQVFSVELGWLPTVGA--- 167

Query: 186 GTIPNLSWSFFVDVLKHYIMPFASIVVSAMGGWAIGMRLMVIYELGSDYAMFSEYLGMKD 245
                       D  +HYI+P  ++  +     A   R   +  L  DY   +   G+ +
Sbjct: 168 ------------DSWQHYILPSLTLGAAVAAVMARFTRASFVDVLSEDYMRTARAKGVSE 215

Query: 246 KRI-FKYVFRNSLLPQITGLALSLGGVLGGALITEIVFNYPGTGYLLFRALTTLDYPLIQ 304
             +  K+  RN+++P +T + L  G +LGG+++ E VFN+PG G LL  ++   DYP+IQ
Sbjct: 216 TWVVLKHGLRNAMIPVVTMMGLQFGFLLGGSIVVEKVFNWPGLGRLLVDSVEMRDYPVIQ 275

Query: 305 GIFVILIASIYLANFIVDFLYALIDPRIR 333
              ++      L N +VD LYA I+P IR
Sbjct: 276 AEILLFSLEFILINLVVDVLYAAINPAIR 304


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: 306
Number of extensions: 14
Number of successful extensions: 5
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: 306
Length adjustment: 28
Effective length of query: 310
Effective length of database: 278
Effective search space:    86180
Effective search space used:    86180
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