GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0030 in Synechococcus elongatus PCC 7942

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 Synpcc7942_0822 Synpcc7942_0822 permease protein of oligopeptide ABC

Query= TCDB::Q9WXN7
         (338 letters)



>FitnessBrowser__SynE:Synpcc7942_0822
          Length = 341

 Score =  177 bits (449), Expect = 3e-49
 Identities = 107/346 (30%), Positives = 177/346 (51%), Gaps = 24/346 (6%)

Query: 3   SKSMFKYLLRRFIFLLVTYIVATTIVFILPRAIPGNPLSQILSGLSRVAQANPEAIRAAE 62
           ++ + +YLL R + L +      T++F+L RA PG+P+  IL          P+A  AA 
Sbjct: 4   ARDLGRYLLARLLLLPLMLWTIATLIFLLLRATPGDPIDAILG---------PKAPAAAR 54

Query: 63  RTLMEEFGLGKPWYVQYFEFITKALRGDLGTSITFYPRKVIDLIIPVIPWTLILLLPATI 122
             L  + GL +P + QYF+++ + L+GDLG S++   + V  +I    P T  L + +  
Sbjct: 55  LALRSQLGLDRPLWQQYFDYLGQLLKGDLGQSLSSQGQSVRQIIGEYFPATAELAIASLA 114

Query: 123 VAWILGNSLGALAAYKRNTWIDKGVLTTSLIVSQIPYYWLGMIFIFLFGVKLGWLPV--- 179
           +A  +G  LG +AA K N+  +       ++   +P +W  M+   LF V LGW PV   
Sbjct: 115 IAIAIGLGLGLMAAAKPNSRRETASRLFGILTYALPTFWAAMLAQLLFAVDLGWFPVGTR 174

Query: 180 -----------QGAYSQGTIPNLSWSFFVDVLKHYIMPFASIVVSAMGGWAIGMRLMVIY 228
                       G Y    +    W      L++  +P  ++ +   G +   +R+ +  
Sbjct: 175 YPVTLDPPLGPTGLYVLDALLKADWRAAGLALRYLALPALTLGLLLSGVFERLVRVNLGQ 234

Query: 229 ELGSDYAMFSEYLGMKDKRIF-KYVFRNSLLPQITGLALSLGGVLGGALITEIVFNYPGT 287
            L +DY       G+ ++R+   +  RN+L+P +T L L+L  +LGGAL+TE+ F++PG 
Sbjct: 235 SLQADYIDAGRSRGLSERRLLLNHALRNALIPVVTLLGLTLASLLGGALLTEVAFSWPGL 294

Query: 288 GYLLFRALTTLDYPLIQGIFVILIASIYLANFIVDFLYALIDPRIR 333
              L+ A++  DY  +QGI V     + LA+ +VDF+ ALIDPRIR
Sbjct: 295 ANRLYEAISLRDYSTVQGIIVFFGCLVVLASIVVDFINALIDPRIR 340


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: 314
Number of extensions: 17
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: 341
Length adjustment: 28
Effective length of query: 310
Effective length of database: 313
Effective search space:    97030
Effective search space used:    97030
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