GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0030 in Sinorhizobium meliloti 1021

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 SMc00787 SMc00787 peptide ABC transporter permease

Query= TCDB::Q9WXN7
         (338 letters)



>FitnessBrowser__Smeli:SMc00787
          Length = 334

 Score =  164 bits (416), Expect = 2e-45
 Identities = 110/344 (31%), Positives = 178/344 (51%), Gaps = 27/344 (7%)

Query: 6   MFKYLLRRFIFLLVTYIVATTIVFILPRAIPGNPLSQILSGLSRVAQANPEAIRAAER-- 63
           MF++LL R   L+ T+I  + I F   R +PG+P++ +LSG         E + + ER  
Sbjct: 1   MFRFLLGRLAVLIPTFIGVSIIAFSFIRLLPGDPVA-LLSG---------ERVMSPERHA 50

Query: 64  TLMEEFGLGKPWYVQYFEFITKALRGDLGTSITFYPRKVIDLIIPVIPWTLILLLPATIV 123
            +  + G  +P  +QY +++   L+GD GTSI    + VID  + + P T+ L L A I 
Sbjct: 51  EISHQLGFDRPIVMQYLDYLWGVLQGDFGTSIVT-KKPVIDQFMELFPATVELSLCAIIF 109

Query: 124 AWILGNSLGALAAYKRNTWIDKGVLTTSLIVSQIPYYWLGMIFIFLFGVKLGWLPVQGAY 183
           A ++G   G +AA KR +  D+ ++ T+LI   +P +W G++ I +    L W PV G  
Sbjct: 110 AVVVGIPAGVVAAVKRGSIFDQIIMGTALIGFSMPIFWWGLLLIIVVSGILQWTPVSGRI 169

Query: 184 S-QGTIPNLSWSFFVDVL------------KHYIMPFASIVVSAMGGWAIGMRLMVIYEL 230
           S     P+++    VD L             H I+P   +    +   A   R  ++  L
Sbjct: 170 SLMFFFPSVTGFMLVDSLLSGQEGAFQSAFNHLILPTIVLGTIPLAVIARQTRSAMLEVL 229

Query: 231 GSDYAMFSEYLGMKDKRIFK-YVFRNSLLPQITGLALSLGGVLGGALITEIVFNYPGTGY 289
             DY   +   G+   R+   +  RN+++P +T + L +G +L GA++TE +F++PG G 
Sbjct: 230 SEDYVRTARAKGLSTFRVVGIHALRNAMIPVVTTIGLQIGVMLAGAILTETIFSWPGIGK 289

Query: 290 LLFRALTTLDYPLIQGIFVILIASIYLANFIVDFLYALIDPRIR 333
            +  ++   DY +IQG  +I+ A I L N  VD LY LI+PRIR
Sbjct: 290 WMVDSVFRRDYAVIQGGLLIIAAVIMLVNLAVDLLYGLINPRIR 333


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: 311
Number of extensions: 21
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: 334
Length adjustment: 28
Effective length of query: 310
Effective length of database: 306
Effective search space:    94860
Effective search space used:    94860
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