GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylHsa in Sinorhizobium meliloti 1021

Align Xylose/arabinose import permease protein XylH (characterized, see rationale)
to candidate SMa0070 SMa0070 ABC transporter permease

Query= uniprot:Q4J711
         (356 letters)



>FitnessBrowser__Smeli:SMa0070
          Length = 327

 Score =  149 bits (376), Expect = 1e-40
 Identities = 94/316 (29%), Positives = 161/316 (50%), Gaps = 18/316 (5%)

Query: 14  LFLVNVIIALFFYFENSAYFSSNNITTIFQYLAEIGIIAIGEAMLMLCGEIDLSPPALAN 73
           L L+ V++ +F    N    S  N+  +   L E+ ++AIG  +LM+CGE DLS  ++  
Sbjct: 17  LALLFVLVLVFQAKSNGILLSFENMRGVMGLLPEMALVAIGVTLLMICGEFDLSVGSVFA 76

Query: 74  FVPLITLTIYNSIYQAISPTPAIVVSILLSLGLASLIGLMNGLITTKAKVNSLITTVGTL 133
            +P+    + NS            V++LL L +   IG +NG +T +  + S ITT+G L
Sbjct: 77  LMPMSMAVLLNS-------GVPFTVAVLLGLMICGAIGFINGYVTLQFSIPSFITTLGML 129

Query: 134 FLFNGIALIYSGGYPESFP------YFRFLGGTVSILPVPFIWSLGALVFLILLLHYTKI 187
           F+   + ++ SGG+P   P       F       S   + F+W +     +  LL  T  
Sbjct: 130 FIARSLTIVISGGFPPLLPPDLPTWLFTDYIWQGSPFRMSFLWFVVIAALVAALLSLTNF 189

Query: 188 GVWTIAAGSNPTGASEVGVPVDRVKIINFIIMANIGALVGIIQGSRVLTIGAT--NFTAD 245
           G W  A G     A+ +G+PV RVKI+ F++ + +    G++Q   VL +G+   +    
Sbjct: 190 GNWIRATGGFNEAAASMGIPVKRVKIVCFMLCSVLAGFAGLLQ---VLRLGSPLPSIGEG 246

Query: 246 VVLEGIAAAVIGGTSLVGGKGSLVGAFLGSVFISELLNGFNILGINAYEFDAILGGAIVV 305
           + L+ +AAAVIGGT+L GG G++ GA +G++ I  + NG  +  ++A  F   +G   + 
Sbjct: 247 LELQAVAAAVIGGTALAGGIGTVFGAIIGTLLIRTIDNGLVLSRVDANWFKFAIGVLTMF 306

Query: 306 VMVLSYYAKRASYKLK 321
            ++ + +  + S K+K
Sbjct: 307 AVIANAWMGKMSRKIK 322


Lambda     K      H
   0.325    0.143    0.404 

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: 15
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: 356
Length of database: 327
Length adjustment: 29
Effective length of query: 327
Effective length of database: 298
Effective search space:    97446
Effective search space used:    97446
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 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