GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fecC in Sinorhizobium meliloti 1021

Align Fe(3+) dicitrate transport system permease protein FecC; Iron(III) dicitrate transport system permease protein FecC (characterized)
to candidate SMa1745 SMa1745 ABC transporter permease, Fe3+-siderophore transport system

Query= SwissProt::P15030
         (332 letters)



>FitnessBrowser__Smeli:SMa1745
          Length = 366

 Score =  191 bits (484), Expect = 3e-53
 Identities = 118/322 (36%), Positives = 175/322 (54%), Gaps = 3/322 (0%)

Query: 10  LWGLPVAALIIIFWLSLFCYSAIPVSGADATRALLPGHTPTLPEALVQNLRLPRSLVAVL 69
           LW   + AL+I+   +        V G D   A + G    +  A V  LR+PR+++A+L
Sbjct: 43  LWLAALFALVIVLLAASVTVGTRNV-GWDDVAAAMGGAQNNIDRASVA-LRIPRTVLALL 100

Query: 70  IGASLALAGTLLQTLTHNPMASPSLLGINSGAALAMALTSALSPTPIAGYSLSFIAACGG 129
            G +L LAG ++Q +T NP+A P +LG+N GA+LA+ +  A        Y+  ++A  G 
Sbjct: 101 AGGALGLAGAIMQGVTRNPLADPGILGVNMGASLAVVVGVAWFGMSSL-YAYIWVAILGA 159

Query: 130 GVSWLLVMTAGGGFRHTHDRNKLILAGIALSAFCMGLTRITLLLAEDHAYGIFYWLAGGV 189
           G + + V   G   R      K+ LAG A S     +    +L   D A GI  W  GGV
Sbjct: 160 GCAAIFVYAIGSLGRGGATPLKMALAGAATSVAFASMVIAVVLPRGDIAGGIHSWQIGGV 219

Query: 190 SHARWQDVWQLLPVVVTAVPVVLLLANQLNLLNLSDSTAHTLGVNLTRLRLVINMLVLLL 249
             A ++ +  +LP ++    + LL A +LN L L D  A  LG ++   R V ++  +LL
Sbjct: 220 GGATYERILPVLPFLLVGFVISLLSARKLNSLALGDELATGLGESVATARAVASLGAILL 279

Query: 250 VGACVSVAGPVAFIGLLVPHLARFWAGFDQRNVLPVSMLLGATLMLLADVLARALAFPGD 309
            GA  ++ GP+ F+GL+VPHL R   G D R +LP S L GA L+L ADVL R +A P +
Sbjct: 280 CGATTAICGPIGFLGLVVPHLCRLLVGVDHRWLLPFSTLAGACLLLAADVLGRIVARPAE 339

Query: 310 LPAGAVLALIGSPCFVWLVRRR 331
           +  G V A+IG+P F+W+VRR+
Sbjct: 340 IDVGIVTAMIGAPFFIWIVRRQ 361


Lambda     K      H
   0.327    0.140    0.436 

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: 358
Number of extensions: 24
Number of successful extensions: 2
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: 332
Length of database: 366
Length adjustment: 29
Effective length of query: 303
Effective length of database: 337
Effective search space:   102111
Effective search space used:   102111
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 (21.7 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