GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01112 in Sinorhizobium meliloti 1021

Align deoxynucleoside transporter, permease component 2 (characterized)
to candidate SM_b20318 SM_b20318 sugar ABC transporter permease

Query= reanno::Burk376:H281DRAFT_01112
         (364 letters)



>FitnessBrowser__Smeli:SM_b20318
          Length = 343

 Score =  399 bits (1025), Expect = e-116
 Identities = 206/342 (60%), Positives = 254/342 (74%), Gaps = 3/342 (0%)

Query: 25  MTTPTVVEIAPSVEAPG-LRTR--LARNPEWFTVALIVVTCLIVGAINPRFFQFATLFDL 81
           M       ++ S E P  +RT     R+P   T  L+V+ C++VG INP F+Q + LFD+
Sbjct: 1   MADVAATPVSGSEEVPAAIRTMRWFIRHPPAVTFLLVVIVCIVVGTINPDFWQVSNLFDM 60

Query: 82  LHSATTMSLFALGTLVVLASGGIDVSFTAIAALTMYGITKAVFAWWPDAPFALILVTGAL 141
             S     LFALG LVVLASGG+DVSFTAIAAL MY IT  V  + PD     IL   A 
Sbjct: 61  ARSTVVRGLFALGVLVVLASGGLDVSFTAIAALVMYVITMLVTNYVPDLSIWPILGIAAA 120

Query: 142 GGVVLGMVNGLLVHRLKAPSLIVTIGTQYLYRGLLLTFIGTTFFMNIPHSMDRFGRIPLF 201
           GG +LG+ NGLLVH L+APSLIVTIGTQY  RG LLTFIGT  FMNIP SMD FG++ LF
Sbjct: 121 GGAILGICNGLLVHALQAPSLIVTIGTQYAIRGFLLTFIGTALFMNIPESMDAFGKLALF 180

Query: 202 FYHTADGLRAVLPVSVLALVAAAVVTWWLLNRTMMGRAVYAMGGSLAIAERLGYNLRAIH 261
            Y  A+G  + LP   L LV AA+ TW++L RT++GRA+YA+GG+ +IA RLGYNLR +H
Sbjct: 181 RYEGANGAVSTLPAYFLVLVVAALATWYILKRTLIGRAIYAVGGNASIASRLGYNLRTVH 240

Query: 262 LFVFGYTGMLAGIAGILHVSNNRLANPFDLVGSELDVIAAVILGGARITGGTGTVVGTLL 321
           +FVF Y G+LAGIAGI+HVS+NRLANPFDL GSELDVIAAV+LGGARITGG+GTV+GTLL
Sbjct: 241 VFVFAYAGLLAGIAGIMHVSSNRLANPFDLAGSELDVIAAVVLGGARITGGSGTVLGTLL 300

Query: 322 GVVLVTLIKSVLILVGVPSTWQKVIIGAFILLAGTLFALQRK 363
           GV+L+TL+ +VLILVG+PST Q  IIG FI++AG +F+++ K
Sbjct: 301 GVLLITLVNNVLILVGIPSTLQLAIIGLFIVVAGAMFSIRPK 342


Lambda     K      H
   0.328    0.141    0.426 

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: 416
Number of extensions: 10
Number of successful extensions: 1
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: 364
Length of database: 343
Length adjustment: 29
Effective length of query: 335
Effective length of database: 314
Effective search space:   105190
Effective search space used:   105190
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