GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01112 in Paraburkholderia bryophila 376MFSha3.1

Align deoxynucleoside transporter, permease component 2 (characterized)
to candidate H281DRAFT_03225 H281DRAFT_03225 mannose ABC transporter membrane protein /fructose ABC transporter membrane protein /ribose ABC transporter membrane protein

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



>FitnessBrowser__Burk376:H281DRAFT_03225
          Length = 328

 Score =  147 bits (371), Expect = 4e-40
 Identities = 105/340 (30%), Positives = 173/340 (50%), Gaps = 13/340 (3%)

Query: 25  MTTPTVVEIAPSVEAPGLRTRLARNPEWFTVALIVVTCLIVGAINPRFFQFATLFDLLHS 84
           M+TP+    AP+        RL    E   +  +V+ C    + + RF  F  L  +L  
Sbjct: 1   MSTPS----APAGHPRHFSDRLPSLAEVGPLIALVLACGFFISQSSRFLSFQNLSLILQQ 56

Query: 85  ATTMSLFALGTLVVLASGGIDVSFTAIAALTMYGITKAVFAWWPDAPFALILVTGALGGV 144
              +++ A+G  +++ +GGID+S   + A     +TK  FA     P AL ++ G     
Sbjct: 57  TMVVAVIAIGQTLIVLTGGIDLSCGMVMAFGSIIMTK--FAVTLGLPPALAILCGIGAST 114

Query: 145 VLGMVNGLLVHRLKAPSLIVTIGTQYLYRGLLLTFIGTTFFMNIPHSMDRFGRIPLFFYH 204
           + G++NG+L+ R+K P+ IVT+GT  +   L   +       N+P ++  FG    F   
Sbjct: 115 LFGVLNGVLITRIKLPAFIVTLGTLNIAFALTQIYSNAESVSNLPDAIMFFGNT--FKLG 172

Query: 205 TADGLRAVLPVSVLALVAAAVVTWWLLNRTMMGRAVYAMGGSLAIAERLGYNLRAIHLFV 264
            AD    V   +VL L+   + TW++L  T+ GR +YA+G +   A  +G + + I L V
Sbjct: 173 PAD----VTYGTVLTLLMY-LATWFVLRDTVPGRHLYALGNNAEAARLMGLSSQKILLTV 227

Query: 265 FGYTGMLAGIAGILHVSNNRLANPFDLVGSELDVIAAVILGGARITGGTGTVVGTLLGVV 324
           +   G + G+A +L VS   + +P       LD I AV+LGG  + GG G++ GTLLG +
Sbjct: 228 YTLAGAIYGVAALLSVSRTGVGDPQAGQTENLDSITAVVLGGTSLFGGRGSISGTLLGAL 287

Query: 325 LVTLIKSVLILVGVPSTWQKVIIGAFILLAGTLFALQRKR 364
           +V + ++ L L+GV S +Q +I G  ++LA     L  +R
Sbjct: 288 IVGVFRNGLTLIGVSSVYQVLITGMLVILAVAADKLSHRR 327


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: 296
Number of extensions: 11
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: 364
Length of database: 328
Length adjustment: 29
Effective length of query: 335
Effective length of database: 299
Effective search space:   100165
Effective search space used:   100165
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