GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01112 in Brucella inopinata BO1

Align deoxynucleoside transporter, permease component 2 (characterized)
to candidate WP_008511382.1 BIBO1_RS19480 ABC transporter permease

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



>NCBI__GCF_000182725.1:WP_008511382.1
          Length = 332

 Score =  153 bits (386), Expect = 7e-42
 Identities = 107/321 (33%), Positives = 164/321 (51%), Gaps = 32/321 (9%)

Query: 57  LIVVTCLIVGAINPRFFQFAT---LFDLLHSATTMSLFALGTLVVLASGGIDVSFTAIAA 113
           L+V+  L+VG    R   FA+   L ++ +  + + + ALG + V+ +  ID+S  A  A
Sbjct: 12  LLVIIALMVGLFTSRAPGFASAHNLANIFNDTSILIIIALGQMAVILTKAIDLSVAANLA 71

Query: 114 LTMYGITKAVF-AWWPDAPFALILVTGALGGVVLGMVNGLLVHRLKAPSLIVTIGTQYLY 172
            T  G+  A+  A +P  P  L++V     G VLG +NG+LV +L  P+++VT+GT  +Y
Sbjct: 72  FT--GMAVAMLNATYPGLPLVLLIVLAIGIGAVLGAINGILVWKLNIPAIVVTLGTLTIY 129

Query: 173 RGLLLTFIG---------TTFFMNIPHSMDRFGRIPLFFYHTADGLRAVLPVSVLALVAA 223
           RG+     G         T  F+N P +   F  +PL       G  A+L ++ + +   
Sbjct: 130 RGMAFVLSGGAWVNAHQMTAPFLNTPRTP--FLGLPLL------GWTAILIIAFIYV--- 178

Query: 224 AVVTWWLLNRTMMGRAVYAMGGSLAIAERLGYNLRAIHLFVFGYTGMLAGIAGILHVSNN 283
                 L+ RT  GRA+YA GG+   A   G ++     F F  +G LAG+ G L VS  
Sbjct: 179 ------LMTRTFFGRALYASGGNPTAAVYTGIDVGRTRFFAFVLSGALAGLCGYLWVSRY 232

Query: 284 RLANPFDLVGSELDVIAAVILGGARITGGTGTVVGTLLGVVLVTLIKSVLILVGVPSTWQ 343
            +A      G ELD +AA ++GG    GG GTV G +LG + + +IK+ L ++ +   WQ
Sbjct: 233 AVAYVDVAAGFELDSVAACVIGGISTLGGIGTVAGAVLGALFLGVIKNALPVIDISPFWQ 292

Query: 344 KVIIGAFILLAGTLFALQRKR 364
             I G+ I+LA    A Q KR
Sbjct: 293 MAISGSVIILAVIFNARQEKR 313


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: 324
Number of extensions: 15
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 364
Length of database: 332
Length adjustment: 29
Effective length of query: 335
Effective length of database: 303
Effective search space:   101505
Effective search space used:   101505
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 24 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