GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS03645 in Brucella inopinata BO1

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate WP_008511382.1 BIBO1_RS19480 ABC transporter permease

Query= uniprot:D8IZC8
         (344 letters)



>NCBI__GCF_000182725.1:WP_008511382.1
          Length = 332

 Score =  197 bits (502), Expect = 2e-55
 Identities = 118/306 (38%), Positives = 177/306 (57%), Gaps = 10/306 (3%)

Query: 40  VLYLLFYGLTLYLSGDGTSNFASAENTMNILRQVAINLVLAAGMTFVILTAGIDLSVGSV 99
           +L L+   L + L       FASA N  NI    +I +++A G   VILT  IDLSV + 
Sbjct: 10  LLLLVIIALMVGLFTSRAPGFASAHNLANIFNDTSILIIIALGQMAVILTKAIDLSVAAN 69

Query: 100 LAVSAVLGMQVSLGAAPGWAIPMFIFS------GLVMGMVNGAMVALLNINAFVVTLGTM 153
           LA +   GM V++  A    +P+ +        G V+G +NG +V  LNI A VVTLGT+
Sbjct: 70  LAFT---GMAVAMLNATYPGLPLVLLIVLAIGIGAVLGAINGILVWKLNIPAIVVTLGTL 126

Query: 154 TAFRGAAYLLADGTTVLNNDIPS-FEWIGNGDFLHVPWLIWVAVAVVLLSWVILRKTVLG 212
           T +RG A++L+ G  V  + + + F       FL +P L W A+ ++   +V++ +T  G
Sbjct: 127 TIYRGMAFVLSGGAWVNAHQMTAPFLNTPRTPFLGLPLLGWTAILIIAFIYVLMTRTFFG 186

Query: 213 MHIYAIGGNLQAARLTGIRVGLVLLFVYSISGLFSGLAGAMSASRLYGANGNWGSGYELD 272
             +YA GGN  AA  TGI VG    F + +SG  +GL G +  SR   A  +  +G+ELD
Sbjct: 187 RALYASGGNPTAAVYTGIDVGRTRFFAFVLSGALAGLCGYLWVSRYAVAYVDVAAGFELD 246

Query: 273 AIAAVVLGGTSLMGGVGSIWGTVVGALIIGVMNNGLTILGLSSFWQYVAKGAVIVLAVIL 332
           ++AA V+GG S +GG+G++ G V+GAL +GV+ N L ++ +S FWQ    G+VI+LAVI 
Sbjct: 247 SVAACVIGGISTLGGIGTVAGAVLGALFLGVIKNALPVIDISPFWQMAISGSVIILAVIF 306

Query: 333 DKWRQK 338
           +  ++K
Sbjct: 307 NARQEK 312


Lambda     K      H
   0.324    0.138    0.417 

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: 289
Number of extensions: 17
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: 344
Length of database: 332
Length adjustment: 28
Effective length of query: 316
Effective length of database: 304
Effective search space:    96064
Effective search space used:    96064
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 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