GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01115 in Dinoroseobacter shibae DFL-12

Align deoxynucleoside transporter, permease component 1 (characterized)
to candidate 3607106 Dshi_0528 Monosaccharide-transporting ATPase (RefSeq)

Query= reanno::Burk376:H281DRAFT_01115
         (357 letters)



>FitnessBrowser__Dino:3607106
          Length = 334

 Score =  241 bits (614), Expect = 3e-68
 Identities = 136/303 (44%), Positives = 198/303 (65%), Gaps = 8/303 (2%)

Query: 19  LLIVNVLVVLVATWLSRGQFVDIDNLQSMGGQLPELGLLALGIMLSMVSGNGGIDLSGVG 78
           LLI+ V V  + + LS  +F+   NL SM  Q PE  +LAL + ++M++G  GIDLS VG
Sbjct: 16  LLIIMVFVFGLMSVLSPDRFLSSQNLTSMAFQFPEFAILALAMTIAMMTG--GIDLSVVG 73

Query: 79  LANLSGMVAAMLVPRLVNGDDSPVLYTSLFCAIV----LMMGLLGGLLNGVVIARLRLTP 134
           +ANLS +VAA+++    N +  P   ++++ AI     L +G + GL+NG ++A   L P
Sbjct: 74  IANLSAVVAALILTHFSNAE-MPAAQSAIWLAIAITAALCIGAIAGLINGSLVAFFGLPP 132

Query: 135 ILCTLGTQLLFTGFAVVISNGASVHVDYVEPLSDIGNGTVLQVPIAFCIFLAAVIVLGWL 194
           IL TLG+ L+FTGFA+ ++ G++V + + + ++ IGN T+  VP+   +F     +L  +
Sbjct: 133 ILATLGSGLVFTGFAIAMTGGSAV-MGFPDTVALIGNATLAGVPVPLILFAVLAFLLHLV 191

Query: 195 LKRSPFGLRLYLMGTNPKAAFYAGIPRARMLITTYAMCGVLASLAGLISATHTSSAKWDY 254
           L R+ FGLR+ + G NP AA YA I   RML+  Y + G+ AS+AGLI  +  +SAK DY
Sbjct: 192 LTRTAFGLRVTMYGANPLAALYAAIDINRMLLKVYVIAGMFASVAGLIIMSRANSAKADY 251

Query: 255 GNSYLLIAILIAVMGGVNPAGGHGRIICVFFAATVLQFLSSLFNLLGVSQFFGDCAWGFL 314
           G+SYLL+A+LIAV+GGVNP GG+GR+I V  A   +QFLSS  N+LGVS F  +  WG L
Sbjct: 252 GSSYLLLAVLIAVLGGVNPYGGYGRVIGVVLAVLSMQFLSSGLNMLGVSNFARELIWGAL 311

Query: 315 LLL 317
           L+L
Sbjct: 312 LIL 314


Lambda     K      H
   0.327    0.143    0.429 

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: 322
Number of extensions: 17
Number of successful extensions: 4
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: 357
Length of database: 334
Length adjustment: 29
Effective length of query: 328
Effective length of database: 305
Effective search space:   100040
Effective search space used:   100040
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