GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01114 in Dinoroseobacter shibae DFL-12

Align deoxynucleoside transporter, substrate-binding component (characterized)
to candidate 3609045 Dshi_2434 rhamnose ABC transporter, periplasmic rhamnose-binding protein (RefSeq)

Query= reanno::Burk376:H281DRAFT_01114
         (334 letters)



>FitnessBrowser__Dino:3609045
          Length = 333

 Score =  129 bits (323), Expect = 1e-34
 Identities = 95/305 (31%), Positives = 150/305 (49%), Gaps = 6/305 (1%)

Query: 4   TRLGAALAAAALTVGVIAAAQAATNETIVTVVKVTGINWFNRMDEGVKEFAKDNPGVTAY 63
           T+L A L+ AA   G  A AQ      I  VVK  GI +F    +G +E A +  GV   
Sbjct: 7   TKLTAGLSLAASLFGTTAMAQDEMR--IALVVKALGIGFFEAAAQGAEEAAAELGGVEII 64

Query: 64  QTGPGRADAAQQLKIIEDLIAKKVNAIAVVPYDPPTLEPALKKAMDRGIKVVTHEADNA- 122
            TGP    A  Q+++I  LIA+ V+AIAV   D   L P LKKAM RGI V++ ++  A 
Sbjct: 65  YTGPTDTTAEGQIEVINSLIAQGVDAIAVSANDTDALVPTLKKAMQRGITVISWDSGVAP 124

Query: 123 KNTMVDIEAFDNTAYGAGLNERLASCMHNEGKWAVLVGSLGSRSQVQWADGGIGNAKAKY 182
           +   + +    N   G  + +  A  + + G  AVL  +  S +Q  W +  +      Y
Sbjct: 125 EGRQMHLNPSSNALIGNMIIKLAADHLPDGGDVAVLSATTTSTNQNIWIE-EMTKVLGDY 183

Query: 183 AKMNLVEPKLETNNDGERAYEVAKEVLRKHPDLKGFQGSSSLDVIGIGRAVEEAGMQGKI 242
             +N+V   +  ++  +++Y  A+ +++  PDL      +S+ ++   +AV +AG  G++
Sbjct: 184 PGINVVS-TVYGDDLADKSYREAQGLMQSFPDLDAIIAPTSVGIVAAAQAVADAGKIGQV 242

Query: 243 CVYGTGLPTEAGKFLESGAINGIAFWDPKLAGIAMNKVAKMLVDG-KTVENGADLGIPGY 301
            V G GLP+E    +ESGA    A W+P   G +   +A  L  G  T E G ++ I   
Sbjct: 243 NVTGLGLPSEMAGAIESGASKSFAIWNPIDLGYSAAMIAHALASGAATAEPGTEISIGRV 302

Query: 302 TKVTV 306
             +T+
Sbjct: 303 GTITL 307


Lambda     K      H
   0.314    0.133    0.385 

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: 228
Number of extensions: 15
Number of successful extensions: 2
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: 334
Length of database: 333
Length adjustment: 28
Effective length of query: 306
Effective length of database: 305
Effective search space:    93330
Effective search space used:    93330
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 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