GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c07310 in Dinoroseobacter shibae DFL-12

Align Inositol transport system permease protein (characterized)
to candidate 3607867 Dshi_1275 Monosaccharide-transporting ATPase (RefSeq)

Query= reanno::Phaeo:GFF716
         (373 letters)



>FitnessBrowser__Dino:3607867
          Length = 374

 Score =  593 bits (1528), Expect = e-174
 Identities = 292/370 (78%), Positives = 326/370 (88%)

Query: 4   APTQFAEDERIKTRSKFREAMIRPELGGIIGTITVFAMFLIFAGDSGMFNSQGVMNWSQI 63
           AP     DERIK  SKFR+A+IRPELGGI GT+ VF  F + A DSGMF  QGV+NW+ +
Sbjct: 5   APPAPVVDERIKQTSKFRQALIRPELGGICGTVIVFVFFFLTAFDSGMFTPQGVLNWTLV 64

Query: 64  SAQFMIIAVGACLLMIAGEFDLSVGSMIGFAGMLIAIFSVTLGWPVWLAILVTFAIATAI 123
           SAQFMIIAVGACLLMIAGEFDLSVGSMIGFAGM+IA+F V L WP+W+AIL+TFAI  +I
Sbjct: 65  SAQFMIIAVGACLLMIAGEFDLSVGSMIGFAGMMIAVFGVVLAWPMWIAILITFAICLSI 124

Query: 124 GALNGFIVVRTGLPSFIVTLAFLFILRGFAIYLPQTIERKTIIGGVADAAEGDWLAALFG 183
           GALNG IV+RTGLPSFIVTLAFLFILRGF I++PQT+E KTIIGG+ DAAEGDWLA +FG
Sbjct: 125 GALNGAIVIRTGLPSFIVTLAFLFILRGFTIFIPQTLESKTIIGGIRDAAEGDWLAPVFG 184

Query: 184 GKILTGLFQWFGDNGWIAVFERGTRKGQPVVEGLPMLIVWAILLVIIGHVILTKTRFGNW 243
           GKI  G FQW GD G I  F RG R G+ V++GLPML++WA+LL+  GH++LT+TRFGNW
Sbjct: 185 GKIGNGFFQWLGDIGVIETFSRGNRAGEAVIDGLPMLVIWALLLIAFGHILLTRTRFGNW 244

Query: 244 IFAAGGDAEAARNSGVPVNRVKILMFMFTAFCATVFATCQVMEFGGAGSDRGLLKEFEAI 303
           IFAAGGDAEAARNSGVPVN+VKILMFMFTAFCA VFATCQVMEFG AG+DRGLLKEFEAI
Sbjct: 245 IFAAGGDAEAARNSGVPVNKVKILMFMFTAFCACVFATCQVMEFGSAGADRGLLKEFEAI 304

Query: 304 IAVVIGGALLTGGYGSVLGAALGALIFGVVQQGLFFAGVESSLFRVFLGLILLFAVILNT 363
           IAVVIGGALLTGGYGSV+GAALGALIFGVVQQGLFFAGVESSLFRVFLG+ILL AVILNT
Sbjct: 305 IAVVIGGALLTGGYGSVIGAALGALIFGVVQQGLFFAGVESSLFRVFLGVILLGAVILNT 364

Query: 364 YIRRVITGER 373
           YIRR+ITGER
Sbjct: 365 YIRRMITGER 374


Lambda     K      H
   0.330    0.145    0.443 

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: 728
Number of extensions: 40
Number of successful extensions: 1
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: 373
Length of database: 374
Length adjustment: 30
Effective length of query: 343
Effective length of database: 344
Effective search space:   117992
Effective search space used:   117992
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 (21.8 bits)
S2: 50 (23.9 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