GapMind for catabolism of small carbon sources

 

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

Align iron(III) dicitrate transport system permease protein FecD (characterized)
to candidate 3607140 Dshi_0562 transport system permease protein (RefSeq)

Query= CharProtDB::CH_004160
         (318 letters)



>FitnessBrowser__Dino:3607140
          Length = 348

 Score =  179 bits (454), Expect = 9e-50
 Identities = 119/334 (35%), Positives = 183/334 (54%), Gaps = 32/334 (9%)

Query: 10  TLALAGCALLSLH------MGVIPVP----WR--------ALLT-DWQAGHEHYYVLMEY 50
           +L +AG A+L L       +G + VP    W          LLT DW  G     ++ E 
Sbjct: 18  SLTVAGVAVLLLSISVAVSLGAVAVPLGTVWGIMADRILPGLLTPDWTTGQAA--IVWEI 75

Query: 51  RLPRLLLALFVGAALAVAGVLIQGIVRNPLASPDILGVNHAASLASVGALLLMPS-LPVM 109
           RLPR LLA  VGA LA+ G  +Q + RNPLA P +LG++  A+  ++ ALL     L ++
Sbjct: 76  RLPRALLAAMVGAGLALVGASLQSVTRNPLADPHLLGISSGAAFGAILALLHTGLFLGLL 135

Query: 110 VLPLLAFAGGMAGLILLKMLAKTHQPM---KLALTGVALSACWASLTDYLM-LSRPQDVN 165
            +PLLAFAG +A  +L+  +    Q     +L L GVA+S    S  + L+ +  P+  +
Sbjct: 136 TVPLLAFAGALAATLLVLGVTSFAQATGADRLVLAGVAVSFIVMSCANILIFIGDPRATH 195

Query: 166 NALLWLTGSLWGRDWSFVKIAIPLMILFLPLSLSFCRD---LDLLALGDARATTLGVSVP 222
             + W+ G L    W   ++  P +IL +   L F  +   L+ + +GD  A+TLG+ + 
Sbjct: 196 TVVFWMLGGLGLAQWD--QLLFPAVIL-VGCGLWFLANASRLNAMTIGDETASTLGIPIA 252

Query: 223 HTRFWALLLAVAMTSTGVAACGPISFIGLVVPHMMRSITGGRHRRLLPVSALTGALLLVV 282
             R    ++   +T   VA  G I F+GL++PH++R + GG + R+LP SAL GA+ LV 
Sbjct: 253 RFRLSVFVVGALLTGCMVAFSGIIGFVGLMIPHIVRMLVGGDYARVLPASALVGAIFLVW 312

Query: 283 ADLLARIIHPPLELPVGVLTAIIGAPWFVWLLVR 316
           AD+ AR +  P ++P+G++T +IG  +FVWLL R
Sbjct: 313 ADIAARTVMAPEDIPIGIVTGLIGGAFFVWLLRR 346


Lambda     K      H
   0.330    0.142    0.447 

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: 339
Number of extensions: 11
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: 318
Length of database: 348
Length adjustment: 28
Effective length of query: 290
Effective length of database: 320
Effective search space:    92800
Effective search space used:    92800
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: 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