GapMind for catabolism of small carbon sources

 

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

Align Glutamate:Na+ symporter (characterized)
to candidate 3607853 Dshi_1261 sodium/glutamate symporter (RefSeq)

Query= TCDB::P73275
         (402 letters)



>FitnessBrowser__Dino:3607853
          Length = 402

 Score =  343 bits (880), Expect = 5e-99
 Identities = 174/391 (44%), Positives = 265/391 (67%), Gaps = 4/391 (1%)

Query: 11  TIIVAILVLYIGKYLTKKIKFLQSFNIPDAVSGGVLASLFFGLIYGIFRTEVAFNFPIRD 70
           ++ + +LV +IG +LT+K++FL+ +NIP+ VSGG+  +L     + +   ++ F+  +RD
Sbjct: 11  SVTLGLLVYFIGAFLTRKVQFLKDYNIPEPVSGGLAIALVTWAFFALTGRQIVFDLAVRD 70

Query: 71  AFLIIFFTCIGLSSKLKVLLQGGKPLLILLATAVSFLVIQNFVGVGMASLLGQALPVGLL 130
             L++FF+ IGL+++L  LL+GG+ LL+LL   V F+V+QN VG+    L     P+ +L
Sbjct: 71  YLLVLFFSTIGLNARLADLLRGGRLLLVLLGLTVGFMVLQNLVGLVGTILFDLPTPMAVL 130

Query: 131 SGSISLSGGHGTAIAWSPVFYDNHGIRNASEIAIACATFGLVFGGIVGGPIAKFLIIRNK 190
            GS +L GGHGTAIAW P   +  G   A+E+ IA AT GLVF  ++GGPIAK LI RN 
Sbjct: 131 LGSAALIGGHGTAIAWGPEIEEVTGFAAAAEVGIAAATLGLVFAALIGGPIAKRLIDRNG 190

Query: 191 LEPDCDTKDLTIGIRRDQDNVQ---IDYNTMLHTILVIGVTIGLGYEINDLVAKLGLMLP 247
           L  +     + +G+  ++       +++ +++ ++L   V I LG+  +  +A  G+MLP
Sbjct: 191 LSGEEGAAPV-VGLEFEEPGEAPEVVNHVSLMRSMLAAHVAILLGFLAHGAIAAAGVMLP 249

Query: 248 AFVSCLLAGIVLTNTIPLAFKKFPWPAETPSLALISDVSLGLFLAISLMSLQLWTLADIG 307
            FV CLL GIV +NTIP  F +  WPA + +LA++SD SL +FLA+SLMS+QLWTL ++G
Sbjct: 250 LFVPCLLVGIVTSNTIPYLFPRLTWPAGSRALAVVSDYSLSVFLAMSLMSMQLWTLTELG 309

Query: 308 GVIALILLVQFMATVLYSIAVVFPLMGRDYNAAVVCSGYSGLTLGATPTAIANMTAVTEK 367
           G +  +L +Q   TV + + VVF  +GR++ AAV+ +G++G  LGATPTAIANM++VT++
Sbjct: 310 GPLLGVLAMQVAMTVAFILLVVFAALGRNFTAAVLSAGFAGFALGATPTAIANMSSVTKR 369

Query: 368 FGAAPQAFIVVPLVGAFFIDIANAFVIQQFL 398
           +G AP AFIV+PLV AFF+D+ANA +IQ F+
Sbjct: 370 YGPAPLAFIVLPLVSAFFVDLANAVIIQVFV 400


Lambda     K      H
   0.329    0.145    0.427 

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: 528
Number of extensions: 33
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: 402
Length of database: 402
Length adjustment: 31
Effective length of query: 371
Effective length of database: 371
Effective search space:   137641
Effective search space used:   137641
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: 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