GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tyt1 in Pseudomonas fluorescens FW300-N2E3

Align The 11 TMS Na+-dependent tyrosine transporter, Tyt1 (characterized)
to candidate AO353_05685 AO353_05685 symporter

Query= TCDB::Q8RHM5
         (438 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_05685
          Length = 467

 Score =  166 bits (421), Expect = 1e-45
 Identities = 109/348 (31%), Positives = 173/348 (49%), Gaps = 8/348 (2%)

Query: 14  FILTCVGSAVGMANIWAFPYRVGKYGGAVFLLIYFMFIALFSYVGLSAEYLIGRRAETGT 73
           FIL   GSAVG+ +IW FPY VG YGG  F+L++   IAL     + AE LIGRRA    
Sbjct: 18  FILAATGSAVGLGSIWKFPYMVGVYGGGAFVLVFLACIALIGVPVMLAETLIGRRARQSP 77

Query: 74  LGSYEYAWKDVG-KGKLGYGLAYIPLLGSMSIAIGYAVIAAWVLRTFGAAVTGKILEVDT 132
             + +    + G   K  +G A+  ++ ++ I   Y+V+  W L        G    V  
Sbjct: 78  ANALKVLALEAGHSAKWSWG-AFAGMITALLILSFYSVVGGWSLDYIIDMGRGDFQGVTA 136

Query: 133 AQ---FFGEAVTGNFVIMPWHIAVIVLTLLTLFAGAKS-IEKTNKIMMPAFFVLFFILAV 188
            Q   +FG  +   + +  WH   ++L+   +  G  + +E++ +IMMP  FV+  IL  
Sbjct: 137 DQVGAYFGGVIADPWRLTLWHTLFMLLSAFVIARGVVAGLERSLRIMMPLLFVMLVILLG 196

Query: 189 RVAFLPGAIEGYKYLFVPDWSYLSNVETWINAMGQAFFSLSITGSGMIVCGAYLDKKEDI 248
                   +EG  ++F  D++    ++  + AMG AFFSLS+    +++ GAY+ K   I
Sbjct: 197 YSLTTGHFMEGVHFMF--DFNPDKLLDGLLPAMGHAFFSLSVGVGSIMIYGAYMPKHSSI 254

Query: 249 INGALQTGVFDTIAAMIAAFVVIPASFAFGYPASAGPSLMFMTIPEVFKQMPFGQLLAIL 308
               +   + DT  +++A   + P  FA G   S GP LMF+++P  F  + FGQL+ ++
Sbjct: 255 SGTIVGVALLDTFVSLLAGLALFPIVFAAGLNPSEGPGLMFVSLPFAFGNVAFGQLMGVV 314

Query: 309 FFVSVVFAAISSLQNMFEVVGESIQTRFKMTRKSVIVLLGIIALVIGI 356
           FFV V  AA SS  ++ E +   +  R  + R  V   L      +G+
Sbjct: 315 FFVLVAIAAWSSAISLLEPMVAYLVERTNIRRGWVTFWLAFSCWFVGL 362


Lambda     K      H
   0.328    0.143    0.434 

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: 607
Number of extensions: 29
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 438
Length of database: 467
Length adjustment: 33
Effective length of query: 405
Effective length of database: 434
Effective search space:   175770
Effective search space used:   175770
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: 51 (24.3 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