GapMind for catabolism of small carbon sources

 

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

Align Serine/threonine transporter SstT; Na(+)/serine-threonine symporter (characterized)
to candidate AO353_20105 AO353_20105 serine/threonine protein kinase

Query= SwissProt::P0AGE4
         (414 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_20105
          Length = 410

 Score =  553 bits (1425), Expect = e-162
 Identities = 282/409 (68%), Positives = 341/409 (83%)

Query: 3   TQRSPGLFRRLAHGSLVKQILVGLVLGILLAWISKPAAEAVGLLGTLFVGALKAVAPILV 62
           T   P L +RL H SLV QI++GL++GI LA  +   A++   +G +FV ALKAVAPILV
Sbjct: 2   TAAPPTLLQRLKHTSLVTQIVIGLIVGIALALFAPEVAKSTAFIGKVFVSALKAVAPILV 61

Query: 63  LMLVMASIANHQHGQKTNIRPILFLYLLGTFSAALAAVVFSFAFPSTLHLSSSAGDISPP 122
            +LVMASIANH+HGQ+T+I+PILFLYLLGTF+AA+ AVV S  FPS+L LS+    IS P
Sbjct: 62  FVLVMASIANHKHGQETHIKPILFLYLLGTFAAAVVAVVASSLFPSSLVLSTHDVAISAP 121

Query: 123 SGIVEVMRGLVMSMVSNPIDALLKGNYIGILVWAIGLGFALRHGNETTKNLVNDMSNAVT 182
            GI EV++ L++S+V NPI AL+  N+IGIL WAIG+G A+RH  ETT+ ++ D+SN VT
Sbjct: 122 GGISEVLQSLLLSVVDNPISALMNANFIGILAWAIGMGIAIRHAGETTRTVLGDLSNGVT 181

Query: 183 FMVKLVIRFAPIGIFGLVSSTLATTGFSTLWGYAQLLVVLVGCMLLVALVVNPLLVWWKI 242
            +V+LVIRFAP+GIFGLV+STLAT+GF  L GY  LL VL+GCML VALV+NP +V+WK+
Sbjct: 182 LIVRLVIRFAPLGIFGLVASTLATSGFGALIGYLHLLAVLLGCMLFVALVMNPAIVYWKL 241

Query: 243 RRNPFPLVLLCLRESGVYAFFTRSSAANIPVNMALCEKLNLDRDTYSVSIPLGATINMAG 302
           RRNP+PLVL CLRESG+ AFFTRSSAANIPVN+ L ++L L  DTYSVSIPLGATINMAG
Sbjct: 242 RRNPYPLVLTCLRESGITAFFTRSSAANIPVNLELSKRLGLHEDTYSVSIPLGATINMAG 301

Query: 303 AAITITVLTLAAVNTLGIPVDLPTALLLSVVASLCACGASGVAGGSLLLIPLACNMFGIS 362
           AAITITVLTLAAV+TLGI VD+PTA+LLSVVA++CACGASGVAGGSLLLIPLAC++FGI 
Sbjct: 302 AAITITVLTLAAVHTLGIAVDIPTAVLLSVVAAICACGASGVAGGSLLLIPLACSLFGIP 361

Query: 363 NDIAMQVVAVGFIIGVLQDSCETALNSSTDVLFTAAACQAEDDRLANSA 411
           ++IAMQVVAVGFIIGVLQDS ETALNSSTDVLFTAAAC  ED+++   A
Sbjct: 362 SEIAMQVVAVGFIIGVLQDSAETALNSSTDVLFTAAACLGEDEKVQRLA 410


Lambda     K      H
   0.325    0.138    0.405 

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: 438
Number of extensions: 7
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: 414
Length of database: 410
Length adjustment: 31
Effective length of query: 383
Effective length of database: 379
Effective search space:   145157
Effective search space used:   145157
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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