GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB in Phaeobacter inhibens BS107

Align L-serine ammonia-lyase (EC 4.3.1.17) (characterized)
to candidate GFF448 PGA1_c04590 putative threonine dehydratase

Query= BRENDA::A0QY48
         (316 letters)



>FitnessBrowser__Phaeo:GFF448
          Length = 324

 Score =  200 bits (508), Expect = 4e-56
 Identities = 130/314 (41%), Positives = 174/314 (55%), Gaps = 21/314 (6%)

Query: 9   ISGAAARIAADIVRTPLLAADWGDPRCP--LWLKAETLQPIGAFKIRGAFNALGRLDTHT 66
           I+ AA R++     TPLL++ + D      + +KAE LQ  G+FK RG + AL  L    
Sbjct: 7   IAAAADRLSGHARETPLLSSPFLDEIAGRRVLIKAECLQHTGSFKFRGGWAALSALTDEQ 66

Query: 67  RARGVVAYSSGNHAQAVAYAAAAYGVPAHIVMPEETPAVKVEATRRRGAHVVLCGAGERE 126
           R RGV+AYSSGNHAQ VA AAAA+  PA I+MP++ PA+K+  TR  GA VVL    +  
Sbjct: 67  RHRGVLAYSSGNHAQGVAAAAAAHTTPAVILMPQDAPAIKIANTRALGAEVVLFDRAKDN 126

Query: 127 RTA--AELVEKTGAVLIPPFDHPDIIAGQGTIGIEIAEDLPEL----ATVLIPVSGGGLA 180
           R A  AEL E  G  LI P+D  +++AGQGT+G+EIA    +L    A VL+   GGGL 
Sbjct: 127 RDAIGAELAEARGLTLIKPYDDVEVVAGQGTVGLEIARQAADLDVTEADVLVCCGGGGLT 186

Query: 181 SGIGTAIRALRPKAKIFAVEPELAADTAESLALGSIVEWPVAKRNRTIADG-----LRST 235
           +G+  A+    PK K+   EPE   D   SL  G I       RN   A       L   
Sbjct: 187 AGVALALEQTAPKMKVSPCEPERFDDVTRSLVAGKIC------RNEASAGSLCDAILTPA 240

Query: 236 PSELTFAHLRQVIDDVITVSEDEIRSAVRELALRARLVAEPSGAVSLAG--YRKAALPDG 293
           P E+TF  L ++    I VSE++   A+    LR ++V EP GAVSLA   +    L   
Sbjct: 241 PGEITFPILARLCGSGIVVSEEDAMRAMVLAFLRLKIVLEPGGAVSLAAALFHGDQLSGP 300

Query: 294 SAVAIVSGGNIEPA 307
           +A+AI +GGN++ A
Sbjct: 301 AAIAIATGGNVDAA 314


Lambda     K      H
   0.318    0.134    0.384 

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: 313
Number of extensions: 19
Number of successful extensions: 6
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: 316
Length of database: 324
Length adjustment: 28
Effective length of query: 288
Effective length of database: 296
Effective search space:    85248
Effective search space used:    85248
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 48 (23.1 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