GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Pseudomonas fluorescens FW300-N1B4

Align serine racemase (EC 5.1.1.18) (characterized)
to candidate Pf1N1B4_2280 Threonine dehydratase biosynthetic (EC 4.3.1.19)

Query= BRENDA::O59791
         (323 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_2280
          Length = 504

 Score =  203 bits (516), Expect = 8e-57
 Identities = 109/306 (35%), Positives = 176/306 (57%), Gaps = 3/306 (0%)

Query: 17  SERIKKFANKTPVLTSSTVNKEFVAEVFFKCENFQKMGAFKFRGALNALSQLNEAQRKAG 76
           + R+   A +TP+ T+  +++    +++ K E+ Q + +FK RGA N L+QL++ +R  G
Sbjct: 11  TSRVYDVAVETPLQTARQLSERLGNDIWLKREDLQPVFSFKIRGAYNKLTQLSDEERARG 70

Query: 77  VLTFSSGNHAQAIALSAKILGIPAKIIMPLDAPEAKVAATKGYGGQVIMYDRYKDDREKM 136
           V+T S+GNHAQ +AL+AK+LG+ A I+MP   PE KV   +  GG+V+++     +    
Sbjct: 71  VVTASAGNHAQGLALAAKVLGVKATIVMPKTTPEIKVEGVRSRGGKVVLHGDSFPEALAY 130

Query: 137 AKEISEREGLTIIPPYDHPHVLAGQGTAAKELF-EEVGPLDALFVCLGGGGLLSGSALAA 195
           + ++ + +G   I PYD PH +AGQGT A E+  +  G LDA+FV +GGGGL++G A   
Sbjct: 131 SLKLVDEKGYVYIHPYDDPHTIAGQGTVAMEILRQHPGRLDAIFVPVGGGGLIAGIAAYV 190

Query: 196 RHFAPNCEVYGVEPEAGNDGQQSFRKGSIVHIDTPKTIADGAQTQHLGNYTFSIIKEKVD 255
           ++  P+ ++ GVEP+  N  Q +   G  V + T    ADG     +G +TF I K+ VD
Sbjct: 191 KYLRPDIKIIGVEPDDSNCLQAAMAAGERVVLPTVGLFADGVAVAQIGQHTFDICKDYVD 250

Query: 256 DILTVSDEELIDCLKFYAARMKIVVEPTGCLSFAAARAMKEK--LKNKRIGIIISGGNVD 313
           +++TVS +E+   +K      + + EP G L  A  +   E+  +       I SG NV+
Sbjct: 251 EVITVSTDEICAAIKDIYDDTRSITEPAGALGVAGIKKYVEQRGVTGHTFVAIDSGANVN 310

Query: 314 IERYAH 319
            +R  H
Sbjct: 311 FDRLRH 316


Lambda     K      H
   0.318    0.135    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: 360
Number of extensions: 14
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: 323
Length of database: 504
Length adjustment: 31
Effective length of query: 292
Effective length of database: 473
Effective search space:   138116
Effective search space used:   138116
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: 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