GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Pseudomonas fluorescens GW456-L13

Align serine racemase (EC 5.1.1.18) (characterized)
to candidate PfGW456L13_3031 Threonine dehydratase biosynthetic (EC 4.3.1.19)

Query= BRENDA::O59791
         (323 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3031
          Length = 337

 Score =  183 bits (465), Expect = 4e-51
 Identities = 103/303 (33%), Positives = 164/303 (54%), Gaps = 3/303 (0%)

Query: 20  IKKFANKTPVLTSSTVNKEFVAEVFFKCENFQKMGAFKFRGALNALSQLNEAQRKAGVLT 79
           + + A +TP+  +  +++    ++  K E+ Q   +FK RGA N L QL+E Q+  GV+T
Sbjct: 23  VYELAVRTPLQPAPALSEALGNQILLKREDLQPTFSFKIRGAYNKLVQLSEVQKARGVVT 82

Query: 80  FSSGNHAQAIALSAKILGIPAKIIMPLDAPEAKVAATKGYGGQVIMYDRYKDDREKMAKE 139
            S+GNHAQ +AL+A+ LGI A I+MP   P+ KV   +  G   +++          A +
Sbjct: 83  ASAGNHAQGVALAARELGINATIVMPCTTPQLKVIGVRSRGADAVLHGESFPFALACALD 142

Query: 140 ISEREGLTIIPPYDHPHVLAGQGTAAKELFEE-VGPLDALFVCLGGGGLLSGSALAARHF 198
           ++   G T + P+D P V+AGQGT A E+  +  GPLDA+FV +GGGGL++G A   ++ 
Sbjct: 143 LARETGRTFVSPFDDPEVIAGQGTVAMEILRQHQGPLDAIFVPVGGGGLIAGIAAYVKYL 202

Query: 199 APNCEVYGVEPEAGNDGQQSFRKGSIVHIDTPKTIADGAQTQHLGNYTFSIIKEKVDDIL 258
            P   V GVE E     Q +   G  V + +  T ADG     +G Y F + +  VDD++
Sbjct: 203 RPEVRVIGVESEHSACLQAAMHAGERVVLPSVGTFADGVAVAQIGAYGFEVCRFCVDDVV 262

Query: 259 TVSDEELIDCLKFYAARMKIVVEPTGCLSFAAAR--AMKEKLKNKRIGIIISGGNVDIER 316
           TVS++EL   +K      + + EP+G L+ A  +    +     + +  I SG N++ + 
Sbjct: 263 TVSNDELCAAIKNIYDDTRSITEPSGALAVAGIKRYVAQTGALGQTLVAIDSGANINFDS 322

Query: 317 YAH 319
             H
Sbjct: 323 LGH 325


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: 243
Number of extensions: 11
Number of successful extensions: 3
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: 337
Length adjustment: 28
Effective length of query: 295
Effective length of database: 309
Effective search space:    91155
Effective search space used:    91155
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: 49 (23.5 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