GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Echinicola vietnamensis KMM 6221, DSM 17526

Align serine racemase (EC 5.1.1.18) (characterized)
to candidate Echvi_3354 Echvi_3354 threonine dehydratase

Query= BRENDA::O59791
         (323 letters)



>FitnessBrowser__Cola:Echvi_3354
          Length = 416

 Score =  176 bits (446), Expect = 9e-49
 Identities = 103/316 (32%), Positives = 169/316 (53%), Gaps = 7/316 (2%)

Query: 9   TYDDVASASERIKKFANKTPVLTSSTVNKEFVAEVFFKCENFQKMGAFKFRGALNALSQL 68
           ++  +  ASE +++  + TP+  +  +++E+   V+ K E+ Q + ++K RGA + +S L
Sbjct: 5   SFQGIIEASEALQEVLHPTPLQFNEQLSEEYGCRVYLKREDLQAVRSYKIRGAYHKISSL 64

Query: 69  NEAQRKAGVLTFSSGNHAQAIALSAKILGIPAKIIMPLDAPEAKVAATKGYGGQ----VI 124
           +E ++  GV+  S+GNHAQ +A + K LGI   I +P      K+   K +G +    V+
Sbjct: 65  SEEEKSRGVVCASAGNHAQGVAFACKKLGIKGTIFIPSTTSAQKINRMKLFGKEMVEIVL 124

Query: 125 MYDRYKDDREKMAKEISEREGLTIIPPYDHPHVLAGQGTAAKELFEEVG-PLDALFVCLG 183
             D Y DD  + A E  E  G   + P+D P V+ GQGT AKE+ ++   P+D LF+ +G
Sbjct: 125 SGDTY-DDAYQTAAEYCEERGAVFVHPFDDPKVIEGQGTIAKEILDDAEFPVDYLFLPIG 183

Query: 184 GGGLLSGSALAARHFAPNCEVYGVEPEAGNDGQQSFRKGSIVHIDTPKTIADGAQTQHLG 243
           GGG+ +G +      +P  ++ G EP+       S +      +D      DGA  + +G
Sbjct: 184 GGGMAAGVSTYFEQSSPETKLIGTEPKGAPSMLTSIQNLKNTVLDEIDGFVDGAAVKKVG 243

Query: 244 NYTFSIIKEKVDDILTVSDEELIDCLKFYAARMKIVVEPTGCLSFAAARAM-KEKLKNKR 302
           N TF I ++ +D++L V +  +   +        IVVEP G ++ AA     KEKLK K 
Sbjct: 244 NITFEICRKSLDEMLLVPEGRICTTILNLYNNEGIVVEPAGAMTLAALSLYDKEKLKGKN 303

Query: 303 IGIIISGGNVDIERYA 318
           +  ++SGGN DI R A
Sbjct: 304 VVCVVSGGNNDIMRTA 319


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: 318
Number of extensions: 13
Number of successful extensions: 4
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: 416
Length adjustment: 30
Effective length of query: 293
Effective length of database: 386
Effective search space:   113098
Effective search space used:   113098
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.

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