GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Acidovorax sp. GW101-3H11

Align serine racemase (EC 5.1.1.18) (characterized)
to candidate Ac3H11_37 Threonine dehydratase, catabolic (EC 4.3.1.19)

Query= BRENDA::O59791
         (323 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_37
          Length = 324

 Score =  465 bits (1197), Expect = e-136
 Identities = 224/317 (70%), Positives = 271/317 (85%)

Query: 7   LPTYDDVASASERIKKFANKTPVLTSSTVNKEFVAEVFFKCENFQKMGAFKFRGALNALS 66
           LPTYDDV +A+ RI   A++TPVLTS TVN+EF A+VFFKCEN Q+MGAFKFRGA NAL+
Sbjct: 8   LPTYDDVVAAAGRIAGVAHRTPVLTSRTVNEEFGAQVFFKCENLQRMGAFKFRGAYNALA 67

Query: 67  QLNEAQRKAGVLTFSSGNHAQAIALSAKILGIPAKIIMPLDAPEAKVAATKGYGGQVIMY 126
           Q + AQRKAGV+ FSSGNHAQ IAL+A+ LGIPA I+MP DAP AKVAAT+GYG QV+ +
Sbjct: 68  QFSPAQRKAGVVAFSSGNHAQGIALAARELGIPATILMPQDAPAAKVAATQGYGAQVVFF 127

Query: 127 DRYKDDREKMAKEISEREGLTIIPPYDHPHVLAGQGTAAKELFEEVGPLDALFVCLGGGG 186
           DRY  DRE++ ++++ER GLT+IPPYDH  VLAGQGTAAKELFEEVGPLDA FVCLGGGG
Sbjct: 128 DRYTQDREQLTRDLAERHGLTLIPPYDHADVLAGQGTAAKELFEEVGPLDAFFVCLGGGG 187

Query: 187 LLSGSALAARHFAPNCEVYGVEPEAGNDGQQSFRKGSIVHIDTPKTIADGAQTQHLGNYT 246
           LLSGSALA R  +P  ++YGVEP AGNDGQQSFR GSIVHIDTP TIADGAQTQHLG+ T
Sbjct: 188 LLSGSALATRALSPQTKLYGVEPAAGNDGQQSFRSGSIVHIDTPTTIADGAQTQHLGHIT 247

Query: 247 FSIIKEKVDDILTVSDEELIDCLKFYAARMKIVVEPTGCLSFAAARAMKEKLKNKRIGII 306
           F+II+  VDDILTV+DE+L+D ++F+A RMK+VVEPTGCL FAAARAM+ +LK +R+G++
Sbjct: 248 FAIIRRDVDDILTVTDEQLVDAMRFFAERMKLVVEPTGCLGFAAARAMQSELKGQRVGVL 307

Query: 307 ISGGNVDIERYAHFLSQ 323
           ISGGNVD+ R+   +++
Sbjct: 308 ISGGNVDLARFCALVAR 324


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: 349
Number of extensions: 9
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: 323
Length of database: 324
Length adjustment: 28
Effective length of query: 295
Effective length of database: 296
Effective search space:    87320
Effective search space used:    87320
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.

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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