GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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