GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Geobacter lovleyi SZ

Align Putative UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate WP_012471395.1 GLOV_RS16655 NAD-dependent epimerase

Query= curated2:Q57664
         (305 letters)



>NCBI__GCF_000020385.1:WP_012471395.1
          Length = 335

 Score =  165 bits (417), Expect = 2e-45
 Identities = 106/317 (33%), Positives = 171/317 (53%), Gaps = 19/317 (5%)

Query: 2   ILVTGGAGFIGSHIVDKLIENNYDVIILDNLTT---GNKNNINPKAEFVNADIRDKDLDE 58
           +L+TGG GFIGS++  +L++    V ++D+L     GN  NI P  E V  +I D   + 
Sbjct: 9   VLITGGLGFIGSNLAIRLVQLGAQVTLVDSLIPEYGGNLWNIEPVKEQVRVNISDVRDEH 68

Query: 59  KINF--KDVEVVIHQAAQINVRNSVENPVYDGDINVLGTINILEMMRKYD-IDKIVFASS 115
            + +  +  + + + A Q +  +S++NP  D +IN    ++ILE  R ++   K+VFAS+
Sbjct: 69  AMKYLIQGQDFLFNLAGQTSHLDSMQNPYPDLEINARAQLSILEACRHHNPAIKLVFAST 128

Query: 116 GGAVYGEPNYLPVDENHPINPLSPYGLSKYVGEEYIKLYNRLYGIEYAILRYSNVYGERQ 175
              +YG P YLPVDE HP+ P+   G++K  GE Y  +YN +YGI  ++LR +N YG R 
Sbjct: 129 R-QMYGAPRYLPVDEKHPLAPVDVNGINKMAGEWYHLVYNNVYGIRASVLRLTNTYGPRM 187

Query: 176 DPK-GEAGVISIFIDKMLKNQSPIIFGDGNQTRDFVYVGDVAKANLMAL---NWKNEIVN 231
             K      + I+I  +L  Q  ++FGDG Q RDF YV DV +A L+         EI N
Sbjct: 188 RVKDARQTFLGIWIRNILTGQPVLVFGDGRQVRDFNYVDDVVEAMLLCAASDAANGEIFN 247

Query: 232 IGTGKETSVNELFDIIKHEIGFRGEAIYDKPRE------GEVYRIYLDIKKAESLGWKPE 285
           +G     ++ +   ++    G    A+   P +      G+ Y  Y  IK   +LGW+P 
Sbjct: 248 LGADDPANLQDTAQLLVQAAGQGSFALVPFPPDRKAIDIGDYYADYGKIK--ATLGWQPA 305

Query: 286 IDLKEGIKRVVNWMKNN 302
           + L+EG++R + + + +
Sbjct: 306 VALQEGLQRTLAYYRTD 322


Lambda     K      H
   0.317    0.140    0.405 

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: 271
Number of extensions: 11
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: 305
Length of database: 335
Length adjustment: 28
Effective length of query: 277
Effective length of database: 307
Effective search space:    85039
Effective search space used:    85039
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 (21.6 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 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