GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Methanosarcina mazei Go1

Align Putative UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate WP_011033111.1 MM_RS06035 UDP-glucose 4-epimerase

Query= curated2:Q57664
         (305 letters)



>NCBI__GCF_000007065.1:WP_011033111.1
          Length = 334

 Score =  212 bits (540), Expect = 8e-60
 Identities = 120/317 (37%), Positives = 180/317 (56%), Gaps = 18/317 (5%)

Query: 2   ILVTGGAGFIGSHIVDKLIENNYDVIILDNLTTG-----NKNNIN-----PKAEFVNADI 51
           I++TGGAGFIGSHI + L ++ ++++I+DNL         K N+N       A F+NAD+
Sbjct: 4   IVITGGAGFIGSHIAENLAKDGHEIVIVDNLDPYYSVDLKKKNLNIALNSGDATFINADV 63

Query: 52  RDKDLDEKINFKDVEVVIHQAAQINVRNSVENPVYDGDINVLGTINILEMMRKYDIDKIV 111
            D    + +    V+ V H+AAQ  VR SVE+P    D+NV GT+N+L+      + K++
Sbjct: 64  TDLSGIKDVIDSTVDYVYHEAAQAGVRISVEDPFKPNDVNVHGTLNVLKASLDAGVKKVI 123

Query: 112 FASSGGAVYGEPNYLPVDENHPINPLSPYGLSKYVGEEYIKLYNRLYGIEYAILRYSNVY 171
            ASS  +VYG+  YLP DE HP  P+SPYG+SK   E Y +++  +YG+    LRY  VY
Sbjct: 124 NASSS-SVYGKVKYLPFDEQHPTEPVSPYGVSKLAAEHYCRVFYEVYGLPTTSLRYFTVY 182

Query: 172 GERQDPKGEAGVISIFIDKMLKNQSPIIFGDGNQTRDFVYVGDVAKANLMALNWK---NE 228
           G R  P      ISIF  KML N+   +FGDG QTRDF Y+ DV +AN   L  +    +
Sbjct: 183 GPRMRPD---LAISIFTRKMLANEPITVFGDGEQTRDFTYIEDVVEANKRLLYNRATDGK 239

Query: 229 IVNIGTGKETSVNELFDIIKHEIGFRGEAIYDKPREGEVYRIYLDIKKAES-LGWKPEID 287
           ++NIG G   SVN L + ++   G   E I    ++G+      ++    + +G+ P  +
Sbjct: 240 VLNIGGGNRISVNNLIENLRFITGSTSEIINADKQKGDTEDTLANVDLGNNMIGYTPLFN 299

Query: 288 LKEGIKRVVNWMKNNNR 304
           + +G+ + V+W K  N+
Sbjct: 300 INKGLNKFVDWFKTENQ 316


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: 343
Number of extensions: 22
Number of successful extensions: 5
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: 334
Length adjustment: 28
Effective length of query: 277
Effective length of database: 306
Effective search space:    84762
Effective search space used:    84762
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.

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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