GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Shewanella oneidensis MR-1

Align Putative UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate 202299 SO3189 polysaccharide biosynthesis protein (NCBI ptt file)

Query= curated2:Q57664
         (305 letters)



>FitnessBrowser__MR1:202299
          Length = 340

 Score =  190 bits (483), Expect = 3e-53
 Identities = 114/320 (35%), Positives = 177/320 (55%), Gaps = 24/320 (7%)

Query: 3   LVTGGAGFIGSHIVDKLIENNYDVIILDNLTTGNKNNINP-----------KAEFVNADI 51
           L+TG AGFIGS+++++L++ N  VI LDN  TG ++N++            +  F+N DI
Sbjct: 19  LITGVAGFIGSNLLEQLLKLNQTVIGLDNFATGRQHNLDEVQSLVTSEQWMRFSFINGDI 78

Query: 52  RDKDLDEKINFKDVEVVIHQAAQINVRNSVENPVYDGDINVLGTINILEMMRKYDIDKIV 111
           RD  + E +    V+ V+HQAA  +V  S+ +P+     N+ G +N+L+  ++ ++    
Sbjct: 79  RDYAICEAV-VNGVDYVLHQAALGSVPRSIADPITTNAANITGFLNMLQAAKEAEVKSFT 137

Query: 112 FASSGGAVYGEPNYLPVDENHPINPLSPYGLSKYVGEEYIKLYNRLYGIEYAILRYSNVY 171
           +A+S  + YG+   LP  E +  NPLSPY ++KYV E Y  +Y R YG E   LRY NV+
Sbjct: 138 YAASS-STYGDHPALPKVEQNIGNPLSPYAVTKYVNELYASVYARTYGFETIGLRYFNVF 196

Query: 172 GERQDPKGE-AGVISIFIDKMLKNQSPIIFGDGNQTRDFVYVGDVAKANLMAL----NWK 226
           G RQDP G  A VI  +   M+K +   I GDG  +RDF Y+ +V + N++A       K
Sbjct: 197 GRRQDPNGAYAAVIPKWTSSMIKGEDVFINGDGETSRDFCYIDNVVQMNILAATAASEAK 256

Query: 227 NEIVNIGTGKETSVNELFDIIKHEIGFRGEAIYDKP-----REGEVYRIYLDIKKAES-L 280
           NE+ N+  G  T++N+L+  IK  +   G  +   P     R G+V     D+ KA + L
Sbjct: 257 NEVYNVAVGDRTTLNDLYFAIKDSLNANGINVNQNPNYRDFRAGDVRHSQADVSKAVTRL 316

Query: 281 GWKPEIDLKEGIKRVVNWMK 300
           G++    + EGI   + W K
Sbjct: 317 GYQYTHKILEGISEAMPWYK 336


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: 306
Number of extensions: 19
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: 340
Length adjustment: 28
Effective length of query: 277
Effective length of database: 312
Effective search space:    86424
Effective search space used:    86424
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 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