GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Desulfovibrio vulgaris Hildenborough

Align UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate 208509 DVU2996 NAD-dependent epimerase/dehydratase family protein

Query= curated2:Q59083
         (348 letters)



>MicrobesOnline__882:208509
          Length = 307

 Score =  113 bits (283), Expect = 6e-30
 Identities = 104/320 (32%), Positives = 149/320 (46%), Gaps = 29/320 (9%)

Query: 11  VLVTGGAGYIGSHVLHALTDAGIPAVTIDDLSAGRREAIPAAVPLVEGDIGSAELLDRVM 70
           VLVTG  G+IGSHV+ AL     P   +  L++    +   AV  V   +   +L + ++
Sbjct: 4   VLVTGATGFIGSHVVEALA----PRHDVVGLASSVYPSPRDAVRHVRMTLPHPDL-EELV 58

Query: 71  RDHRVDAVMHFAGSIVVPESVVKPLDYYRNNTANSLTLLGACLRAGI-DKVVFSSTAAVY 129
              R D V+H AG   V  S+  P   +++       L  A  +AG+  KVV  S+AAVY
Sbjct: 59  ATLRPDVVVHCAGVASVGLSMHSPGVDFQSGPPVVFQLFDAIRKAGLASKVVLLSSAAVY 118

Query: 130 GAPESVPIREDAPTVPINPYGASKLMTEQMLRDAGAAHGLRSVILRYFNVAGADPAGRTG 189
           G P+S+P+ EDAP  PI+PYG  K M E + ++    +G+RS +LR F+  GA       
Sbjct: 119 GNPQSLPVGEDAPRAPISPYGWHKGMCEDIAQEFHGTYGIRSAVLRIFSCYGAG------ 172

Query: 190 QATPVATHLIKVACQALLGRRPPLAIFGTDYDTPDGTCIRDYIHVSDLADAHVLALLHLR 249
               +   L+  A   LL         GT  +T      RD+IHV D+A A V  L+   
Sbjct: 173 ----LRKQLLWDAAHKLL--EGAFVFDGTGDET------RDFIHVRDVA-AFVTRLVEGW 219

Query: 250 RGGGSLLMNCGYGRGASVREVVRTLEEVSGEQ--VPATFADRRPGDPPQLVAGADRIREQ 307
             GG ++ N   G    + +++  L E  G    VP      R GDP    A   R R Q
Sbjct: 220 PDGGCVVCNVASGEATRIADLLALLPEAFGLSGVVPVFTGRVRGGDPHHWRADISRAR-Q 278

Query: 308 LGWVPKHDRLDGIVRSALSW 327
           +G  P     +G VR   +W
Sbjct: 279 MGLAPAVSLEEG-VREYATW 297


Lambda     K      H
   0.319    0.136    0.401 

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: 286
Number of extensions: 15
Number of successful extensions: 3
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: 348
Length of database: 307
Length adjustment: 28
Effective length of query: 320
Effective length of database: 279
Effective search space:    89280
Effective search space used:    89280
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 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