GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Allochromatium vinosum DSM 180

Align Putative UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate WP_012969466.1 ALVIN_RS01120 epimerase

Query= curated2:Q57664
         (305 letters)



>NCBI__GCF_000025485.1:WP_012969466.1
          Length = 328

 Score =  184 bits (466), Expect = 3e-51
 Identities = 118/325 (36%), Positives = 176/325 (54%), Gaps = 34/325 (10%)

Query: 2   ILVTGGAGFIGSHIVDKLIEN--NYDVIILDNLTTGNKNNINPKAEF------------- 46
           +L+TGG GFIG+ ++ KL+       + I+DN  TG+  ++     F             
Sbjct: 5   VLITGGCGFIGTSLIHKLLARYPTAHIRIVDNFVTGSPADLAEVCVFQSTQAADLAQATL 64

Query: 47  ------VNADIRDKDLDEKINFKDVEVVIHQAAQINVRNSVENPVYDGDINVLGTINILE 100
                 +  DIRD D   +   + V+ ++H AA   V  SVE+P  D D NV+GT N LE
Sbjct: 65  TAGVFLLEGDIRDADFLLQCA-QGVDCIVHLAANTGVGPSVEDPRLDMDCNVVGTFNALE 123

Query: 101 MMRKYDIDKIVFASSGG-AVYGEPNYLPVDENHPINPLSPYGLSKYVGEEYIKLYNRLYG 159
             R   + + +FASSG  A   EP   P+ E  P +P+SPYG SK  GE Y   Y R +G
Sbjct: 124 AARLNGVKRFIFASSGAPAGEVEP---PIHEELPPHPVSPYGASKLAGEGYCSAYYRTFG 180

Query: 160 IEYAILRYSNVYGERQDPKGEAGVISIFIDKMLKNQSPIIFGDGNQTRDFVYVGDVAKAN 219
           IE   LR+ NVYG R   K ++ V++ FI + L+ +  II+GDG QTRDF+Y+ D+ +A 
Sbjct: 181 IETICLRFGNVYGPRS--KKKSSVVAKFIRQALQGEPCIIYGDGTQTRDFLYIDDLVRAV 238

Query: 220 LMALNWK--NEIVNIGTGKETSVNELFDIIKHEIGFRG---EAIYDKPREGEVYRIYLDI 274
           ++A+      E   I TG E +V E+  ++   +  RG   +  +D PR G+V R + D 
Sbjct: 239 MLAMEQPVGGETFQIATGMERTVGEVATLLAKALEKRGTHMDIQHDSPRLGDVRRNFSDT 298

Query: 275 KK-AESLGWKPEIDLKEGIKRVVNW 298
            K A  L W+ E+++ EGI+R ++W
Sbjct: 299 SKAARLLEWRTEVEVPEGIERTLDW 323


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: 264
Number of extensions: 17
Number of successful extensions: 6
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: 328
Length adjustment: 27
Effective length of query: 278
Effective length of database: 301
Effective search space:    83678
Effective search space used:    83678
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