GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Desulfatibacillum aliphaticivorans DSM 15576

Align Putative UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate WP_028313395.1 G491_RS0102035 KR domain-containing protein

Query= curated2:Q57664
         (305 letters)



>NCBI__GCF_000429905.1:WP_028313395.1
          Length = 306

 Score =  197 bits (501), Expect = 3e-55
 Identities = 127/304 (41%), Positives = 179/304 (58%), Gaps = 14/304 (4%)

Query: 3   LVTGGAGFIGSHIVDKLIENNYDVIILDNLTTGNKNNINP---KAEFVNADIRDKDLDEK 59
           LVTGG GFIGSHI + L E    V ILD+L++G + NI     K EF+  DIRD +   K
Sbjct: 4   LVTGGCGFIGSHISEVLAEKGEKVRILDDLSSGYEANIADFADKVEFIKGDIRDPEAVAK 63

Query: 60  INFKDVEVVIHQAAQINVRNSVENPVYDGDINVLGTINILEMMRKYDIDKIVFASSGGAV 119
              K V+ V H A  ++  +SVE P+   DINV GT+NIL   R   + ++VFASS  AV
Sbjct: 64  A-MKGVDGVFHLAGMVSAFDSVERPLVCHDINVTGTLNILTAARDAGVKRVVFASSC-AV 121

Query: 120 YGEPNYLPVDENHPINPLSPYGLSKYVGEEYIKLYNRLYGIEYAILRYSNVYGERQDPKG 179
           YG     P  E     P SPY  SK   E Y++++  LYG++   LR+ NV+G RQDP  
Sbjct: 122 YGNNPESPKVEAMTRAPASPYAASKAASELYMRVFAELYGVQTVCLRFFNVFGPRQDPSS 181

Query: 180 E-AGVISIFIDKMLKNQSPIIFGDGNQTRDFVYVGDVAKANLMALN----WKNEIVNIGT 234
           + +GVIS F++   +  +  I+GDG QTRDF++V DV +ANL+A+        E VN+GT
Sbjct: 182 QYSGVISRFVNDTAEGYA-CIYGDGLQTRDFIFVRDVVRANLLAMTSNKAGAGEAVNVGT 240

Query: 235 GKETSVNELFDIIKHEIGFRG-EAIYDKPREGEVYRIYLDIKKA-ESLGWKPEIDLKEGI 292
           G E S+ +L D ++ E+G R  E ++   R G+V     DI KA E LG++P   ++ G+
Sbjct: 241 GVEISLLDLLDYMR-ELGDREFEVMFKDARAGDVRHSRADISKAQELLGFEPAYTIRNGL 299

Query: 293 KRVV 296
             ++
Sbjct: 300 AELL 303


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: 280
Number of extensions: 11
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: 306
Length adjustment: 27
Effective length of query: 278
Effective length of database: 279
Effective search space:    77562
Effective search space used:    77562
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