GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Azohydromonas australica DSM 1124

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate WP_029000185.1 H537_RS0125960 NAD-dependent epimerase

Query= BRENDA::P9WN67
         (314 letters)



>NCBI__GCF_000430725.1:WP_029000185.1
          Length = 335

 Score =  144 bits (364), Expect = 2e-39
 Identities = 106/334 (31%), Positives = 160/334 (47%), Gaps = 29/334 (8%)

Query: 1   MRALVTGAAGFIGSTLVDRLLADGHSVVGLDNF-----ATGRATNLEHLADNSAHVFVEA 55
           M+ LVTGAAGFIG   V RLL  G  VVG+DN         +   L+ L  ++   F++ 
Sbjct: 1   MKVLVTGAAGFIGMATVLRLLERGDEVVGVDNLNDYYDVNLKLARLQQLQPHAGFRFLKL 60

Query: 56  DIV-TADLHAILEQHRPEVVFHLAAQIDVRRSVADPQFDAAVNVIGTVRLAEAARQTGVR 114
           DI   A +  + +  R + V HLAAQ  VR S+ +P      N++G V + E  R T V+
Sbjct: 61  DIADRAGMETLFKAERFDRVVHLAAQAGVRYSLLNPNAYVDSNLVGFVNVLEGCRHTQVQ 120

Query: 115 KIVHTSSGGSIYGTPPEYPTPETAPTD-PASPYAAGKVAGEIYLNTFRHLYGLDCSHIAP 173
            +V+ SS  S+YG   + P  E+   D P S YAA K A E+  +T+ HLY L  + +  
Sbjct: 121 HLVYASS-SSVYGGNVKMPFSESDGVDHPVSLYAATKKANELMAHTYSHLYKLPTTGLRF 179

Query: 174 ANVYGPRQDPHGEAGVVAIFAQALLSGKPTRVFGDGTNTRDYVFVDDVVDAFVRV----- 228
             VYGP   P        +F +A+L  +P  VF  G   RD+ +VDD+V+  +RV     
Sbjct: 180 FTVYGPWGRPD---MAPILFTKAILENRPIDVFNQGRMRRDFTYVDDIVEGVIRVLDRAA 236

Query: 229 ---------SADVGGGLR----FNIGTGKETSDRQLHSAVAAAVGGPDDPEFHPPRLGDL 275
                    + D G         NIG  +  S  +    +  A+G   D    P + GD+
Sbjct: 237 TPDEGFDPHAPDPGRSHAPYRVVNIGNNEPVSLMEFIECIEQALGRQADKRMLPMQNGDV 296

Query: 276 KRSCLDIGLAERVLGWRPQIELADGVRRTVEYFR 309
             +  D+   +  + + P+  + +GV R V ++R
Sbjct: 297 PATYADVDALKAWVDFAPRTGIREGVARFVAWYR 330


Lambda     K      H
   0.320    0.137    0.410 

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: 241
Number of extensions: 16
Number of successful extensions: 4
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: 314
Length of database: 335
Length adjustment: 28
Effective length of query: 286
Effective length of database: 307
Effective search space:    87802
Effective search space used:    87802
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 (21.8 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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