GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Dyella japonica UNC79MFTsu3.2

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate N515DRAFT_3549 N515DRAFT_3549 UDP-glucuronate 4-epimerase

Query= BRENDA::F6DEY6
         (311 letters)



>FitnessBrowser__Dyella79:N515DRAFT_3549
          Length = 336

 Score =  147 bits (372), Expect = 3e-40
 Identities = 110/341 (32%), Positives = 162/341 (47%), Gaps = 43/341 (12%)

Query: 1   MRVLVTGGAGFIGSHIVEDLLARGLEVAVLDNL----------ATGKRENVPKGVPFFQV 50
           M+VLVTG AGFIGSH+   LLARG EV  LDNL          A   R     G      
Sbjct: 1   MKVLVTGTAGFIGSHVARKLLARGDEVIGLDNLNDYYDVGLKQARLARVQAYPGYTHVHA 60

Query: 51  DLRDKEEVERAFREFRPTHVSHQAAQASVKVSVEDPVLDFEVNLLGGLNLLEACRQYGVE 110
           DL D+  VE+ F   +P  V + AAQA V+ +  +P +    N+ G L++LE CRQ+GV+
Sbjct: 61  DLADRAAVEKLFATHKPERVVNLAAQAGVRYAATNPHVYVSSNVTGFLHILEGCRQHGVQ 120

Query: 111 KLVFASTGGAIYGEVPEGERAEETWPPRPKSPYAASKAAFEHYLSVYGQSYGLKWVSLRY 170
            LVFAST  ++YG   +   +E      P + YAA+K A E     Y   YG+    LR+
Sbjct: 121 HLVFAST-SSVYGANRDLPFSEHRPAEHPLTLYAATKKANEQMAHSYAHLYGVPATGLRF 179

Query: 171 GNVYGPRQDPHGEAGVVAIFAERVLNGLPVTLYARKTPGDEG-CVRDYVYVGDVAEAHAL 229
             VYGP   P      + +F + +L G P+ ++      +EG   R + Y+ D+ E    
Sbjct: 180 FTVYGPWGRPD---MALFLFTKAILAGEPIRVF------NEGRHKRSFTYIDDIVEGVVR 230

Query: 230 ALFSLEG---------------------IYNVGTGEGHTTREVLEAVAEAAGKAPQVQPA 268
           AL ++ G                     +YN+G  +       +E + +  G+   ++  
Sbjct: 231 ALDTVPGKDPAWDATQPDPSTSGVAPYRLYNIGNEQPVELLRYIEVLEQCLGRKATMELL 290

Query: 269 PPRPGDLERSVLSPLKLMAH-GWRPKVGFQEGIRLTVDHFR 308
           P + GD+  +      L+A  G+RPKV  +EGI   V  +R
Sbjct: 291 PLQAGDVPETEADVSSLVAAVGYRPKVSVEEGIAAFVKWYR 331


Lambda     K      H
   0.318    0.138    0.411 

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: 318
Number of extensions: 22
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: 311
Length of database: 336
Length adjustment: 28
Effective length of query: 283
Effective length of database: 308
Effective search space:    87164
Effective search space used:    87164
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 (21.7 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