GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Acidovorax sp. GW101-3H11

Align UDP-glucose 4-epimerase; UDP-galactose 4-epimerase; Uridine diphosphate galactose 4-epimerase; EC 5.1.3.2 (characterized)
to candidate Ac3H11_1880 dTDP-glucose 4,6-dehydratase (EC 4.2.1.46)

Query= SwissProt::A0R5C5
         (313 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1880
          Length = 363

 Score =  129 bits (325), Expect = 8e-35
 Identities = 103/330 (31%), Positives = 148/330 (44%), Gaps = 30/330 (9%)

Query: 4   LVTGAAGFIGSTLV-DRLLADGHGVVGLDDLS-SGRAENLHSAENSDKFEFVKADIVDAD 61
           LVTG AGFIG+  V D L A    VV LD L+ +G   NL S +   +  FV+ DI D  
Sbjct: 3   LVTGGAGFIGANFVLDWLAASSEPVVNLDKLTYAGNLHNLDSVQGDARHIFVQGDIGDTA 62

Query: 62  LTG-LLAEFKPEVIFHLAAQISVKRSVDDPPFDATVNVVGTVRLAEAARL---------A 111
           L   LLAE KP  + + AA+  V RS+  P      N+VG+ RL EA R           
Sbjct: 63  LVARLLAECKPRAVVNFAAESHVDRSIHGPEDFIQTNIVGSFRLLEAVRAYWGALPEGDR 122

Query: 112 GVRKVVHTSSG---GSVYGTPPAYPTSEDMPVNPASPYAAGKVAGEVYLNMYRNLYDLDC 168
              + +H S+    GS+  T PA+  +E     P SPY+A K A +  +  + + Y L  
Sbjct: 123 AAFRFLHVSTDEVYGSLAPTDPAF--AETRGFEPNSPYSASKAASDHLVRAWHHTYGLPV 180

Query: 169 SHIAPANVYGPRQDPHGEAGVVAIFSEALLAGRTTKIFGDGSDTRDYVFVDDVVDAFVRA 228
                +N YGP   P     ++ +     LAG+   ++GDG   RD+++V D   A  R 
Sbjct: 181 LTTNCSNNYGPYHFPE---KLIPLMIVNALAGKNLPVYGDGMQVRDWLYVKDHCSAIRRV 237

Query: 229 GGPAGGGQRFNVGTGVETSTRELHTAI----------AGAVGAPDEPEFHPPRLGDLRRS 278
                 G+ +NVG   E    E+   +          A       +  +   R G  RR 
Sbjct: 238 LEAGAPGETYNVGGWNEKPNIEIVNMVCSLLDELRPRADGQSYRTQITYVKDRPGHDRRY 297

Query: 279 RLDNTRAREVLGWQPQVALAEGIAKTVEFF 308
            +D  +    LGW+P      GI KTV+++
Sbjct: 298 AIDARKIERELGWKPAETFDTGIRKTVQWY 327


Lambda     K      H
   0.317    0.136    0.396 

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: 265
Number of extensions: 17
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: 313
Length of database: 363
Length adjustment: 28
Effective length of query: 285
Effective length of database: 335
Effective search space:    95475
Effective search space used:    95475
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: 49 (23.5 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