GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Methylocella silvestris BL2

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate WP_012590207.1 MSIL_RS06020 UDP-glucuronate 5-epimerase

Query= BRENDA::A3MUJ4
         (312 letters)



>NCBI__GCF_000021745.1:WP_012590207.1
          Length = 337

 Score =  126 bits (317), Expect = 6e-34
 Identities = 104/333 (31%), Positives = 155/333 (46%), Gaps = 42/333 (12%)

Query: 1   MRIVVTGGAGFIGSHLVDKLVELGYEVVVVDNLS-------SGRREFV---NPSAELHVR 50
           MRI+VTG AGFIG H+  +L+  G+EVV VD  +         RR  +   NP    H  
Sbjct: 1   MRILVTGSAGFIGFHMAARLLADGHEVVGVDGFTHYYDPELKRRRNAILSQNPYFTSHAI 60

Query: 51  DLKDYS-----WGAGIKGDVVFHFAANPEVRLSTTEPIVHFNENVVATFNVLEWARQTGV 105
            L+D S     + AG   D V+HFAA   VR S   P  + + N+   FN+LE  R+   
Sbjct: 61  LLEDASALKRVYDAGF--DAVYHFAAQAGVRYSLENPRAYVDANLTGAFNLLELMREAPP 118

Query: 106 RTVVFASSSTVYGDADVIPTPE-EEPYKPISVYGAAKAAGEVMCATYARLFGVRCLAVRY 164
           +  + AS+S+VYG    IP  E +    P++ Y A K A E M  +YA LF +    +R+
Sbjct: 119 KHALMASTSSVYGANTKIPFHETDRADHPLTFYAATKKANEEMAHSYAHLFKIPVTMLRF 178

Query: 165 ANVVGPRLRHGVIYDFIMKLRRNPNVLEVLGDGTQRKSYLYVRDAVEATLAAWKK----- 219
             V GP  R  +     +        ++V   G  ++ + +V D VEA      K     
Sbjct: 179 FTVYGPWGRPDMALFKFVDAMVEGRPIDVFNHGKMKRDFTFVGDLVEAMALLIDKAPPAP 238

Query: 220 ---------FEEMD--APFLALNVGNVDAVRVLDIAQIVAEVLGLRPEIRLVPSTPDGRG 268
                    ++ +   AP+  +N+G    V ++D  + +    GL+ E   +        
Sbjct: 239 DSRTSPTPDYDSLSPVAPWRIVNIGTERPVGLMDFIEAIETATGLKAERNYLEMQ----- 293

Query: 269 WPGDVKYMTLAVTKLM-KLTGWRPTMTSAEAVK 300
             GDV  +T A T+L+ +LTG+RP  T AE VK
Sbjct: 294 -KGDVP-LTFASTRLLFELTGYRPATTLAEGVK 324


Lambda     K      H
   0.320    0.137    0.409 

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: 276
Number of extensions: 19
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: 312
Length of database: 337
Length adjustment: 28
Effective length of query: 284
Effective length of database: 309
Effective search space:    87756
Effective search space used:    87756
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.

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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