GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Klebsiella michiganensis M5al

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate BWI76_RS19065 BWI76_RS19065 dTDP-glucose 4,6-dehydratase

Query= BRENDA::F6DEY6
         (311 letters)



>FitnessBrowser__Koxy:BWI76_RS19065
          Length = 354

 Score =  130 bits (327), Expect = 5e-35
 Identities = 107/345 (31%), Positives = 166/345 (48%), Gaps = 53/345 (15%)

Query: 1   MRVLVTGGAGFIGSHIVEDLLARGL-EVAVLD------NLATGKRENVPKGVPFFQVDLR 53
           M++LVTGGAGFIGS +V  ++     EV V+D      NL +  + +V     F +V++ 
Sbjct: 1   MKILVTGGAGFIGSAVVRHIINDTTDEVVVVDCLTYAGNLESLTQVSVSDRFSFEKVNIC 60

Query: 54  DKEEVERAFREFRPTHVSHQAAQASVKVSVEDPVLDFEVNLLGGLNLLEACRQYGVE-KL 112
           DK+E+ R F   +P  V H AA++ V  S++ P    E N++G   LLE  R Y  + + 
Sbjct: 61  DKDELNRIFHYHKPDAVMHLAAESHVDRSIDGPAAFIETNIVGTYTLLEVARAYWNQLEE 120

Query: 113 VFAS-------TGGAIYGEV-PEGERAEETWPPRPKSPYAASKAAFEHYLSVYGQSYGLK 164
            F S       +   +YG++    +   E     P SPY+ASKA+ +H +  + ++YGL 
Sbjct: 121 QFKSNFRFHHISTDEVYGDLHGTDDLFTEKTSYSPSSPYSASKASSDHLVRAWLRTYGLP 180

Query: 165 WVSLRYGNVYGPRQDPHGEAGVVAIFAERVLNGLPVTLYARKTPGDEGCVRDYVYVGDVA 224
            +     N YGP   P     ++ +     L G P+ +Y     GD G +RD++YV D  
Sbjct: 181 TIVTNCSNNYGPFHFPE---KLIPLIILNALEGKPLPVY-----GDGGQIRDWLYVED-- 230

Query: 225 EAHALALFSL--EGI----YNVGTGEGHTTREVLEAVAEAAGKAPQVQPAPP-------- 270
             HA AL+ +  EGI    YN+G   GH  R+ ++ V        +  P  P        
Sbjct: 231 --HARALYKVVTEGIVGETYNIG---GHNERKNIDVVKTICLLLEEYVPTKPKGLNNYCD 285

Query: 271 -------RPGDLERSVLSPLKLMAH-GWRPKVGFQEGIRLTVDHF 307
                  RPG   R  +   K++   GW+P+  F+ GIR TV+ +
Sbjct: 286 LITYVKDRPGHDVRYAIDATKILNELGWKPQETFESGIRKTVEWY 330


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: 261
Number of extensions: 15
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: 354
Length adjustment: 28
Effective length of query: 283
Effective length of database: 326
Effective search space:    92258
Effective search space used:    92258
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: 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