GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Desulfobacca acetoxidans DSM 11109

Align UDP-glucose 4-epimerase; Galactowaldenase; UDP-galactose 4-epimerase; EC 5.1.3.2 (characterized)
to candidate WP_013706824.1 DESAC_RS09365 UDP-N-acetylglucosamine 4,6-dehydratase (inverting)

Query= SwissProt::Q9ZDJ5
         (341 letters)



>NCBI__GCF_000195295.1:WP_013706824.1
          Length = 326

 Score =  218 bits (555), Expect = 2e-61
 Identities = 142/340 (41%), Positives = 197/340 (57%), Gaps = 23/340 (6%)

Query: 1   MFVDKTLMITGGTGSFGNA----VLSRFLKSNIINDIKEIRIFSRDEKKQEDMRIALNNS 56
           MF DK ++ITGGTGSFG      +L R+    II       IFSRDE KQ +M    ++ 
Sbjct: 1   MFDDKAILITGGTGSFGRKCAQILLERYAPRKII-------IFSRDEYKQFEMGRIFSHE 53

Query: 57  K---LKFYIGDVRNYQSIDDAMHGVDYVFHAAALKQVPTCEFYPMEAINTNVLGAENVLS 113
           K   +++++GDVR+ + +  A H VDY+ HAAALKQ+P  E+ P EA+ TN+LGA+NV++
Sbjct: 54  KYPNMRYFLGDVRDKERLYRAFHEVDYIIHAAALKQIPAAEYNPFEAVKTNILGAQNVIN 113

Query: 114 AAINNKVTKVIVLSTDKAVYPINAMGLSKALMEKLAIAKARMRSPGETILCVTRYGNVMA 173
            AI+ KV KVI LSTDKA  P+N  G +K   +KL IA         TI  V RYGNV+ 
Sbjct: 114 VAIDQKVKKVIALSTDKAANPVNLYGATKLCSDKLFIAGNAYVGRDHTIFSVVRYGNVVG 173

Query: 174 SRGSVIPLFIHQIKQGKELTITEPSMTRFLMSLVDSVDLVLYAFEHGRQGDIFVQKSPAS 233
           SRGSVIPLF+ +  +G  L IT+P MTRF ++L  +V  VL   E    G++FV K P+ 
Sbjct: 174 SRGSVIPLFLRERAKG-VLPITDPRMTRFWITLEQAVLFVLDCLERMVGGELFVPKLPSM 232

Query: 234 TIEVLAKALQEIFGSKNAIRFIGTRHGEKHYESLVSSEDMAKADDLGGYYRIPMDGRDLN 293
            I  LA A+    G +   + IG R GEK +E +++ +D     +   YY I  D R   
Sbjct: 233 NIMDLAAAI----GPECQTKIIGIRPGEKLHELMITKDDARNTIEFKDYYVIKPDFR--Y 286

Query: 294 YAKYFVTGEKKVALLD-DYTS-HNTKRLNLKEVKELLLTL 331
           +A+ F          D +Y S +N  RL  +E++EL+  L
Sbjct: 287 FARRFQEEAGTPTPPDFEYDSLNNPWRLQPEELRELIQDL 326


Lambda     K      H
   0.319    0.135    0.373 

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: 288
Number of extensions: 9
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: 341
Length of database: 326
Length adjustment: 28
Effective length of query: 313
Effective length of database: 298
Effective search space:    93274
Effective search space used:    93274
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: 49 (23.5 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