GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Sulfuritalea hydrogenivorans DSM 22779

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate WP_041098319.1 SUTH_RS07575 dTDP-glucose 4,6-dehydratase

Query= BRENDA::F2NQX6
         (314 letters)



>NCBI__GCF_000828635.1:WP_041098319.1
          Length = 355

 Score =  121 bits (303), Expect = 3e-32
 Identities = 100/334 (29%), Positives = 154/334 (46%), Gaps = 37/334 (11%)

Query: 3   VLVTGGAGFIGSHLVHAL-HQKGIPVAVLDDLSTGKRAHIPPDVP------LYQTDIRDL 55
           + VTGGAGFIGS L+  L  +    +  +D L+         D+         +TDI D 
Sbjct: 4   LFVTGGAGFIGSALIRLLIAESDWRIVNIDKLTYAGNLESLADIADSDRHVFSRTDICDR 63

Query: 56  NAVLHAFQDFQPTHVAHQAAQASVKHSVQNPCKDAEINLLGGLNILEAMRA--------- 106
            A+   F + QP  V H AA++ V  S+  P    E N+ G   +LEA RA         
Sbjct: 64  AALDALFAEHQPAGVIHLAAESHVDRSIHGPGDFIETNISGTYTLLEAARAHWSALDPEP 123

Query: 107 TGTQKIVFASTGGAIYGEVPEGRRAPETWPPKPKSPYAASKAAFEHYLEVYRQTHGLTYT 166
             T +    ST   ++G +       ET P +P SPY+ASKAA +H +  +  T+GL   
Sbjct: 124 KATFRFHHVSTD-EVFGSLGATGLFVETSPYQPNSPYSASKAASDHLVRAWHHTYGLPTV 182

Query: 167 TLRYANVYGPRQDPHGEAGVVAIFTNRLLHAQPVTLYARKEPGDPGCIRDYIHVEDVTRA 226
               +N YGP Q P     ++ +  +  +  +P+ +Y +   GD   +RD+++V+D  RA
Sbjct: 183 ITNCSNNYGPCQFPE---KLIPLMIHNAVSDKPLPIYGK---GDN--VRDWLYVDDHARA 234

Query: 227 NLLALETNLEG-TYNVSTGQGRTTEDVLYTIARALG-TTPRVTYAPPRDGDLEVS----- 279
             L  E    G TYN+     +T  +V+ T+   L    PR      R+  + V+     
Sbjct: 235 LRLVFERGSVGETYNIGGHNEKTNLEVVDTLCALLDELKPRHDRRSYREQKISVADRPGH 294

Query: 280 ----VLDPTQLQAH-GWRPQVPFEEGIRRTVAWF 308
                +D  ++Q   GW PQ  FE G+ +TV W+
Sbjct: 295 DQRYAIDAGKIQRELGWTPQETFESGLAKTVRWY 328


Lambda     K      H
   0.318    0.135    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: 289
Number of extensions: 25
Number of successful extensions: 6
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: 314
Length of database: 355
Length adjustment: 28
Effective length of query: 286
Effective length of database: 327
Effective search space:    93522
Effective search space used:    93522
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 Apr 09 2024. 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