GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Saccharomonospora cyanea NA-134

Align Putative UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate WP_005453649.1 SACCYDRAFT_RS03525 dTDP-glucose 4,6-dehydratase

Query= curated2:Q57664
         (305 letters)



>NCBI__GCF_000244975.1:WP_005453649.1
          Length = 330

 Score =  140 bits (353), Expect = 4e-38
 Identities = 103/319 (32%), Positives = 165/319 (51%), Gaps = 21/319 (6%)

Query: 2   ILVTGGAGFIGSHIVDKLIENNY------DVIILDNLT-TGNKNNINPKAE-----FVNA 49
           +LVTGGAGFIGSH V + +   Y      ++++LD LT  G+++N++P A+     FV  
Sbjct: 3   VLVTGGAGFIGSHYVRQALSGEYAALRDAEIVVLDKLTYAGSRSNLDPVADSPRLRFVRG 62

Query: 50  DIRDKDLDEKINFKDVEVVIHQAAQINVRNSVENPVYDGDINVLGTINILEMMRKYDIDK 109
           DI D  +  +     V++V+H AA+ +V  S+         NVLGT  +L+      + +
Sbjct: 63  DICDPAVVVEA-MAGVDLVVHFAAESHVDRSILGAADFVLTNVLGTQTLLQAALDAGVGR 121

Query: 110 IVFASSGGAVYGEPNYLPVDENHPINPLSPYGLSKYVGEEYIKLYNRLYGIEYAILRYSN 169
            V  S+   VYG        E+H + P SPY  SK   +   + ++R YG+   I R SN
Sbjct: 122 FVHVSTD-EVYGSIERGSWSEDHVLEPNSPYSASKASSDLVARSFHRTYGLPVCITRCSN 180

Query: 170 VYGERQDPKGEAGVISIFIDKMLKNQSPIIFGDGNQTRDFVYVGDVAKA-NLMALNWK-N 227
            YG  Q P+    VI +F+  +L  +S  ++GDG   RD+++V D  +   L+A   +  
Sbjct: 181 NYGPYQFPE---KVIPLFVTNLLDGKSVPLYGDGLNVRDWLHVDDHCRGIQLVAEGGRPG 237

Query: 228 EIVNIGTGKETSVNELFDIIKHEIGFRGEAIYD-KPREGEVYRIYLDIKK-AESLGWKPE 285
           EI NIG G E +  EL + +   +G   E +   + R+G   R  +DI K +  LG+ P+
Sbjct: 238 EIYNIGGGTELTNRELTERLLAAVGVGWEMVERVEDRKGHDRRYSVDITKISRELGYSPK 297

Query: 286 IDLKEGIKRVVNWMKNNNR 304
           +D + G+   V W  +N +
Sbjct: 298 VDFETGLADTVRWYADNRQ 316


Lambda     K      H
   0.317    0.140    0.405 

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: 256
Number of extensions: 18
Number of successful extensions: 4
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: 305
Length of database: 330
Length adjustment: 27
Effective length of query: 278
Effective length of database: 303
Effective search space:    84234
Effective search space used:    84234
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: 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