GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Desulfobacca acetoxidans DSM 11109

Align UDP-glucose 4-epimerase; UDP-galactose 4-epimerase; Uridine diphosphate galactose 4-epimerase; EC 5.1.3.2 (characterized)
to candidate WP_013706597.1 DESAC_RS08145 nucleotide sugar epimerase

Query= SwissProt::A0R5C5
         (313 letters)



>NCBI__GCF_000195295.1:WP_013706597.1
          Length = 347

 Score =  167 bits (422), Expect = 4e-46
 Identities = 111/312 (35%), Positives = 172/312 (55%), Gaps = 9/312 (2%)

Query: 4   LVTGAAGFIGSTLVDRLLADGHG-VVGLDDLSSGRAENLHSAENSDKFEFVKADIVD-AD 61
           LVTG AG IGS L   L   G   V+ LDDLSS    N+ +  N     FV+  I+D  +
Sbjct: 14  LVTGGAGAIGSNLTRALGELGARLVIVLDDLSSASRWNVPALPN---VLFVEGSILDEVE 70

Query: 62  LTGLLAEFKPEVIFHLAAQISVKRSVDDPPFDATVNVVGTVRLAEAARLAGVRKVVHTSS 121
           L  +  E +P++++HLAA  + + S+D P  D  VN +GT+++ +  ++AGV++ V+ SS
Sbjct: 71  LKRVFFE-RPDIVYHLAALFANQNSLDHPETDLLVNGLGTLKILQYCQMAGVQRCVYASS 129

Query: 122 GGSVYGTPPAYPTSED-MPVNPASPYAAGKVAGEVYLNMYRNLYDLDCSHIAPANVYGPR 180
           G S+YG+    P +E+ M ++ +SPY   K+ GE+Y N + + YDL        N YGP 
Sbjct: 130 GCSIYGSSAPLPLTEEFMSLHLSSPYQITKMLGELYGNFFHHHYDLPVVKARFFNSYGPG 189

Query: 181 QDPHGEAGVVAIFSEALLAGRTTKIFGDGSDTRDYVFVDDVVDAFVRAG-GPAGGGQRFN 239
           + P     V+  F    + G+T  I G G +TRD+ +V D+VD  +RAG   +  GQ FN
Sbjct: 190 EIPGQYRNVIPNFIYWAMQGQTLPITGTGEETRDFTYVGDIVDGLLRAGYFESAIGQEFN 249

Query: 240 VGTGVETSTRELHTAIAGAVGAPDEPEFHPPRLGDLRRSRLDNT-RAREVLGWQPQVALA 298
           + +GVET   +L   I   VG     +F   R  D +   L +  RA+ ++G+QP     
Sbjct: 250 LASGVETRIGDLAQMINDQVGNEAGVKFTERRKWDTKPRLLASVDRAQNLIGYQPHTPFE 309

Query: 299 EGIAKTVEFFRN 310
           EG+  T+ +F++
Sbjct: 310 EGLKNTIAWFKD 321


Lambda     K      H
   0.317    0.136    0.396 

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: 273
Number of extensions: 23
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: 313
Length of database: 347
Length adjustment: 28
Effective length of query: 285
Effective length of database: 319
Effective search space:    90915
Effective search space used:    90915
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: 49 (23.5 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