GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Thermovibrio ammonificans HB-1

Align UDP-glucose 4-epimerase (EC 5.1.3.2); UDP-N-acetylglucosamine 4-epimerase (EC 5.1.3.7) (characterized)
to candidate WP_013536844.1 THEAM_RS00425 nucleotide sugar epimerase

Query= BRENDA::Q9WYX9
         (309 letters)



>NCBI__GCF_000185805.1:WP_013536844.1
          Length = 324

 Score =  188 bits (478), Expect = 1e-52
 Identities = 117/319 (36%), Positives = 172/319 (53%), Gaps = 22/319 (6%)

Query: 2   NILVTGGAGFIGSHVVDKLIENGYGVIVVDNLSSGKVENL----------NRNALFYEQS 51
           ++L+TG AGFIG      L+E GY VI VDNL++     L          NRN  FY   
Sbjct: 3   SVLLTGAAGFIGYRTAKLLLEKGYKVIGVDNLNNYYDPKLKEYRLNLLKENRNFKFYRLD 62

Query: 52  IEDEEMMERIFSLHRPEYVFHLAAQASVAISVREPARDAKTNIIGSLVLLEKSIKYGVKK 111
           IE+ E ++ +F  +  E + +LAA+A V  S+  P     TN +G+L LLE   ++G+KK
Sbjct: 63  IENFEALKVVFEENSFEGIINLAARAGVRYSIENPFVYETTNSLGTLNLLELMKEFGLKK 122

Query: 112 FIFSSTGGAIYGENVKVFPTPETE---IPHPISPYGIAKYSTEMYLEFFAREYGLKYTVL 168
           F+ +ST     G+     P P  E   +  PISPY  +K + E+    +   YG   TV+
Sbjct: 123 FVLASTSSLYAGQ-----PMPFKEDLPVNTPISPYAASKKAAEVMSYTYHYLYGFDVTVV 177

Query: 169 RYANVYGPRQDPYGEAGVVAIFTERMLRGEEVHIFGDGEYVRDYVYVDDVVRANLLAMEK 228
           RY  VYGP   P      +  F + +  G  V ++GDG   RD+ YVDD+    + A E 
Sbjct: 178 RYFTVYGPAGRPDMS---IFRFIKWIDEGRPVEVYGDGTQSRDFTYVDDIAEGTIRAYET 234

Query: 229 GDN-EVFNIGTGRGTTVNQLFKLLKEITGYDKEPVYKPPRKGDVRKSILDYTKAKEKLGW 287
               ++ N+G  R   + ++ +L++E  G   E +YKP  K D++ +  D TKA+E LGW
Sbjct: 235 ETGYQIINLGGNRPHQLKEVIRLIEEYLGKKAEIIYKPFHKADLKATWADITKAREILGW 294

Query: 288 EPKVSLEEGLKLTVEYFRK 306
           EPKV LEEGL+ TVE+ ++
Sbjct: 295 EPKVPLEEGLRRTVEWHKE 313


Lambda     K      H
   0.318    0.139    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: 265
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: 309
Length of database: 324
Length adjustment: 27
Effective length of query: 282
Effective length of database: 297
Effective search space:    83754
Effective search space used:    83754
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