GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Echinicola vietnamensis KMM 6221, DSM 17526

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate Echvi_3438 Echvi_3438 thioredoxin-disulfide reductase

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__Cola:Echvi_3438
          Length = 314

 Score =  296 bits (757), Expect = 6e-85
 Identities = 156/313 (49%), Positives = 213/313 (68%), Gaps = 11/313 (3%)

Query: 3   EVRHSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTG 62
           E    +V+I+GSGPAGY+AA+YA+RA L P+L TG Q GGQLT T +V+N+PG   G+ G
Sbjct: 4   EAEKIKVLIVGSGPAGYTAAIYASRAGLSPVLYTGGQPGGQLTITNDVENYPGYPDGVMG 63

Query: 63  PALMERMREHAERFETEIVFDHINAVDFAAKPY-TLTGDSATYTCDALIIATGASARYLG 121
           P +ME  ++ AERF T++ +  + AVDF+  P+  +  D      D +II+TGASA++LG
Sbjct: 64  PQMMEDFKKQAERFGTDVRYGLVTAVDFSTGPHKVIVDDKDEILADTVIISTGASAKWLG 123

Query: 122 LPSEEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETF 181
           L SE    GKGVSACA CDGFF+RN+ VA+VG G+TA EEA YLANI   V ++ RR+  
Sbjct: 124 LESETKLNGKGVSACAVCDGFFFRNQKVAIVGAGDTACEEASYLANICEKVYMLVRRDEM 183

Query: 182 RAEKILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKNND-GSFDELKVDGVFI 240
           RA +I+  ++    +  KI +  N   +E+LG+   VTG R+KNN  G   EL+V G F+
Sbjct: 184 RASQIMQKRV---TSNPKIEILWNTETEEILGEE-EVTGVRVKNNQTGEEQELEVTGFFV 239

Query: 241 AIGHTPNTSLFEGQLTLKD-GYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAG 299
           AIGH PNT +F+  L + + GY+  Q G    +T T++EG+FA GD  DHVYRQA+T+AG
Sbjct: 240 AIGHKPNTDIFKDFLDMNEAGYINTQPG----STKTNIEGVFACGDAQDHVYRQAVTAAG 295

Query: 300 AGCMAALDTERYL 312
            GCM+ALD ER+L
Sbjct: 296 TGCMSALDAERFL 308


Lambda     K      H
   0.318    0.135    0.386 

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: 307
Number of extensions: 18
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 320
Length of database: 314
Length adjustment: 27
Effective length of query: 293
Effective length of database: 287
Effective search space:    84091
Effective search space used:    84091
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: 48 (23.1 bits)

This GapMind analysis is from Sep 17 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