GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Bacteroides thetaiotaomicron VPI-5482

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate 353862 BT4336 thioredoxin reductase (NCBI ptt file)

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__Btheta:353862
          Length = 316

 Score =  293 bits (749), Expect = 5e-84
 Identities = 162/319 (50%), Positives = 215/319 (67%), Gaps = 16/319 (5%)

Query: 1   MVEVRHSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGL 60
           M E+   + +I+GSGPAGY+AA+YA RANL P+L  G+Q GGQLTTTT+V+N+PG   G+
Sbjct: 1   MAEIEKVKCLIIGSGPAGYTAAIYAGRANLCPVLYEGLQPGGQLTTTTDVENFPGYPEGI 60

Query: 61  TGPALMERMREHAERFETEIVFDHINAVDFAAKPY--TLTGDSATYTCDALIIATGASAR 118
           +GP LME +R  A RF T++ F    A D +  PY  T+ GD    T +ALII+TGA+A+
Sbjct: 61  SGPQLMEDLRAQASRFGTDVRFGIATAADLSKAPYQITIDGDKVIET-EALIISTGATAK 119

Query: 119 YLGLPSEEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRR 178
           YLGL  E+ + G GVSACATCDGFFYR K VAVVGGG+TA EEA+YLA +AS V L+ R+
Sbjct: 120 YLGLEDEKKYAGMGVSACATCDGFFYRKKVVAVVGGGDTACEEAIYLAGLASKVYLVVRK 179

Query: 179 ETFRAEKILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKNNDGSFDE----LK 234
              RA KI+ +++       KI +    N+  + GDN GV G  +    G  DE    L 
Sbjct: 180 PYLRASKIMQERVQ---KHEKIEVLFEHNVVGLFGDN-GVEGMNVVKRWGESDEERYSLP 235

Query: 235 VDGVFIAIGHTPNTSLFEGQL-TLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQ 293
           +DG F+AIGH PN+ +F+  + T + GY++     DG++  T V G+FAAGDVAD  YRQ
Sbjct: 236 IDGFFLAIGHKPNSDIFKEYIDTDEVGYIIT----DGDSPRTKVPGVFAAGDVADPHYRQ 291

Query: 294 AITSAGAGCMAALDTERYL 312
           AIT+AG+GC AA++ ERYL
Sbjct: 292 AITAAGSGCKAAIEAERYL 310


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: 317
Number of extensions: 16
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: 320
Length of database: 316
Length adjustment: 27
Effective length of query: 293
Effective length of database: 289
Effective search space:    84677
Effective search space used:    84677
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.

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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