GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Desulfovibrio vulgaris Hildenborough

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate 209312 DVU0377 thioredoxin reductase

Query= curated2:Q93HX6
         (320 letters)



>MicrobesOnline__882:209312
          Length = 305

 Score =  140 bits (354), Expect = 3e-38
 Identities = 106/311 (34%), Positives = 159/311 (51%), Gaps = 24/311 (7%)

Query: 9   VIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTGPALMER 68
           +IILG G AG ++A+YAARANL+ L++     GG +  T  V+N P     + G  L +R
Sbjct: 7   LIILGGGVAGMTSAIYAARANLRVLILDENACGGLVNWTKVVENMP-SYTSIGGMELAQR 65

Query: 69  MREHAERFETEI-VFDHINAVDFAAKPYTLTGDSATYTCDALIIATGASARYLGLPSEEA 127
           M+E        +     I+++D       +  D   YT  A+I+ATG       +P E A
Sbjct: 66  MQEQVNNLGVTVEEAVCIDSMDLTGPEKRVEADGEVYTAKAVIVATGRKP----VPLEAA 121

Query: 128 FMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIA-STVTLIHRRETF----R 182
              + V  CA CDG  Y  K V VVGGGN+  +E+L L +   + +TL+ R + F    +
Sbjct: 122 GECEQVHFCAICDGAPYIGKRVLVVGGGNSGFDESLALLDQGIAELTLVERMDRFFAAQK 181

Query: 183 AEKILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKNNDGSFDELKVDGVFIAI 242
           A+ +L  + NA +     +  ++ + DE L     VT   +    G     + DG+F+ +
Sbjct: 182 AQDLLAARPNATLMRSTEV--VSVDYDETL---RSVTLRDVAT--GEVFTREFDGIFVFM 234

Query: 243 GHTPNTSLFEGQLTL-KDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAGAG 301
           G  P T +F GQ  +   GY+V     D N  ATS+ G++AAGDV    YRQ  T+   G
Sbjct: 235 GQKPGTEVFRGQFDMDAQGYIVT----DEN-MATSLSGVYAAGDVRQKKYRQLTTAMADG 289

Query: 302 CMAALDTERYL 312
            MAAL+ ER++
Sbjct: 290 TMAALEAERFI 300


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: 282
Number of extensions: 16
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: 320
Length of database: 305
Length adjustment: 27
Effective length of query: 293
Effective length of database: 278
Effective search space:    81454
Effective search space used:    81454
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