GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gci in Sphingomonas koreensis DSMZ 15582

Align D-galactarolactone cycloisomerase (EC 5.5.1.27) (characterized)
to candidate Ga0059261_2635 Ga0059261_2635 L-alanine-DL-glutamate epimerase and related enzymes of enolase superfamily

Query= BRENDA::A9CEQ8
         (378 letters)



>FitnessBrowser__Korea:Ga0059261_2635
          Length = 402

 Score =  146 bits (368), Expect = 1e-39
 Identities = 115/358 (32%), Positives = 174/358 (48%), Gaps = 51/358 (14%)

Query: 32  VLVEIECDDGTVGWGECLGPARPNAAVVQAY-SGWLIGQDPRQTEKIWAVLYNALRDQGQ 90
           ++VE+E +DGT+G+    G   P   +V+ + S +LIG+DP   E IW  +Y + +  G+
Sbjct: 65  LVVELEAEDGTIGFAVTTG-GEPACFIVEKHLSRFLIGRDPSDYETIWDQMYFSTQYYGR 123

Query: 91  RGLSLTALSGIDIALWDIKGKHYGASISMLLGGRWRESVRAYATGSFKRDNVDRVSDNAS 150
           +GL + A+SG+D+A+WD+ GK     +  LLGG  R+ ++ YATG+          D A 
Sbjct: 124 KGLVVNAISGVDLAIWDLLGKLRQEPVYHLLGGAVRDEMQFYATGA--------RPDLAK 175

Query: 151 EMAERRAEGFHACKIKIGF-------GVEEDLRVIAAVREAIGPDMRLMIDANHGYTVTE 203
           EM      GF   K+ +         G+E+++ ++A +R   G D  LM D      +  
Sbjct: 176 EM------GFIGGKLPLHHGPAEGEEGMEKNIALLADMRAKCGDDFWLMYDCWMALDIDY 229

Query: 204 AITLGDRAAG-FGIDWFEEPVVPEQLDAYARVRAGQP--IPVAGGETWHGRYGMWQALSA 260
           A  L  RA    G+ W EE + P+    YA+++   P  + V  GE    R+G    L  
Sbjct: 230 ATRLAHRAWNECGLKWIEEALSPDDYWGYAQLKKNAPDGLLVTTGEHESTRWGFRMLLEM 289

Query: 261 GAVDILQPDLCGCGGFSEIQKIATLATLHGVRIVPHVWGTGV--------QIAAALQFMA 312
              DI+QPD+  CGG +E+ KIA  A   GV +VPH  G+ V        +  +      
Sbjct: 290 ECCDIIQPDVGWCGGVTELIKIADDADRKGVLMVPH--GSSVYSYHFVVTRHNSPFAEFL 347

Query: 313 AMTPDPVRVNPIEPIMEFDRTHNPFRQAVLREPLEAVNGVVTIP--DGPGLGIEINRD 368
            M P P  V P+            F   +L EP+  VNG +     D PG G+E+NRD
Sbjct: 348 MMHPGPTEVVPM------------FAPQLLGEPV-PVNGKIRASELDKPGFGVELNRD 392


Lambda     K      H
   0.321    0.138    0.431 

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: 482
Number of extensions: 32
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: 378
Length of database: 402
Length adjustment: 30
Effective length of query: 348
Effective length of database: 372
Effective search space:   129456
Effective search space used:   129456
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 50 (23.9 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