GapMind for catabolism of small carbon sources

 

Alignments for a candidate for LRA3 in Dinoroseobacter shibae DFL-12

Align L-rhamnonate dehydratase (EC 4.2.1.90) (characterized)
to candidate 3609058 Dshi_2447 Mandelate racemase/muconate lactonizing protein (RefSeq)

Query= BRENDA::A3LZU6
         (429 letters)



>FitnessBrowser__Dino:3609058
          Length = 391

 Score =  188 bits (477), Expect = 3e-52
 Identities = 111/332 (33%), Positives = 175/332 (52%), Gaps = 14/332 (4%)

Query: 68  EIEATNGVKGFATGFGGPPAC-WLVANHFRRFLIGADPRDTTLLWDKMFRASMFYGRKGL 126
           E+E  +G  G       P      +   +   +IG DP D   LW+KM+R +  +GRKG+
Sbjct: 52  EVETEDGTIGIGNAALAPNVVKQAIDEWYAPLVIGEDPFDYAYLWEKMYRRTHAWGRKGI 111

Query: 127 TVAVISVIDLAIWDLLGKLRNEPVYKMIGGATRERLDFYCTGCRPDI----------AKE 176
            +  IS ID+AIWDL+GKL  +PV+K++GG T+E++  Y +    D           A++
Sbjct: 112 GMTAISAIDIAIWDLMGKLVGKPVFKLLGGRTKEKIPVYYSKLYADSIPAMQAEAEEAQK 171

Query: 177 VGFWGGKVALPYGPAEGHDGLRRNVEFLRKHRKSVGPDFPIMVDCYMSLNVSYVIDLVNA 236
            G+ G K    YGP +G  G+R N++ +   R+ +G D  +M++CYM  N+ Y   ++  
Sbjct: 172 HGYQGYKTRFGYGPKDGPAGMRENLKRVEALREVLGYDVDLMLECYMGWNLDYTKRMLPK 231

Query: 237 CKDLNINWFEEVLHPDDFDGFQKLKSACPWMKFTTGEHEYSKYGFRKLIEGRNVDILQPD 296
            +     W EE +  DD  G+ +L +A   +  + GEHE+S  G  +LI  + V +LQ D
Sbjct: 232 LERFEPRWLEEPVIADDVAGYAEL-NAMGIVPISGGEHEFSVMGCAELINRKAVSVLQYD 290

Query: 297 IMWVGGLTEILKISHQAAAYDIPVVPHASGPYSYHFVISQENTPFHEYLSNSPDSMSVLP 356
              VGG+T   KI+  A A  I V+PHA   ++YH  ++  N P  EY     D      
Sbjct: 291 TNRVGGITAAQKINAIAEAAQIIVIPHAGQMHNYHLTMANMNCPISEYFPVF-DVEVGNE 349

Query: 357 VFGELFTDEPVPTEGYLSITEFDKPGFGLTLN 388
           +F  +F  +P   +GYL + + D PG G+T++
Sbjct: 350 LFYYIFDGDPEAVDGYLQLDD-DTPGLGITIS 380


Lambda     K      H
   0.321    0.141    0.454 

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: 467
Number of extensions: 24
Number of successful extensions: 3
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: 429
Length of database: 391
Length adjustment: 31
Effective length of query: 398
Effective length of database: 360
Effective search space:   143280
Effective search space used:   143280
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 (21.8 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