GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Marinobacter adhaerens HP15

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate GFF56 HP15_56 acyl-CoA dehydrogenase domain protein

Query= reanno::psRCH2:GFF1051
         (387 letters)



>FitnessBrowser__Marino:GFF56
          Length = 374

 Score =  250 bits (639), Expect = 4e-71
 Identities = 138/371 (37%), Positives = 220/371 (59%), Gaps = 3/371 (0%)

Query: 12  ETIDMLREQVQAFVAAEIAPRAEAIDQENLFPADMWRKFGEMGLLGVTVSEEYGGAGLGY 71
           E  +M REQ + F+  EI P  E  ++  + P ++WRK GEMGLL  TV EEYGGAG  +
Sbjct: 7   EDHNMFREQARRFIEREICPHLEEWEKSGIVPKEIWRKAGEMGLLCSTVPEEYGGAGGDF 66

Query: 72  LAHVVAMEEISRGSASVALSYGAHSNLCVNQINRNGNPEQKARYLPKLISGEHVGALAMS 131
               V +EE++R +A+ A+ +  HS +    I   G  EQK ++LP+++SGE +G +AMS
Sbjct: 67  GHSAVMIEELARVNAT-AIGFTTHSEIVAPYIVAYGTEEQKQKWLPRMVSGEIIGVIAMS 125

Query: 132 EPNAGSDVVSMKLRAEKRGDRYVLNGSKTWITNGPDANTYVIYAKTDLDKGAHGITAFIV 191
           EP  GSD+ SM+ +  + GD+Y+++G KT+ITNG +A+  ++   T +D  +  +T   V
Sbjct: 126 EPGIGSDLRSMRTQLRRDGDQYIISGQKTFITNGGNAD--LVVTATKVDPASKDLTLVCV 183

Query: 192 ERDWKGFSRGNKFDKLGMRGSNTCELFFDDVEVPQENVLGAENGGVKVLMSGLDYERVVL 251
           E D  GF++G   DK+G++G +T ELFFDDV VP  N LG EN G   L   L +ER+++
Sbjct: 184 ETDRDGFAKGRLLDKIGLKGQDTAELFFDDVRVPVSNRLGEENEGFGYLTHQLAWERLII 243

Query: 252 AGGPTGIMQSCLDVVVPYIHDRKQFGQSIGEFQFIQGKVADMYTQLNASRAYLYAVAQAC 311
           A      + S LD+ + Y  +RK FG+++ +FQ  + K+A++  Q    R ++    +  
Sbjct: 244 AIRAAESIDSFLDMTIGYTKERKVFGKTVFDFQNTRFKLAEIKAQATMLRVFVDNCLERV 303

Query: 312 DRGETTRKDAAGVILYTAENATQMALQAIQILGGNGYINEFPTGRLLRDAKLYEIGAGTS 371
              +     AA   L  +E   ++  + +Q+ GG G+++E+  G+   DA++  I  GTS
Sbjct: 304 MNNDLPADVAAMAKLMGSELQGKLLDEMLQLHGGYGFMSEYRIGQAWIDARVARIYGGTS 363

Query: 372 EIRRMLIGREL 382
           EI + +I R+L
Sbjct: 364 EIMKEIISRKL 374


Lambda     K      H
   0.318    0.135    0.391 

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: 356
Number of extensions: 15
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: 387
Length of database: 374
Length adjustment: 30
Effective length of query: 357
Effective length of database: 344
Effective search space:   122808
Effective search space used:   122808
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: 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