GapMind for catabolism of small carbon sources

 

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

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate 3607889 Dshi_1297 acyl-CoA dehydrogenase domain protein (RefSeq)

Query= reanno::Phaeo:GFF1011
         (386 letters)



>FitnessBrowser__Dino:3607889
          Length = 387

 Score =  648 bits (1671), Expect = 0.0
 Identities = 319/386 (82%), Positives = 346/386 (89%)

Query: 1   MFNASMTFDLGEDVNALRDMVHRWAQERVRPMAQEIDQKNEFPAELWQEMGELGLLGITV 60
           MF ASM FDLGE+V ALR+MVHRWAQERV+P+A E D+ N FP  LW EMGELGLLGITV
Sbjct: 1   MFMASMKFDLGEEVEALREMVHRWAQERVKPLAAETDRSNAFPNALWPEMGELGLLGITV 60

Query: 61  PEEFGGAGMSYLAHTVAVEEIARASASVSLSYGAHSNLCVNQIKLNGNAEQKAKYLPRLV 120
            E +GGAGM YLAHTVAVEEI+RASAS+ LSYGAHSNLCVNQIKLNG   QK KYLP+LV
Sbjct: 61  DEAYGGAGMGYLAHTVAVEEISRASASIGLSYGAHSNLCVNQIKLNGTDAQKEKYLPKLV 120

Query: 121 SGEHVGALAMSEAGAGSDVVSMSLRAEKRNDHYRLNGNKYWITNGPDADTLVVYAKTDPD 180
           SG HVGALAMSEAGAGSDVV M LRAEKRNDHYRLNG KYWITNGPDADTLVVYAKTDP+
Sbjct: 121 SGAHVGALAMSEAGAGSDVVGMKLRAEKRNDHYRLNGTKYWITNGPDADTLVVYAKTDPE 180

Query: 181 AGSKGMTAFLIEKEFKGFSTSQHFDKLGMRGSNTAELVFEDVEVPFENVLGEEGKGVRVL 240
           AGSKG+TAFLIEKE  GFSTS HFDKLGMRGSNTAEL+FEDVEVPFENVLGEEG+GV VL
Sbjct: 181 AGSKGITAFLIEKEMAGFSTSPHFDKLGMRGSNTAELIFEDVEVPFENVLGEEGRGVAVL 240

Query: 241 MSGLDYERVVLAGIGTGIMAACMDEMMPYMKERKQFGQPIGNFQLMQGKIADMYTAMNTA 300
           MSGLDYERVVL+G+  GIMA C+DE+MPYM ER+QFG+PIGNFQLMQGKIADMYTAMN+A
Sbjct: 241 MSGLDYERVVLSGVNIGIMAGCLDEVMPYMTERRQFGEPIGNFQLMQGKIADMYTAMNSA 300

Query: 301 RAYVYEVAKACDKGTVTRQDAAACCLYASEVAMTQAHQAVQAFGGAGYLSDNPVGRIFRD 360
           RAY YEVAKACD+G VTRQDAAAC LYASE  M  AHQAVQA GGAG+L+D+PV R+FRD
Sbjct: 301 RAYAYEVAKACDRGEVTRQDAAACVLYASEEGMKVAHQAVQAMGGAGFLNDSPVARMFRD 360

Query: 361 AKLMEIGAGTSEIRRMLIGRELMSQM 386
           AKLMEIGAGTSEIRRML+GRELM+ M
Sbjct: 361 AKLMEIGAGTSEIRRMLVGRELMAAM 386


Lambda     K      H
   0.318    0.132    0.382 

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: 598
Number of extensions: 19
Number of successful extensions: 1
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: 386
Length of database: 387
Length adjustment: 30
Effective length of query: 356
Effective length of database: 357
Effective search space:   127092
Effective search space used:   127092
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