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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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