GapMind for catabolism of small carbon sources

 

Aligments for a candidate for liuA in Pseudomonas fluorescens FW300-N2E2

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate Pf6N2E2_1146 Butyryl-CoA dehydrogenase (EC 1.3.99.2)

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



>lcl|FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1146 Butyryl-CoA
           dehydrogenase (EC 1.3.99.2)
          Length = 375

 Score =  288 bits (738), Expect = 1e-82
 Identities = 153/372 (41%), Positives = 230/372 (61%), Gaps = 2/372 (0%)

Query: 12  EDVNALRDMVHRWAQERVRPMAQEIDQKNEFPAELWQEMGELGLLGITVPEEFGGAGMSY 71
           E+   +RDM  ++A+ER++P A E D+++ FP E   EM ELG  G+ VPE++GG    Y
Sbjct: 5   EEQTQIRDMARQFAEERLKPFAAEWDREHRFPREAIDEMAELGFFGMLVPEQWGGCDTGY 64

Query: 72  LAHTVAVEEIARASASVSLSYGAHSNL-CVNQIKLNGNAEQKAKYLPRLVSGEHVGALAM 130
           LA+ + +EEIA    + S     H+++ CV  +K  GN EQKAK+L  L SG  +GA A+
Sbjct: 65  LAYAMTLEEIAAGDGACSTIMSVHNSVGCVPILKF-GNDEQKAKFLTPLASGAMLGAFAL 123

Query: 131 SEAGAGSDVVSMSLRAEKRNDHYRLNGNKYWITNGPDADTLVVYAKTDPDAGSKGMTAFL 190
           +E  AGSD  S+  RA    DHY LNG K +IT+G +A  ++V+A TDP AG +G++AF+
Sbjct: 124 TEPQAGSDASSLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFI 183

Query: 191 IEKEFKGFSTSQHFDKLGMRGSNTAELVFEDVEVPFENVLGEEGKGVRVLMSGLDYERVV 250
           +  +  G+S ++  DKLG   S+T +++FED++VP  N LGEEG+G ++ ++ L+  RV 
Sbjct: 184 VPTDSPGYSVARVEDKLGQHASDTCQILFEDLKVPVGNRLGEEGEGYKIALANLEGGRVG 243

Query: 251 LAGIGTGIMAACMDEMMPYMKERKQFGQPIGNFQLMQGKIADMYTAMNTARAYVYEVAKA 310
           +A    G+  A  +    Y +ER  FG+PI   Q +  ++ADM T +  AR  V+  A  
Sbjct: 244 IAAQAVGMARAAFEAARDYARERSSFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAAL 303

Query: 311 CDKGTVTRQDAAACCLYASEVAMTQAHQAVQAFGGAGYLSDNPVGRIFRDAKLMEIGAGT 370
            D G     +A+   L+ASE+A      A+Q  GG GYL+D P+ RI+RD ++ +I  GT
Sbjct: 304 RDSGQPALVEASMAKLFASEMAEKVCSMALQTLGGYGYLNDFPLERIYRDVRVCQIYEGT 363

Query: 371 SEIRRMLIGREL 382
           S+I+RM+I R L
Sbjct: 364 SDIQRMVISRNL 375


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: 334
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: 375
Length adjustment: 30
Effective length of query: 356
Effective length of database: 345
Effective search space:   122820
Effective search space used:   122820
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 against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer. 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. 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 preprint 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