GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimD in Pseudomonas fluorescens GW456-L13

Align pimeloyl-CoA dehydrogenase large subunit (EC 1.3.1.62) (characterized)
to candidate PfGW456L13_2536 Butyryl-CoA dehydrogenase (EC 1.3.99.2)

Query= metacyc::MONOMER-20676
         (396 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2536
          Length = 388

 Score =  237 bits (604), Expect = 5e-67
 Identities = 150/408 (36%), Positives = 223/408 (54%), Gaps = 35/408 (8%)

Query: 1   MDLNFSKEEIAFRDEVRQFFKDNVPAKTRQKLIEGRHNTKEEMVE---WYRILNKKGWAV 57
           MDL ++  + AFR + R +   NVP++  Q       +T++   E   W   LN+  W +
Sbjct: 1   MDLTYTPAQQAFRFDARTWLAANVPSEPLQSF-----DTEQGFAEHRAWEAKLNEGRWGM 55

Query: 58  THWPKEYGGTGWSSVQHYIFNEELQAAPAPQPL-AFGVSMVGPVIYTFGSEEQKKRFLPR 116
             WP E GG G   ++  IF EE   + AP  +   G+ ++GP +  +GSEEQK RFLPR
Sbjct: 56  VTWPTELGGRGCDLIEWLIFEEEYYRSGAPARVNQNGIFLLGPTLMEYGSEEQKARFLPR 115

Query: 117 IANVDDWWCQGFSEPGSGSDLASLKTKAEKKGDKWIINGQKTWTTLAQHADWIFCLCRTD 176
           +A  +D W Q +SEPG+GSD+A++++KAE+ GD ++INGQKTW+T A  ADW F + RTD
Sbjct: 116 MATGEDIWAQAWSEPGAGSDMAAIRSKAERVGDHYVINGQKTWSTRAVWADWAFGIFRTD 175

Query: 177 PAAKKQEGISFILVDMKTKGITVRPIQTIDGGHEVNEVFFDDVEVPLENLVGQENKGWDY 236
           P +++  G++FIL+ + T GITVRPI  ++G     E+FFDDV+VP+EN +G E  GW  
Sbjct: 176 PQSQRHHGLTFILLPLNTPGITVRPIPQLNGLPGFAEIFFDDVKVPVENALGGEGMGWHV 235

Query: 237 AKFLLGNERTGIAR-VGMSKERIRRIKQ--LAAQVESGGKPVIEDPKFRDKLAAVEIELK 293
           A    G ER  + R     +E  +R+ Q  LA + ++   P I +   R  L A E    
Sbjct: 236 AMSTAGFERGLLLRSPARFQETAKRLVQLYLANREQADRDPAIGEAVMRAWLDA-EAYTL 294

Query: 294 ALELTQLRVVADEGKHGKGKPNPASSVLKIKGSEIQQATTELLMEVIGPFAAPYDVHGD- 352
              +T  ++V        GK  P SS  KI  SE+ Q   +  M ++G       + G+ 
Sbjct: 295 GTYMTASQLVQG------GKIGPESSTNKIFWSELDQRMHDTAMSILG-------LRGEL 341

Query: 353 ----DDSNETMDWTAQIAPGYFNNRKVSIYGGSNEIQRNIICKAVLGL 396
                 + +   W      G+   +   IY G+NEIQRNII + +LG+
Sbjct: 342 LPQAPAAGDVGHW----LEGFLFAQAGPIYAGTNEIQRNIIAERMLGM 385


Lambda     K      H
   0.317    0.135    0.411 

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: 434
Number of extensions: 22
Number of successful extensions: 5
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: 396
Length of database: 388
Length adjustment: 31
Effective length of query: 365
Effective length of database: 357
Effective search space:   130305
Effective search space used:   130305
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 (21.6 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