GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Phaeobacter inhibens BS107

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate GFF2829 PGA1_c28750 aminotransferase class-III

Query= BRENDA::P42588
         (459 letters)



>FitnessBrowser__Phaeo:GFF2829
          Length = 440

 Score =  193 bits (491), Expect = 8e-54
 Identities = 123/350 (35%), Positives = 187/350 (53%), Gaps = 24/350 (6%)

Query: 70  AGSLNTLVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPL-HSQELLDPLRAM 128
           AG    L+D  G+ ++D  GG  +  +GH +  V++AVQ Q+ K    H+  L       
Sbjct: 18  AGDGCYLIDANGKRYLDGSGGAAVSCLGHSDAEVIAAVQEQVGKLAFAHTGFLTSEPAEA 77

Query: 129 LAKTLAALTPGKLKYSFFCNSGTESVEAALKLAKAYQSPRGKFT---FIATSGAFHGKSL 185
           LA  L +  PG L   +F + G+E+ EAA+KLA+ Y   RG  T    IA   ++HG +L
Sbjct: 78  LADLLISQAPGDLHRVYFVSGGSEATEAAIKLARQYHLERGDTTRRHVIARRQSYHGNTL 137

Query: 186 GALSATAKSTFRKPFMPLL-------PGFRHVPFGNIEAM----RTALNECKKT-----G 229
           GAL+A   +  R+ F PLL       P + +V  G+ E+     +   NE +        
Sbjct: 138 GALAAGGNAWRRQQFAPLLIDISHIAPCYEYVDRGDGESRYDYGQRVANELEAEILRLGP 197

Query: 230 DDVAAVILEPIQGE-GGVILPPPGYLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEH 288
           + V A + EP+ G   G +    GY   +R++CD++G L+ILDEV  GMGRTG +FACE 
Sbjct: 198 ETVMAFMAEPVVGATSGAVPAVEGYFKRIREICDQYGVLLILDEVMCGMGRTGHLFACEA 257

Query: 289 ENVQPDILCLAKALGGGVMPIGATIATEEVFSVLFDNP--FLHTTTFGGNPLACAAALAT 346
           + V PDILC+AK LG G  PIGA + + +++  +      F H  T+ G+P+A AA LA 
Sbjct: 258 DGVAPDILCIAKGLGAGYQPIGAMLCSRQIYDAIEGGSGFFQHGHTYIGHPVATAAGLAV 317

Query: 347 INVLLEQNLPAQAEQKGDMLLDGFRQLAREYPDLVQEARGKGMLMAIEFV 396
           +  LL++ L  ++ + G+ L         ++P  V + RG+G+   IE V
Sbjct: 318 VRALLDRGLVQRSAEMGETLHAALVARFGQHPH-VGDLRGRGLFRGIELV 366


Lambda     K      H
   0.320    0.135    0.393 

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: 493
Number of extensions: 27
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: 459
Length of database: 440
Length adjustment: 33
Effective length of query: 426
Effective length of database: 407
Effective search space:   173382
Effective search space used:   173382
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 51 (24.3 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