GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dpkA in Pseudomonas fluorescens FW300-N2E2

Align Delta(1)-pyrroline-2-carboxylate/Delta(1)-piperideine-2-carboxylate reductase; Pyr2C/Pip2C reductase; N-methyl-L-amino acid dehydrogenase; EC 1.5.1.21; EC 1.4.1.17 (characterized)
to candidate Pf6N2E2_1089 Delta 1-piperideine-2-carboxylate reductase (EC 1.5.1.21) / Delta 1-pyrroline-2-carboxylate reductase (EC 1.5.1.1)

Query= SwissProt::Q4U331
         (343 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1089
          Length = 343

 Score =  523 bits (1347), Expect = e-153
 Identities = 255/331 (77%), Positives = 291/331 (87%)

Query: 12  TVSYPQLIDLLRRIFVVHGTSPEVADVLAENCASAQRDGSHSHGIFRIPGYLSSLASGWV 71
           T+S+  L+ LL +IF+ HGTS EVA  LAENCA A+RDG+HSHG+FRIPGY+S+L SGWV
Sbjct: 12  TLSFDALVSLLEKIFLRHGTSTEVARCLAENCAGAERDGAHSHGVFRIPGYVSTLDSGWV 71

Query: 72  DGKAVPVVEDVGAAFVRVDACNGFAQPALAAARSLLIDKARSAGVAILAIRGSHHFAALW 131
           +GKAVP+VEDV + FV VDACNGFAQPALAAAR LL+ KARSAG+A+LAIR SHHFAALW
Sbjct: 72  NGKAVPMVEDVASGFVAVDACNGFAQPALAAARPLLVAKARSAGIAVLAIRNSHHFAALW 131

Query: 132 PDVEPFAEQGLVALSMVNSMTCVVPHGARQPLFGTNPIAFGAPRAGGEPIVFDLATSAIA 191
           PDVEPFA +GLVALS+VNSMTCVVPHGA +PLFGTNPIAF APRA GEPIVFDLATSAIA
Sbjct: 132 PDVEPFAYEGLVALSVVNSMTCVVPHGADRPLFGTNPIAFAAPRADGEPIVFDLATSAIA 191

Query: 192 HGDVQIAAREGRLLPAGMGVDRDGLPTQEPRAILDGGALLPFGGHKGSALSMMVELLAAG 251
           HGDVQIAAR+G LLP GMGVD  G PT++P+AIL+GGALLPFGGHKGSALSMMVELLAA 
Sbjct: 192 HGDVQIAARKGELLPPGMGVDSLGQPTRDPKAILEGGALLPFGGHKGSALSMMVELLAAA 251

Query: 252 LTGGNFSFEFDWSKHPGAQTPWTGQLLIVIDPDKGAGQHFAQRSEELVRQLHGVGQERLP 311
           LTGGNFSFEFDW  HPGA+TPWTGQLLIVIDP K AGQ+FA+RS+ELVRQ+HGVG  RLP
Sbjct: 252 LTGGNFSFEFDWHNHPGAKTPWTGQLLIVIDPSKTAGQNFAERSQELVRQMHGVGLRRLP 311

Query: 312 GDRRYLERARSMAHGIVIAQADLERLQELAG 342
           GDRR+ ER++S  HGI + +  L +L+ELAG
Sbjct: 312 GDRRHRERSKSNEHGISLDEQTLAQLRELAG 342


Lambda     K      H
   0.320    0.137    0.412 

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: 511
Number of extensions: 16
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: 343
Length of database: 343
Length adjustment: 29
Effective length of query: 314
Effective length of database: 314
Effective search space:    98596
Effective search space used:    98596
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: 49 (23.5 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