GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaE in Pseudomonas stutzeri RCH2

Align ring 1,2-phenylacetyl-CoA epoxidase PaaE subunit (EC 1.14.13.149) (characterized)
to candidate GFF3388 Psest_3453 Flavodoxin reductases (ferredoxin-NADPH reductases) family 1

Query= metacyc::MONOMER-15950
         (357 letters)



>FitnessBrowser__psRCH2:GFF3388
          Length = 518

 Score =  191 bits (484), Expect = 5e-53
 Identities = 124/354 (35%), Positives = 190/354 (53%), Gaps = 25/354 (7%)

Query: 4   FHSLTIKEVRPETRDAVSIAFDVPAELADSFRFTQGQHLVMRTQLDGEEVRRSYSICTGV 63
           F +LT+   + ET DA S +  VPAEL + F    GQ + +R       + RSYS+   +
Sbjct: 187 FAALTVIARQAETADAASFSLQVPAELRERFAAQPGQFVTLRVPCSEPPLLRSYSLSKPL 246

Query: 64  -NDGELRVAIKRVAGGRFSAYANESLKAGQRLEVMPPSGHFHV-ELDAARHGNYLAVAAG 121
            +DG LR++++RV GGR S +  ++L+ GQR++V+PP+G     +LD    G+ L + AG
Sbjct: 247 GSDGVLRISVRRVPGGRASNWLLDNLQVGQRIDVLPPAGRLVPHDLD----GDLLLLGAG 302

Query: 122 SGITPILSIIKTTLETEPHSRVTLLYGNRSSASTLFREQLEDLKNRYLQRLNLIFLFSRE 181
           SGITP+ +I++  LE +   RV L Y +R +AS +F E+L D   RY +RL L      E
Sbjct: 303 SGITPLRAILQAALE-QGRGRVFLFYASRDAASLIFAEELADFAARYPERLQLRIWLDAE 361

Query: 182 QQDVDLYNGRIDADKCGQLFSRWIDVKALDAAFICGPQAMTETVRDQLKANGMAAERIHF 241
           Q       G   A         W   +A    F+CGPQ   +     L    ++++ IH 
Sbjct: 362 Q-------GIPSAPAIAAKIGDWPQGEA----FVCGPQPFMDGASVALAELDVSSDAIHV 410

Query: 242 ELF-AAAGSAQKREARESAAQDSSVSQITVISDGRELSFELPRNSQSILDAGNAQGAELP 300
           E F  AA  A   E R+        S++ V  DGR  + ++ +  + +LDA    G + P
Sbjct: 411 ERFNTAAPVAPLSELRQPLH-----SRLQVALDGRRHALDV-QQGEVLLDAMEQAGLQPP 464

Query: 301 YSCKAGVCSTCKCKVVEGEVEMDSNFALEDYEVAAGYVLSCQTFPISDKVVLDF 354
            +C+AGVC+ C+C+VVEG V M SN  L D +V  G+ L+CQ  P S ++ +++
Sbjct: 465 SACRAGVCAACRCRVVEGSVSMRSNQVLSDQQVRQGWTLACQAVPTSTRLAVEY 518


Lambda     K      H
   0.319    0.133    0.377 

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: 376
Number of extensions: 18
Number of successful extensions: 6
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: 357
Length of database: 518
Length adjustment: 32
Effective length of query: 325
Effective length of database: 486
Effective search space:   157950
Effective search space used:   157950
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