GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuC in Pseudomonas fluorescens FW300-N2C3

Align 3-hydroxy-3-methylglutaryl-coenzyme A lyase/3-methylglutaconyl-coenzyme A hydratase; EC 4.1.3.4; EC 4.2.1.18 (characterized)
to candidate AO356_24105 AO356_24105 hydroxymethylglutaryl-CoA lyase

Query= CharProtDB::CH_122457
         (599 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_24105
          Length = 306

 Score =  271 bits (693), Expect = 3e-77
 Identities = 146/306 (47%), Positives = 201/306 (65%), Gaps = 8/306 (2%)

Query: 7   TVRIVEVGPRDGLQNIPQSIDSTIKLDLIRRLRDAGLQTIELTSFVSPRAIPQLADAQVV 66
           +VR+VEVG RDGLQN  +++   I+++L+++L +AGL+T+E  +FVS R +P +A +   
Sbjct: 8   SVRLVEVGARDGLQNENRTLAPAIRVELLKKLANAGLRTLEAGAFVSERWVPHMAGS--- 64

Query: 67  VQNADIQKLLKN-PKLRLPVLVPNLKGLERALHNGIKEVAVFISATEGFSRANINCTVDE 125
               D+ K L + P +    LVPN +GLE AL  G +EVAVF +A+E FS+ NINC++ E
Sbjct: 65  ---GDVFKALPDLPDVTWTALVPNARGLEEALAAGCREVAVFAAASEAFSQKNINCSIAE 121

Query: 126 GLERARQVASRAASAGLSVRGYVSCIFADPYDGPTRPSSVLRCTKALLDAGCYEVSLGDT 185
            LER   V  RA  A + VRGYVSC+   P+ G  +P +V   + AL   GCYE+SLGDT
Sbjct: 122 SLERFEAVMVRARDADVRVRGYVSCVMGCPFTGHVKPETVAAVSAALYGMGCYEISLGDT 181

Query: 186 LGIGTPADVRWLITYLQDNGVPLEMLAGHFHDTYGGAVANVWEAYKCGLRMFDSSVAGLG 245
           +G GTPA  + L+       VP+  LAGHFHDTYG A+AN+  A   G+R+FDSSVAGLG
Sbjct: 182 IGTGTPAATKALLDAC-TRVVPVNALAGHFHDTYGMAIANIHTALGMGVRVFDSSVAGLG 240

Query: 246 GCPXALGAKGNVASEDLVYMFERSGIHTGVDLSKLVETGEWISRQLSIAISSRAGAALWA 305
           GCP + GA GNVA+ED++Y+ +  GI  GVDL  +V+ GE+I   L    +SR   AL A
Sbjct: 241 GCPYSPGATGNVATEDVLYLLDGLGIKHGVDLDAVVDAGEFIDAHLGRETASRVARALLA 300

Query: 306 MRKQTA 311
            R++ A
Sbjct: 301 KRRREA 306


Lambda     K      H
   0.318    0.134    0.389 

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: 422
Number of extensions: 16
Number of successful extensions: 3
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: 599
Length of database: 306
Length adjustment: 32
Effective length of query: 567
Effective length of database: 274
Effective search space:   155358
Effective search space used:   155358
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 (21.7 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