GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ligI in Derxia gummosa DSM 723

Align 2-pyrone-4,6-dicarbaxylate hydrolase; PDC hydrolase; 2-pyrone-4,6-dicarboxylate lactonase; EC 3.1.1.57 (characterized)
to candidate WP_028310842.1 H566_RS0106740 2-pyrone-4,6-dicarboxylate hydrolase

Query= SwissProt::Q93PS7
         (305 letters)



>NCBI__GCF_000482785.1:WP_028310842.1
          Length = 312

 Score =  578 bits (1489), Expect = e-170
 Identities = 269/302 (89%), Positives = 284/302 (94%)

Query: 4   FEKTPGWLDWYANPSKPQFKLPAGAVDAHCHVFGPGNEFPFAPERKYTPCDASKAQLYAL 63
           F KT GWLDWY  PSKP F LPAGAVDAHCHVFGPG EFP+APERKYTPCDASKA+LYAL
Sbjct: 9   FTKTAGWLDWYTGPSKPAFTLPAGAVDAHCHVFGPGAEFPYAPERKYTPCDASKAELYAL 68

Query: 64  RDHLGFARNVVVQATCHGADNRAMVDACKSSGGKARGVATVKRSISDAELQQLHDAGVRG 123
           RDHLGFARNV+VQATCHGADNRAMVDAC +SGGKARGVATV+RS++D E+Q +HDAGVRG
Sbjct: 69  RDHLGFARNVIVQATCHGADNRAMVDACVNSGGKARGVATVRRSVTDEEIQAMHDAGVRG 128

Query: 124 VRFNFVKRLVDFTPKDELMEIAGRIAKLGWHVVIYFEAVDLPELWDFFTALPTTVVVDHM 183
           VRFNFVKRLVDFTPKDELMEIAGRIAK GWHVVIYFEAVDLPELWDFFTALPTTVVVDHM
Sbjct: 129 VRFNFVKRLVDFTPKDELMEIAGRIAKWGWHVVIYFEAVDLPELWDFFTALPTTVVVDHM 188

Query: 184 GRPDVTKGVDSEEFALFLKFMREHQNVWSKVSCPERLSVTGPKALNGEQNAYRDVVPFAR 243
           GRPDV+K +D  EF LFLKFMREH NVWSKVSCPERLSVTGPKAL+GE+NAY DV+PFAR
Sbjct: 189 GRPDVSKPIDGPEFELFLKFMREHGNVWSKVSCPERLSVTGPKALDGERNAYTDVIPFAR 248

Query: 244 RVVEEFPDRVLWGTDWPHPNLKDHMPDDGLLVDFIPHIAPTAELQQKLLVDNPMRLYWPE 303
           RVVEEFPDRVLWGTDWPHPNLKDHMPDDGLLVDFIPHIAPTAELQQKLLV NPMRLYWP+
Sbjct: 249 RVVEEFPDRVLWGTDWPHPNLKDHMPDDGLLVDFIPHIAPTAELQQKLLVANPMRLYWPD 308

Query: 304 EV 305
           EV
Sbjct: 309 EV 310


Lambda     K      H
   0.322    0.138    0.445 

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: 514
Number of extensions: 12
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: 305
Length of database: 312
Length adjustment: 27
Effective length of query: 278
Effective length of database: 285
Effective search space:    79230
Effective search space used:    79230
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 (21.9 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 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