GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lpd in Pseudomonas benzenivorans DSM 8628

Align dihydrolipoamide dehydrogenase (EC 1.8.1.4) (characterized)
to candidate WP_090440669.1 BLS63_RS05065 dihydrolipoyllysine-residue acetyltransferase

Query= metacyc::MONOMER-18551
         (613 letters)



>NCBI__GCF_900100495.1:WP_090440669.1
          Length = 553

 Score =  100 bits (249), Expect = 2e-25
 Identities = 61/129 (47%), Positives = 83/129 (64%), Gaps = 2/129 (1%)

Query: 6   IKVPDIGDFDAVEVIEVLVAQGDTVKEEQSLITVESDKASMEIPSSAAGKVVSLSVKVGD 65
           I+VPDIG  +  EVIE++V  GD ++ +QSL+T+ESDKASMEIP+  AG + SL VK+GD
Sbjct: 5   IRVPDIGSGEG-EVIELMVKVGDRIEADQSLLTLESDKASMEIPAPKAGVIKSLKVKLGD 63

Query: 66  KVSEGTVILMLEAAAAGAQAAASDKAAAQPAAKSEAAAQKPAASSAAAEQASAAADQRPA 125
           ++ EG  +L LE   A A AA   +AAA PAA  +AAA  P A+ AA   +S      P 
Sbjct: 64  RLKEGDELLELEVEGASAPAAQPAQAAA-PAAAPQAAAAAPVAAPAAPVASSVQDVHVPD 122

Query: 126 QAAADSSEV 134
             +A  ++V
Sbjct: 123 IGSAGKAKV 131



 Score = 98.6 bits (244), Expect = 6e-25
 Identities = 71/164 (43%), Positives = 91/164 (55%), Gaps = 13/164 (7%)

Query: 5   EIKVPDIGDFDAVEVIEVLVAQGDTVKEEQSLITVESDKASMEIPSSAAGKVVSLSVKVG 64
           ++ VPDIG     +VIEVLV  GDTV+ +QSLIT+ESDKASMEIPS AAG V S+ VK+ 
Sbjct: 117 DVHVPDIGSAGKAKVIEVLVKAGDTVETDQSLITLESDKASMEIPSPAAGVVESVEVKLD 176

Query: 65  DKVSEGTVILMLEAAAAGAQAAASDKAAAQPAAKSEAAAQKPAAS-------SAAAEQAS 117
            +V  G +IL L+   AGA AAA+  AA  PAA        P A+       +A A+ A+
Sbjct: 177 AEVGTGDLILKLK--VAGAAAAAAPAAAPAPAAAPALHTTPPGAAPEVVAEVNAIAKLAA 234

Query: 118 AAADQRPAQAAADSSEVRYSPPASAPADGCDV---LVLGAGPGG 158
           AAA   P    +  + V   P     A    V    + G+GP G
Sbjct: 235 AAASVAP-PTLSSGARVHAGPAVRQLARDFGVELGAIGGSGPKG 277


Lambda     K      H
   0.314    0.131    0.364 

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: 714
Number of extensions: 38
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 613
Length of database: 553
Length adjustment: 36
Effective length of query: 577
Effective length of database: 517
Effective search space:   298309
Effective search space used:   298309
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 53 (25.0 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