GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimC in Caulobacter crescentus NA1000

Align pimeloyl-CoA dehydrogenase small subunit (EC 1.3.1.62) (characterized)
to candidate CCNA_01875 CCNA_01875 acyl-CoA dehydrogenase, short-chain specific

Query= metacyc::MONOMER-20677
         (380 letters)



>FitnessBrowser__Caulo:CCNA_01875
          Length = 381

 Score =  129 bits (323), Expect = 2e-34
 Identities = 103/316 (32%), Positives = 143/316 (45%), Gaps = 21/316 (6%)

Query: 51  GLLGLPFSEEDGGFGAGAVETMIVMEALGHSLVL--EPYLPTVVIGGGFLRRAGSAAQKA 108
           GL GL   E  GG G    E   V+ A  H+       +   V IG   L   G  AQKA
Sbjct: 47  GLFGLSIPESYGGLGLSLEEEARVIVAFCHTAPAFRSTFGTNVGIGSQGLVMFGDEAQKA 106

Query: 109 AHLPGIIDGSKTFAFAQLEKNSRWDLGDVSTTAKKSGDGWVIDGEKFVVLNGEAADTLIV 168
             LP I  G    AFA  E  +  D   V T A + GD +V++G K  + N   A+   V
Sbjct: 107 RWLPSIASGETITAFALTEAEAGSDSASVQTRAVRDGDHYVLNGVKRYITNAGRANLFTV 166

Query: 169 TARTKGGQRDRTGVGVFLVPADAKGITRKGYPT----QDGLHAADITFTGVQVGADAAIG 224
            ART    +   GV  FLVPAD  G++  G P     Q G H  D+ F  V+V  +  +G
Sbjct: 167 MARTDPNTKGGAGVSAFLVPADLPGLS-VGKPEKKMGQQGAHIHDVVFEDVRVPVENRLG 225

Query: 225 DPENALELIEAVVDDARTALCAEAVGLMDESLTTTVEYIKTRKQFGVPIGSFQVLQHRAA 284
                  +   V+D  R  + A  VG+ +  +   V Y   RKQFG PI SFQ++Q   A
Sbjct: 226 AEGEGFTVAMRVLDRGRVHISAVCVGVAERLIADCVAYASERKQFGQPIASFQLIQAMIA 285

Query: 285 DMFVATEQARSMAMFATMAAEFDDAKER-AGA-----IAAAKVQIGKSGKFVGQQSIQLH 338
           D       +++ A+ A  A  FD A++R AGA      AA K+   +    V  +++Q+ 
Sbjct: 286 D-------SKTEAL-AAKALVFDTARKRDAGANVTLEAAATKLFASEMVGRVADRAVQVF 337

Query: 339 GGIGMTMEAKIGHYFK 354
           GG G   +  I   ++
Sbjct: 338 GGAGYVADYGIERLYR 353


Lambda     K      H
   0.318    0.135    0.388 

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: 324
Number of extensions: 19
Number of successful extensions: 2
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: 380
Length of database: 381
Length adjustment: 30
Effective length of query: 350
Effective length of database: 351
Effective search space:   122850
Effective search space used:   122850
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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