GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ketodeoxyribonate-cleavage in Pseudomonas putida KT2440

Align 2-deoxy-3-keto-D-ribonate cleavage enzyme (characterized)
to candidate PP_0303 PP_0303 dehydrocarnitine cleavage enzyme

Query= reanno::Burk376:H281DRAFT_00641
         (312 letters)



>FitnessBrowser__Putida:PP_0303
          Length = 294

 Score =  160 bits (405), Expect = 3e-44
 Identities = 105/317 (33%), Positives = 162/317 (51%), Gaps = 48/317 (15%)

Query: 8   VIISCAITGATHVPSMSEFLPITPEQIRDQAIEAAQAGAAIIHLHARDPVDGRPTPSPEI 67
           VII+CA+TGA    S S  +P+TP+QI + A+EAA+AGA ++H H RDP  GR +    +
Sbjct: 5   VIITCALTGAGDTASKSHLVPVTPKQIAESAVEAAKAGATVVHCHVRDPQTGRFSRDVAL 64

Query: 68  FKAFVPAIAEA-TDAVINITTG---------GSTRMTLE---------ERLAYPRLARPE 108
           ++  +  I EA  D ++N+T G         G T +            ERLA+     PE
Sbjct: 65  YREVMERIREADVDIIVNLTAGMGGDLEIGPGETPLAFGPGTDLIGPLERLAHVEALLPE 124

Query: 109 MCSLNMGSMNFSIHPVAAKISSWRYGWEKDYIEGMEDMIFRNTFRDIRNILLELGESGTR 168
           +C+L+ G++NF                      G  + I+ +T   +R     + E G +
Sbjct: 125 ICTLDCGTLNF----------------------GDGNSIYVSTPAQLRAGAKRITELGVK 162

Query: 169 FEFECYDVGHLYNLAHFVDQGLVKPPFFIQSVFGILGGLGADPENMLLMRSTADRLFGRE 228
            E E +D GHL+     + +GL++ P F Q   GI  G  AD      M++  D L    
Sbjct: 163 AELEIFDTGHLWFAKQMMKEGLLEDPLF-QLCLGIPWGAPADTTT---MKAMVDNL--PA 216

Query: 229 NYHFSVLGAGRHQMPLVTMSAIMGGNVRVGLEDSVYLAKGVKAETNAQQVRKIRRILEEL 288
           N  ++  G GR QMP+   + ++GGNVRVGLED++YL +GV A +N Q V +   I+  +
Sbjct: 217 NVTWAGFGIGRMQMPMAAQAVLLGGNVRVGLEDNLYLDRGVLA-SNGQLVERASEIITRM 275

Query: 289 SLEIATPADARKMLGLK 305
              + +PA+ R+ + LK
Sbjct: 276 GGRVLSPAEGREKMNLK 292


Lambda     K      H
   0.321    0.137    0.400 

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: 234
Number of extensions: 13
Number of successful extensions: 5
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: 312
Length of database: 294
Length adjustment: 27
Effective length of query: 285
Effective length of database: 267
Effective search space:    76095
Effective search space used:    76095
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 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