GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ketodeoxyribonate-cleavage in Neptunomonas antarctica S3-22

Align 2-deoxy-3-keto-D-ribonate cleavage enzyme (characterized)
to candidate WP_054340607.1 Nant_RS05340 3-keto-5-aminohexanoate cleavage protein

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



>NCBI__GCF_001305295.1:WP_054340607.1
          Length = 296

 Score =  144 bits (362), Expect = 3e-39
 Identities = 101/321 (31%), Positives = 155/321 (48%), Gaps = 47/321 (14%)

Query: 5   SRKVIISCAITGATHVPSMSEFLPITPEQIRDQAIEAAQAGAAIIHLHARDPVDGRPTPS 64
           ++ VII+CA+ GA      S  +P+TPE+I + AIEA  AGAAI H+H R+P   + +  
Sbjct: 2   NQDVIITCALNGAADTAHRSPHVPVTPEEIANAAIEAWNAGAAIAHIHVREPDTKQGSRR 61

Query: 65  PEIFKAFVPAI-AEATDAVINITTG-----------GSTRMTLE-------ERLAYPRLA 105
            E++      + A   D +IN+T G             T    E       ERL +    
Sbjct: 62  VELYAEVCERLRASDCDIIINLTAGMGGDLYIGPDENPTAFAKETDLVGATERLIHIEAL 121

Query: 106 RPEMCSLNMGSMNFSIHPVAAKISSWRYGWEKDYIEGMEDMIFRNTFRDIRNILLELGES 165
           +PE+C+L+ GS+NF                      G  ++++ +T   +R     + E 
Sbjct: 122 KPEICTLDCGSVNF----------------------GDSNLVYVSTPEMLRQGAARIKEL 159

Query: 166 GTRFEFECYDVGHLYNLAHFVDQGLVKPPFFIQSVFGILGGLGADPENMLLMRSTADRLF 225
           G   E E +D G+L+     + +GL+      Q   GI  G    P    L++   D L 
Sbjct: 160 GVTVELEIFDTGNLWFALQMMKEGLLDDNAMFQLCQGIPWG---TPPEFSLLKGMVDML- 215

Query: 226 GRENYHFSVLGAGRHQMPLVTMSAIMGGNVRVGLEDSVYLAKGVKAETNAQQVRKIRRIL 285
             +N +++    GR+Q+P V  SA++GG+ RVGLED++YL KG  A TN Q V +   I+
Sbjct: 216 -PDNTNWTAFALGRNQLPWVAQSALLGGHARVGLEDNLYLGKGQMA-TNGQLVERAVNII 273

Query: 286 EELSLEIATPADARKMLGLKG 306
           E +   I TP  AR+ L L+G
Sbjct: 274 ENMGGRIMTPTQAREKLCLRG 294


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: 247
Number of extensions: 16
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: 296
Length adjustment: 27
Effective length of query: 285
Effective length of database: 269
Effective search space:    76665
Effective search space used:    76665
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