GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ketodeoxyribonate-cleavage in Halomonas xinjiangensis TRM 0175

Align 2-deoxy-3-keto-D-ribonate cleavage enzyme (characterized)
to candidate WP_043532163.1 JH15_RS16010 3-keto-5-aminohexanoate cleavage protein

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



>NCBI__GCF_000759345.1:WP_043532163.1
          Length = 292

 Score =  187 bits (476), Expect = 2e-52
 Identities = 123/319 (38%), Positives = 166/319 (52%), Gaps = 48/319 (15%)

Query: 5   SRKVIISCAITGATHVPSMSEFLPITPEQIRDQAIEAAQAGAAIIHLHARDPVDGRPTPS 64
           +R VI++CAITGA    +    LP+TP QI D AIEAA+AGA+I+HLH RDP  G  + S
Sbjct: 2   NRDVILTCAITGAGDTANKHPELPVTPRQIADSAIEAARAGASIVHLHVRDPETGGISHS 61

Query: 65  PEIFKAFVPAIAEA-TDAVINITTG-----------------GSTRMTLEERLAYPRLAR 106
              F+  V  I EA  D VIN+T G                 G+   T  ER A      
Sbjct: 62  TAHFREAVSRIREADIDVVINLTAGGGGDWVPHPDDPTRGGEGTDMQTPAERHAPIGELL 121

Query: 107 PEMCSLNMGSMNFSIHPVAAKISSWRYGWEKDYIEGMEDMIFRNTFRDIRNILLELGESG 166
           PE+C+L+ GS+NF                         D ++ NT   +R     + E+G
Sbjct: 122 PELCTLDCGSLNFG------------------------DTVYLNTADWLREHARLVKEAG 157

Query: 167 TRFEFECYDVGHLYNLAHFVDQGLVKPPFFIQSVFGILGGLGADPENMLLMRSTADRLFG 226
            + E EC+D+GH++     +++GL++     Q   GI  G  AD E ML MR+       
Sbjct: 158 VKPELECFDLGHVWFARQLIEEGLIEGDPLFQLCLGIPWGAEADTETMLAMRNKLP---- 213

Query: 227 RENYHFSVLGAGRHQMPLVTMSAIMGGNVRVGLEDSVYLAKGVKAETNAQQVRKIRRILE 286
             N H+S  G GR +MP+V  S ++GG+VRVGLED++YL+KGV A TNAQ V K   I E
Sbjct: 214 -ANAHWSAFGIGRTEMPMVAQSILLGGHVRVGLEDNLYLSKGVFA-TNAQLVEKAANIAE 271

Query: 287 ELSLEIATPADARKMLGLK 305
            L   I TPA  R+ L L+
Sbjct: 272 NLGSRILTPAQTRQKLDLR 290


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: 273
Number of extensions: 17
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: 292
Length adjustment: 27
Effective length of query: 285
Effective length of database: 265
Effective search space:    75525
Effective search space used:    75525
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