GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ketodeoxyribonate-cleavage in Sulfuritalea hydrogenivorans DSM 22779

Align 2-deoxy-3-keto-D-ribonate cleavage enzyme (characterized)
to candidate WP_041100197.1 SUTH_RS14325 3-keto-5-aminohexanoate cleavage protein

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



>NCBI__GCF_000828635.1:WP_041100197.1
          Length = 294

 Score =  113 bits (283), Expect = 5e-30
 Identities = 94/314 (29%), Positives = 145/314 (46%), Gaps = 32/314 (10%)

Query: 4   TSRKVIISCAITGATHVPSMSEFLPITPEQIRDQAIEAAQAGAAIIHLHARDPVDGR--- 60
           T  K I++CA+TG    P     +P+TP Q+   A EA  AGA+I+H+H R    G    
Sbjct: 3   THDKAILTCALTGVLTDPKQHP-VPVTPSQMAAAAREAFDAGASIMHVHLRRQEPGMGHL 61

Query: 61  PTPSPEIFKAFVPAIAEATDAVINITTGGSTRMTLEERLAYPRLARPEMCSLNMGSMNFS 120
           P+  P +    V AI  A   VI   T G     +    A  R  +PE+ + N G++N+ 
Sbjct: 62  PSWDPAVAAEIVDAIRAACPGVIINLTTGVIGADISGPAACIRRVKPEIAACNAGTLNY- 120

Query: 121 IHPVAAKISS-WRYGWEKDYIEGMEDMIFRNTFRDIRNILLELGESGTRFEFECYDVGHL 179
                 K+    R+ W          M+F N    ++  L  + E+GTR EFEC+DVG +
Sbjct: 121 -----LKLKDDGRWAWPP--------MVFDNPVEKVQAFLDVMAETGTRPEFECFDVGIV 167

Query: 180 YNLAHFVDQGLVKPPFFIQS----VFGILGGLGADPENM-LLMRSTADRLFGRENYHFSV 234
            ++  +  +  + P     +    V G+  G+  D + + LL+R      + +    +  
Sbjct: 168 RSVGMY-RKAAMSPQLANHAEYNFVMGVASGMPVDADLLQLLLR------WIQPGSSWQA 220

Query: 235 LGAGRHQM-PLVTMSAIMGGNVRVGLEDSVYLAKGVKAETNAQQVRKIRRILEELSLEIA 293
              GR ++ PL    A +GG +R GLEDS YL  G +A  N   +  +         E+A
Sbjct: 221 TLIGRAEIWPLHQRVAELGGMLRTGLEDSFYLPDGSRAAGNGAMIEALAACARRAGREVA 280

Query: 294 TPADARKMLGLKGA 307
           +PA+AR  LGL  A
Sbjct: 281 SPAEARVALGLPAA 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: 209
Number of extensions: 11
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 Apr 09 2024. 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