GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ketodeoxyribonate-cleavage in Phyllobacterium brassicacearum STM 196

Align 2-deoxy-3-keto-D-ribonate cleavage enzyme (characterized)
to candidate WP_106710555.1 CU102_RS07810 3-keto-5-aminohexanoate cleavage protein

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



>NCBI__GCF_003010955.1:WP_106710555.1
          Length = 301

 Score =  159 bits (401), Expect = 1e-43
 Identities = 104/320 (32%), Positives = 153/320 (47%), Gaps = 48/320 (15%)

Query: 5   SRKVIISCAITGATHVPSMSEFLPITPEQIRDQAIEAAQAGAAIIHLHARDPVDGRPTPS 64
           +R+V I+CA+TGA      S+ +P+TP QI D+ I AA AGAAI H+H RDP  G+ +  
Sbjct: 6   NREVFITCAVTGAGDTTGRSDKVPVTPRQIADECIAAANAGAAIAHIHVRDPKTGKGSRD 65

Query: 65  PEIFKAFVPAI-AEATDAVINITTGGSTRMTL-------------------EERLAYPRL 104
             ++   V  I A   D V+N+T G    +TL                    ERL +   
Sbjct: 66  VALYAEVVEHIKASGVDMVLNLTAGMGGDLTLGSVEQPMPPSPNGTDMAGATERLEHVAK 125

Query: 105 ARPEMCSLNMGSMNFSIHPVAAKISSWRYGWEKDYIEGMEDMIFRNTFRDIRNILLELGE 164
            RPE+C+L+ G+MNF                      G  D +  NT   ++ +  ++  
Sbjct: 126 LRPEICTLDCGTMNF----------------------GEGDYVMTNTPAMLKAMAAQIKA 163

Query: 165 SGTRFEFECYDVGHLYNLAHFVDQGLVKPPFFIQSVFGILGGLGADPENMLLMRSTADRL 224
            G R E E +D GHL       DQ L++ P  +Q   GI  G   D   +L + +     
Sbjct: 164 LGVRPEVEIFDTGHLLLAKWLYDQKLLEDPVMVQLCMGIPWGAPDDINTLLALTNNLP-- 221

Query: 225 FGRENYHFSVLGAGRHQMPLVTMSAIMGGNVRVGLEDSVYLAKGVKAETNAQQVRKIRRI 284
               N+ FS    GR+QMP   M+ + GGN+RVGLED+++L KGV A TN   V +  ++
Sbjct: 222 ---SNWTFSAFSIGRNQMPYAAMAMLAGGNIRVGLEDTIWLDKGVLA-TNGPLVERAVKV 277

Query: 285 LEELSLEIATPADARKMLGL 304
            E +   I  P + R+ + L
Sbjct: 278 AEGMGARILGPNEVRERMKL 297


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: 251
Number of extensions: 14
Number of successful extensions: 4
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: 301
Length adjustment: 27
Effective length of query: 285
Effective length of database: 274
Effective search space:    78090
Effective search space used:    78090
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