GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ketodeoxyribonate-cleavage in Brevibacterium jeotgali SJ5-8

Align 2-deoxy-3-keto-D-ribonate cleavage enzyme (characterized)
to candidate WP_101590062.1 BJEO58_RS13895 3-keto-5-aminohexanoate cleavage protein

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



>NCBI__GCF_900169175.1:WP_101590062.1
          Length = 318

 Score =  150 bits (380), Expect = 3e-41
 Identities = 105/318 (33%), Positives = 158/318 (49%), Gaps = 46/318 (14%)

Query: 5   SRKVIISCAITGATHVPSMSEFLPITPEQIRDQAIEAAQAGAAIIHLHARDPVDGRPTPS 64
           +R VI++CA+TGA      SE +P+TP++I +  I AA+AGA+IIH+H RDP   + +  
Sbjct: 2   NRSVILTCALTGAGDTAGKSEHVPVTPQEIANSGIAAARAGASIIHIHVRDPQTKQGSRD 61

Query: 65  PEIFKAFVPAI-AEATDAVINITTG-----------------GSTRMTLEERLAYPRLAR 106
            E++      I A   D VIN+T G                 G+  +   ERL +    R
Sbjct: 62  TELYAEVARLIRASDVDPVINMTAGMGGDLVIDPENPTAQLEGTDLVNQAERLTHVEALR 121

Query: 107 PEMCSLNMGSMNFSIHPVAAKISSWRYGWEKDYIEGMEDMIFRNTFRDIRNILLELGESG 166
           PE+C+L+ G++NF                     EG    I  +T   +R     + E G
Sbjct: 122 PEICTLDCGTLNFG--------------------EGSNTYI--STPDMMRAGAARIRELG 159

Query: 167 TRFEFECYDVGHLYNLAHFVDQGLVKPPFFIQSVFGILGGLGADPENMLLMRSTADRLFG 226
            + E E +D G+L+      ++GL+  P F Q   GI  G   D   +  M +       
Sbjct: 160 VKPELEIFDTGNLWFANVLYEEGLLDDPPFYQLCQGIPYGAPVDTGLLTAMVNMLP---- 215

Query: 227 RENYHFSVLGAGRHQMPLVTMSAIMGGNVRVGLEDSVYLAKGVKAETNAQQVRKIRRILE 286
            E   F+    GR+Q+  V  S + GG+VRVGLED++YL+KGVK  TNAQ   +   ++E
Sbjct: 216 -ETAQFTSFAIGRNQLAWVAQSVLAGGHVRVGLEDNLYLSKGVKG-TNAQLTERAVGVIE 273

Query: 287 ELSLEIATPADARKMLGL 304
            +   +A+P +AR+MLGL
Sbjct: 274 GMGSAVASPDEAREMLGL 291


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: 293
Number of extensions: 17
Number of successful extensions: 6
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: 318
Length adjustment: 27
Effective length of query: 285
Effective length of database: 291
Effective search space:    82935
Effective search space used:    82935
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