GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iolJ in Caulobacter crescentus NA1000

Align 6-phospho-5-dehydro-2-deoxy-D-gluconate aldolase; DKGP aldolase; EC 4.1.2.29 (characterized)
to candidate CCNA_03360 CCNA_03360 tagatose-1,6-bisphosphate aldolase

Query= SwissProt::P42420
         (290 letters)



>FitnessBrowser__Caulo:CCNA_03360
          Length = 363

 Score =  157 bits (396), Expect = 4e-43
 Identities = 108/333 (32%), Positives = 170/333 (51%), Gaps = 49/333 (14%)

Query: 1   MAFVSMKELLEDAKREQYAIGQFNINGLQWTKAILQAAQKEQSPVIAAASDRLVDYLGGF 60
           MA +++++LL+ A   +Y +  FNIN ++   AI++AA    SPVI  AS    +Y    
Sbjct: 1   MARITLRQLLDHAAEHEYGLPAFNINNMEQGLAIMEAADAVNSPVIIQASRGARNYANDI 60

Query: 61  KTIAAMVGALIEDMAITVPVVLHLDHGSSAERCRQAIDAGFSSVMIDGSHQP-------I 113
             +A M+ AL+ D+   +PV +H DHG+    C  AI  GF+SVM+DGS           
Sbjct: 61  M-LAKMIDALV-DIYPHIPVCMHQDHGNGPATCATAIQYGFTSVMMDGSLMEDAKTPASY 118

Query: 114 DENIAMTKEVTDYAAKHGVSVEAEVGTVGGMEDGL---------VGGVRY----ADITEC 160
           + N+ +T++V   A   GVSVE E+G +G +E G+          G + +     D  + 
Sbjct: 119 EYNVEVTRKVVQMAHSCGVSVEGELGVLGSLETGMGEAEDGHGFEGKLSHDELLTDPDQA 178

Query: 161 ERIVKETNIDALAAALGSVHGKYQ--GEPNLGFKEMEAIS----RMTDIPLVLHGASGIP 214
              V +T +DALA A+G+ HG Y+   +P+     M  I     R+ +  LV+HG+S +P
Sbjct: 179 VDFVAQTGVDALAIAMGTSHGAYKFTRKPDGDVLAMNVIEEIHRRLPNTHLVMHGSSSVP 238

Query: 215 QD---------------------QIKKAITLGHAKININTECMVAWTDETRRMFQENSDL 253
           QD                     +I++ I  G  KIN++T+  +A T   R++  E    
Sbjct: 239 QDLQDIINQYGGEMPQTWGVPVEEIQRGIKHGVRKINVDTDNRMAITGAIRKLLVEKPGE 298

Query: 254 YEPRGYLTPGIEAVEETVRSKMREFGSAGKAAK 286
           ++PR YL P  EA+ +  +++  EFGSAG A K
Sbjct: 299 FDPRAYLKPAKEAMRKVCQARFVEFGSAGHADK 331


Lambda     K      H
   0.316    0.132    0.372 

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: 265
Number of extensions: 18
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: 290
Length of database: 363
Length adjustment: 28
Effective length of query: 262
Effective length of database: 335
Effective search space:    87770
Effective search space used:    87770
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 17 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