GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iolJ in Marinobacter adhaerens HP15

Align 6-phospho-5-dehydro-2-deoxy-D-gluconate aldolase; DKGP aldolase; EC 4.1.2.29 (characterized)
to candidate GFF2966 HP15_2910 fructose-1,6-bisphosphate aldolase

Query= SwissProt::P42420
         (290 letters)



>FitnessBrowser__Marino:GFF2966
          Length = 354

 Score =  162 bits (410), Expect = 1e-44
 Identities = 111/333 (33%), Positives = 172/333 (51%), Gaps = 49/333 (14%)

Query: 1   MAFVSMKELLEDAKREQYAIGQFNINGLQWTKAILQAAQKEQSPVIAAASDRLVDYLGGF 60
           MA +SM+++L+ A    Y +  FN+N L+  +AI++AA +  SPVI  AS     Y G  
Sbjct: 1   MALISMRQMLDHAAEHGYGVPAFNVNNLEQMRAIMEAADRTDSPVIVQASAGARKYAGA- 59

Query: 61  KTIAAMVGALIEDMAITVPVVLHLDHGSSAERCRQAIDAGFSSVMIDGS-----HQPIDE 115
             +  ++ A IE+    +PVV+H DHG+S   C+++I  GFSSVM+DGS       P D 
Sbjct: 60  PFLRHLILAAIEEFP-HIPVVMHQDHGTSPSVCQRSIQLGFSSVMMDGSLGEDGKTPTDY 118

Query: 116 --NIAMTKEVTDYAAKHGVSVEAEVGTVGGMEDGLVG-------------GVRYADITEC 160
             N+ +T+   + A   GVSVE E+G +G +E G  G                  D  E 
Sbjct: 119 EYNVDVTRRTVEMAHACGVSVEGELGCLGSLETGQAGEEDGIGAEGTLDHSQMLTDPEEA 178

Query: 161 ERIVKETNIDALAAALGSVHGKYQ--GEPN---LGFKEMEAI-SRMTDIPLVLHGASGIP 214
              VK+T++DALA A+G+ HG Y+    P    L   +++AI +R+ D  LV+HG+S +P
Sbjct: 179 ADFVKKTHVDALAIAIGTSHGAYKFTRPPTGDILAIDQIKAIHARIPDTHLVMHGSSSVP 238

Query: 215 QDQIK---------------------KAITLGHAKININTECMVAWTDETRRMFQENSDL 253
           Q+ +K                     + I  G  K+NI+T+  +A T   RR   EN   
Sbjct: 239 QEWLKIINEYGGEIPETYGVPVEEIVEGIKHGVRKVNIDTDLRLASTGAVRRFLAENPAE 298

Query: 254 YEPRGYLTPGIEAVEETVRSKMREFGSAGKAAK 286
           ++PR +L   ++A+ +   ++   FG AG A+K
Sbjct: 299 FDPRKFLKETMKAMTDVCIARYEAFGCAGNASK 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: 275
Number of extensions: 12
Number of successful extensions: 8
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: 354
Length adjustment: 28
Effective length of query: 262
Effective length of database: 326
Effective search space:    85412
Effective search space used:    85412
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