GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ivdG in Phaeobacter inhibens BS107

Align 3-hydroxyacyl-CoA dehydrogenase type-2; 17-beta-hydroxysteroid dehydrogenase 10; 17-beta-HSD 10; 3-hydroxy-2-methylbutyryl-CoA dehydrogenase; 3-hydroxyacyl-CoA dehydrogenase type II; Mitochondrial ribonuclease P protein 2; Mitochondrial RNase P protein 2; Scully protein; Type II HADH; EC 1.1.1.35; EC 1.1.1.51; EC 1.1.1.178 (characterized)
to candidate GFF328 PGA1_c03390 acetoacetyl-CoA reductase PhaB

Query= SwissProt::O18404
         (255 letters)



>FitnessBrowser__Phaeo:GFF328
          Length = 240

 Score = 94.4 bits (233), Expect = 2e-24
 Identities = 84/261 (32%), Positives = 124/261 (47%), Gaps = 36/261 (13%)

Query: 1   MIKNAVSLVTGGASGLGRATAERLAKQGASVILADLPSSKGNEVA-----KELGDKVVFV 55
           M +NA  LVTGG+ G+G A ++ L  +G +V      +  GN+ A      E G K    
Sbjct: 1   MARNA--LVTGGSRGIGAAISQALKAEGYTVAA----TYAGNDEAAAKFTNETGIKTY-- 52

Query: 56  PVDVTSEKDVSAALQTAKDKFGRLDLTVNCAGTATAVKTFNFNKNVAHRLEDFQRVININ 115
             DV S +D +A +   +   G +D+ V  AG     +   F+K     LE +Q+VI+ N
Sbjct: 53  KWDVASYEDSAAGIAKVEADIGPIDIVVANAGIT---RDAPFHKMT---LEQWQQVIDTN 106

Query: 116 TVGTFNVIRLSAGLMGANEPNQDGQR----GVIVNTASVAAFDGQIGQAAYSASKAAVVG 171
             G FN +           P   G R    G ++  +S+    GQ  Q  Y+A+KA  +G
Sbjct: 107 LTGVFNTVH----------PIWPGMRERKFGRVIVISSINGQKGQFAQVNYAATKAGDLG 156

Query: 172 MTLPIARDLSTQGIRICTIAPGLFNTPMLAALPEKVRTFLAKSIPFPQRLGEPSEYAHLV 231
           +   +A++ +  GI    I PG   T M+ A+PEKVR  +   IP   RLGEP E A  V
Sbjct: 157 IVKSLAQEGARAGITANAICPGYIATEMVMAVPEKVRESIIGQIP-AGRLGEPEEIARCV 215

Query: 232 Q--AIYENPLLNGEVIRIDGA 250
              A  ++  +NG  I  +GA
Sbjct: 216 AFLASEDSGFINGSTISANGA 236


Lambda     K      H
   0.317    0.133    0.369 

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: 143
Number of extensions: 7
Number of successful extensions: 2
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: 255
Length of database: 240
Length adjustment: 24
Effective length of query: 231
Effective length of database: 216
Effective search space:    49896
Effective search space used:    49896
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 (21.7 bits)
S2: 46 (22.3 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