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 GFF2277 PGA1_c23090 putative acetoin(diacetyl) reductase

Query= SwissProt::O18404
         (255 letters)



>FitnessBrowser__Phaeo:GFF2277
          Length = 263

 Score = 92.8 bits (229), Expect = 6e-24
 Identities = 77/265 (29%), Positives = 120/265 (45%), Gaps = 29/265 (10%)

Query: 8   LVTGGASGLGRATAERLAKQGASVILADLPSSKGNEVAK-----ELGDKVVFVPVDVTSE 62
           +VTG A G+GRA AE L  +GASV  AD+   K  EVA          +V    VDVT  
Sbjct: 10  IVTGAAQGIGRAIAEALLDEGASVCFADINGIKVAEVASLNRSTHGESRVTHAQVDVTDR 69

Query: 63  KDVSAALQTAKDKFGRLDLTVNCAGTATAVKTFNFNKNVAHRLEDFQRVININTVGTFNV 122
           + V A +      FG+LD+  N AG    +   +  +      E+++ V ++N +G    
Sbjct: 70  ETVRALIDHTVAMFGKLDVKFNNAGVNKPMNFLDVTE------ENWRFVNDVNGLGC--- 120

Query: 123 IRLSAGLMGANEPNQDGQRGVIVNTASVAAFDGQIGQAAYSASKAAVVGMTLPIARDLST 182
             L      A +  + G  G I+NTAS+A+  G    A Y ASK  VV +T   ARDL+ 
Sbjct: 121 --LIGMQEAAKQFIRQGTFGKIINTASIASRQGFDNVAPYCASKFGVVALTQSGARDLAK 178

Query: 183 QGIRICTIAPGLFNTPMLAALPEKVRTFLAKSIP-----------FPQRLGEPSEYAHLV 231
             I +   APG+ +T M   + + +    A   P              R+ +P +     
Sbjct: 179 HNITVTGFAPGVVDTEMWEQVDQDLMDIGAAERPGQAMEEFSADILKGRVAKPQDITGTT 238

Query: 232 Q--AIYENPLLNGEVIRIDGALRMM 254
              A  ++  + G+++ IDG + ++
Sbjct: 239 TFLAAPDSDYMTGQIVMIDGGMTLV 263


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: 170
Number of extensions: 7
Number of successful extensions: 3
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: 263
Length adjustment: 24
Effective length of query: 231
Effective length of database: 239
Effective search space:    55209
Effective search space used:    55209
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: 47 (22.7 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