GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ivdG in Methylocella silvestris BL2

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; Endoplasmic reticulum-associated amyloid beta-peptide-binding protein; Mitochondrial ribonuclease P protein 2; Mitochondrial RNase P protein 2; Type II HADH; EC 1.1.1.35; EC 1.1.1.51; EC 1.1.1.178 (characterized)
to candidate WP_012589851.1 MSIL_RS04185 3-hydroxybutyrate dehydrogenase

Query= SwissProt::O08756
         (261 letters)



>NCBI__GCF_000021745.1:WP_012589851.1
          Length = 261

 Score = 89.4 bits (220), Expect = 7e-23
 Identities = 65/205 (31%), Positives = 105/205 (51%), Gaps = 17/205 (8%)

Query: 7   SVKGLVAVVTGGASGPWLATAKRLVGQGATAVLLDVPDSEG-ESQAKKL----GESCIFA 61
           ++K   A+VTG  SG  LA A+     GA   +  + D+   E++  K+    G    ++
Sbjct: 2   TLKSRNAIVTGSTSGIGLAIAREFAKDGANVTINGLGDAAAIEAERAKIEADFGVKAAYS 61

Query: 62  PANVTSEKEIQAALTLAKEKFGRIDVAVNCAGIAVAIKTYHQKKNKIHTLEDFQRVINVN 121
           PAN+T  +EI+A +T A++ FG +D+ VN AGI       H    +   ++ +  +I +N
Sbjct: 62  PANMTKPEEIRAMVTDAEKAFGSVDILVNNAGIQ------HVAPIEDFPIDTWNLIIAIN 115

Query: 122 LIGTFNVIRLVAGEMGQNEPDQGGQRGVIINTASVAAFEGQVGQAAYSASKGGIDGMTLP 181
           L   F+ I      M      +  + G II+TAS  +      ++AY ++K GIDG+T  
Sbjct: 116 LSAAFHAIAAAIPGM------KARKWGRIISTASAHSKVASPFKSAYVSAKHGIDGLTKT 169

Query: 182 IARDLAPTGIRVVTIAPGLFATPLL 206
            A +LA  G+ V  I+PG   TPL+
Sbjct: 170 AALELATFGVTVNCISPGYVWTPLV 194


Lambda     K      H
   0.317    0.134    0.380 

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: 160
Number of extensions: 12
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: 261
Length of database: 261
Length adjustment: 25
Effective length of query: 236
Effective length of database: 236
Effective search space:    55696
Effective search space used:    55696
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 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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