GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fadB in Chromobacterium vaccinii MWU205

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_082113695.1 VL52_RS09785 SDR family oxidoreductase

Query= SwissProt::O08756
         (261 letters)



>NCBI__GCF_000971335.1:WP_082113695.1
          Length = 251

 Score = 97.1 bits (240), Expect = 3e-25
 Identities = 75/250 (30%), Positives = 122/250 (48%), Gaps = 22/250 (8%)

Query: 14  VVTGGASGPWLATAKRLVGQGATAVLLDVPDSEGESQAKKLGESCI----FAPANVTSEK 69
           VV+GG+    L   + L+  G         D+   ++  +L +S      +  A+VT   
Sbjct: 16  VVSGGSRSLGLKICESLLAGGYRVATFSRNDT---AELSRLRDSAAGDFHWEAADVTDAP 72

Query: 70  EIQAALTLAKEKFGRIDVAVNCAGIAVAIKTYHQKKNKIHTLEDFQRVINVNLIGTFNVI 129
            +   L  A+EK G +   VN AG+      YH+    +   +D  R++ VNL G   + 
Sbjct: 73  ALSRFLGRAREKLGPLRGLVNNAGV------YHEGLLAMSRPDDIARLLEVNLGGAIRLA 126

Query: 130 RLVAGEMGQNEPDQGGQRGVIINTASVAAFEGQVGQAAYSASKGGIDGMTLPIARDLAPT 189
           +L A +M        G  G I+N +SVA   G  G AAYSA+K  +DG+T  +AR+L P 
Sbjct: 127 QLCAKQM------MVGGGGAIVNVSSVAGVRGFEGVAAYSATKAALDGLTRSLARELGPM 180

Query: 190 GIRVVTIAPGLFATPLLTTLPEKVRNFLASQVPFPSRLGDPAEYAHLVQTII--ENPFLN 247
            IRV  +APGL  T +++ +  + +  L  Q P   RL    + A +V+ ++  E  F+ 
Sbjct: 181 RIRVNAVAPGLMETEMVSGMVARQKEQLVRQTPL-GRLTTVDDAASVVRFLLSDEAGFVT 239

Query: 248 GEVIRLDGAI 257
           G+ + +DG +
Sbjct: 240 GQTLIVDGGL 249


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: 174
Number of extensions: 10
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: 251
Length adjustment: 24
Effective length of query: 237
Effective length of database: 227
Effective search space:    53799
Effective search space used:    53799
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.

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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