GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fadB in Phyllobacterium leguminum ORS 1419

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 WP_110749380.1 C7477_RS03820 SDR family oxidoreductase

Query= SwissProt::O18404
         (255 letters)



>NCBI__GCF_003217235.1:WP_110749380.1
          Length = 245

 Score = 94.0 bits (232), Expect = 3e-24
 Identities = 78/255 (30%), Positives = 121/255 (47%), Gaps = 22/255 (8%)

Query: 2   IKNAVSLVTGGASGLGRATAERLAKQGASVILADLPSSKGNEVAKE----LGDKVVFVPV 57
           +K+ +++VTG   G+G A A RLA++GA+V++          V  E     G + V V  
Sbjct: 3   LKDKIAIVTGAGKGIGAAIAHRLAEEGAAVVVNYARDEAAARVVVEEIVKAGGRAVAVQA 62

Query: 58  DVTSEKDVSAALQTAKDKFGRLDLTVNCAGTATAVKTFNFNKNVAHRLEDFQRVININTV 117
           DV +   ++A    A+  FG+ D+ VN AG          +        D    I IN  
Sbjct: 63  DVAAPSAITALFDAAEAAFGQADILVNNAGM------MRLSPLAEATDADLDNHIAINLG 116

Query: 118 GTFNVIRLSAGLMGANEPNQDGQRGVIVNTASVAAFDGQIGQAAYSASKAAVVGMTLPIA 177
           GTF  +R      GA     DG+  +I  ++SV  F  Q G   Y+A+KAA+  MT  +A
Sbjct: 117 GTFRGMR-----EGAKRLRDDGR--IISLSSSVVGFY-QPGYGLYAATKAAIEAMTHVLA 168

Query: 178 RDLSTQGIRICTIAPGLFNTP-MLAALPEKVRTFLAKSIPFPQRLGEPSEYAHLVQAIY- 235
           ++L  +GI +  IAPG   T   +    +++   + K IP   RLG P + A  V  +  
Sbjct: 169 KELGPRGITVNAIAPGPVETDFFMRGKSDELVANITKMIPL-GRLGRPDDIADAVAFLAG 227

Query: 236 -ENPLLNGEVIRIDG 249
            +   +NG+ IR +G
Sbjct: 228 PDGRWINGQTIRANG 242


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: 149
Number of extensions: 8
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: 245
Length adjustment: 24
Effective length of query: 231
Effective length of database: 221
Effective search space:    51051
Effective search space used:    51051
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 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