GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ivdG in Salinicoccus carnicancri Crm

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_017549801.1 C792_RS0112530 3-hydroxybutyrate dehydrogenase

Query= SwissProt::O08756
         (261 letters)



>NCBI__GCF_000330705.1:WP_017549801.1
          Length = 258

 Score = 94.0 bits (232), Expect = 3e-24
 Identities = 80/270 (29%), Positives = 129/270 (47%), Gaps = 30/270 (11%)

Query: 8   VKGLVAVVTGGASGPWLATAKRLVGQGATAVLLDVPDSEGESQAKKL---GESCIFAPAN 64
           VK  V ++TG ASG  L  +K  +  GA  VL D+   + +   + L      C+   A+
Sbjct: 2   VKDKVTIITGAASGLGLEISKVFLKNGAKVVLSDINQEKLDEIVEDLKAKAYDCLGIRAD 61

Query: 65  VTSEKEIQAALTLAKEKFGRIDVAVNCAGIAVAIKTYHQKKNKIHTLEDFQRVINVNLIG 124
           VTSE +I+  +   KE++GRIDV  N AG+       H    +    + F+++I++ L+ 
Sbjct: 62  VTSEDDIENLIDRTKEEYGRIDVLFNNAGLQ------HVSDIEEFPTDKFRQMIDIMLVA 115

Query: 125 TFNVIRLVAGEMGQNEPDQGGQRGVIINTASVAAFEGQVGQAAYSASKGGIDGMTLPIAR 184
            F   + V   M     +QG   G I+N AS+    G  G+AAY+++K G+ G+T   A 
Sbjct: 116 PFIGTKHVMPIM----KEQGS--GTILNMASINGVIGFAGKAAYNSAKHGVIGLTKVAAL 169

Query: 185 DLAPTGIRVVTIAPGLFATPLLTTLPEKV-------RNFLASQVPFP-------SRLGDP 230
           + A  GI V  I PG   TPL+    E +        + +  +V FP         +G+ 
Sbjct: 170 EAAEHGITVNAICPGYVDTPLVRGQMEDLAQSRGVAADKVIEEVLFPLIPQKRLIEIGEI 229

Query: 231 AEYAHLVQTIIENPFLNGEVIRLDGAIRMQ 260
           A+YA +  T      + G+ + +DG   +Q
Sbjct: 230 ADYA-MFLTSDSAKGVTGQAVLIDGGYTVQ 258


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: 159
Number of extensions: 9
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: 258
Length adjustment: 24
Effective length of query: 237
Effective length of database: 234
Effective search space:    55458
Effective search space used:    55458
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