GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaH in Stenotrophomonas chelatiphaga DSM 21508

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_057506951.1 ABB28_RS01610 3-oxoacyl-ACP reductase FabG

Query= SwissProt::O18404
         (255 letters)



>NCBI__GCF_001431535.1:WP_057506951.1
          Length = 247

 Score =  110 bits (274), Expect = 4e-29
 Identities = 78/259 (30%), Positives = 129/259 (49%), Gaps = 24/259 (9%)

Query: 2   IKNAVSLVTGGASGLGRATAERLAKQGASVILADLPSSKGNEVAKELGDKVVFV-PVDVT 60
           ++  ++LVTG + G+G A A+ LA QGA+VI      S    + + L  +      ++VT
Sbjct: 5   LQGEIALVTGASRGIGAAIADLLAAQGATVIGTATTDSGAAAIGERLAAQGGHGRALNVT 64

Query: 61  SEKDVSAALQTAKDKFGRLDLTVNCAGTATAVKTFNFNKNVAHRL--EDFQRVININTVG 118
               +   L     +FG + + VN AG            N+  R+  ED+  +I+ N   
Sbjct: 65  DAAALETVLADIAKEFGAISILVNNAGIT--------RDNLLMRMKDEDWASIIDTNLTS 116

Query: 119 TFNVIR-LSAGLMGANEPNQDGQRGVIVNTASVAAFDGQIGQAAYSASKAAVVGMTLPIA 177
            F   + +  G+M A       ++G I+N ASV    G  GQA Y+A+KA ++G +  +A
Sbjct: 117 VFRTSKAVMRGMMKA-------RKGRIINIASVVGVTGNAGQANYAAAKAGIIGFSKSLA 169

Query: 178 RDLSTQGIRICTIAPGLFNTPMLAALPEKVRTFLAKSIPFPQRLGEPSEYAHLVQAIYEN 237
           +++ ++G+ +  +APG  +T M  AL ++ R  L  SI   +RLG P + AH V A    
Sbjct: 170 KEIGSRGVTVNVVAPGFIDTDMTKALTDEARAALVNSIAL-ERLGSPEDIAHAV-AFLAG 227

Query: 238 PLLN---GEVIRIDGALRM 253
           P  N   GE + ++G + M
Sbjct: 228 PAANYITGETLHVNGGMYM 246


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: 160
Number of extensions: 10
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: 247
Length adjustment: 24
Effective length of query: 231
Effective length of database: 223
Effective search space:    51513
Effective search space used:    51513
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