GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fadB in Shewanella halifaxensis HAW-EB4

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_012277208.1 SHAL_RS11070 SDR family oxidoreductase

Query= SwissProt::O18404
         (255 letters)



>NCBI__GCF_000019185.1:WP_012277208.1
          Length = 247

 Score =  125 bits (314), Expect = 8e-34
 Identities = 82/258 (31%), Positives = 136/258 (52%), Gaps = 20/258 (7%)

Query: 3   KNAVSLVTGGASGLGRATAERLAKQGASVILADLPSSKGNEVAK----ELGDKVVFVPVD 58
           K+ V  VTG   G+G A  +  A+QGA V   D+  +   +VA+    E G +V+ +  D
Sbjct: 4   KDKVIFVTGAGQGMGLAMVKLFAEQGAKVAAIDINEAAAKQVAEQQSAESGSEVIGIGCD 63

Query: 59  VTSEKDVSAALQTAKDKFGRLDLTVNCAGTATAVKTFNFNKNVAHRLEDFQRVININTVG 118
           ++    V  A+     + G +D+ +N AG  + + +F    +     E++ +VIN+N  G
Sbjct: 64  ISQSSSVRDAIAEVVQRLGSVDVVINNAGIGS-IDSFIDTPD-----ENWHKVINVNLTG 117

Query: 119 TFNVIRLSAGLMGANEPNQDGQRGVIVNTASVAAFDGQIGQAAYSASKAAVVGMTLPIAR 178
           TF   R +A +M      ++   G I+N +S A   G  G + Y ASKA V+G+T  IA+
Sbjct: 118 TFYCCREAARVM------KEQGSGCIINISSTAVMSGD-GPSHYCASKAGVIGLTRSIAK 170

Query: 179 DLSTQGIRICTIAPGLFNTPMLAALPEKVRTFLAKSIPFPQRLGEPSEYAHLVQ--AIYE 236
           +L+  GIR+ TI PG  NTPM+A +PE+    +  +IP   R+GEP + A L    A  +
Sbjct: 171 ELAASGIRVNTIVPGPTNTPMMADIPEEWTQQMINAIPL-GRMGEPEDIAKLASFIASED 229

Query: 237 NPLLNGEVIRIDGALRMM 254
              + G+ + ++G +  +
Sbjct: 230 ASFITGQNLAVNGGMAFL 247


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: 151
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: 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.

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