GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ivdG in Mycolicibacterium vanbaalenii PYR-1

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_011781406.1 MVAN_RS21320 short-chain dehydrogenase

Query= SwissProt::O18404
         (255 letters)



>NCBI__GCF_000015305.1:WP_011781406.1
          Length = 254

 Score =  211 bits (537), Expect = 1e-59
 Identities = 116/254 (45%), Positives = 153/254 (60%), Gaps = 3/254 (1%)

Query: 2   IKNAVSLVTGGASGLGRATAERLAKQGASVILADLPSSKGNEVAKELGDKVVFVPVDVTS 61
           I  + +LV GGA GLG AT  RL   GA V++ADL   KG ++  ELG  V +V  D TS
Sbjct: 3   IAGSSALVVGGAGGLGEATVRRLHDAGAKVVIADLADDKGRQLESELG--VRYVRTDATS 60

Query: 62  EKDVSAALQTAKDKFGRLDLTVNCAGTATAVKTFNFNKNVAHRLEDFQRVININTVGTFN 121
           E+ V+AA+ T  +  G L ++V+  G                 +E F+  I       FN
Sbjct: 61  EESVNAAI-TEAESLGPLRISVDTHGGPAGGGRLVGKDGSPLSMEAFETTIKFYLTAVFN 119

Query: 122 VIRLSAGLMGANEPNQDGQRGVIVNTASVAAFDGQIGQAAYSASKAAVVGMTLPIARDLS 181
           ++RLSA  +   EP ++G RGVIVNTASVA ++GQIGQ  YSA+K  V+GMTL  ARDLS
Sbjct: 120 IMRLSAAAIAKTEPLEEGGRGVIVNTASVAGYEGQIGQLPYSAAKGGVIGMTLVAARDLS 179

Query: 182 TQGIRICTIAPGLFNTPMLAALPEKVRTFLAKSIPFPQRLGEPSEYAHLVQAIYENPLLN 241
             GIR+ TIAPG  NTP      +++  +    +PFP+R+G  +EYA L Q++ EN  LN
Sbjct: 180 PLGIRVVTIAPGTINTPAYGKAADQLEQYWGPQVPFPKRMGRSTEYAQLAQSVIENDYLN 239

Query: 242 GEVIRIDGALRMMP 255
           GEVIR+DGALR  P
Sbjct: 240 GEVIRLDGALRFPP 253


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: 182
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: 254
Length adjustment: 24
Effective length of query: 231
Effective length of database: 230
Effective search space:    53130
Effective search space used:    53130
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