GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fadB 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; 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_017547482.1 C792_RS0100525 SDR family oxidoreductase

Query= SwissProt::O18404
         (255 letters)



>NCBI__GCF_000330705.1:WP_017547482.1
          Length = 257

 Score =  106 bits (264), Expect = 5e-28
 Identities = 82/259 (31%), Positives = 127/259 (49%), Gaps = 25/259 (9%)

Query: 6   VSLVTGGASGLGRATAERLAKQGASVILADLPSSKGNEVAKELG--DKVVFVPVDVTSEK 63
           V ++TGG+ G+G+ TA +  ++GA V + D+         +EL    +V+ V  DV+ E 
Sbjct: 9   VVIITGGSGGIGKQTALQFLQEGAKVTIVDINEESLTSAREELSRQGEVLAVQADVSDEA 68

Query: 64  DVSAALQTAKDKFGRLDLTVNCAGTATAVKTFNFNKNVAHRLEDFQRVININTVGTFNVI 123
           DV   ++   +KFG++D+  N AG    V +      V    ++F+ V  +N  G F   
Sbjct: 69  DVENYIRATVEKFGKVDVLFNNAGIIGKVGSL-----VDQEYDNFKAVTGVNMNGVF--- 120

Query: 124 RLSAGLMGA-NEPNQDGQRGVIVNTASVAAFDGQIGQAAYSASKAAVVGMTLPIARDLST 182
               GL  A  +  + G  G I+NT SV +F G   Q+AYSA+K AVVG+T   A + + 
Sbjct: 121 ---LGLKHAIKQMIKQGTPGSIINTGSVDSFRGSPEQSAYSATKHAVVGLTKTAAVEAAG 177

Query: 183 QGIRICTIAPGLFNTPMLAALPE--------KVRTFLAKSIPFPQRLGEPSEYAHLV--Q 232
             IR+ +I P   +TPM+A + E         VR      IP   R  + S+ A LV   
Sbjct: 178 HNIRVNSIHPAPVDTPMMAHVEESRDKKNSASVREKFTSGIPL-NRYADSSDIADLVLFL 236

Query: 233 AIYENPLLNGEVIRIDGAL 251
           A  ++  + G    IDG +
Sbjct: 237 ASDDSKFVTGSQYSIDGGM 255


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: 8
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: 257
Length adjustment: 24
Effective length of query: 231
Effective length of database: 233
Effective search space:    53823
Effective search space used:    53823
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