GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Archaeoglobus sulfaticallidus PM70-1

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_015590688.1 ASULF_RS05400 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000385565.1:WP_015590688.1
          Length = 328

 Score =  280 bits (716), Expect = 4e-80
 Identities = 162/331 (48%), Positives = 211/331 (63%), Gaps = 8/331 (2%)

Query: 4   RICLIEGDGIGHEVIPAARRVLEATGLPLEFVEAEAGWETFERRGTSVPEETVEKILSCH 63
           +I +I GDGIG EV+ A  +VLEA   P E+V AEAG ET E+ G ++P+ET++      
Sbjct: 3   KIAVIPGDGIGKEVMSACLKVLEAFDFPFEYVFAEAGDETKEKTGEALPDETLQICKESS 62

Query: 64  ATLFGAATSPTRKVPGFFGAIRYLRRRLDLYANVRPAKS-RPVPGSRPGVDLVIVRENTE 122
           A LFGAA      V      I  LR  L+ +AN+RPAKS + V      VD+V+VRENTE
Sbjct: 63  AVLFGAAGETAADV------IVRLRLELETFANLRPAKSYKGVKCLFDNVDIVVVRENTE 116

Query: 123 GLYVEQERRYLD-VAIADAVISKKASERIGRAALRIAEGRPRKTLHIAHKANVLPLTQGL 181
            LY   E      V     +I++KASERI R A  +A    RK +   HKANV+  T GL
Sbjct: 117 CLYKGLEFEVKKGVTEGIRIITEKASERIARYAFELARRDGRKRVTALHKANVMKKTCGL 176

Query: 182 FLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTNLLGDILSDLAAGLVGGL 241
           F D  + VA+D+  +   D  +D   M LV+ P RFDVIVTTN+ GDI+SDL AGLVGGL
Sbjct: 177 FRDVCRRVARDYDDIEFSDYYIDAGCMYLVLDPWRFDVIVTTNMFGDIVSDLIAGLVGGL 236

Query: 242 GLAPSGNIGDTTAVFEPVHGSAPDIAGKGIANPTAAILSAAMMLDYLGEKEAAKRVEKAV 301
           GLAPS NIG+  A+FEPVHGSAPDIAGKGIANP+A ILS+ +ML + G    A+R+EKA+
Sbjct: 237 GLAPSANIGEKYAIFEPVHGSAPDIAGKGIANPSAMILSSTLMLRHFGYISEAERIEKAL 296

Query: 302 DLVLERGPRTPDLGGDATTEAFTEAVVEALK 332
           +  +  G  TPDLGG+  T+   E +++ ++
Sbjct: 297 EKTIAEGKTTPDLGGNLKTDEMVEEIIKNIE 327


Lambda     K      H
   0.319    0.137    0.391 

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: 292
Number of extensions: 11
Number of successful extensions: 4
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: 334
Length of database: 328
Length adjustment: 28
Effective length of query: 306
Effective length of database: 300
Effective search space:    91800
Effective search space used:    91800
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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