GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Salinicoccus carnicancri Crm

Align isocitrate-homoisocitrate dehydrogenase (EC 1.1.1.286) (characterized)
to candidate WP_017548413.1 C792_RS0105310 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5JFV8
         (347 letters)



>NCBI__GCF_000330705.1:WP_017548413.1
          Length = 368

 Score =  192 bits (488), Expect = 1e-53
 Identities = 140/349 (40%), Positives = 195/349 (55%), Gaps = 36/349 (10%)

Query: 3   RVAVIPGDGIGPEVIDGAVRVLKAVTGRVRFEY----YEGGVDVFQECGSPIREEDLEEI 58
           ++ ++PGDG+G E+++GA  VL AV G    E+    +  G       G+P+ EE ++  
Sbjct: 4   QIIMLPGDGVGKEIMEGARAVLNAVAGEHHHEFIFHEHAIGGSAIDRYGTPLPEETVKAC 63

Query: 59  RRSDAVLFGATTTP------FDLPGYRSLILTLRKELGLYANLRIIP------------- 99
             +D+VL GA   P            R L L +RK LGL+ANLR +              
Sbjct: 64  SSADSVLLGAVGGPKWDHVEASKRPERGL-LGIRKSLGLFANLRPVTGFSSLVHSSPLKT 122

Query: 100 DLRTGREIVIVRENSEGLYFGIGAV--VNGRAV-DVRLITREGAERIARFAVEQAKARGS 156
           ++  G +I+IVRE + GLYFG  +     GR V D    TRE  ERI     E AK R  
Sbjct: 123 EIVDGCDILIVRELTGGLYFGKPSERREGGRTVIDTLKYTREEMERIVDKGFESAKMRRG 182

Query: 157 FITFVHKANVLTGDKFFRRIVREVAGEEG-VEVRDAIIDSFTIKLVRNPWEHGVILSENL 215
            +T V KANVL   + +R +V E A +   VEV   ++D+  +KL+ NP +  VI++ENL
Sbjct: 183 KLTSVDKANVLESSRMWREVVDEKARDHPEVEVEHLLVDAAAMKLIINPRQFDVIVTENL 242

Query: 216 FGDILSDLATVHAGSIGIVPSGNYG-DGIALFEPVHGSAPDIAGKGIANPIGAILSGAML 274
           FGDILSD A+V  GS+G++PS +   DGI L+EPVHGSAPDIAG+ IANP+G ILS AM+
Sbjct: 243 FGDILSDEASVLTGSLGMLPSASIRTDGIGLYEPVHGSAPDIAGQDIANPLGMILSAAMM 302

Query: 275 LDY-LGLDGSL--IRAAVRGYVVNGELTPDM---GGR-ARTEDVVRGII 316
           L +  G++     I  AV   +  G  T D+   GGR   T ++V  +I
Sbjct: 303 LRHSFGMEDEADEIERAVSDTLEGGYHTADLDIEGGRIVGTREMVEKVI 351


Lambda     K      H
   0.321    0.143    0.411 

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: 340
Number of extensions: 23
Number of successful extensions: 7
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: 347
Length of database: 368
Length adjustment: 29
Effective length of query: 318
Effective length of database: 339
Effective search space:   107802
Effective search space used:   107802
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 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Jul 26 2024. The underlying query database was built on Jul 25 2024.

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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