GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Sphingomonas koreensis DSMZ 15582

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate Ga0059261_3190 Ga0059261_3190 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>FitnessBrowser__Korea:Ga0059261_3190
          Length = 348

 Score =  209 bits (533), Expect = 6e-59
 Identities = 150/348 (43%), Positives = 195/348 (56%), Gaps = 25/348 (7%)

Query: 5   ICLIEGDGIGHEVIPAARRVLEATGLPLEFVEAEAGWETFERRGTSVPEETVEKILSCHA 64
           I ++ GDGIG EV   ARRVL+A  L L F EA  G   +   G  +P  T++      A
Sbjct: 4   IAILPGDGIGPEVTAQARRVLDALDLGLSFEEAPVGGAAYFSDGHPLPARTLDLAKRADA 63

Query: 65  TLFGAATSPTRKVPGFFG------AIRYLRRRLDLYANVRPAKSRP--------VPGSRP 110
            LFGA   P  +  G         AI  LR+ L+L+AN+RPA+  P         P    
Sbjct: 64  LLFGAVGDP--RCDGLDRHLRPEQAILGLRKELELFANLRPARLFPGLEDASALKPEVAG 121

Query: 111 GVDLVIVRE-NTEGLYVEQERRYLDVAIADA--VISKKASE--RIGRAALRIAEGRPRKT 165
            +D+VIVRE N +  + E+  R       +   ++S    E  RI R     A+ R RK 
Sbjct: 122 AIDMVIVRELNGDVYFGEKGMRTTASGRREGYDIMSYNEDEVARIARVGFETAQVRNRKL 181

Query: 166 LHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTNL 225
             +  KANVL  +Q L+ D V EV+ +FP V +  + VDN AMQLV  P +FDVIVT NL
Sbjct: 182 CSV-DKANVLETSQ-LWRDVVIEVSAEFPDVELTHMYVDNAAMQLVRNPGQFDVIVTGNL 239

Query: 226 LGDILSDLAAGLVGGLGLAPSGNI-GDTTAVFEPVHGSAPDIAGKGIANPTAAILSAAMM 284
            GDILSD A+   G +G+ PS  + G    ++EP+HGSAPDIAG+G ANP A ILSAAM+
Sbjct: 240 FGDILSDQASMCAGSIGMLPSAALNGSGKGLYEPIHGSAPDIAGQGKANPCATILSAAML 299

Query: 285 LDY-LGEKEAAKRVEKAVDLVLERGPRTPDLGGDATTEAFTEAVVEAL 331
           L Y L  + AA +VE AV   L  G RT DLGG  +TEA  +AV++AL
Sbjct: 300 LRYSLDMEAAADKVEAAVTAALAGGARTADLGGALSTEAMGDAVLKAL 347


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: 321
Number of extensions: 20
Number of successful extensions: 5
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: 348
Length adjustment: 29
Effective length of query: 305
Effective length of database: 319
Effective search space:    97295
Effective search space used:    97295
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 Apr 09 2024. The underlying query database was built on Apr 09 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