GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Methanococcus aeolicus Nankai-3

Align 3-isopropylmalate/3-methylmalate dehydrogenase; 3-isopropylmalate dehydrogenase; 3-IPM-DH; IMDH; IPMDH; Beta-IPM dehydrogenase; D-malate dehydrogenase [decarboxylating]; EC 1.1.1.85; EC 1.1.1.n5; EC 1.1.1.83 (characterized)
to candidate WP_157196862.1 MAEO_RS07600 homoisocitrate dehydrogenase

Query= SwissProt::Q58130
         (333 letters)



>NCBI__GCF_000017185.1:WP_157196862.1
          Length = 344

 Score =  326 bits (835), Expect = 6e-94
 Identities = 174/343 (50%), Positives = 238/343 (69%), Gaps = 19/343 (5%)

Query: 3   KICVIEGDGIGKEVVPATIQVLEATGLPFEFVYAEAGDEVYKRTGKALPEETIETALDCD 62
           KICVIEGDGIGKEV+P T+++L+  G  FEF+Y  AG E +KR G A+PE+T++TA +CD
Sbjct: 6   KICVIEGDGIGKEVIPETVRILKEIG-DFEFIYEHAGYECFKRCGDAIPEKTLKTAKECD 64

Query: 63  AVLFGAAGETAADV---------IVKLRHILDTYANIRPVKAYKGVKCLRPDIDYVIVRE 113
           A+LFGA      D          I+ LR  LD YAN+RP+           +ID++I+RE
Sbjct: 65  AILFGAVSTPKLDETERKPYKSPILTLRKELDLYANVRPIHKLDNSDSSN-NIDFIIIRE 123

Query: 114 NTEGLYKGIEAEIDEG-ITIATRVITEKACERIFRFAFNLARERKKMGKEGKVTCAHKAN 172
           NTEGLY G+E   +E  + I+ R I++K  +RI +FAF  A +  +     KV+C HK+N
Sbjct: 124 NTEGLYSGVEYYDEEKELAISERHISKKGSKRIIKFAFEYAVKHHRK----KVSCIHKSN 179

Query: 173 VLKLTDGLFKKIFYKVAEEYDD---IKAEDYYIDAMNMYIITKPQVFDVVVTSNLFGDIL 229
           +L++TDGLF  IF +  E+Y +   I+  DY +DA  MYI+  PQ+FDV+VT+NLFGDIL
Sbjct: 180 ILRITDGLFLNIFNEFKEKYKNEYNIEGNDYLVDATAMYILKSPQMFDVIVTTNLFGDIL 239

Query: 230 SDGAAGTVGGLGLAPSANIGDEHGLFEPVHGSAPDIAGKKIANPTATILSAVLMLRYLGE 289
           SD A+G +GGLGLAPSANIGD +GLFEPVHGSAPDIAGK +ANP A +LSA +ML YL  
Sbjct: 240 SDEASGLLGGLGLAPSANIGDNYGLFEPVHGSAPDIAGKGVANPIAAVLSASMMLYYLDM 299

Query: 290 YEAADKVEKALEEVLALGLTTPDLGGNLNTFEMAEEVAKRVRE 332
            E +  ++ A+++VLA    TPDLGGNL T E+++++ + +R+
Sbjct: 300 KEKSRLLKDAVKQVLAHKDITPDLGGNLKTKEVSDKIIEELRK 342


Lambda     K      H
   0.318    0.138    0.390 

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: 372
Number of extensions: 16
Number of successful extensions: 6
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: 333
Length of database: 344
Length adjustment: 28
Effective length of query: 305
Effective length of database: 316
Effective search space:    96380
Effective search space used:    96380
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: 49 (23.5 bits)

This GapMind analysis is from Jul 25 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