GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Teredinibacter turnerae T7901

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_015818168.1 TERTU_RS11085 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000023025.1:WP_015818168.1
          Length = 357

 Score =  203 bits (517), Expect = 5e-57
 Identities = 142/357 (39%), Positives = 201/357 (56%), Gaps = 30/357 (8%)

Query: 1   MAYRICLIEGDGIGHEVIPAARRVLEATG----LPLEFVEAEAGWETFERRGTSVPEETV 56
           M+ +I L+ GDGIG E++  A +VLE       L L+F E   G    +  G  +   T+
Sbjct: 1   MSKKIVLLPGDGIGPEIVAEAVKVLEVVDKKHKLGLKFEEELIGGSAIDVHGVPLASSTL 60

Query: 57  EKILSCHATLFGAATSPTRKVPGFFGAIR------YLRRRLDLYANVRPAKSRPV----- 105
           EK  +  A L G+   P  K      +IR       +R  + L+ N+RPA   P      
Sbjct: 61  EKCQAADAVLMGSVGGP--KWDTLDSSIRPEKGLLKIRYEMGLFGNLRPAILYPQLADAS 118

Query: 106 ---PGSRPGVDLVIVRENTEGLYVEQER--RYLDVAIADA----VISKKASERIGRAALR 156
              P    G+D++IVRE T G+Y  + R  R LD          V ++   ERIGR A  
Sbjct: 119 SLKPELVAGLDILIVRELTGGIYFGEPRGIRLLDNGERQGYNTYVYAEHEIERIGRMAFE 178

Query: 157 IAEGRPRKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPER 216
           +A  R +K   +  KANVL  T  L+ + V+ +++++P V +  + VDN AMQLV +P++
Sbjct: 179 MAMKRNKKVCSV-DKANVLEATV-LWREVVQSLSREYPEVELSHMYVDNAAMQLVRQPKQ 236

Query: 217 FDVIVTTNLLGDILSDLAAGLVGGLGLAPSGNIG-DTTAVFEPVHGSAPDIAGKGIANPT 275
           FDVIVT N+ GDILSD AA L G +G+ PS ++  D   ++EPVHGSAPDIAG+GIANP 
Sbjct: 237 FDVIVTGNMFGDILSDTAAMLTGSIGMLPSASLNKDKRGLYEPVHGSAPDIAGQGIANPL 296

Query: 276 AAILSAAMMLDY-LGEKEAAKRVEKAVDLVLERGPRTPDLGGDATTEAFTEAVVEAL 331
           A ILSAAMML Y L + EAA  +E AV  VL+ G R+ D+  +  T+  T+ + +A+
Sbjct: 297 ATILSAAMMLRYSLDQGEAADAIEAAVGKVLDDGYRSADIFSEGCTKVSTKEMGDAV 353


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: 303
Number of extensions: 13
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: 357
Length adjustment: 29
Effective length of query: 305
Effective length of database: 328
Effective search space:   100040
Effective search space used:   100040
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 10 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