GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Pyrolobus fumarii 1A

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_014027430.1 PYRFU_RS09335 isocitrate/isopropylmalate dehydrogenase family protein

Query= SwissProt::Q58130
         (333 letters)



>NCBI__GCF_000223395.1:WP_014027430.1
          Length = 349

 Score =  298 bits (762), Expect = 2e-85
 Identities = 172/336 (51%), Positives = 219/336 (65%), Gaps = 15/336 (4%)

Query: 3   KICVIEGDGIGKEVVPATIQVLEAT----GLPFEFVYAEAGDEVYKRTGKALPEETIETA 58
           + C+IEGDGIG EV  AT++VLEA     G+ FE V  EAGDE  KR G  LPEET+  A
Sbjct: 16  RFCLIEGDGIGPEVSRATLRVLEAVSKRFGIGFEPVLCEAGDEAAKRRGSPLPEETLRKA 75

Query: 59  LDCDAVLFGAAGETAADVIVKLRHILDTYANIRPVKAYKGV--KCLRPDIDYVIVRENTE 116
            +   VL G  GETA +V+  LR  L TYA IRP K   GV  +C +P +D VIVRE  E
Sbjct: 76  KEIGIVLKGPVGETAGEVVTVLRRELGTYAAIRPAKTLPGVSPRCGKP-LDVVIVRELLE 134

Query: 117 GLYKGIEAE--IDEGITIATRVITEKACERIFRFAFNLARERKKMGKEGKVTCAHKANVL 174
           G+Y   E    +     +A RV + +  ER+ R A  +AR     G+ G V+  HKANVL
Sbjct: 135 GVYVQTEYVDVVSNSFAVALRVASARETERVARLAARIAR-----GRRGIVSIIHKANVL 189

Query: 175 KLTDGLFKKIFYKVAEEYDDIKAEDYYIDAMNMYIITKPQVFDVVVTSNLFGDILSDGAA 234
             T GLF+ +  +V EE + +  E+YY+DA    ++  P+ FDV++T NLFGDILSD AA
Sbjct: 190 HGTCGLFRDVAKRVLEE-EGVVVEEYYVDAAAALLVRTPERFDVMLTPNLFGDILSDLAA 248

Query: 235 GTVGGLGLAPSANIGDEHGLFEPVHGSAPDIAGKKIANPTATILSAVLMLRYLGEYEAAD 294
              G LGL+PSAN+GD+ G+FEPVHG+A DIAG  IANPTA +L+A +ML +LG  +AA 
Sbjct: 249 ELAGSLGLSPSANVGDKTGIFEPVHGAAFDIAGMGIANPTAMMLAAAMMLDWLGYRDAAR 308

Query: 295 KVEKALEEVLALGLTTPDLGGNLNTFEMAEEVAKRV 330
            +EKA+E+ LA G  TPDLGGNL T E AEEVAKR+
Sbjct: 309 AIEKAIEDALASGARTPDLGGNLKTMEFAEEVAKRI 344


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: 295
Number of extensions: 11
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: 349
Length adjustment: 29
Effective length of query: 304
Effective length of database: 320
Effective search space:    97280
Effective search space used:    97280
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 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