GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Ferroglobus placidus DSM 10642

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_012966595.1 FERP_RS10670 3-isopropylmalate dehydrogenase

Query= SwissProt::Q58130
         (333 letters)



>NCBI__GCF_000025505.1:WP_012966595.1
          Length = 325

 Score =  403 bits (1035), Expect = e-117
 Identities = 210/328 (64%), Positives = 254/328 (77%), Gaps = 5/328 (1%)

Query: 3   KICVIEGDGIGKEVVPATIQVLEATGLPFEFVYAEAGDEVYKRTGKALPEETIETALDCD 62
           +I VI GDGIGKEV  A + +LE   LPFE+V+ EAGDE  K+ GK LP+ET+E    C 
Sbjct: 2   RIAVIPGDGIGKEVTEAAMLILENLDLPFEYVWLEAGDEAEKKYGKPLPDETLEEVKRCK 61

Query: 63  AVLFGAAGETAADVIVKLRHILDTYANIRPVKAYKGVKCLRPDIDYVIVRENTEGLYKGI 122
           AVLFGAAGETAADVIVKLR  L+TYAN+RP K+++GVK +  ++D VIVRENTE LYKGI
Sbjct: 62  AVLFGAAGETAADVIVKLRQELETYANVRPAKSFEGVKSIHKNVDMVIVRENTECLYKGI 121

Query: 123 EAEIDEGITIATRVITEKACERIFRFAFNLARERKKMGKEGKVTCAHKANVLKLTDGLFK 182
           E E+D G+  A R+I+ KA ERI RFAF LA+  K+     +VT  HKANV++ T GLFK
Sbjct: 122 EFEVD-GVAEAVRIISRKASERIVRFAFELAKREKRK----RVTALHKANVMRKTCGLFK 176

Query: 183 KIFYKVAEEYDDIKAEDYYIDAMNMYIITKPQVFDVVVTSNLFGDILSDGAAGTVGGLGL 242
           ++FY+VA EY+ I+A DYYIDA  MYI   P  FDV+VT+N+FGDI+SD AAG VGGLGL
Sbjct: 177 RVFYEVAREYERIEANDYYIDAACMYIAMDPWRFDVIVTTNMFGDIVSDLAAGIVGGLGL 236

Query: 243 APSANIGDEHGLFEPVHGSAPDIAGKKIANPTATILSAVLMLRYLGEYEAADKVEKALEE 302
           APSANIGDE+ +FEPVHG+A DIAGK IANPTA IL+A +MLR+LG  E A KVEKA+E+
Sbjct: 237 APSANIGDEYAIFEPVHGAAFDIAGKGIANPTAMILTASMMLRHLGFEEEAKKVEKAVEK 296

Query: 303 VLALGLTTPDLGGNLNTFEMAEEVAKRV 330
           VLA G TTPDLGGNL T EMAEE+ K +
Sbjct: 297 VLAEGKTTPDLGGNLKTMEMAEEILKAI 324


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: 359
Number of extensions: 12
Number of successful extensions: 3
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: 325
Length adjustment: 28
Effective length of query: 305
Effective length of database: 297
Effective search space:    90585
Effective search space used:    90585
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