GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Ammonifex degensii KC4

Align 3-isopropylmalate dehydrogenase; 3-IPM-DH; IMDH; EC 1.1.1.85; Beta-IPM dehydrogenase (uncharacterized)
to candidate WP_015739105.1 ADEG_RS05580 isocitrate/isopropylmalate dehydrogenase family protein

Query= curated2:O29627
         (326 letters)



>NCBI__GCF_000024605.1:WP_015739105.1
          Length = 334

 Score =  303 bits (775), Expect = 5e-87
 Identities = 157/327 (48%), Positives = 220/327 (67%), Gaps = 6/327 (1%)

Query: 3   KIVVIPGDGIGKEVMEAAMLILEKLDLPFEYSYYDAGDEALEKYGKALPDETLEACRKSD 62
           ++ +IPGDGIG E+  AA  +L+      E+   +AG++ + +YG  LP+  L++ R++ 
Sbjct: 4   RVTLIPGDGIGPEITAAARQVLDASGAEIEWEVVEAGEKVIPEYGTPLPEHVLDSIRRNR 63

Query: 63  AVLFGAA----GETAADVIVRLRRELGTFANVRPAKAIEGIECLYPGLDIVVVRENTECL 118
             L G      G     V V LR+EL  +A VRPAK + GI+  +  +D++VVRENTE L
Sbjct: 64  VALKGPLTTPIGHGFRSVNVTLRQELDLYACVRPAKTLPGIKTRFDHVDLIVVRENTEDL 123

Query: 119 YMGFEFGFG-DVTEAIRVITREASERIARYAFELAKREGRKKVTALHKANVMKKTCGLFR 177
           Y G E   G +  E+I+++TREAS RI R+AFELA+REGR+KVTA+HKAN+MK T GLF 
Sbjct: 124 YAGIEHRVGKNAAESIKIVTREASTRIVRFAFELARREGRRKVTAVHKANIMKLTDGLFL 183

Query: 178 DVCREVAKDYPEIQYNDYYIDAACMYLVMDPFRFDVIVTTNMFGDIVSDLAAGLVGGLGL 237
           +  REVA +YP+I + +  +DA CM LV  P  +DVIVT N++GDI+SDLAAGLVGGLG+
Sbjct: 184 ECAREVAAEYPDIAFEEMIVDAMCMKLVQSPENYDVIVTLNLYGDIISDLAAGLVGGLGV 243

Query: 238 APSANVGERTAIFEPVHGAAFDIAGKGIANPTAMILTACMMLRHFGYVEEAKKVEEAVEK 297
           AP AN+G+  A+FEPVHG+A   AG+   NP A IL+  MML+H G +E A++V   +  
Sbjct: 244 APGANIGDEAAVFEPVHGSAPKHAGQDKVNPLATILSGVMMLKHLGEMEAAERVMRGIIG 303

Query: 298 TIKEGKK-TPDLGGNLKTMEFANEVAS 323
            ++EGK  T DLGG+ +T E A  + +
Sbjct: 304 VLQEGKALTYDLGGSARTSEMAAAIVA 330


Lambda     K      H
   0.321    0.139    0.399 

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: 299
Number of extensions: 9
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: 326
Length of database: 334
Length adjustment: 28
Effective length of query: 298
Effective length of database: 306
Effective search space:    91188
Effective search space used:    91188
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 (21.8 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