GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Billgrantia desiderata SP1

Align 3-isopropylmalate dehydrogenase; 3-IPM-DH; IMDH; Beta-IPM dehydrogenase; EC 1.1.1.85 (characterized)
to candidate WP_086510509.1 BZY95_RS13880 isocitrate/isopropylmalate family dehydrogenase

Query= SwissProt::P50455
         (337 letters)



>NCBI__GCF_002151265.1:WP_086510509.1
          Length = 363

 Score =  191 bits (485), Expect = 2e-53
 Identities = 115/347 (33%), Positives = 180/347 (51%), Gaps = 23/347 (6%)

Query: 4   TVALIQGDGIGPEIVSKSKRILAKINELYSLPIEYIEVEAGDRALARYGEALPKDSLKII 63
           T+ ++ GD IG EIV  +  +     E   L I++  +  G +AL  +G  +P  +L+ +
Sbjct: 7   TLGVLNGDDIGHEIVPAAVEVAQAAAERCGLVIDWRHMPLGRKALDEFGTTMPDGTLETL 66

Query: 64  DKADIILKGPVG-------ESAADVVVKLRQIYDMYANIRPAKSIPGIDTKYGNVDILIV 116
              D  + GP+G       E A +    LR+ +D++AN+RP +S P I   Y ++D++IV
Sbjct: 67  STFDGFILGPIGHREYPKVEGAINPHPILRKHFDLFANVRPTRSYPDIGCIYDDIDLVIV 126

Query: 117 RENTEDLYKGFEHIVSDG-------VAVGMKIITRFASERIAKVGLNFALRRRKKVTCVH 169
           REN E        +   G       V + +++ITR  S ++A   L  A  R K++T VH
Sbjct: 127 RENNEGFQPDRNVVAGSGEFRPTEDVTISVRVITREGSRKVATAALELARARNKRLTVVH 186

Query: 170 KANVMRITDGLFAEACRSVLKG--KVEYSEMYVDAAAANLVRNPQMFDVIVTENVYGDIL 227
           K  V ++  G+F E C    +    V+  E  VD  A +L+RNPQ +DV+VT N++GDIL
Sbjct: 187 KNTVYKLGCGMFVEECYKAAEAYPDVKVDEAIVDTFAMHLIRNPQQYDVVVTTNMFGDIL 246

Query: 228 SDEASQIAGSLGIAPSANIG-DKKALFEPVHGAAFDIAGKNIGNPTAFLLSVSMMYE--- 283
           +DEA+ + G LG+AP   IG    A+ +  HG+A DIAG  + NP A + S  M+ E   
Sbjct: 247 TDEAAGLVGGLGMAPGLCIGRGNMAMAQATHGSAPDIAGTGLANPYAMIESTRMLIEWLG 306

Query: 284 RMYELSNDDRYIKASRALENAIYLVYKERKALTPDVGGNATTDDLIN 330
           R +EL        A+  +   I     + +  TPD+ G     D++N
Sbjct: 307 RRHELPGAQ---AAAALMAKGIQAALADPRTRTPDIRGQGRLSDMVN 350


Lambda     K      H
   0.318    0.137    0.380 

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: 268
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: 337
Length of database: 363
Length adjustment: 29
Effective length of query: 308
Effective length of database: 334
Effective search space:   102872
Effective search space used:   102872
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 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