GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Magnetospirillum magneticum AMB-1

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_011386420.1 AMB_RS20570 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000009985.1:WP_011386420.1
          Length = 369

 Score =  186 bits (473), Expect = 6e-52
 Identities = 137/370 (37%), Positives = 189/370 (51%), Gaps = 42/370 (11%)

Query: 2   AYRICLIEGDGIGHEVIPAARRVLEATG----LPLEFVEAEAGWETFERRGTSVPEETVE 57
           A ++ ++ GDGIG EV+   RR+++  G    +  E  E   G   ++  GT  P ET+E
Sbjct: 3   AKKLLILPGDGIGVEVMAQVRRIIDWMGRKRKIEFEITEGLLGGAAYDVHGTPYPAETLE 62

Query: 58  KILSCHATLFGAATSPT--------RKVPGFFGAIRYLRRRLDLYANVRPAKSRPVPGSR 109
             L+  A L GA   P         +   G  G    +R+ + L+AN+RPA         
Sbjct: 63  AALAADAVLLGAVGGPKWDDLPFDKKPERGLLG----IRKDMGLFANLRPATVLEALADA 118

Query: 110 P--------GVDLVIVRENTEGLYVEQERRYLDV------AIADAVISKKASERIGRAAL 155
                    G+D++I+RE T GLY  Q R    +           V +    +RIGR A 
Sbjct: 119 STLKAEVVSGLDIMILRELTGGLYFGQPRGIDTLPDGTRKGYNTLVYTTPEIQRIGRVAF 178

Query: 156 RIAEGRPRKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPE 215
            +A  R +K   +  KANVL  T     + +K   ++FP V +  + VDN AMQLV  P+
Sbjct: 179 DLARKRNKKLCSV-DKANVLECTVLWREEMIKLQKEEFPDVELTHMYVDNAAMQLVRNPK 237

Query: 216 RFDVIVTTNLLGDILSDLAAGLVGGLGLAPSGNIGDT------TAVFEPVHGSAPDIAGK 269
           +FDV+VT N+ GDILSD AA L G LG+ PS ++G+        A++EPVHGSAPDIAGK
Sbjct: 238 QFDVMVTENMFGDILSDCAAMLTGSLGMLPSASLGEADAQGKRKALYEPVHGSAPDIAGK 297

Query: 270 GIANPTAAILSAAMMLDYLGEKEA-AKRVEKAVDLVLERGPRTPDL----GGDATTEAFT 324
            +ANP A I+S AM L Y  +  A A  +E AV  VL+ G RT D+        +T    
Sbjct: 298 DMANPLATIMSFAMCLRYSFDMAAEADLIETAVKNVLKGGLRTADIMQPGKAKVSTTVMG 357

Query: 325 EAVVEALKSL 334
           EAVV  L  L
Sbjct: 358 EAVVRELDKL 367


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: 300
Number of extensions: 21
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: 334
Length of database: 369
Length adjustment: 29
Effective length of query: 305
Effective length of database: 340
Effective search space:   103700
Effective search space used:   103700
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 Sep 17 2021. The underlying query database was built on Sep 17 2021.

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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