GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Pseudomonas stutzeri RCH2

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate GFF2539 Psest_2589 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>FitnessBrowser__psRCH2:GFF2539
          Length = 360

 Score =  190 bits (482), Expect = 5e-53
 Identities = 137/357 (38%), Positives = 198/357 (55%), Gaps = 30/357 (8%)

Query: 1   MAYRICLIEGDGIGHEVIPAARRVLEATG----LPLEFVEAEAGWETFERRGTSVPEETV 56
           M+ +I ++ GDGIG E++  A +VL+       L  E    E G    ++ G  + +ET+
Sbjct: 1   MSKQILVLPGDGIGPEIMAEAVKVLQLANDKFQLDFELSYDELGGAAVDKYGVPLADETL 60

Query: 57  EKILSCHATLFGAATSPTRKVPGFFGAIR------YLRRRLDLYANVRPAKSRPV----- 105
           E+  +  A L GA   P  K      AIR       +R +L L+ N+RPA   P      
Sbjct: 61  ERARAADAILLGAVGGP--KWDTIDPAIRPERGLLKIRSQLGLFGNLRPALLYPQLAEAS 118

Query: 106 ---PGSRPGVDLVIVRENTEGLYVEQER--RYLD----VAIADAVISKKASERIGRAALR 156
              P    G+D++IVRE T G+Y  Q R  + L+    +A      S+    RI +    
Sbjct: 119 SLKPEIVAGLDILIVRELTGGIYFGQPRESKVLESGERMAYDTLPYSESEIRRIAKVGFD 178

Query: 157 IAEGRPRKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPER 216
           +A  R +K   +  KANVL  +Q L+   V+EVAK +P V +  + VDN AMQLV  P++
Sbjct: 179 MAMVRNKKLCSV-DKANVLASSQ-LWRAVVEEVAKYYPDVELSHMYVDNAAMQLVRAPKQ 236

Query: 217 FDVIVTTNLLGDILSDLAAGLVGGLGLAPSGNI-GDTTAVFEPVHGSAPDIAGKGIANPT 275
           FDVIVT N+ GDILSD A+ L G +G+ PS ++      ++EP HGSAPDIAG+GIANP 
Sbjct: 237 FDVIVTDNMFGDILSDEASMLTGSIGMLPSASLDAGNKGMYEPCHGSAPDIAGQGIANPL 296

Query: 276 AAILSAAMMLDY-LGEKEAAKRVEKAVDLVLERGPRTPDLGGDATTEAFTEAVVEAL 331
           A ILS +MML Y   +  AA  +E+AV  VL++G RT D+  +  T+  T+A+ +A+
Sbjct: 297 ATILSVSMMLRYSFNQVAAADAIEQAVSDVLDQGLRTGDIWSEGCTKVGTQAMGDAV 353


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: 291
Number of extensions: 15
Number of successful extensions: 4
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: 360
Length adjustment: 29
Effective length of query: 305
Effective length of database: 331
Effective search space:   100955
Effective search space used:   100955
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