GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Shewanella sp. ANA-3

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate 7026627 Shewana3_3760 3-isopropylmalate dehydrogenase (RefSeq)

Query= BRENDA::Q5SIJ1
         (334 letters)



>FitnessBrowser__ANA3:7026627
          Length = 364

 Score =  196 bits (499), Expect = 6e-55
 Identities = 138/339 (40%), Positives = 190/339 (56%), Gaps = 27/339 (7%)

Query: 1   MAYRICLIEGDGIGHEVIPAARRVLEAT----GLPLEFVEAEAGWETFERRGTSVPEETV 56
           M+Y+I ++ GDGIG EV+  AR+VL+A     GL +E+ E + G    +  G  +PE T+
Sbjct: 1   MSYQIAVLAGDGIGPEVMAEARKVLKAVEARFGLNIEYSEYDVGGIAIDNHGCPLPEATL 60

Query: 57  EKILSCHATLFGAATSPT-RKVPGFF----GAIRYLRRRLDLYANVRPAKSR-------P 104
           +   +  A LFG+   P   K+P       GA+  LR   +L+ N+RPAK         P
Sbjct: 61  KGCEAADAILFGSVGGPKWEKLPPNEQPERGALLPLRGHFELFCNLRPAKLHDGLEHMSP 120

Query: 105 VPG--SRPGVDLVIVRENTEGLYV-----EQERRYLDVAIADAVISKKASERIGRAALRI 157
           +    S  G D++ VRE T G+Y       Q     + A      S++   RI R A   
Sbjct: 121 LRSDISARGFDVLCVRELTGGIYFGKPKGRQGEGESEEAFDTMRYSRREIARIARIAFEA 180

Query: 158 AEGRPRKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERF 217
           A GR +K   +  KANVL  +  L+   V+EVA DFP V ++ I +DN  MQL+ RP+ F
Sbjct: 181 ARGRRKKVTSV-DKANVLACSV-LWRQVVEEVAVDFPDVELEHIYIDNATMQLLRRPDEF 238

Query: 218 DVIVTTNLLGDILSDLAAGLVGGLGLAPSGNIGDT-TAVFEPVHGSAPDIAGKGIANPTA 276
           DV++ +NL GDILSD  A L G +GL  S ++  T   +FEP  GSAPDIAGKGIANP A
Sbjct: 239 DVMLCSNLFGDILSDEIAMLTGSMGLLSSASMNSTGFGLFEPAGGSAPDIAGKGIANPIA 298

Query: 277 AILSAAMMLDY-LGEKEAAKRVEKAVDLVLERGPRTPDL 314
            ILSAA+ML + L ++EAA  +E+AV   L  G  T +L
Sbjct: 299 QILSAALMLRHSLKQEEAASAIERAVSKALNSGYLTGEL 337


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: 272
Number of extensions: 17
Number of successful extensions: 7
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: 364
Length adjustment: 29
Effective length of query: 305
Effective length of database: 335
Effective search space:   102175
Effective search space used:   102175
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