GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Escherichia coli BW25113

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate 15918 b1800 predicted dehydrogenase (NCBI)

Query= BRENDA::Q5SIJ1
         (334 letters)



>FitnessBrowser__Keio:15918
          Length = 361

 Score =  221 bits (563), Expect = 2e-62
 Identities = 138/355 (38%), Positives = 201/355 (56%), Gaps = 28/355 (7%)

Query: 4   RICLIEGDGIGHEVIPAARRVLEAT----GLPLEFVEAE-AGWETFERRGTSVPEETVEK 58
           RI  I GDGIG EV+P   RVL+A     G  L F + E A  E +   G  +P++  E+
Sbjct: 6   RIAAIPGDGIGKEVLPEGIRVLQAAAERWGFALSFEQMEWASCEYYSHHGKMMPDDWHEQ 65

Query: 59  ILSCHATLFGAATSPTRKVP---GFFGAIRYLRRRLDLYANVRPAK-----SRPVPGSRP 110
           +    A  FGA   P   VP     +G++   RR  D Y N+RP +       P+ G +P
Sbjct: 66  LSRFDAIYFGAVGWPDT-VPDHISLWGSLLKFRREFDQYVNLRPVRLFPGVPCPLAGKQP 124

Query: 111 G-VDLVIVRENTEGLYVE-----QERRYLDVAIADAVISKKASERIGRAALRIAEGRPRK 164
           G +D  +VRENTEG Y        E    +V I ++V +++  +RI R A  +A+ RPRK
Sbjct: 125 GDIDFYVVRENTEGEYSSLGGRVNEGTEHEVVIQESVFTRRGVDRILRYAFELAQSRPRK 184

Query: 165 TLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTN 224
           TL  A K+N L ++   + + V+ +A+++P +      +D    + VM+PERFDV+V +N
Sbjct: 185 TLTSATKSNGLAISMPYWDERVEAMAENYPEIRWDKQHIDILCARFVMQPERFDVVVASN 244

Query: 225 LLGDILSDLAAGLVGGLGLAPSGNIGDT---TAVFEPVHGSAPDIAGKGIANPTAAILSA 281
           L GDILSDL     G +G+APS N+       ++FEPVHGSAPDI GK IANP A I + 
Sbjct: 245 LFGDILSDLGPACTGTIGIAPSANLNPERTFPSLFEPVHGSAPDIYGKNIANPIATIWAG 304

Query: 282 AMMLDYLGE-----KEAAKRVEKAVDLVLERGPRTPDLGGDATTEAFTEAVVEAL 331
           AMMLD+LG      ++A   +  A++ V+  GP+TPD+ G+ATT    +A+ + +
Sbjct: 305 AMMLDFLGNGDERFQQAHNGILAAIEEVIAHGPKTPDMKGNATTPQVADAICKII 359


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: 310
Number of extensions: 15
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: 361
Length adjustment: 29
Effective length of query: 305
Effective length of database: 332
Effective search space:   101260
Effective search space used:   101260
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