GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Hafnia paralvei ATCC 29927

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_004094577.1 M988_RS03500 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_001655005.1:WP_004094577.1
          Length = 363

 Score =  174 bits (442), Expect = 2e-48
 Identities = 124/348 (35%), Positives = 184/348 (52%), Gaps = 27/348 (7%)

Query: 3   YRICLIEGDGIGHEVIPAARRVLEAT----GLPLEFVEAEAGWETFERRGTSVPEETVEK 58
           + I ++ GDGIG E++  A + ++A     GL +   E + G    ++ GT +P  T+  
Sbjct: 5   HHIAVLPGDGIGPEIMAQAYKTIDAVRQRFGLRISTSEYDVGGAAIDKHGTPLPAATIAG 64

Query: 59  ILSCHATLFGAATSPT-RKVPGFF----GAIRYLRRRLDLYANVRPAKSR-------PVP 106
                A LFG+   P    +P       GA+  LR+   L++N+RPA+         P+ 
Sbjct: 65  CEQASAILFGSVGGPKWENLPPAQQPERGALLPLRKHFKLFSNLRPARLYEGLEEFCPLR 124

Query: 107 G--SRPGVDLVIVRENTEGLYVEQERR-----YLDVAIADAVISKKASERIGRAALRIAE 159
              +  G D++ VRE T G+Y  Q +        + A    V  +   ERI R A   A 
Sbjct: 125 SDIAARGFDILCVRELTGGIYFGQPKGREGQGMHERAFDTEVYHRFEIERIARIAFEAAR 184

Query: 160 GRPRKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDV 219
            R  K   I  KANVL  +  L+ +   E+ KD+P V +  + +DN  MQL+  P +FDV
Sbjct: 185 KRRGKVTSI-DKANVLQ-SSILWREIATEIGKDYPDVALNHMYIDNATMQLIKDPSQFDV 242

Query: 220 IVTTNLLGDILSDLAAGLVGGLGLAPSGNIGDT-TAVFEPVHGSAPDIAGKGIANPTAAI 278
           ++ +N+ GDILSD  A + G +G+ PS ++ +    ++EP  GSAPDIAGK IANP A I
Sbjct: 243 MLCSNIFGDILSDECAMITGSMGMLPSASLNEQGFGLYEPAGGSAPDIAGKNIANPIAQI 302

Query: 279 LSAAMMLDY-LGEKEAAKRVEKAVDLVLERGPRTPDLGGDATTEAFTE 325
           LS A++L Y L   +AA  VE+AV+  LE+G RT DL GD    + +E
Sbjct: 303 LSFALLLRYSLNADDAANAVEQAVNKALEQGFRTGDLAGDGQAISTSE 350


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: 18
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: 363
Length adjustment: 29
Effective length of query: 305
Effective length of database: 334
Effective search space:   101870
Effective search space used:   101870
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 24 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