GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Escherichia coli BW25113

Align isocitrate-homoisocitrate dehydrogenase (EC 1.1.1.286) (characterized)
to candidate 14219 b0073 3-isopropylmalate dehydrogenase (VIMSS)

Query= BRENDA::Q5JFV8
         (347 letters)



>FitnessBrowser__Keio:14219
          Length = 363

 Score =  184 bits (467), Expect = 3e-51
 Identities = 133/344 (38%), Positives = 184/344 (53%), Gaps = 37/344 (10%)

Query: 2   YRVAVIPGDGIGPEVIDGAVRVLKAVTGR----VRFEYYEGGVDVFQECGSPIREEDLEE 57
           Y +AV+PGDGIGPEV+  A++VL AV  R    +   +Y+ G       G P+    +E 
Sbjct: 5   YHIAVLPGDGIGPEVMTQALKVLDAVRNRFAMRITTSHYDVGGAAIDNHGQPLPPATVEG 64

Query: 58  IRRSDAVLFGATTTPF------DLPGYRSLILTLRKELGLYANLR-------------II 98
             ++DAVLFG+   P       D    R  +L LRK   L++NLR             + 
Sbjct: 65  CEQADAVLFGSVGGPKWEHLPPDQQPERGALLPLRKHFKLFSNLRPAKLYQGLEAFCPLR 124

Query: 99  PDLRT-GREIVIVRENSEGLYFGI-----GAVVNGRAVDVRLITREGAERIARFAVEQAK 152
            D+   G +I+ VRE + G+YFG      G+    +A D  +  R   ERIAR A E A+
Sbjct: 125 ADIAANGFDILCVRELTGGIYFGQPKGREGSGQYEKAFDTEVYHRFEIERIARIAFESAR 184

Query: 153 ARGSFITFVHKANVLTGDKFFRRIVREVAGE-EGVEVRDAIIDSFTIKLVRNPWEHGVIL 211
            R   +T + KANVL     +R IV E+A E   VE+    ID+ T++L+++P +  V+L
Sbjct: 185 KRRHKVTSIDKANVLQSSILWREIVNEIATEYPDVELAHMYIDNATMQLIKDPSQFDVLL 244

Query: 212 SENLFGDILSDLATVHAGSIGIVPSGNYGD-GIALFEPVHGSAPDIAGKGIANPIGAILS 270
             NLFGDILSD   +  GS+G++PS +  + G  L+EP  GSAPDIAGK IANPI  ILS
Sbjct: 245 CSNLFGDILSDECAMITGSMGMLPSASLNEQGFGLYEPAGGSAPDIAGKNIANPIAQILS 304

Query: 271 GAMLLDYLGLDGSLIRAAVRGYVVNGELTPDMGGRARTEDVVRG 314
            A+LL Y  LD      A+    +N  L   +    RT D+ RG
Sbjct: 305 LALLLRY-SLDADDAACAIE-RAINRALEEGI----RTGDLARG 342


Lambda     K      H
   0.321    0.143    0.411 

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: 311
Number of extensions: 19
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: 347
Length of database: 363
Length adjustment: 29
Effective length of query: 318
Effective length of database: 334
Effective search space:   106212
Effective search space used:   106212
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 (21.8 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