GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Dyella japonica UNC79MFTsu3.2

Align isocitrate dehydrogenase (NAD+) subunit 2; EC 1.1.1.41 (characterized)
to candidate N515DRAFT_1138 N515DRAFT_1138 isocitrate dehydrogenase (NAD+)

Query= CharProtDB::CH_125980
         (378 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1138
          Length = 338

 Score =  315 bits (807), Expect = 1e-90
 Identities = 162/335 (48%), Positives = 224/335 (66%), Gaps = 5/335 (1%)

Query: 47  TVTMIAGDGIGPEIAQSVERIFKAAKVPIEWERVKVYPI-LKNGTTTIPDDAKESVRKNK 105
           T+ +I GDGIGPEI ++  R+  A    + +E V    + L+     +P D  +++ ++ 
Sbjct: 4   TIAVIPGDGIGPEIMKATLRVLDALDCGLSYEFVDAGMVALEKHGDLLPKDTLDAIARHT 63

Query: 106 VALKGPLATPIGKGHVSMNLTLRRTFGLFANVRPCVSITGYKTPYDNVNTVLIRENTEGE 165
           +ALKGPL TPIG G  S+N+TLRR F L+ANVRP +S  G K  ++N++ + +RENTEG 
Sbjct: 64  IALKGPLTTPIGGGFTSINVTLRRHFDLYANVRPAISFPGTKARFENIDIITVRENTEGA 123

Query: 166 Y--SGIEHEVIPGVVQSIKLITRAASERVIRYAFQYARQTGKNNITVVHKATIMRMADGL 223
           Y   G        V  S+   TR  S R+++YAF+ ARQ G+  IT VHKA IM+ + GL
Sbjct: 124 YLSEGQTLSEDGEVATSMVRNTRKGSTRIVKYAFEMARQKGRKKITAVHKANIMKTSSGL 183

Query: 224 FLECAKELAPEYPDIELREEILDNACLKIVTDPVPYNNTVMVMPNLYGDIVSDMCAGLIG 283
           FL  A+E+A EYPDIE  E I+DN C+++V  P  ++  V+V  NL+GDI+SD+CAGL+G
Sbjct: 184 FLNVAREVAKEYPDIEFNEMIVDNTCMQLVMKPEQFD--VIVTTNLFGDILSDLCAGLVG 241

Query: 284 GLGLTPSGNIGNQASIFEAVHGTAPDIAGKGLANPTALLLSSVMMLKHMNLNDYAKRIES 343
           GLGL P  NIG  A+IFEAVHG+APDIAGKG+ANP ALLL++  ML H+ + D   ++ +
Sbjct: 242 GLGLAPGDNIGAGAAIFEAVHGSAPDIAGKGIANPCALLLAAADMLDHLGMADKGNKVRA 301

Query: 344 AIFDTLANNPDARTKDLGGKSNNVQYTDAIISKLK 378
           AI DTL N+ DA T DLGGK N   + DAI+ ++K
Sbjct: 302 AIRDTLTNDRDAVTPDLGGKGNTDSFGDAIVKRVK 336


Lambda     K      H
   0.317    0.133    0.381 

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: 365
Number of extensions: 13
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: 378
Length of database: 338
Length adjustment: 29
Effective length of query: 349
Effective length of database: 309
Effective search space:   107841
Effective search space used:   107841
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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