GapMind for catabolism of small carbon sources

 

Alignments for a candidate for icd in Stenotrophomonas chelatiphaga DSM 21508

Align isocitrate dehydrogenase (NAD+) (EC 1.1.1.41) (characterized)
to candidate WP_057506985.1 ABB28_RS01900 isocitrate dehydrogenase

Query= BRENDA::Q945K7
         (374 letters)



>NCBI__GCF_001431535.1:WP_057506985.1
          Length = 334

 Score =  310 bits (793), Expect = 5e-89
 Identities = 161/330 (48%), Positives = 217/330 (65%), Gaps = 3/330 (0%)

Query: 47  TLFPGDGIGPEIAESVKKVFTTAGVPIEWEEHYVGTEIDPRTQSFLTWESLESVRRNKVG 106
           T+  GDGIGPEI ++   V       +E+E+   G     +    +   +LES+ RNK+ 
Sbjct: 6   TVIRGDGIGPEIMDATLYVLDKLNAGLEYEDADAGLVALEKHGDLMPASTLESIARNKIA 65

Query: 107 LKGPMATPIGKGHRSLNLTLRKELNLYANVRPCYSLPGYKTRYDDVDLITIRENTEGEY- 165
           LK P++TPIG G  S+N++LR+  +LYANVRP ++ P  K+R+D+V+L+T+RENTEG Y 
Sbjct: 66  LKSPLSTPIGGGFTSINVSLRRHFDLYANVRPAHTFPNTKSRFDNVNLVTVRENTEGAYL 125

Query: 166 -SGLEHQVVRGVVESLKIITRQASLRVAEYAFLYAKTHGRERVSAIHKANIMQKTDGLFL 224
             G E         S   ITR+ S R+  YAF  A++ GR++V+A+HKANI++ T GLFL
Sbjct: 126 AEGQEVSPDGETAFSGTRITRKGSERIVRYAFELARSTGRKKVTAVHKANIIKSTSGLFL 185

Query: 225 KCCREVAEKYPEITYEEVVIDNCCMMLVKNPALFDVLVMPNLYGDIISDLCAGLVGGLGL 284
              REVA KYP+I ++E+++DNCCM LV  P  FDV+V  NL+GDIISDLCAGLVGGLGL
Sbjct: 186 AVAREVAAKYPDIEFQEMIVDNCCMQLVMRPEQFDVIVTTNLFGDIISDLCAGLVGGLGL 245

Query: 285 TPSCNIGEDGVALAEAVHGSAPDIAGKNLANPTALLLSGVMMLRHLKFNEQAEQIHSAII 344
            P  NIGE+  A+ EAVHG+APDIAG+  ANP ALLL+   ML H+   E AE++  AI+
Sbjct: 246 APGANIGEN-AAIFEAVHGTAPDIAGQGKANPCALLLAAAQMLDHIGQPENAERLRKAIV 304

Query: 345 NTIAEGKYRTADLGGSSTTTEFTKAICDHL 374
            T+      T DLGG+  T  F +AI   L
Sbjct: 305 ATLEAKDSLTGDLGGTGNTMGFAQAIASRL 334


Lambda     K      H
   0.318    0.134    0.389 

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: 340
Number of extensions: 13
Number of successful extensions: 3
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: 374
Length of database: 334
Length adjustment: 29
Effective length of query: 345
Effective length of database: 305
Effective search space:   105225
Effective search space used:   105225
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 (21.7 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