GapMind for catabolism of small carbon sources

 

Alignments for a candidate for LRA5 in Echinicola vietnamensis KMM 6221, DSM 17526

Align 2-dehydro-3-deoxy-L-rhamnonate dehydrogenase (NAD(+)); 2-keto-3-deoxy-L-rhamnonate dehydrogenase; KDRDH; L-KDR dehydrogenase; EC 1.1.1.401 (characterized)
to candidate Echvi_0507 Echvi_0507 Threonine dehydrogenase and related Zn-dependent dehydrogenases

Query= SwissProt::P0DOW0
         (331 letters)



>FitnessBrowser__Cola:Echvi_0507
          Length = 337

 Score =  123 bits (308), Expect = 7e-33
 Identities = 92/301 (30%), Positives = 132/301 (43%), Gaps = 9/301 (2%)

Query: 1   MKTLTWTAKETMSILSAPAPVPEPGWIALRVAGVGICGSELSGYLGHNELRKPPLVMGHE 60
           MK LT T            P   PG   +++  +GICG++L  Y G       P V+GHE
Sbjct: 1   MKILTCTEPGNFEYSEGEKPTLSPGRAIIKIKRIGICGTDLHAYEGTQPFFNYPRVLGHE 60

Query: 61  FSGVVEEVGHGVTNVKIGDLVTANPLVTCGRCIHCLRGERQRCESRRIIGIDFPGAYAER 120
            SG + EV  G      GDLVT  P   CG C+ C  G+   C +  + G+   G   E 
Sbjct: 61  LSGELVEV-DGAEGFVPGDLVTIIPYFNCGECVACKAGKPNCCATISVFGVHEDGGMKEF 119

Query: 121 VLVPSNQCYAVK--DAIDGALVEPLACAVRAVGLARIKVGDTAVVIGAGIIGLMTVRLLG 178
           + VPS+     +       AL EPLA     V  A ++ G+  VV+GAG IGL  +    
Sbjct: 120 ISVPSSSLVKQEGLSLEQLALAEPLAIGAHGVRRAGVQPGEFVVVMGAGPIGLGVMEFAR 179

Query: 179 LSGAKRIAVVDPNDERLKISQLWGATEMAPN----LGALLTDNHPQSF-DCVIDAVGLST 233
           ++G K IA +D N++RL   +     E   N      A + D    SF + VIDA G S 
Sbjct: 180 IAGGKVIA-MDINEDRLAFCRETLGVEYTVNAKGDFKAAIADITGGSFAESVIDATGSSV 238

Query: 234 TRRDSLNALIRGGRAVWIGLHEALTHLDGNQIVRDELEVRGSFCYTDDEFIRAVSLINSQ 293
                   +  GGR V +GL +     +  +  + E  +  S   T ++F   +  +  Q
Sbjct: 239 AIHHGFGLMAHGGRYVLVGLQKGPIEFNHPEFHKRESTLMSSRNATREDFDTVLKALKEQ 298

Query: 294 K 294
           K
Sbjct: 299 K 299


Lambda     K      H
   0.322    0.139    0.424 

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: 293
Number of extensions: 14
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: 331
Length of database: 337
Length adjustment: 28
Effective length of query: 303
Effective length of database: 309
Effective search space:    93627
Effective search space used:    93627
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 (21.9 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