GapMind for catabolism of small carbon sources

 

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

Align D-xylose reductase (EC 1.1.1.307) (characterized)
to candidate Echvi_4178 Echvi_4178 Aldo/keto reductases, related to diketogulonate reductase

Query= BRENDA::A9QVV8
         (324 letters)



>FitnessBrowser__Cola:Echvi_4178
          Length = 283

 Score =  187 bits (476), Expect = 2e-52
 Identities = 114/300 (38%), Positives = 167/300 (55%), Gaps = 44/300 (14%)

Query: 10  IKLNSGYEMPLVGFGCWKVTNATAADQ-IYNAIKTGYRLFDGAEDYGNEKEVGEGINRAI 68
           IKLN+G EMPL+GFG +++ +    ++ + +AI  GYRL D A  Y NE  VG  I   I
Sbjct: 4   IKLNNGLEMPLLGFGVFQIPDLKECERAVMDAINIGYRLIDTASAYMNEAAVGNAI---I 60

Query: 69  KDGLVKREELFITSKLWNNFHDPKNVETALNKTLSDLNLDYVDLFLIHFPIAFKFVPIEE 128
           K G V R+ELFITSKLW      ++ + A  +TL  L LDY+DL+LIH P          
Sbjct: 61  KSG-VARKELFITSKLWVQDMGYESTKAAFRRTLERLQLDYLDLYLIHQP---------- 109

Query: 129 KYPPGFYCGDGDNFHYEDVPLLDTWKALEKLVEAGKIKSIGISNFTGALIYDLIRGATIK 188
                          Y DV    +WKA+++L +AGKIK+IG++NF    + DL   +   
Sbjct: 110 ---------------YGDV--FGSWKAMQELYQAGKIKAIGVANFQPDRVVDLTINSGFA 152

Query: 189 PAVLQIEHHPYLQQPKLIEYVQKAGIAITGYSSFGPQSFLELESKRALNTPTLFEHETIK 248
           PA+ QIE HP+ QQ +  +++    + +  +  F        E K  +     F++E + 
Sbjct: 153 PAINQIETHPFHQQQESHDFLIDHNVQMQSWGPFA-------EGKNGI-----FQNEVLS 200

Query: 249 SIADKHGKSPAQVLLRWATQRNIAVIPKSNNPERLAQNLSVVDFDLTKDDLDNIAKLDIG 308
            I  K+ KS AQV+LRW  QRN+  IPKS + ER+ +N  + DF+++K+D+ +IA LD G
Sbjct: 201 EIGRKYNKSIAQVILRWLIQRNVIAIPKSVHKERIEENFRIFDFEISKEDMHSIAALDTG 260


Lambda     K      H
   0.318    0.138    0.419 

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: 241
Number of extensions: 9
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: 324
Length of database: 283
Length adjustment: 27
Effective length of query: 297
Effective length of database: 256
Effective search space:    76032
Effective search space used:    76032
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: 48 (23.1 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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