GapMind for catabolism of small carbon sources

 

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

Align L-talarate dehydratase (EC 4.2.1.156); galactarate dehydratase (EC 4.2.1.42) (characterized)
to candidate Echvi_2941 Echvi_2941 L-alanine-DL-glutamate epimerase and related enzymes of enolase superfamily

Query= BRENDA::Q8ZL58
         (398 letters)



>FitnessBrowser__Cola:Echvi_2941
          Length = 448

 Score =  105 bits (263), Expect = 2e-27
 Identities = 97/347 (27%), Positives = 152/347 (43%), Gaps = 67/347 (19%)

Query: 44  VSDAKVLTGRQK---------PLTEVAIIIAEIRSRDGFEGVGFSYSKRAGGQGIYAHAK 94
           V D +  T R+K         P    A II +    D  EG G +++   G +   A  +
Sbjct: 21  VKDIRFPTSREKHGSDAMNPDPDYSAAYIILKTNQPD-LEGHGLTFTIGRGNEICCAALE 79

Query: 95  EIADNLLGED----PNDIDKIY------TKLLWAGASVGRSGMAVQAISPIDIALWDMKA 144
            IA +++G+D      D+   +      +++ W G   G   +A  A+     A+WD+ A
Sbjct: 80  AIAHHVIGKDLAALTADMGAFWRTVNSDSQIRWLGPEKGVVHLATGALVN---AVWDLYA 136

Query: 145 KRAGLPLAKLLGA------------------------------------------HRDSV 162
           K    PL KLLG                                             +  
Sbjct: 137 KVEQKPLWKLLGEMTPEQLLSCIDFSYITDVLTKEEALDILKESEKGKKERIRYLEENGY 196

Query: 163 QCYNTSGGFLHTPLDQVLKNVVISRENGIGGIKLKVGQPNCAEDIRRLTAVREALGDEFP 222
             Y TS G+L    +++ +    +++ G   IK+KVG  N  +DIRR   +RE +G++  
Sbjct: 197 PGYTTSAGWLGYTDEKIRRLCREAKQEGWKHIKMKVGA-NLQDDIRRAGIIREEIGEDMY 255

Query: 223 LMVDANQQWDRETAIRMGRKMEQFNLIWIEEPLDAYDIEGHAQLAAALD-TPIATGEMLT 281
           LM+DANQ+W+   AI   +++ +FN +WIEEP    DI GH  +A A+    +ATGE   
Sbjct: 256 LMMDANQRWEVAEAIENMKELAKFNPLWIEEPTSPDDILGHKAIADAVQPILVATGEHCQ 315

Query: 282 SFREHEQLILGNASDFVQPDAPRVGGISPFLKIMDLAAKHGRKLAPH 328
           +    +QL+   A    Q D+ RVGG++  L IM +A K    + PH
Sbjct: 316 NRVIFKQLMQAGALQICQIDSCRVGGVNENLAIMLIAKKFDIPVCPH 362


Lambda     K      H
   0.319    0.136    0.410 

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: 424
Number of extensions: 23
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 398
Length of database: 448
Length adjustment: 32
Effective length of query: 366
Effective length of database: 416
Effective search space:   152256
Effective search space used:   152256
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: 50 (23.9 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