GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Sphingomonas koreensis DSMZ 15582

Align D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate Ga0059261_3694 Ga0059261_3694 threonine ammonia-lyase, medium form

Query= BRENDA::Q54HH2
         (324 letters)



>FitnessBrowser__Korea:Ga0059261_3694
          Length = 420

 Score =  190 bits (482), Expect = 6e-53
 Identities = 106/318 (33%), Positives = 182/318 (57%), Gaps = 7/318 (2%)

Query: 7   VTLKDIKEAHKRIEKYIHKTPVLTNSTINELAGKELYFKCENLQKTGSFKMRGACNAIFS 66
           VTL D++ A  RI   +  TP L + T+++L G  +Y K ENLQ T ++K RGA N +  
Sbjct: 20  VTLADVQAAAARIMGAVVHTPTLHSKTLSDLTGATVYLKFENLQFTAAYKERGALNTLLQ 79

Query: 67  LDEEELSKGVVTHSSGNHGQALSYASKVRCVKCYVVVPEDAPSVKLNAICGYGATVTKCK 126
           LD+   +KGV+  S+GNH Q L+Y      +   +V+P+  P+VK+     +GAT+    
Sbjct: 80  LDDAARAKGVIAASAGNHAQGLAYHGNRLGIPVTIVMPKSTPTVKVMQTESHGATIILEG 139

Query: 127 ATLEARESNTKQLIEQHSCKLIHPFDNLQVIAGQGTASLELMEQVENLDAIITPVGGGGL 186
            T +   ++ +QL   +    +HPFD+ ++IAGQGT  LE++     +D +I P+GGGGL
Sbjct: 140 ETFDEAYAHARQLEASNGYTFVHPFDDPRIIAGQGTVFLEMLADAPAIDTLIVPIGGGGL 199

Query: 187 LSGTCITAKSLNPNIKVFAAEPLGADDTYRSLLSGEIQKHTPGKPNTIADGL-LTTVGSL 245
           +SG    AK+ +  I+V   +     + + S+ +     H P   +T+A+G+ +   G L
Sbjct: 200 ISGALTVAKAADKPIEVVGVQA----ELFPSMFNRFTGAHEPIGGDTLAEGIAVKEPGGL 255

Query: 246 TFPIIKENCDGVILVTEDEIKYAMKLVWERMKIIIEPSSATTLAAILKQEFKDKKDIKKV 305
           T  I++   D ++LV+E  ++ A+ L+ +  K ++E + A  LAA++ Q  + +   K V
Sbjct: 256 TAQIVEALVDEIMLVSERSLEEAVSLLLQIEKTVVEGAGAAGLAALMTQPERFRG--KTV 313

Query: 306 GIIISGGNVDLSSISKIL 323
           G+I++GGN+D   ++ +L
Sbjct: 314 GVILTGGNIDTRLLANVL 331


Lambda     K      H
   0.315    0.132    0.374 

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: 263
Number of extensions: 14
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: 324
Length of database: 420
Length adjustment: 30
Effective length of query: 294
Effective length of database: 390
Effective search space:   114660
Effective search space used:   114660
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 (21.5 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