GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaK' in Paraburkholderia bryophila 376MFSha3.1

Align triokinase (EC 2.7.1.28); glycerone kinase (EC 2.7.1.29); FAD-AMP lyase (cyclizing) (EC 4.6.1.15) (characterized)
to candidate H281DRAFT_05885 H281DRAFT_05885 dihydroxyacetone kinase DhaK subunit

Query= BRENDA::Q3LXA3
         (575 letters)



>FitnessBrowser__Burk376:H281DRAFT_05885
          Length = 329

 Score =  228 bits (581), Expect = 3e-64
 Identities = 139/337 (41%), Positives = 198/337 (58%), Gaps = 15/337 (4%)

Query: 4   KKLVNSVAGCADDALAGLVACNPNLQLLQGHRVALRSDLDSLKGRVALLSGGGSGHEPAH 63
           KK +N V     ++LAG  A + +L +L    V +R   D   G+VAL+SGGGSGHEP H
Sbjct: 2   KKFINHVDDFLAESLAGFAAAHGDLVVLNREPVFVRRK-DLKPGKVALISGGGSGHEPLH 60

Query: 64  AGFIGKGMLTGVIAGAVFTSPAVGSILAAIRAVAQAGTVGTLLIVKNYTGDRLNFGLARE 123
           +GF+G GML     G +FTSP    ++AA +AV      G L IVKNY+GD +NF +A E
Sbjct: 61  SGFVGHGMLDAACPGQIFTSPTPDQMMAAAKAVDTG--AGVLFIVKNYSGDLMNFEMASE 118

Query: 124 QARAEGIPVEMVVIGDDSAF-TVLKKAGRRGLCGTVLIHKVAGALAEAGVGLEEIAKQVN 182
            +    +P  MV+I DD A        GRRG+ G V++ K+ G+LAE+G  L+E     N
Sbjct: 119 MSE---VPNAMVLINDDVAVENSSYTTGRRGVAGAVIVEKLVGSLAESGASLDECKAFGN 175

Query: 183 VVAKAMGTLGVSLSSCSVPGSKP-TFELSADEVELGLGIHGEAGVRRIKMATADEIVKLM 241
            + K   ++GV+ SSC+VP +   TF++  DE+E+G+GIHGE G RR K A+AD I   +
Sbjct: 176 RINKRTASMGVAFSSCTVPAAGTLTFKIGDDEIEVGVGIHGEPGRRRAKFASADTIAAEL 235

Query: 242 LDHMTNTTNASHVPVQPGSSVVMMVNNLGGLSFLELGIIADATVRSLEGRGVKIARALVG 301
           L     T     +    G+ V+++VN LGG    EL ++ ++T   LE R +KIAR  VG
Sbjct: 236 L-----TAIVDDLKPAAGAGVLVLVNGLGGTPLGELYLLFNSTRAWLEKRDLKIARVQVG 290

Query: 302 TFMSALEMPGISLTLLLVDEPLLKLIDA--ETTAAAW 336
           +  ++LEM G S+TL ++DE + K  D+   T A  W
Sbjct: 291 SLTTSLEMAGASITLCMLDEQMTKHWDSAVHTPALRW 327


Lambda     K      H
   0.315    0.130    0.365 

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: 432
Number of extensions: 21
Number of successful extensions: 5
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: 575
Length of database: 329
Length adjustment: 32
Effective length of query: 543
Effective length of database: 297
Effective search space:   161271
Effective search space used:   161271
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 (21.6 bits)
S2: 51 (24.3 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