GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucO in Paraburkholderia bryophila 376MFSha3.1

Align NADH-dependent aldehyde reductase (EC 1.1.1.77; EC 1.1.1.244; EC 1.1.1.1) (characterized)
to candidate H281DRAFT_02547 H281DRAFT_02547 Nucleoside-diphosphate-sugar epimerase

Query= metacyc::G3O-32155-MONOMER
         (298 letters)



>FitnessBrowser__Burk376:H281DRAFT_02547
          Length = 297

 Score =  238 bits (606), Expect = 2e-67
 Identities = 127/296 (42%), Positives = 177/296 (59%), Gaps = 4/296 (1%)

Query: 1   MKVFITGASGFIGSAVLSELISSGHEVVGLARSDEAAAKIKSIDPAAKILRGDLKDLEIL 60
           M++ +TGASG+IGSA ++ELI +GH V+GLAR+DEAAAKI ++   A+++RG L +L+ L
Sbjct: 1   MRILVTGASGWIGSASVTELIDAGHHVLGLARNDEAAAKIAAL--GAEVVRGSLDNLDSL 58

Query: 61  KKGATESDGVIHLGFVHDFKNFEQCCEIDRQATVAMLESLKGSNKPFLYTNGTLSLRPNK 120
           +  AT ++GV+HLG+ HDF       + DR A     + L G+  P L  +GTL L   +
Sbjct: 59  RVAATMAEGVVHLGYNHDFSQMAAAAQTDRAAIETFADVLTGTGGPLLIASGTLGLATGR 118

Query: 121 VANEQDGIDEDSKILRAVTEQVALSYKDKGVSARIVRLPFSVHGKG-DKAFVPILMNIAK 179
           V  E D    D    R       L  +++G+ + +VR   +VHG G D  FV +L  IA+
Sbjct: 119 VGIESDTPAPDGHP-RLANAAYVLGLRERGIRSMVVRFAPTVHGAGGDHGFVAVLARIAR 177

Query: 180 AAGKSGYVGQGTNAWAAVHRLDTAPLFRLVLEKGKTGQVYHCVGEQGIPFKDIARVIGEI 239
            +G S Y+G G N W AV+RLD   L RL ++K   G   H V E+G+  ++IA  +G  
Sbjct: 178 QSGASAYIGDGQNRWPAVNRLDAGKLVRLAVDKAPAGSALHAVAEEGVATREIAGALGRF 237

Query: 240 LNVPVASIPVDDAESHFGFLTCFVTRDGPVSSEGTRKELGWQPQQIGLLEDIRANY 295
           LNVPV SIP D A+S F +L+ F   D P SS  TR  LGW+P    LLEDI A +
Sbjct: 238 LNVPVESIPADQAQSRFDWLSMFFGADIPASSAHTRSLLGWEPVHPTLLEDIAAGH 293


Lambda     K      H
   0.318    0.136    0.393 

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: 256
Number of extensions: 10
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: 298
Length of database: 297
Length adjustment: 26
Effective length of query: 272
Effective length of database: 271
Effective search space:    73712
Effective search space used:    73712
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.

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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