GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pco in Geotalea uraniireducens Rf4

Align decanoate oxidase (EC 1.3.3.6; EC 5.3.3.14) (characterized)
to candidate WP_041245487.1 GURA_RS15315 nitronate monooxygenase family protein

Query= metacyc::HP0773-MONOMER
         (363 letters)



>NCBI__GCF_000016745.1:WP_041245487.1
          Length = 362

 Score =  230 bits (587), Expect = 4e-65
 Identities = 136/363 (37%), Positives = 202/363 (55%), Gaps = 23/363 (6%)

Query: 6   KPLKIGKHTIKFPIFQGGMGVGISWDELAGNVAKEGALGVISAVGTG----YYKNMRFVE 61
           KPLKIGK+ +K+P+ QGGMGV IS   LAG+VAK G +G+++A G      +Y    +++
Sbjct: 3   KPLKIGKYEVKYPLIQGGMGVRISAGSLAGHVAKCGGVGLVAAPGIALNSEFYDGTNYMQ 62

Query: 62  RIVAKKPFEALNFYSKKALNEIFANARKICGNNPLGANILYAINDYGRVLRDSCEAGANI 121
              A    E    Y+             I  +  +G N++ A++D+ ++++ + E GA +
Sbjct: 63  ADAAAFKAELQKAYA-------------IAPDGVIGVNVMVALSDFEQLVQAAIEGGAKV 109

Query: 122 IITGAGLPTNMPEFAKDFSDVALIPIISSAKALKILCKRWSDRYKRIPDAFIVEGP-LSG 180
           ++ GAGLP  +P       DVAL+PI+SS +A +++ K+W   Y R+PDA +VE P  +G
Sbjct: 110 VVCGAGLPMTLPGLTAHAPDVALVPIVSSVRAAQLIAKKWDKGYNRLPDAVVVEDPDTAG 169

Query: 181 GHQGFKYEDCFKEEFRLENLVPKVVE-ASKEWG-NIPIIAAGGIWDRKDIDTMLSLGASG 238
           GH G K E+    ++     V  V E    E+G ++P+IAAGGIWDR D+   L  GA G
Sbjct: 170 GHLGEKMENIGTGDYDQYATVRGVKEFFLAEYGIDMPVIAAGGIWDRADLLHALEQGADG 229

Query: 239 VQMATRFLGTKECDA-KVYADLLPTLKKEDILLIKSPVGYPARAINTGVIKRIEEGNAPK 297
           VQMA+RF+ T ECDA   +       KKEDI LI SP G P RAI T     +       
Sbjct: 230 VQMASRFVPTVECDADDAFKQAYLKCKKEDIGLIMSPAGLPGRAILTNQEDIVLYDQVRS 289

Query: 298 IACVSNCVAPCNRGEEAKKVGYCIADGLGRSYLGNREEGLYFTGANGYRVDKIISVHELI 357
             C + C+  C+  E  ++  +CI   L R+  G+ + GL F G N ++ D+I +V E+ 
Sbjct: 290 SVCTTGCLKKCSFKESGER--FCIVKALDRAQRGDVDTGLIFCGTNAWKADRIGTVQEIF 347

Query: 358 KEL 360
            EL
Sbjct: 348 DEL 350


Lambda     K      H
   0.319    0.139    0.418 

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: 366
Number of extensions: 17
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: 363
Length of database: 362
Length adjustment: 29
Effective length of query: 334
Effective length of database: 333
Effective search space:   111222
Effective search space used:   111222
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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