GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pco in Paraburkholderia phymatum STM815

Align decanoate oxidase (EC 1.3.3.6; EC 5.3.3.14) (characterized)
to candidate WP_012400680.1 BPHY_RS06510 nitronate monooxygenase

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



>NCBI__GCF_000020045.1:WP_012400680.1
          Length = 396

 Score =  164 bits (415), Expect = 4e-45
 Identities = 122/372 (32%), Positives = 194/372 (52%), Gaps = 35/372 (9%)

Query: 18  PIFQGGMGVGISWDELAGNVAKEGALGVISAVGTGYYKNMRFVERIVAKKPFEALNFYSK 77
           PI QGGMGVG+S   LAG+VA+EGALG I+++   ++ +   +ER  A      L   ++
Sbjct: 19  PIVQGGMGVGVSAHRLAGSVAREGALGTIASIDLRHHHD-DLLERCRATPDRATLEDANR 77

Query: 78  KALNEIFANARKIC-GNNPLGANILYAINDYGRVLRDSCEAGANIIITGAGLPTNMPEFA 136
            AL      AR +  G   +  N++ A+N +   +R +CE GA+ I+ GAGLP ++P+  
Sbjct: 78  AALVREIRAARNLSEGRGMIAVNVMKAVNAHADYVRIACEEGADAIVMGAGLPLDLPDLT 137

Query: 137 KDFSDVALIPIISSAKALKILCKRWSDRYKRIPDAFIVEGPL-SGGHQGF-KYEDCFKEE 194
           +   D+AL+PI+S ++ + ++ K+W  +  R+PDA ++E P  +GGH G    +D     
Sbjct: 138 QG-HDIALVPILSDSRGVGVVLKKWMKK-GRLPDAIVIEHPAHAGGHLGVTNLDDMHDTR 195

Query: 195 FRLENLVPKV------VEASKEWGNIPIIAAGGIWDRKDIDTMLSLGASGVQMATRFLGT 248
           F    ++ +V      ++ S+    +P+I AGGI   + + T L  GA+GVQ+ T F  T
Sbjct: 196 FDFARVLKEVDQLFTSLQISRT--QVPLILAGGINSHEAVRTCLEAGANGVQIGTPFAVT 253

Query: 249 KECDA-----KVYADLLPTLKKEDILLIKSPVGYPARAINTGVIKRI--------EEGNA 295
           +E DA     +V AD  P    +DI+   S  G PARA+ T  + R          +  A
Sbjct: 254 EEGDAHPRFKRVLADATP----DDIVEFVSVTGLPARAVKTPWLDRYLRNETRIRTKVGA 309

Query: 296 PKIACVS--NCVAPCNRGEEAKKVG-YCIADGLGRSYLGNREEGLYFTGANGYRVDKII- 351
            K AC +   C++ C   +  +K G +CI   L  +  G+   GL+F G         I 
Sbjct: 310 LKRACPTALECLSACGLRDGIEKFGHFCIDTRLAAALRGDVNNGLFFRGREALPFGNAIR 369

Query: 352 SVHELIKELTEG 363
           SV +L++ L  G
Sbjct: 370 SVRDLLELLLTG 381


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: 353
Number of extensions: 19
Number of successful extensions: 6
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: 396
Length adjustment: 30
Effective length of query: 333
Effective length of database: 366
Effective search space:   121878
Effective search space used:   121878
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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