GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pco in Desulfovibrio vulgaris Miyazaki F

Align decanoate oxidase (EC 1.3.3.6; EC 5.3.3.14) (characterized)
to candidate 8500002 DvMF_0766 2-nitropropane dioxygenase NPD (RefSeq)

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



>FitnessBrowser__Miya:8500002
          Length = 373

 Score =  262 bits (670), Expect = 1e-74
 Identities = 155/372 (41%), Positives = 214/372 (57%), Gaps = 36/372 (9%)

Query: 8   LKIGKHTIKFPIFQGGMGVGISWDELAGNVAKEGALGVISAVGTGYYKNMRFVERIVAKK 67
           L IG    + PI QGGMGVGIS   LA  VA EG +GVI+A   G        E  VAK 
Sbjct: 6   LNIGDLVARIPIVQGGMGVGISLSRLASAVANEGGIGVIAAAMIG------MKEPDVAKN 59

Query: 68  PFEALNFYSKKALNEIFANARKICGNNPLGANILYAINDYGRVLRDSCEAGANIIITGAG 127
           P EA    + +AL      AR++     +G NI+ A+  +G ++R S E  A+II +GAG
Sbjct: 60  PIEA----NVRALRRELQKAREMT-QGIVGVNIMVALTTFGEMVRTSIEERADIIFSGAG 114

Query: 128 LPTNMPEFAKDFSD-------VALIPIISSAKALKILCKRWSDRYKRIPDAFIVEGPLSG 180
           LP ++P   ++  D         L+PI+SSA+A  ++ K+W  R+  +PDAF+VEGP +G
Sbjct: 115 LPLDLPRHLREACDQKKEEFRTKLVPIVSSARAASVIAKKWITRFDYVPDAFVVEGPKAG 174

Query: 181 GHQGFKYEDCFKEEFRLENLVPKVVEASKEWGN-----IPIIAAGGIWDRKDIDTMLSLG 235
           GH GFK E+       LE ++P+VVEA K + +     IP+IAAGG++  +DI   + LG
Sbjct: 175 GHLGFKAEEIDDPNHSLEAVIPQVVEAVKPFEDQKGCRIPVIAAGGVYTGEDITRFMELG 234

Query: 236 ASGVQMATRFLGTKECDA-----KVYADLLPTLKKEDILLIKSPVGYPARAINTGVIKRI 290
           A+GVQM TRF+ T ECDA     + Y D      ++D+ +IKSPVG P RAI    I  +
Sbjct: 235 AAGVQMGTRFVATHECDADDRFKQAYVD----ATEQDVTIIKSPVGMPGRAIGNSFIDSM 290

Query: 291 EEGNAPKIACVSNCVAPCNRGEEAKKVGYCIADGLGRSYLGNREEGLYFTGANGYRVDKI 350
            EG      CV  C++ C    E ++  YCIA  L  +  GN E+G  F+GAN +RVD+I
Sbjct: 291 REGAKKPFKCVFKCISTC----EQEQTPYCIAAALINAMKGNLEKGFAFSGANVFRVDRI 346

Query: 351 ISVHELIKELTE 362
            SVHEL+  L +
Sbjct: 347 QSVHELVSSLQQ 358


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: 383
Number of extensions: 26
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: 373
Length adjustment: 30
Effective length of query: 333
Effective length of database: 343
Effective search space:   114219
Effective search space used:   114219
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 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