GapMind for catabolism of small carbon sources

 

Alignments for a candidate for puuB in Halomonas desiderata SP1

Align Gamma-glutamylputrescine oxidoreductase; Gamma-Glu-Put oxidase; Gamma-glutamylputrescine oxidase; EC 1.4.3.- (characterized)
to candidate WP_086509629.1 BZY95_RS09110 FAD-binding oxidoreductase

Query= SwissProt::P37906
         (426 letters)



>NCBI__GCF_002151265.1:WP_086509629.1
          Length = 426

 Score =  137 bits (345), Expect = 6e-37
 Identities = 108/357 (30%), Positives = 170/357 (47%), Gaps = 6/357 (1%)

Query: 29  DVCVVGGGYTGLSSALHLAEAGFDVVVLEASRIGFGASGRNGGQLVNSYSRDIDVIEKSY 88
           DV V+GGG TG+++ALHLAEAG DV ++EA  +  GASGRN G +        D I +  
Sbjct: 28  DVLVIGGGITGINTALHLAEAGVDVTLIEAGDVPSGASGRNVGLVNAGMWIPPDDIREVL 87

Query: 89  GMDTARMLGSMMFEGGEIIRERIKRYQIDCD-YRPGGLFVAMNDKQLATLEEQKENWERY 147
           G +      +++ +   ++   I+R+ I C   R G L +A N +    L  + E  +R 
Sbjct: 88  GEEIGERANTILGDAPAVVFSLIERHGIACQATRTGTLHLAHNGRGEQELARRAEQLQRR 147

Query: 148 GNKQLELLDANAIRREVASDRYTGALLDHSGGHIHPLNLAIGEADAIRLNGGRVYELSAV 207
           G   +ELL+A A +  + + R   ALLDH  G ++P     G A A +  G R++  SA 
Sbjct: 148 G-APVELLEAAACQERLGTRRIHRALLDHRAGTLNPSAYTRGLARAAKAAGARLHTHSAA 206

Query: 208 TQIQHTTPA-VVRTAKGQVTAKYVIVAGNAYLGDKVEPELAKRSMPCGTQVITTERLSED 266
           T +        V TA G V A+ +++A NAY  D+   E+ +         + +  LS +
Sbjct: 207 TGVARAGDGWRVTTAHGSVQAQRLVLATNAYTEDRWN-EVRRHFFVGHFYQVASRPLSGE 265

Query: 267 LARSLIPKNYCVEDCNYLLDYYRLTADNRLLYGGGVVYGARDPDDVERLVVPKLLK-TFP 325
            A  ++P +    D   +L   R  A+ RL+  G +  G   P    R    ++ +  FP
Sbjct: 266 AADEILPGHQGAWDTRMVLSSIRRDAEGRLIL-GSLGKGEGKPAAFLRCWANRIQRHYFP 324

Query: 326 QLKGVKIDYRWTGNFLLTLSRMPQFGRLDTNIYYMQGYSGHGVTCTHLAGRLIAELL 382
           QL  V+ +  WTG    T     +   L   +  + GY+G G+T   + G+  A  L
Sbjct: 325 QLGSVEWECSWTGRIGFTPDHTLRLFELAPGVLGVSGYNGRGITTGTVVGKGFARYL 381


Lambda     K      H
   0.320    0.138    0.411 

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: 421
Number of extensions: 22
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: 426
Length of database: 426
Length adjustment: 32
Effective length of query: 394
Effective length of database: 394
Effective search space:   155236
Effective search space used:   155236
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 (21.8 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Sep 24 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