GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Phyllobacterium brassicacearum STM 196

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_106710418.1 CU102_RS07270 PQQ-dependent sugar dehydrogenase

Query= BRENDA::I7A144
         (352 letters)



>NCBI__GCF_003010955.1:WP_106710418.1
          Length = 382

 Score =  190 bits (482), Expect = 6e-53
 Identities = 124/342 (36%), Positives = 174/342 (50%), Gaps = 37/342 (10%)

Query: 24  EEVVGGLEVPWALAFLPDGGMLIAERPGRIRLFREGRLST-YAELP-VYHRGESGLLGLA 81
           E V G L  PW+LAFLPDG +L+ ER G +R+   G++S   A +P V   G+ GLL +A
Sbjct: 39  ETVAGSLNHPWSLAFLPDGALLVTERVGNMRIITNGKVSEPIANVPKVAVMGQGGLLDVA 98

Query: 82  LHPRFPEAPYVY-AYRTVAEGGLRNQVVRLRHLGERG---VLDRVVLDGIPARPH-GLHS 136
           L P FP +  +Y  Y    +GG    +   + + ++    + D  VL  +  +   G H 
Sbjct: 99  LAPDFPTSGGIYFTYSQPGKGGAGTALASAKLVRDQNGAALEDVSVLVSMNRKSRRGQHF 158

Query: 137 GGRIAFGPDGMLYVTTGEVYERELAQDLASLGGKILRLTPEGEPAPGNPFLGRRGARPEV 196
           G RI   PDG L+VT GE  E+  AQD     G +LR+  +G     NPF   +   PE+
Sbjct: 159 GSRIVVAPDGKLFVTMGERGEQRRAQDFRDHAGSVLRINADGSIPADNPFADGKLGLPEL 218

Query: 197 YSLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEVNLIVPGGNYGWPRV-------- 248
           +S GHRNPQG  W P T  L++ EHG       G DEVN   PG NYGWP +        
Sbjct: 219 WSKGHRNPQGAFWDPVTQSLWTVEHG-----AMGGDEVNQPQPGKNYGWPVITYGKDYSG 273

Query: 249 --VGRGNDPR-YRDPLYFWPQGFPPGNLAFF--------RGDLYVAGLRGQALLRLVLEG 297
             +G+G   + Y  PLY+W     P   A +        +GDL V  L+ + L RL    
Sbjct: 274 AKIGKGTAAKGYEQPLYYWDPSIAPSGAAVYEGAMFPEWKGDLLVGSLKFELLSRL---- 329

Query: 298 ERGRWRVLRVETAL--SGFGRLREVQVGPDGALYVTTSNRDG 337
           +R    V+  E  +    FGR+R+V+V PDG++Y+ T   +G
Sbjct: 330 DRDEKGVITGEERIFDGEFGRIRDVRVAPDGSVYLLTDESNG 371


Lambda     K      H
   0.322    0.146    0.460 

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: 473
Number of extensions: 28
Number of successful extensions: 7
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: 352
Length of database: 382
Length adjustment: 30
Effective length of query: 322
Effective length of database: 352
Effective search space:   113344
Effective search space used:   113344
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: 49 (23.5 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