GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Flavobacterium beibuense F44-8

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_084596050.1 Q763_RS09610 hypothetical protein

Query= BRENDA::I7A144
         (352 letters)



>NCBI__GCF_000769915.1:WP_084596050.1
          Length = 479

 Score =  159 bits (402), Expect = 1e-43
 Identities = 109/347 (31%), Positives = 164/347 (47%), Gaps = 44/347 (12%)

Query: 21  LRVEEVVGGLEVPWALAFLPDGGMLIAERPGRIRLFREGRLSTYAELP-VYHRGESGLLG 79
           +RV+ +  G+ VPW +AFLPD  +L+  R G++   +  + +    +P V   G+ GLL 
Sbjct: 136 VRVDTIATGIAVPWGIAFLPDNELLVTNRDGQLYRVKNRKNTKVNGVPEVVAEGQGGLLD 195

Query: 80  LALHPRFPEAPYVY-AY--------RTVAEGGLRNQVVRLRHLGERGVLDRVVLDGIPAR 130
           + LHP +     +Y +Y        R +A   +   ++    L ++    +++ +  P  
Sbjct: 196 VILHPDYANNHRIYFSYSKGKKVNGRKLATTAVMTAILEGNSLKQQ----KIIFEANPYA 251

Query: 131 PHGLHSGGRIAFGPDGMLYVTTGEV-YERELAQDLASLG-GKILRLTPEGEPAPGNPFLG 188
               H G R+ F   G L+++ GE   E    Q L     GKI R+  +G     NPF  
Sbjct: 252 STRHHYGSRLVFDDKGYLFISVGERGNENGNPQTLGDNQLGKIHRIKDDGSIPAHNPFKD 311

Query: 189 RRGARPEVYSLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEVNLIVPGGNYGWPRV 248
           + G    +Y  G+RNPQ LA +P T EL+ +EHGP      G DE+N+I PG NYGWP V
Sbjct: 312 KNGKPTSLYCYGNRNPQSLAINPFTKELWETEHGPR-----GGDEINIITPGTNYGWPLV 366

Query: 249 -----------VGRGNDPRYRDPLYFWPQGFPPGNLAFFRGDLY--------VAGLRGQA 289
                        +   P  +DPL++W     P  +AF   D+Y        V  LR + 
Sbjct: 367 SYGINYNGEVITDKTEAPGIQDPLHYWIPSIAPSGMAFVTSDVYKPWKGALLVGSLRFKY 426

Query: 290 LLRLVLEGERGRWRVLRVETALSGFGRLREVQVGPDGALYVTTSNRD 336
           L    L+G     +V   E  L   GRLR+V+ GPDG +YV   + D
Sbjct: 427 LNLCYLDGA----KVTHEEKLLKNIGRLRDVRQGPDGYIYVAVEDTD 469


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: 488
Number of extensions: 27
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: 479
Length adjustment: 31
Effective length of query: 321
Effective length of database: 448
Effective search space:   143808
Effective search space used:   143808
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: 50 (23.9 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