GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Cronobacter condimenti 1330

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_007664530.1 BN137_RS17380 PQQ-dependent sugar dehydrogenase

Query= BRENDA::I7A144
         (352 letters)



>NCBI__GCF_000319285.1:WP_007664530.1
          Length = 370

 Score =  178 bits (451), Expect = 2e-49
 Identities = 122/355 (34%), Positives = 179/355 (50%), Gaps = 55/355 (15%)

Query: 22  RVEEVVGGLEVPWALAFLP-DGGMLIAERPGRIRLFR--EGRLSTYAELP-VYHRGESGL 77
           +V+ +   L+ PW+L+FLP D G LI  + G ++ ++  +G  +  A +P V+H+G+ GL
Sbjct: 25  KVDVLADKLDHPWSLSFLPGDQGALITLKKGELKRWQPDKGLSAAIAGVPTVWHQGQGGL 84

Query: 78  LGLALHPRFPEAPYVY-----------AYRTVAEGGLRNQVVRLRHLGERGVLDRVVLDG 126
             + L P F E+  V+           A   V  G L + + RL +         VV   
Sbjct: 85  FDVVLAPDFNESRRVWLSYAEAGSDGKAGTAVGYGRLSDDLQRLENF-------TVVFRQ 137

Query: 127 IPARPHGLHSGGRIAFGPDGMLYVTTGEVYERELAQDLASLGGKILRLTPEGEPAPGNPF 186
            P    G H GGR+AF   G L++  GE  +R  AQDL  L GK++RLT +GE    NPF
Sbjct: 138 APKLSTGNHFGGRMAFDGKGHLFIALGENNQRPTAQDLDKLQGKVVRLTQDGEVPKDNPF 197

Query: 187 LGRRGARPEVYSLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEVNLIVPGGNYGWP 246
           +G+ G RPE++S G RNPQGLA +P +  ++ +EHGP      G DE+N+   G NYGWP
Sbjct: 198 VGKAGVRPEIWSYGIRNPQGLALNPWSQTIWLNEHGPK-----GGDEINIPQAGKNYGWP 252

Query: 247 RV-------------VGRGNDPRYRDPLYFWPQGFPPGNLAFFRGD--------LYVAGL 285
                             G  P    PL++W        +AF+  D        L++  L
Sbjct: 253 LATWGINYSGEPIPEAKGGEAPGTEQPLFYWKVSPAVSGMAFYNADKFPQWKNKLFIGAL 312

Query: 286 RGQALLRLVLEGER--GRWRVLRVETALSGFGRLREVQVGPDGALYVTTSNRDGR 338
           + Q L++L + G +     R+L  E       R+R+V+VGPDG LYV T   DG+
Sbjct: 313 KEQNLIQLSVNGNKVTEDGRLLARENQ-----RIRDVRVGPDGYLYVLTDESDGQ 362


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: 445
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: 370
Length adjustment: 29
Effective length of query: 323
Effective length of database: 341
Effective search space:   110143
Effective search space used:   110143
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