GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Stenotrophomonas chelatiphaga DSM 21508

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_057508775.1 ABB28_RS11575 PQQ-dependent sugar dehydrogenase

Query= BRENDA::I7A144
         (352 letters)



>NCBI__GCF_001431535.1:WP_057508775.1
          Length = 540

 Score =  202 bits (514), Expect = 2e-56
 Identities = 130/346 (37%), Positives = 189/346 (54%), Gaps = 43/346 (12%)

Query: 23  VEEVVGGLEVPWALAFLPDGGMLIAERPGRIRLFREGRLSTYAEL----PVYHRG-ESGL 77
           +  V  GL  PW+ AFLPDG +L+ E  GR+        S+   L    P++ +G  +GL
Sbjct: 197 IHTVATGLNRPWSAAFLPDGRVLVTEMGGRLLAIGPDGASSEISLDGLRPIFQQGGTTGL 256

Query: 78  LGLALHPRFPEAPYVY---AYRTVAEGGLRNQVVRLRHLGERGVLDRVVLDGIPARPHGL 134
           + +AL PRF +  ++Y    Y   +  G+R  ++R+R  G++    RV+ +  P    G 
Sbjct: 257 MDIALDPRFAQNGWMYLTMGYGEASANGVR--LLRVRLAGDQIEDVRVLFNSTPKASAG- 313

Query: 135 HSGGRIAFGPDGMLYVTTGE-VYERELAQDLASLGGKILRLTPEGEPAPGNPFLGRRGAR 193
           ++GGRIAF PD  L ++ G+    RE AQ+ A+  G ++R+  EG P   NPF+GR G  
Sbjct: 314 NNGGRIAFLPDDSLVLSLGDGSRRREEAQNPANALGTVIRIDREGRPPADNPFVGRAGMA 373

Query: 194 PEVYSLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEVNLIVPGGNYGWPRVVGRGN 253
           PE+YSLGHRNPQG+A  P  G+L  +EHGP      G DE+NLI+PGGNYGWP V G G 
Sbjct: 374 PEIYSLGHRNPQGIAVDPANGDLLLTEHGPR-----GGDEINLILPGGNYGWPIVTG-GM 427

Query: 254 D------------PRYRDPLYFWPQGFPPGNLAFF--------RGDLYVAGLRGQALLRL 293
           D            P Y+D L  W     P  LA +        RGDL V  L+ +A+ R+
Sbjct: 428 DYPFARVSPFRSLPGYQDALLEWTPSIAPAGLAIYNGALFPQWRGDLLVPALKERAVRRV 487

Query: 294 VLEGERGRWRVLRVETALSGFG-RLREVQVGPDGALYVTTSNRDGR 338
           + +G     R++  +  L     R+R+V+V PDG++YV T   + +
Sbjct: 488 IRDGR----RIVGQQLLLGELNERIRDVKVAPDGSVYVLTDGTNAK 529


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: 657
Number of extensions: 44
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: 352
Length of database: 540
Length adjustment: 32
Effective length of query: 320
Effective length of database: 508
Effective search space:   162560
Effective search space used:   162560
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