GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Halomonas desiderata SP1

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_086511877.1 BZY95_RS21205 PQQ-dependent sugar dehydrogenase

Query= BRENDA::I7A144
         (352 letters)



>NCBI__GCF_002151265.1:WP_086511877.1
          Length = 384

 Score =  183 bits (465), Expect = 6e-51
 Identities = 125/343 (36%), Positives = 178/343 (51%), Gaps = 37/343 (10%)

Query: 21  LRVEEVVGGLEVPWALAFLPDGGMLIAERPGRIRLFREGRLSTYAE-LP-VYHRGESGLL 78
           LR+E +  GLE PWA+A LPDG  L+ ERPGR+ L  E    T+ E +P V  +G+ GLL
Sbjct: 44  LRLERIAEGLENPWAVAMLPDGRFLVTERPGRLALIDEDGSITHLEGVPEVSAQGQGGLL 103

Query: 79  GLALHPRFPEAPYVYAYRTVA---EGGLRNQVVRLRHLGERGVLD-RVVLDGIPARPHGL 134
            + LHPR+ +  + + Y T +   +GG    + R R L +  + D   + +       G 
Sbjct: 104 DVTLHPRYGDGEHDWLYFTWSKPGDGGTATALSRAR-LSDDALSDVETLFEQDRFSGPGR 162

Query: 135 HSGGRIAFGPDGMLYVTTGEVYERELAQDLASLGGKILRLTPEGEPAPGNPFLGRRGARP 194
           H G R+A+ PD  L +T G+    E AQ      G +LRL  +G     NPF        
Sbjct: 163 HYGSRLAWLPDETLLMTIGDRGTPERAQAADDHAGSVLRLAADGSAPDDNPFADDDATLA 222

Query: 195 EVYSLGHRNPQGLAWHPKTGELFSSEHGPSGEQGYGHDEVNLIVPGGNYGWPRV------ 248
           E+Y+LG+RN QG+    + GE++++EHGP     +G DE+NLIV G NYGWP V      
Sbjct: 223 EIYTLGNRNIQGMV-VTEQGEIWATEHGP-----FGGDELNLIVAGENYGWPEVSQGRDY 276

Query: 249 -----VGRGNDPRYRDPLYFWPQGFPPGNLA--------FFRGDLYVAGLRGQALLRLVL 295
                +G  + P  +DP++ +   F P  LA         ++GDL   GLRG+ L RL +
Sbjct: 277 GTREPIGEDSLPGMQDPIHVFEAPFAPSGLAQVTSVTFGEWQGDLLAGGLRGERLYRLSI 336

Query: 296 EGERGRWRVLRVETALSG-FGRLREVQVGPDGALYVTTSNRDG 337
           EGE    ++   E  L G  GR+R V  G DGA+Y+      G
Sbjct: 337 EGE----QLADSEVVLDGHIGRIRGVHQGHDGAIYLVNDEAQG 375


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: 528
Number of extensions: 37
Number of successful extensions: 9
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: 384
Length adjustment: 30
Effective length of query: 322
Effective length of database: 354
Effective search space:   113988
Effective search space used:   113988
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