GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdh in Rhodococcus qingshengii djl-6-2

Align glucose 1-dehydrogenase (PQQ, quinone) (EC 1.1.5.2) (characterized)
to candidate WP_050654949.1 C1M55_RS29555 glucose dehydrogenase

Query= BRENDA::Q8ZUN8
         (371 letters)



>NCBI__GCF_002893965.1:WP_050654949.1
          Length = 361

 Score =  221 bits (564), Expect = 2e-62
 Identities = 140/330 (42%), Positives = 182/330 (55%), Gaps = 28/330 (8%)

Query: 41  VASDLEVPWSIAPLGGGRYLVTERPGRLVLISPSG---KKLVASFDVANVGEAGLLGLAL 97
           VA  L+ PWSIA   G   LV+ER    +L   +G   +++     V+  GE GLLG+A+
Sbjct: 52  VADGLDAPWSIA-FHGDTPLVSERDSARILELDAGGNSREVGVVDGVSPRGEGGLLGIAV 110

Query: 98  HPEFPKKSWVYLYASYFAEGGHIRNRVIRGRLDGST--FKLKEVKTLIDGIPGAYIHNGG 155
                      LYA + A G    NR+ R  + G+   F L   +T++DG+  A  HNGG
Sbjct: 111 REN-------RLYAYFTANG---ENRIERFDIIGAPGEFALGPAETILDGLASANYHNGG 160

Query: 156 RIRFGPDGMLYITTGDAADPRLAQDLSSLAGKILRVDEEGRPPADNPFPNSPIWSYGHRN 215
           RI FGPDGMLY+T GDA     AQDL S++GKILR+  +G  P DNPFPNS ++SYGHRN
Sbjct: 161 RIAFGPDGMLYVTVGDAGSRVRAQDLDSMSGKILRMTPDGDVPLDNPFPNSFVYSYGHRN 220

Query: 216 PQGIDWHRASGVMVATEHGPVGHDEVNIILKGGNYGWPLATGKAGRGEFVDPVIDTGSET 275
            QGI W    G M A+E G    DE+N I  GGNYGWP   G  G   F+DP+     + 
Sbjct: 221 SQGIAW-TEDGTMYASEFGQDTWDELNKIEAGGNYGWPEVEGIVGEDGFIDPLQQWSPDD 279

Query: 276 WAPSGASFVHGDMFPGLRGWLLIACLRGSMLAAVNFGDNMEVRKISTFFKNVFGRLRDVV 335
            +PSG +   G ++        IA LRG  L  V   D          F + +GRLRDVV
Sbjct: 280 ASPSGIAIHDGTIY--------IANLRGERLRTVPLTDPATA---DEQFVDEYGRLRDVV 328

Query: 336 IDDDGGILISTSNRDGRGSLRAGDDKILKI 365
           +  DG + I T+N DGRG    GDD+IL++
Sbjct: 329 VAPDGSLWILTNNTDGRGDPNPGDDRILRV 358


Lambda     K      H
   0.320    0.140    0.432 

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: 506
Number of extensions: 31
Number of successful extensions: 4
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: 371
Length of database: 361
Length adjustment: 30
Effective length of query: 341
Effective length of database: 331
Effective search space:   112871
Effective search space used:   112871
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 (21.7 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