GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gntA in Pseudomonas benzenivorans DSM 8628

Align fusion of gluconokinase and the small permease component of the D-gluconate TRAP transporter (characterized)
to candidate WP_090448378.1 BLS63_RS24290 gluconokinase

Query= reanno::psRCH2:GFF2080
         (376 letters)



>NCBI__GCF_900100495.1:WP_090448378.1
          Length = 361

 Score =  469 bits (1207), Expect = e-137
 Identities = 246/361 (68%), Positives = 276/361 (76%), Gaps = 2/361 (0%)

Query: 18  MGVSGSGKTETSHAVADALGLPHIEADNFHPAENVARMRAGTPLSDADRMEWLHALIAEM 77
           MGVSGSGK++ S AVA  LG  HIEAD FHP ENV RMRAG PLSD DR  WL ALI EM
Sbjct: 1   MGVSGSGKSDISQAVARQLGWRHIEADQFHPRENVERMRAGIPLSDDDRSHWLDALIREM 60

Query: 78  QRTLAAGSGFVLACSALKRSYRELLRSAVPELRFAHLAIDYETAVQRVGGRAGHFMPISL 137
           Q   A+G GFVLACSALKRSYRE LR+AVP LRFAHL ID  TA+QRVG R GHFMP SL
Sbjct: 61  QAAEASGEGFVLACSALKRSYRERLRAAVPGLRFAHLDIDQATALQRVGARPGHFMPTSL 120

Query: 138 VDSQFATLESPEGEPGVLTVDASQPREGVLRQIVEWMQGSGLDELIETRVDLSSRPFDSA 197
           VDSQFATLE P GE GVL+VDA+Q R  V+ Q+  W+ G  L+  IE  VD S++ FDSA
Sbjct: 121 VDSQFATLEDPSGEYGVLSVDAAQSRAVVVAQVCAWVHGKSLEVEIEEAVDFSAQTFDSA 180

Query: 198 TT--APPLTNEPIYSGRVAQHFDRLTDWLMAALMAFMVIVVFSSVVLRYAFGTGWTGAEE 255
                  LT EPIY+G +A+ FDRLTD LMA LM FMV+VVF +VVLRYAF +GW GAEE
Sbjct: 181 NKEGGAHLTGEPIYTGALARLFDRLTDGLMAVLMGFMVLVVFGNVVLRYAFDSGWAGAEE 240

Query: 256 LSRLAFVWLVFVGVASSMRRGELMSFSMLRDRFPRLFRRVVDSLSWLLVAAASCLAAWGG 315
           LSRLAFVWLVF+GVASSMRRGELMSFS++RDRFP+  RR++DS SWLLVAAAS LA WG 
Sbjct: 241 LSRLAFVWLVFIGVASSMRRGELMSFSLVRDRFPQAVRRLIDSASWLLVAAASGLATWGA 300

Query: 316 WNQMQFGWTINSPVVGYPLGLAMLPVAASMVALAVLALLQLVNVWRRDQPSATAAANVTA 375
           W QMQFGW   S VVGY L LAMLPV A M  L +LAL+QL+NVWRR    A++ ANVT 
Sbjct: 301 WQQMQFGWGNISAVVGYSLALAMLPVLACMAVLVLLALVQLLNVWRRPYGLASSLANVTV 360

Query: 376 D 376
           D
Sbjct: 361 D 361


Lambda     K      H
   0.322    0.133    0.401 

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: 423
Number of extensions: 8
Number of successful extensions: 2
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: 376
Length of database: 361
Length adjustment: 30
Effective length of query: 346
Effective length of database: 331
Effective search space:   114526
Effective search space used:   114526
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 (22.0 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