GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gntC in Pseudomonas stutzeri RCH2

Align TRAP-type periplasmic solute-binding protein (characterized, see rationale)
to candidate GFF362 Psest_0363 tripartite ATP-independent periplasmic transporter solute receptor, DctP family

Query= uniprot:Q930R1
         (334 letters)



>FitnessBrowser__psRCH2:GFF362
          Length = 323

 Score =  144 bits (364), Expect = 2e-39
 Identities = 99/314 (31%), Positives = 160/314 (50%), Gaps = 21/314 (6%)

Query: 2   RKLLLATTAIAFGLSAAAPAFAEFNDRNIRVSNGINEDHPVGNG-IKAMQAC---LDQKS 57
           RKLL+     AF +S  A A          ++  I E HP G   + AM+     L+  +
Sbjct: 5   RKLLVTALPFAFCISGLAHA----------MTLKIAEIHPAGYPTVVAMENLGKKLETAT 54

Query: 58  GGKLKLTAFWGGALGGDLQATQALRSGVQEAVVTSSSPLVGIIPALGVFDLPFLFANAQE 117
            G++K   F GG LG + +  +  + G  +    S   +  ++PA  VF++PF+F +   
Sbjct: 55  NGEIKSRMFAGGVLGSEKEVIEQTQIGAVQLTRVSLGSVGPVVPATNVFNMPFVFRDIDH 114

Query: 118 AYTVLDGDFGDMMNEKLEAA--GLVNLAYWENGFRNLSNSVRPVTKWEDFEGMKVRVMQN 175
              V+DG+ G  + + +  +   +V LA+ E G R+L    +P+ + ED +GMK+RV+ N
Sbjct: 115 MRKVVDGEIGQEILDAITNSDFNMVGLAWMEAGSRSLYTK-KPIRRIEDLKGMKIRVIGN 173

Query: 176 NIFLDTFQNLGANATPMAFGEVFSALETKAIDAQENPYVTIDTSKFFEVQKYVTETNHAY 235
            +F+DT   +GAN   M  GE+FSAL++  ID  EN   T+     F V K+ T+T+H  
Sbjct: 174 PLFIDTLNAMGANGIAMDTGEIFSALQSGVIDGAENNSPTLLEHNHFRVAKHYTQTHHLI 233

Query: 236 TPFLFLFSKPIFDSYTPEEQAALRECAVVGRDEERKVIQDLNKKSLEKIKEAGLEVNTLS 295
            P   L SK  ++  +PE+QA +++ A   + EER +       S EK+K  G+E   + 
Sbjct: 234 LPEPLLMSKDTWNKLSPEQQATVKKLAKEAQLEERDLWVAKETASNEKLKAEGVEFIEVD 293

Query: 296 A----EEQARIREK 305
                +  A +REK
Sbjct: 294 TKPFYDATAPVREK 307


Lambda     K      H
   0.317    0.133    0.374 

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: 254
Number of extensions: 13
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: 334
Length of database: 323
Length adjustment: 28
Effective length of query: 306
Effective length of database: 295
Effective search space:    90270
Effective search space used:    90270
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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 17 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