GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaM in Pseudomonas simiae WCS417

Align glycerone kinase (EC 2.7.1.29) (characterized)
to candidate GFF4500 PS417_23035 PTS mannose transporter subunit IIC

Query= BRENDA::P37349
         (472 letters)



>FitnessBrowser__WCS417:GFF4500
          Length = 838

 Score =  107 bits (267), Expect = 2e-27
 Identities = 106/348 (30%), Positives = 141/348 (40%), Gaps = 26/348 (7%)

Query: 134 QLGLPSSDTEISDTCPAYDEEAR----SLAVVIKNRNGLHVRPASRLVYTLSTFNADMLL 189
           + G P      S    A DEE      S  + + N NGLH RPA+        FNA + L
Sbjct: 142 ETGQPLLQLSPSGAVEAVDEEEGDALFSKPLTLPNANGLHARPAAVFAQAAKGFNASIYL 201

Query: 190 EKNGKCVTPESINQIALLQVRYNDTLRLIAKGPEAEEALIAFRQLAEDNFGETE-EVAPP 248
            K  +    +S+  I  LQ    DTL++ A G +AE A+ A   L  +  GE    VA P
Sbjct: 202 HKQTQSANAKSLVAIMALQTVQGDTLQVSAAGEDAEAAIKALVALLAEGCGEAVVNVAEP 261

Query: 249 T--------LRPVPPVSGKAFYYQPVLCTVQAKSTLTVEEEQDRLRQAIDFTLLDLMTLT 300
                    LR V    G AF        VQ      V  EQ     A +   L    L 
Sbjct: 262 VATQSSATLLRGVCASPGSAFGQ-----VVQVTDPELVITEQGT-GGATERAALTRGLLA 315

Query: 301 AKAEASGLDDIAA------IFSGHHTLLDDPELLAAASELLQHEHCTAEYAWQQVLKELS 354
           A      L D AA      IF  H  LL+DP LL  A  LL  E  +A +AW        
Sbjct: 316 ANEALQVLQDKAAGSAQAEIFRAHQELLEDPTLLEHAHRLLG-EGKSAAFAWNSATLATV 374

Query: 355 QQYQQLDDEYLQARYIDVDDLLHRTLVHLTQTKEELPQFNSPTILLAENIYPSTVLQLDP 414
             +Q L +  +  R  D+ D+  R L  +   ++         IL+AE + PS    LD 
Sbjct: 375 TLFQGLGNALIAERAADLADVGQRVLKLILGIQDSAWDLPERAILIAEQLTPSQTASLDT 434

Query: 415 AVVKGICLSAGSPVSHSALIARELGIGWICQQGEKLYAIQPEETLTLD 462
             V G    AG   SH A++AR LG+  IC    ++ A+   + + LD
Sbjct: 435 RKVLGFVTVAGGATSHVAILARALGLPAICGVPAQVLALANGKQVLLD 482


Lambda     K      H
   0.316    0.132    0.368 

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: 766
Number of extensions: 29
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: 472
Length of database: 838
Length adjustment: 38
Effective length of query: 434
Effective length of database: 800
Effective search space:   347200
Effective search space used:   347200
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 (21.6 bits)
S2: 54 (25.4 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