GapMind for catabolism of small carbon sources

 

Alignments for a candidate for antA in Pseudomonas fluorescens FW300-N2E2

Align Anthranilate 1,2-dioxygenase (deaminating, decarboxylating) (EC 1.14.12.1) (characterized)
to candidate Pf6N2E2_1863 putative dioxygenase hydroxylase component

Query= reanno::pseudo13_GW456_L13:PfGW456L13_2740
         (461 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1863
          Length = 419

 Score =  195 bits (496), Expect = 2e-54
 Identities = 132/396 (33%), Positives = 193/396 (48%), Gaps = 49/396 (12%)

Query: 28  RVARDMFTEPELFDLEMELIFEKNWIYACHESEIANPNDFLTMRAGRQPMIITRDGNNQL 87
           RV   ++T+ ELF LE+E I+ + W+Y  H SE+   NDF+    G QP+I+TRDG  Q+
Sbjct: 18  RVHGSVYTDEELFQLELERIWYRTWVYVGHVSEVPKLNDFVVKSIGPQPVIMTRDGEGQI 77

Query: 88  HALINACQHRGATLTRVSKGNQSTFTCPFHAWCYKSDGRLVKVKAPGEYPEGFDKATRGL 147
           H L+N C HRG  +     GN+ +FTCP+H W + + G L        Y EG D++T GL
Sbjct: 78  HLLLNRCPHRGNQVCLEHAGNRRSFTCPYHGWTFSNTGTLRGYPFAAGY-EGTDRSTLGL 136

Query: 148 -KKARIESYKGFVFISLDVNGSDSLEDYLGDAKVFFDMMVAQSPTGELEILPGKSTYSYD 206
            K ARI  Y+GFVF S+ V G  +LE++LG A+   D +V  SP GE+EI  G   +   
Sbjct: 137 GKVARIGIYQGFVFGSMAVEG-PTLEEHLGAARGALDALVVTSPEGEVEITAGFLQHKAK 195

Query: 207 GNWKLQHENGLDGYHVSTVHYNYVSTVQHRQQVNAANGGVSD------TLDYSKLGAGDA 260
            NWK   EN  DGYH   VH +           + A+ G+ D      T     +G G  
Sbjct: 196 SNWKFIVENETDGYHPQFVHASI---------FDVASSGIGDLYSADSTAVARDMGGGHT 246

Query: 261 ETD-----------DGWFSFKNGHSLLFSDMPNPTVRAGYATVMPRLIEEYGQQQA-EWM 308
           E D            GWF                T  A     + ++ E YG ++A E M
Sbjct: 247 EIDLRPEFRRIGQPMGWFG---------------TTEARLPEYVSKMREAYGTERANEIM 291

Query: 309 MHRLRNLNIYPSLFFMDQISSQLRIVRPVAWNKTEITSQCIGVKGESDADRENRIRQFED 368
           +    ++ I+P+LF  +    Q+ +++P+A ++T      +  KG  D +R  R +Q   
Sbjct: 292 IDGTPHIMIFPNLFIAE---IQIFVIQPLAVDETVQHVTALQFKGAPDLNRRLR-QQTMG 347

Query: 369 FFNVSGMGTPDDLVEFREAQRGFQARLERWNEVSRG 404
               +G    DD   +   QRG ++R   WN + RG
Sbjct: 348 SVGPAGFLLADDSEMYERTQRGVRSRNPEWNYLGRG 383


Lambda     K      H
   0.318    0.135    0.415 

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: 526
Number of extensions: 20
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: 461
Length of database: 419
Length adjustment: 32
Effective length of query: 429
Effective length of database: 387
Effective search space:   166023
Effective search space used:   166023
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: 51 (24.3 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