GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ARO8 in Dyella japonica UNC79MFTsu3.2

Align Aromatic-amino-acid aminotransferase (EC 2.6.1.57) (characterized)
to candidate N515DRAFT_3488 N515DRAFT_3488 aromatic-amino-acid transaminase

Query= reanno::Cup4G11:RR42_RS33490
         (400 letters)



>FitnessBrowser__Dyella79:N515DRAFT_3488
          Length = 400

 Score =  388 bits (997), Expect = e-112
 Identities = 199/395 (50%), Positives = 262/395 (66%), Gaps = 2/395 (0%)

Query: 2   FEHIDAYPGDPILSLNESFQLDPRTDKVNLSIGIYFDDEGRLPVMQAVREAEAALMADMG 61
           F  ++  PGDPIL L E++  D R  KVNL +GIY+D++GR+P+++AV E E  L  +  
Sbjct: 4   FASVEMTPGDPILGLTEAYLADARPGKVNLGVGIYYDEQGRIPLLRAVHEVEQRLAQEAK 63

Query: 62  PRPYLPMAGFAAYRDAVQALVFGQPCQARAEGRIATVQTLGGSGALRVGADFLKRYFPDA 121
           PR YLP+ G  AY    Q LVFG      A GR+AT QT+GGSGALRVGAD LK+  P A
Sbjct: 64  PRGYLPIDGLPAYTQGTQKLVFGAESPLLAAGRVATSQTIGGSGALRVGADVLKKALPKA 123

Query: 122 QVWISDPSWENHRVIFERTGFTVNTYPYYDDATGGLKFDAMLDALRLIPKRSIVLLHACC 181
           ++ IS+PSWENHRV+F   GF V  Y YYD  T GL F  ML  L  +   ++VLLHACC
Sbjct: 124 KIAISNPSWENHRVVFIAAGFEVVEYTYYDPQTHGLDFAGMLADLGKLEPGTVVLLHACC 183

Query: 182 HNPTGVDLNHDQWRQLITLLKQHELLPFVDMAYQGFGAGLDDDAFAVRELVAQGVPC-LV 240
           HNPTGVDLN  QW+Q++ ++K+ +LLPF+DMAYQGF  G+D DA AVR   A G+   +V
Sbjct: 184 HNPTGVDLNAAQWQQVVEVVKERQLLPFIDMAYQGFDQGIDADATAVRLFAASGIESFVV 243

Query: 241 ANSFSKNFSLYGERCGGLSVVCDSAEETGRVLGQLTGAVRANYSNPPTHGARVVARVLTT 300
            +S++K+FSLYGER G L+ V    +E  RV   +   +R+ YS+P THG  +VA VL +
Sbjct: 244 TSSYAKSFSLYGERAGALTFVAADRDEALRVQSLVKRTIRSIYSSPSTHGGALVAGVLNS 303

Query: 301 PALRTIWERELAGKCERIAKMRAAIHKGLAAHVSGEALSRYLTQRGMFTYTGLTADQVDR 360
           P LR +WE+EL    ERI  MRA + + LAAH      +    Q GMF+Y+GL+  QVDR
Sbjct: 304 PELRAMWEQELGEMRERIHAMRAGMVEKLAAH-GAPQFAFIQQQAGMFSYSGLSKAQVDR 362

Query: 361 LRTEHGVYLLRSGRMCVAGLNERNVTQVAQAIASV 395
           LR E+ +Y + +GR+CVA LN  N+  VA A+A+V
Sbjct: 363 LRDEYAIYAIGTGRICVAALNRSNLDTVAAAVAAV 397


Lambda     K      H
   0.323    0.137    0.417 

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: 422
Number of extensions: 20
Number of successful extensions: 3
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: 400
Length of database: 400
Length adjustment: 31
Effective length of query: 369
Effective length of database: 369
Effective search space:   136161
Effective search space used:   136161
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 (21.9 bits)
S2: 50 (23.9 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