GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Pseudomonas fluorescens FW300-N2C3

Align [amino group carrier protein]-gamma-(L-lysyl)-L-glutamate aminotransferase (EC 2.6.1.118) (characterized)
to candidate AO356_02850 AO356_02850 2,4-diaminobutyrate 4-aminotransferase

Query= BRENDA::Q93R93
         (395 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_02850
          Length = 470

 Score =  238 bits (607), Expect = 3e-67
 Identities = 159/408 (38%), Positives = 226/408 (55%), Gaps = 49/408 (12%)

Query: 29  LLIVRGQGARVWDAEGNEYIDCVGGYGVANLGHGNPEVVEAVKRQ-AETLMAMPQTLPTP 87
           L + R +G  V D EG  +IDC+ G G   LGH +P V++A+++  A+ L      L TP
Sbjct: 51  LALKRAKGLYVEDVEGRTFIDCLAGAGTLALGHNHPVVIDAIQQVLADELPLHTLDLTTP 110

Query: 88  MRGEFYRTLTAILPPELNRVFPVN----SGTEANEAALKFARAHTGRKKFVAAMRGFSGR 143
           ++  F + L  +LP EL     +     +GT+A EAALK  R  TGR   ++   G+ G 
Sbjct: 111 VKDRFVQDLFGLLPVELAAEAKIQFCGPTGTDAVEAALKLVRTATGRSTVLSFQGGYHGM 170

Query: 144 TMGSLSVTWEPKYREPFLPLVEP-VEFIPY----------NDVEALKRAV--------DE 184
           + G+LS+      ++P   L+   V+F+PY            VE +K  +        D 
Sbjct: 171 SQGALSLMGSLGPKKPLGALLSSGVQFMPYPYNYRCPFGLGGVEGVKANLHYLENLLNDP 230

Query: 185 ET-----AAVILEPVQGEGGVRPATPEFLRAAREITQEKGALLILDEIQTGMGRTGKRFA 239
           E      AAVI+E VQGEGGV PA  ++LR  R IT++ G  LI+DEIQ+G GRTGK FA
Sbjct: 231 EAGVQLPAAVIVEVVQGEGGVIPADLDWLRGLRRITEQAGVALIVDEIQSGFGRTGKMFA 290

Query: 240 FEHFGIVPDILTLAKALGGGVPLGVAVMREEVARSMPKGGHGTTFGGNPLAMAAGVAAIR 299
           FEH GI+PD++ L+KA+GG +PL V V R+ +   +P G H  TF GN +AMAAG A +R
Sbjct: 291 FEHAGIIPDVVVLSKAIGGSLPLAVVVYRDWLDTWLP-GAHAGTFRGNQMAMAAGSAVMR 349

Query: 300 YLERTRLWERAAELGPWFMEKLRAIPS--PKIREVRGMGLMVGLELKEKA---------- 347
           YL    L   AA +G    E L  +    P++ ++RG GLM+G+EL + A          
Sbjct: 350 YLREHDLPAHAAAMGERLSEHLHILQRDYPQLGDIRGRGLMLGVELVDPAGKPDAQGHPP 409

Query: 348 --APYIARLEKE--HRVLALQAGPT---VIRFLPPLVIEKEDLERVVE 388
             A    RL++E   R L L+ G     V+RFLPPL+I + +++RV E
Sbjct: 410 VHAQLAPRLQRECLKRGLILELGGRQGGVVRFLPPLIITRAEIDRVAE 457


Lambda     K      H
   0.319    0.137    0.403 

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: 507
Number of extensions: 20
Number of successful extensions: 7
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: 395
Length of database: 470
Length adjustment: 32
Effective length of query: 363
Effective length of database: 438
Effective search space:   158994
Effective search space used:   158994
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 (21.7 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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