GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Dinoroseobacter shibae DFL-12

Align LL-diaminopimelate aminotransferase (EC 2.6.1.83) (characterized)
to candidate 3607347 Dshi_0762 aminotransferase class I and II (RefSeq)

Query= BRENDA::Q8TQ40
         (389 letters)



>FitnessBrowser__Dino:3607347
          Length = 400

 Score =  165 bits (418), Expect = 2e-45
 Identities = 120/381 (31%), Positives = 186/381 (48%), Gaps = 25/381 (6%)

Query: 20  AIDEAKDEMIAKGVDVIDLGVGDPDLPTHPHIVEAMREAVCDPKTHQYPSYAGMPEFREA 79
           A+    +E+ A G DVI LG G+PD  T  +I +A + A+   KT +Y +  G+PE ++A
Sbjct: 18  AVTNMANELKAAGRDVIGLGAGEPDFDTPQNIKDAGKAAIDAGKT-KYTAVDGIPELKKA 76

Query: 80  AAEWCKKYKGIELDPATEVLSLIGSKEAVAHIPLAFVNPGDVVLYTDPGYPVYKIGTLFA 139
                K+  G++ D  T+V    G K+ + +  +A +NPGD V+   P +  Y    L A
Sbjct: 77  IVAKFKRDNGLDYD-TTQVTVANGGKQILINALMATMNPGDEVIIPAPYWVSYPDMVLLA 135

Query: 140 GGEPYSLPLKAENSFLPDLDSIPADILKRAKLFFFNYPNNPTSA---TADMKFFEKVVEF 196
           GGEP       +  F    D + A I  R K F FN P+NPT A    A++K    V+  
Sbjct: 136 GGEPVIAEASIQTGFKLTADQLEAAITPRTKWFIFNSPSNPTGAGYTAAELKELTDVL-- 193

Query: 197 CKKNDIIAVHDNAYSQMVYDGYDAPSFLAAEGAM-DIGIELYSHSKTYNMTGWRLGFAVG 255
            +   +  + D+ Y  +VYD ++  +    E  + +  +     SK Y MTGWR+G+A G
Sbjct: 194 LRHPHVWVMTDDMYEHLVYDDFEFATPAQVEPKLYNRTLTCNGVSKAYAMTGWRIGYAAG 253

Query: 256 SKALIKGLGKVKSNVDSGVFDAIQIAGIAALSSSQACVDDTNKIYEERRNVLIEGLT-AM 314
            K LI  + K++S   S      Q A + AL  +Q  + + NK ++ RR++++  L  A 
Sbjct: 254 PKELIGAMRKIQSQSTSNPCSISQWAAVEALDGTQDYIPENNKTFKRRRDLVVGMLNDAQ 313

Query: 315 GLEVKPPKATFYVWAPV-------PTGFTSI----EFAKLLLEEAGIVATPGVGFGDAGE 363
           G+    P+  FYV+  +         G T I     FAK LLEE G+    G  FG +  
Sbjct: 314 GISCPKPEGAFYVYPSIAGCIGKTSAGGTKITDDEAFAKALLEEKGVAVVFGAAFGLSPN 373

Query: 364 GYVRF-----ALTKPVERIKE 379
             V +     ALT+   RI++
Sbjct: 374 FRVSYATSDDALTEACTRIQD 394


Lambda     K      H
   0.319    0.137    0.409 

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: 391
Number of extensions: 17
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: 389
Length of database: 400
Length adjustment: 31
Effective length of query: 358
Effective length of database: 369
Effective search space:   132102
Effective search space used:   132102
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: 50 (23.9 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