GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Pseudomonas simiae WCS417

Align LL-diaminopimelate aminotransferase; DAP-AT; DAP-aminotransferase; LL-DAP-aminotransferase; EC 2.6.1.83 (characterized)
to candidate GFF2657 PS417_13545 arginine aminotransferase

Query= SwissProt::Q2RK33
         (390 letters)



>FitnessBrowser__WCS417:GFF2657
          Length = 664

 Score =  174 bits (440), Expect = 9e-48
 Identities = 109/367 (29%), Positives = 179/367 (48%), Gaps = 5/367 (1%)

Query: 24  EARERGVDIISLGIGDPDMPTPSHVIDKLVAEAHNPENHRYPTSEGLLAFRQAVADWYQR 83
           +A  +G DII L +GDPD  TPS + D  V+     + H Y    G  A R+A+A  Y +
Sbjct: 26  QAASQGEDIIILSVGDPDFATPSFITDAAVSALREGDTH-YTEIPGRPALREAIAARYSK 84

Query: 84  LYGVDLDPRREVVTLIGSKEGIAHISLCYVDPGDINLVPDPGYPVYNIGTLLAGGESYFM 143
                L     V+T+ G++  +   SLC +  GD  LV DP Y  Y      +G     +
Sbjct: 85  TLARALSAEN-VITVAGAQNALFVTSLCLLQAGDEVLVLDPMYVTYEATLKASGATLVRV 143

Query: 144 PLTAANGFLPDLGAIPSDVARRAKLMFINYPNNPTGAVADLKFFQEVVEFARSYDLIVCH 203
           P +  +GF  D   + + +  R + +F + PNNPTG V +L+  Q + + A + DL V  
Sbjct: 144 PCSPESGFRLDAQLLGAAITPRTRAIFFSNPNNPTGVVLNLQELQAIADLAIARDLWVVV 203

Query: 204 DAAYSEITYDGYRAPSFLQAPGAKEVGIEFNSVSKPYNMTGWRLGWACGRADVIEALARI 263
           D  Y  + +DG    S    PG  E  +   S+SK + MTGWR+GW      ++     +
Sbjct: 204 DEVYESLVFDG-EYHSLAALPGMAERCVVIGSLSKSHAMTGWRIGWIIATPQMVAHAETL 262

Query: 264 KSNIDSGAFQAVQYAGIAALTGPQEGLAEVRRVYQERRDIIVEGFNSL-GWHLEKPKATF 322
             ++  G    V  A  AA+    +    +R +Y+ RRD+++ G ++  G  ++ P+A  
Sbjct: 263 VLSMLYGLPGFVMEAATAAVLAHDDVTQGMREIYRRRRDLVMAGLSACPGIKVQAPQAGM 322

Query: 323 YVWAPV-PRGYTSASFAEMVLEKAGVIITPGNGYGNYGEGYFRIALTISKERMQEAIERL 381
           +V   V   G  S  FA  +  +AGV +     +G   +G+ R++ T+ +ER+ EA +R+
Sbjct: 323 FVLVDVRGTGLGSLDFAWRLFREAGVSVLDAAAFGAPAQGFVRLSFTLGEERLSEACQRI 382

Query: 382 RRVLGKV 388
              + K+
Sbjct: 383 AHFVAKL 389


Lambda     K      H
   0.320    0.139    0.421 

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: 592
Number of extensions: 35
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: 390
Length of database: 664
Length adjustment: 34
Effective length of query: 356
Effective length of database: 630
Effective search space:   224280
Effective search space used:   224280
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 (21.8 bits)
S2: 52 (24.6 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