GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Dechlorosoma suillum PS

Align LL-diaminopimelate aminotransferase; DAP-AT; DAP-aminotransferase; LL-DAP-aminotransferase; EC 2.6.1.83 (uncharacterized)
to candidate Dsui_2708 Dsui_2708 succinyldiaminopimelate transaminase

Query= curated2:C6BUK3
         (388 letters)



>FitnessBrowser__PS:Dsui_2708
          Length = 401

 Score =  179 bits (454), Expect = 1e-49
 Identities = 130/394 (32%), Positives = 197/394 (50%), Gaps = 26/394 (6%)

Query: 10  LATLPPYLFAEIDRLKAEVAAQ-GVDIISLGIGDPDLPTPDFIIEALHKAAKNPVNHQYP 68
           LA L PY F ++ +L   V        I L IG+P   TP FI EAL        N  YP
Sbjct: 5   LAKLQPYPFEKLRQLFQGVTPNPDYQEIKLSIGEPQHATPGFIKEALTANLGGLAN--YP 62

Query: 69  SYVGLLTFRQAVADWYKERFDVE-LDATKEVVSLIGSKEGIAHFPLAFVNP--GDLVLVA 125
           +  G    RQA+A W + R+ +  ++   E++ + GS+E +  F    ++P  G + LV 
Sbjct: 63  TSQGTPALRQAIAAWMERRYGLAGVNPDTEILPVNGSREALFAFAQTVIDPSRGYVPLVV 122

Query: 126 SPN--YPVYPVASGFAGGEVEIVPLLEENDFLPNLDAISDEKWDKCKIFFVNYPNNPTSA 183
           SPN  Y +Y  A+  AG E   +  L ENDF   L+A+S+  W + ++ +V  P NPT  
Sbjct: 123 SPNPFYQIYEGAAYLAGAEPYFLNTLPENDFSLELEALSEADWARVQLLYVCSPGNPTGK 182

Query: 184 TATPEFYAELVAKAKKHNVIIAADAAYTEVYYDEDKKPISILETPGAKDVA------IEF 237
               E + +L A + K+  +IA+D  Y+E+Y+DE K P+  L+   AK +       + F
Sbjct: 183 VLDLEDWKKLFALSDKYGFVIASDECYSEIYFDEAKPPLGGLQ--AAKQLGRGFERLVMF 240

Query: 238 HSLSKTYNMTGWRCGMAVGNASLVAGLGKIKENVDSGIFQAVQEAGIVALKEGEPYVKEF 297
            SLSK  N+ G R G   G+A+++      +      +  AVQ A  +A  E E + +E 
Sbjct: 241 SSLSKRSNVPGLRSGFVAGDAAVLKKFLLYRTYHGGAMNPAVQAASAIAWNE-EAHAREN 299

Query: 298 RKIYKERRDCVIEALEKINISCKVPDASIFVWAKTPEGYTSSEFVSKLLKETGVVVTPGN 357
           R+ YKE+ D V   +  + +   +PDAS ++WA+TP     +EF  +LL +  VVV PG+
Sbjct: 300 RRQYKEKFDAVTPIVASV-LQTGLPDASFYLWARTP--IADTEFARRLLADYNVVVLPGS 356

Query: 358 GFGES------GEGYFRISLTVDTDRLKEAVSRI 385
                      GE + RI+L        EA  RI
Sbjct: 357 YLAREARGVNPGENFVRIALVAPLADCLEAAERI 390


Lambda     K      H
   0.317    0.136    0.398 

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: 477
Number of extensions: 27
Number of successful extensions: 6
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: 388
Length of database: 401
Length adjustment: 31
Effective length of query: 357
Effective length of database: 370
Effective search space:   132090
Effective search space used:   132090
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 (21.6 bits)
S2: 50 (23.9 bits)

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

Links

Downloads

Related tools

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