GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Shewanella sp. ANA-3

Align Acetylornithine/succinyldiaminopimelate aminotransferase; ACOAT; DapATase; Succinyldiaminopimelate transferase; EC 2.6.1.11; EC 2.6.1.17 (characterized)
to candidate 7025360 Shewana3_2520 aminotransferase (RefSeq)

Query= SwissProt::P40732
         (405 letters)



>FitnessBrowser__ANA3:7025360
          Length = 452

 Score =  149 bits (375), Expect = 2e-40
 Identities = 122/352 (34%), Positives = 173/352 (49%), Gaps = 42/352 (11%)

Query: 6   TAITRATFDEVILPVYAPADFIPVKGKGSRVWDQQGKEYIDFAGGIAVTALGHCHPALVE 65
           T++TRA      LPVY          +G  +    G++ ID          G+ HPA++ 
Sbjct: 19  TSMTRA------LPVYGVHS-----AQGCELELVDGRKLIDGTSSWWACVHGYGHPAILT 67

Query: 66  ALKSQGETLWHTS-NVFTNEPALRLGRKLIDATFAE--RVLFMNSGTEANETAFKLARHY 122
           A++ Q   L H      T+EPA+ L +KL+  T     +V   +SG+ A E A K+A  Y
Sbjct: 68  AMERQLHQLSHVMFGGITHEPAITLCKKLLAMTCEPLTKVFLCDSGSIAVEVAIKMALQY 127

Query: 123 ACVRHSPF-----KTKIIAFHNAFHGRSLFTVSV----GGQPKYSDGFGPKPA--DIIHV 171
              +  P      K +I+     +HG +   +SV    GG          K    D    
Sbjct: 128 WQGQDLPLAQKAQKQRILTVKKGYHGDTFAAMSVCDPEGGMHTMFGEAVTKQCFVDAPQT 187

Query: 172 PF------NDLHAVKAVMDDH---TCAVVVEPI-QGEGGVQAATPEFLKGLRDLCDEHQA 221
           PF      +DL  ++ ++ +      AV++EPI QG GG++  + E+L+GLR LCDE+  
Sbjct: 188 PFGEPLRQDDLAPMQRILREQHPEIAAVIIEPIMQGAGGMRFYSSEYLRGLRALCDEYNV 247

Query: 222 LLVFDEVQCGMGRTGDLFAYMHYGVTPDILTSAKALGGGF-PVSAMLTTQEIA-----SA 275
           LL+ DE+  G GRTG LFAY H  +TPDIL   KAL GG+  ++A L T  +A     S 
Sbjct: 248 LLILDEIATGFGRTGKLFAYEHADITPDILCLGKALTGGYISLAATLCTDNVAQGISQSP 307

Query: 276 FHVGSHGSTYGGNPLACAVAGAAFDIINTPEVLQGIHTKRQQFVQHL-QAID 326
             V  HG T+ GNPLACA A A+ D+IN  E    +    QQ  + L  AID
Sbjct: 308 AGVFMHGPTFMGNPLACAAACASLDLINQQEWPAQVAAIEQQMQRELADAID 359


Lambda     K      H
   0.322    0.137    0.412 

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: 445
Number of extensions: 23
Number of successful extensions: 2
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: 405
Length of database: 452
Length adjustment: 32
Effective length of query: 373
Effective length of database: 420
Effective search space:   156660
Effective search space used:   156660
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: 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