GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Hydrogenovibrio halophilus DSM 15072

Align Acetylornithine/succinyldiaminopimelate aminotransferase; ACOAT; DapATase; Succinyldiaminopimelate transferase; EC 2.6.1.11; EC 2.6.1.17 (uncharacterized)
to candidate WP_019894837.1 A377_RS0103865 adenosylmethionine--8-amino-7-oxononanoate transaminase

Query= curated2:P59317
         (406 letters)



>NCBI__GCF_000384235.1:WP_019894837.1
          Length = 433

 Score =  166 bits (420), Expect = 1e-45
 Identities = 110/341 (32%), Positives = 178/341 (52%), Gaps = 29/341 (8%)

Query: 32  QGSRIWDQQGKEYVDFAGGIAVTALGHCHPALVNALKTQGETLWHIS-NVFTNEPALRLG 90
           QGSRI    G+E +D          G+ HP +V A+  Q +T+ HI     T+EPA++L 
Sbjct: 35  QGSRITLANGRELIDGMSSWWAAIHGYNHPDIVRAMHAQIDTMPHIMFGGLTHEPAIQLA 94

Query: 91  RKLIEAT--FAERVVFMNSGTEANETAFKLARHYACVRHSPFKTKIIAFHNAFHGRSLFT 148
           ++L++ +    E+V F++SG+ A E A K+A  Y   R  P K+++++    +HG +  T
Sbjct: 95  QQLVKLSPEGLEKVFFVDSGSVAMEVAIKMALQYQISRGKPSKSRLLSIKGGYHGDTFAT 154

Query: 149 VSVGGQ------------PKYSDGFGPKP-ADIIHVPFNDLHAVKAVMDDH---TCAVVV 192
           +++               P++   F P+P   + +   +D+ A++ ++  H     A+ +
Sbjct: 155 MALCDPDNGMHTTFGPLLPRHF--FAPRPNPGMDNTDNSDIEALETMLAKHHDQIAAITL 212

Query: 193 EPI-QGEGGVTAATPEFLQGLRELCDQHQALLVFDEVQCGMGRTGDLFAYMHYGVTPDIL 251
           EPI QG GG+    P +L+ +R LCD+   LL+ DE+  G GRTG+LF     G+TPDI+
Sbjct: 213 EPIIQGAGGMRPYRPAYLKQVRALCDRFDVLLIADEIATGFGRTGELFGCDWAGITPDIM 272

Query: 252 TSAKAL-GGGFPVSAMLTTAEIASAFHPGS-----HGSTYGGNPLACAVAGAAFDIINTP 305
              K L GG   ++A L T  ++     G      HG TY  NPLACA A A  D +   
Sbjct: 273 ALGKTLTGGHITLAATLATEAVSDTISQGEPGLLMHGPTYMANPLACAAASANIDTLLAS 332

Query: 306 EVLEGIQAKRQHFVDHLQKIDQQYDVFSDIRGMGLLIGAEL 346
              + I   ++HF  HL+ +++Q D   D+R +G +   EL
Sbjct: 333 PWRDNIARIQRHFETHLRPLNEQ-DSVKDVRILGAIAAVEL 372


Lambda     K      H
   0.322    0.138    0.416 

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: 457
Number of extensions: 20
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: 406
Length of database: 433
Length adjustment: 32
Effective length of query: 374
Effective length of database: 401
Effective search space:   149974
Effective search space used:   149974
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: 50 (23.9 bits)

This GapMind analysis is from Apr 10 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