GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Thiomicrospira cyclica ALM1

Align Acetylornithine/succinyldiaminopimelate aminotransferase; ACOAT; DapATase; Succinyldiaminopimelate transferase; EC 2.6.1.11; EC 2.6.1.17 (uncharacterized)
to candidate WP_013834671.1 THICY_RS00550 adenosylmethionine--8-amino-7-oxononanoate transaminase

Query= curated2:P59086
         (404 letters)



>NCBI__GCF_000214825.1:WP_013834671.1
          Length = 443

 Score =  132 bits (332), Expect = 2e-35
 Identities = 103/314 (32%), Positives = 158/314 (50%), Gaps = 29/314 (9%)

Query: 18  LPVYNPAFFIPVKGKGSRLWDQKGKEYIDFSGGIAVTSLGHCHPVLNKVLRQQSKKLWHI 77
           LP   PA       +G  +    G++ +D          G+ HP +     +Q +K+ HI
Sbjct: 18  LPARQPALAAS-STQGCTITLDDGRQLLDAMSSWWSAIHGYNHPTIIAAASEQLQKMPHI 76

Query: 78  S-NIFTNEPALRLADKLISSSFAS--RVFFANSGAEANEAAFKLARYYSSKIYNLKKNKI 134
               F+++PA  LA  LI  S  S    FFA+SG+ A E A K+A  Y   I   +K++ 
Sbjct: 77  MFGGFSHQPATELAQALIDISPPSLTHTFFADSGSIAVEVALKMALQYWKSIGQPRKSRF 136

Query: 135 ISFYNSFHGRTFFTVSV-----GGQAKYSDFFGP----KPPAIMHAKFNEIN------SV 179
           I+  +++HG TF  +SV     G    ++D   P    K P I H     ++      S+
Sbjct: 137 IALQHAYHGDTFGAMSVCDPVDGMHHLFADNLMPNLFAKAPPICHHPSEPLDNQACLASL 196

Query: 180 KSIIDDN---TCAVVME-LIQGEGGIVPADVAFVREIRDLCYKYNALLIFDEIQTGIGRT 235
             I++ +     A + E ++QG GG+      +++E   LC  Y+ LLI DEI TG+GRT
Sbjct: 197 AQILEQHHHEIAAFIFEPIVQGAGGMRFYSADYLKEAAALCRHYDVLLIADEIATGLGRT 256

Query: 236 SKLYAYEHYEVQPDILTIAKSLGSG-FPISATLTTNGIASVIK---PGI--HGTTYGGNP 289
            KL+A E  +++PDILT+ K L +G   ++A L    I + I    PG+  HG T+  NP
Sbjct: 257 GKLFACEWADIEPDILTLGKGLSAGMISLAAVLCNERIRAGISQAAPGLLMHGPTFMANP 316

Query: 290 LACSIAESVVNIVN 303
           LAC IA + V ++N
Sbjct: 317 LACRIAHASVKLLN 330


Lambda     K      H
   0.322    0.139    0.404 

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: 348
Number of extensions: 22
Number of successful extensions: 3
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: 404
Length of database: 443
Length adjustment: 32
Effective length of query: 372
Effective length of database: 411
Effective search space:   152892
Effective search space used:   152892
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 Jul 25 2024. The underlying query database was built on Jul 25 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