GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Nostoc punctiforme PCC 73102 ATCC 29133; PCC 73102

Align succinyldiaminopimelate transaminase (EC 2.6.1.17) (characterized)
to candidate WP_336884956.1 NPUN_RS00030 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= BRENDA::P9WPZ5
         (397 letters)



>NCBI__GCF_000020025.1:WP_336884956.1
          Length = 314

 Score =  207 bits (528), Expect = 3e-58
 Identities = 116/324 (35%), Positives = 177/324 (54%), Gaps = 10/324 (3%)

Query: 70  IAAQRRRHFGVDYDPETEVLVTVGATEAIAAAVLGLVEPGSEVLLIEPFYDSYSPVVAMA 129
           +A++ R + G+D DPET++ VT G+TEA+A+ +L  V+PG EV++ EP+Y++Y P   +A
Sbjct: 1   MASKVRWYLGLDIDPETQITVTCGSTEAMASVMLATVDPGDEVIVFEPYYENYGPDAILA 60

Query: 130 GAHRVTVPLVPDGRGFALDADALRRAVTPRTRALIINSPHNPTGAVLSATELAAIAEIAV 189
           GA    V L P    F  D   L +A    T+A+IIN+PHNPTG V +  EL  IAE+  
Sbjct: 61  GATPRYVTLHPPHWTF--DEAQLHQAFNANTKAIIINTPHNPTGKVFTREELTLIAELCQ 118

Query: 190 AANLVVITDEVYEHLVFDHARHLPLAGFDGMAERTITISSAAKMFNCTGWKIGWACGPAE 249
             +++  TDE+YEH+++D  +H+ LA   GM ERTITI+  +K ++ TGW++G+      
Sbjct: 119 KWDVLAFTDEIYEHILYDGTQHIALATLPGMEERTITINGLSKTYSVTGWRVGYILANPA 178

Query: 250 LIAGVRAAKQYLSYVGGAPFQPAVALALDTEDAWVAALRNSLRARRDRLAAGLTEIGFAV 309
           L   +R    +L+    AP Q A   A+    ++   L      +RD +   L  +G   
Sbjct: 179 LTGAIRKVHDFLTVGAPAPLQRAGVTAMQLPPSYYEELGKLYHQKRDSILQILDGVGIPY 238

Query: 310 HDSYGTYFLCADPRPLGYDDSTEFCAALPEKVGVAAIPMSAFCDPAAGQASQQADVWNHL 369
               G Y++ AD    GY    EF   L + +GVA +P S+F          Q +  + L
Sbjct: 239 FLPQGAYYVLADISKFGYKTDIEFTYHLIKNIGVAVVPGSSF--------FSQPEKGHSL 290

Query: 370 VRFTFCKRDDTLDEAIRRLSVLAE 393
           +RF F K  +TL  A  RL  L++
Sbjct: 291 IRFCFSKTPETLQAASDRLLKLSK 314


Lambda     K      H
   0.321    0.135    0.405 

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: 320
Number of extensions: 13
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: 397
Length of database: 314
Length adjustment: 29
Effective length of query: 368
Effective length of database: 285
Effective search space:   104880
Effective search space used:   104880
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: 49 (23.5 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