GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Sulfuricurvum kujiense DSM 16994

Align LL-diaminopimelate aminotransferase (EC 2.6.1.83) (characterized)
to candidate WP_013459667.1 SULKU_RS04095 hypothetical protein

Query= BRENDA::O66630
         (387 letters)



>NCBI__GCF_000183725.1:WP_013459667.1
          Length = 378

 Score =  137 bits (345), Expect = 5e-37
 Identities = 117/368 (31%), Positives = 182/368 (49%), Gaps = 38/368 (10%)

Query: 34  IDLGVGDPDMPTPKPIVEAAKKALENPENHKYPSYVGKYEFRKAVADWYKRRFDVDLDPN 93
           I L +G+P   TP  I ++  K  E  E  +YP   G+     ++  + +RRF V L  N
Sbjct: 27  IALTIGEPQFETPAFIQKSLAKHSE--ELRRYPKTAGESYLNDSMRGFVERRFGVKLKAN 84

Query: 94  TEVITLIGSKEGIAHFP--LAFVNPGDIVLCPDPAYPVYRIGAIFAGGTPYTVPLKEENN 151
            E+++  G++E + +FP    F     ++   +P Y +Y   AI +      + L E+N 
Sbjct: 85  -ELVSSFGTREVLFNFPQYYLFDKKEPVMAYTNPFYQIYEGSAIASRAKVIHLNLSEQNG 143

Query: 152 FLPDLDSIPEDVAKKAKIIWINYPNNPTSAPPTLEFYKKLVDWAK---EYNVIIASDNAY 208
           F P +D   E       ++ +N+PNNPT++  +LE   +L DW K   +++  + +D  Y
Sbjct: 144 FKPVID---EAELAGCDLVILNFPNNPTASVLSLE---ELGDWVKLALKHDFCLINDECY 197

Query: 209 SEIYTGQEKPPSILQV------PGAKDVAIEFHSLSKTYNMTGWRIGMAVGNKELVAGLG 262
           SEIYT Q K PS+L+          K+V +  +S+SK  +  G R G   G+  ++ G  
Sbjct: 198 SEIYTDQ-KIPSLLEASLYVGNSSFKNVLV-INSISKRSSAPGLRSGFIAGDGSILKGYA 255

Query: 263 KVKTNVDSGQFGAVQDAGIVALNLPEEEVEKIRDVYRERKKIMTEALEKIGLEIYRSDYT 322
           + +T V       +Q A  +A    E  V K R+VY E  K    A E +G+E   SD T
Sbjct: 256 QYRTYVGCASPLPLQAAAAMAW-ADEYHVAKAREVYAENFK---AAQEILGIE--TSDAT 309

Query: 323 FYLWIKVPEGYTSAEFVGRLIDEAGIVCTPG------NGFGEY-GEGYFRISLTVPTERL 375
           FY+W+KVP    + EF  RL  +  +   PG      +  GE  G GY RI+L   T R 
Sbjct: 310 FYVWLKVP---NALEFTQRLYRDYNVKVLPGEFLAREDARGENPGIGYIRIALVEETVRT 366

Query: 376 LEAAERIK 383
           ++A ER+K
Sbjct: 367 IQALERLK 374


Lambda     K      H
   0.317    0.139    0.413 

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: 368
Number of extensions: 26
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: 387
Length of database: 378
Length adjustment: 30
Effective length of query: 357
Effective length of database: 348
Effective search space:   124236
Effective search space used:   124236
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 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