GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD in Escherichia coli BW25113

Align Acetylornithine aminotransferase; ACOAT; EC 2.6.1.11 (uncharacterized)
to candidate 17148 b3073 putrescine:2-oxoglutaric acid aminotransferase, PLP-dependent (RefSeq)

Query= curated2:Q8TUZ5
         (389 letters)



>FitnessBrowser__Keio:17148
          Length = 459

 Score =  317 bits (812), Expect = 4e-91
 Identities = 175/374 (46%), Positives = 240/374 (64%), Gaps = 18/374 (4%)

Query: 32  DDEGNEYIDLVAGIAVNVLGHCHPAVVEAVKEQVERLIHCSNLYYNEPQAEAARLLAEAA 91
           D +G E+ID + G  +  +GH +P VV AV+ Q+ +    S    +  +A  A+ LA   
Sbjct: 78  DTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLRAMLAKTLAALT 137

Query: 92  PKDLNKVFFCNSGTESVECAIKLARKFT---GCTKFIAFEGGFHGRTMGALSATWKPEFR 148
           P  L   FFCNSGTESVE A+KLA+ +    G   FIA  G FHG+++GALSAT K  FR
Sbjct: 138 PGKLKYSFFCNSGTESVEAALKLAKAYQSPRGKFTFIATSGAFHGKSLGALSATAKSTFR 197

Query: 149 EPFEPLVPEFEHVPYGDVNAVEKAID------DDTAAVIVEPVQGEAGVRIPPEGFLREL 202
           +PF PL+P F HVP+G++ A+  A++      DD AAVI+EP+QGE GV +PP G+L  +
Sbjct: 198 KPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQGEGGVILPPPGYLTAV 257

Query: 203 RELCDEHGLLLIVDEVQSGMGRTGQFFAFEHEDVLPDIVCLAKGLGGGV-PVGATIAREE 261
           R+LCDE G L+I+DEVQ+GMGRTG+ FA EHE+V PDI+CLAK LGGGV P+GATIA EE
Sbjct: 258 RKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGGGVMPIGATIATEE 317

Query: 262 VAEAF--EPGDHGSTFGGNPLACAAVCAAVSTVLEENLPEAAERKGKLAM----RILSEA 315
           V       P  H +TFGGNPLACAA  A ++ +LE+NLP  AE+KG + +    ++  E 
Sbjct: 318 VFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQKGDMLLDGFRQLAREY 377

Query: 316 EDVVEEVRGRGLMMGVEVGDDERAKDVAREMLDRGALV--NVTSGDVIRLVPPLVIGEDE 373
            D+V+E RG+G++M +E  D+E   + A EM  +  LV   + +   IR+ PPL +  ++
Sbjct: 378 PDLVQEARGKGMLMAIEFVDNEIGYNFASEMFRQRVLVAGTLNNAKTIRIEPPLTLTIEQ 437

Query: 374 LEKALAELADALRA 387
            E  +     AL A
Sbjct: 438 CELVIKAARKALAA 451


Lambda     K      H
   0.318    0.137    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: 447
Number of extensions: 28
Number of successful extensions: 6
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: 389
Length of database: 459
Length adjustment: 32
Effective length of query: 357
Effective length of database: 427
Effective search space:   152439
Effective search space used:   152439
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 (21.7 bits)
S2: 50 (23.9 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