GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Escherichia coli BW25113

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate 16484 b2379 hypothetical protein (NCBI)

Query= BRENDA::Q56232
         (385 letters)



>FitnessBrowser__Keio:16484
          Length = 412

 Score =  154 bits (390), Expect = 3e-42
 Identities = 115/381 (30%), Positives = 179/381 (46%), Gaps = 17/381 (4%)

Query: 7   RVQAMKPSATVAVNAKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKTK-YA 65
           R+  + P          +  RR+G D++  + G PD  TP H+ E       +  T  Y+
Sbjct: 12  RIDRLPPYVFNITAELKMAARRRGEDIIDFSMGNPDGATPPHIVEKLCTVAQRPDTHGYS 71

Query: 66  PPAGIPELREALAEKFRRENGLSVTPE-ETIVTVGGKQALFNLFQAILDPGDEVIVLSPY 124
              GIP LR A++  ++    + + PE E IVT+G K+ L +L  A LD GD V+V +P 
Sbjct: 72  TSRGIPRLRRAISRWYQDRYDVEIDPESEAIVTIGSKEGLAHLMLATLDHGDTVLVPNPS 131

Query: 125 WVSYPEMVRFAGGVVVEVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKE 184
           +  +      AG  V  V  +    F  + ER  R   P+ K +++  P+NPT      E
Sbjct: 132 YPIHIYGAVIAGAQVRSVPLVEGVDFFNELERAIRESYPKPKMMILGFPSNPTAQCVELE 191

Query: 185 VLEALARLAVEHDFYLVSDEIYEHLLYEGEHFS-----PGRVAPEHTLTVNGAAKAFAMT 239
             E +  LA  +D  +V D  Y  ++Y+G         PG  A +  +     +K++ M 
Sbjct: 192 FFEKVVALAKRYDVLVVHDLAYADIVYDGWKAPSIMQVPG--ARDVAVEFFTLSKSYNMA 249

Query: 240 GWRIGYACGPKEVIKAMASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRR 299
           GWRIG+  G K ++ A+A + S       T  Q A + AL   E  +  V    E Y+RR
Sbjct: 250 GWRIGFMVGNKTLVSALARIKSYHDYGTFTPLQVAAIAAL---EGDQQCVRDIAEQYKRR 306

Query: 300 RDLLLEGLTALGLKAVRPSGAFYV--LMDTSPIAPDEVRAAERLL-EAGVAVVPGTDFAA 356
           RD+L++GL   G     P  + YV   +     A   +  A++LL EA V V PG  F  
Sbjct: 307 RDVLVKGLHEAGWMVEMPKASMYVWAKIPEPYAAMGSLEFAKKLLNEAKVCVSPGIGFGD 366

Query: 357 FG--HVRLSYATSEENLRKAL 375
           +G  HVR +   + + +R+A+
Sbjct: 367 YGDTHVRFALIENRDRIRQAI 387


Lambda     K      H
   0.317    0.133    0.379 

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: 358
Number of extensions: 18
Number of successful extensions: 5
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: 385
Length of database: 412
Length adjustment: 31
Effective length of query: 354
Effective length of database: 381
Effective search space:   134874
Effective search space used:   134874
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