GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Pseudomonas fluorescens GW456-L13

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate PfGW456L13_2943 Aspartate aminotransferase (EC 2.6.1.1)

Query= BRENDA::Q56232
         (385 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2943
          Length = 395

 Score =  248 bits (633), Expect = 2e-70
 Identities = 142/371 (38%), Positives = 211/371 (56%), Gaps = 11/371 (2%)

Query: 14  SATVAVNAKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAGIPEL 73
           +A   ++ +AL LR QGVD++ L+ G+PDFDTP+ + +AA  +L  G T Y    G   L
Sbjct: 15  AAAWQIHDRALALREQGVDVLLLSIGDPDFDTPQPIVQAAIGSLLAGDTHYPAVRGSQGL 74

Query: 74  REALAEKFRRENGLSVTPEETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPEMVR 133
           R+++A   RR +G +V  +  IV  G + A++++ Q +LDPGDEV+V  P +V+Y  +  
Sbjct: 75  RDSIARHHRRRSGQAVDAQHVIVFPGAQCAVYSVAQCLLDPGDEVLVAEPMYVTYEGVFG 134

Query: 134 FAGGVVVEVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALARLA 193
             G  VV V    + GF  DP  V   ITP T+A+++NSPNNP+GA  P    +ALA L 
Sbjct: 135 ACGAKVVPVPVRSQNGFRVDPADVAALITPNTRAMLLNSPNNPSGASLPLTAWKALAALC 194

Query: 194 VEHDFYLVSDEIYEHLLYEGEHFSPGRV--APEHTLTVNGAAKAFAMTGWRIGYACGPKE 251
           + HD +L+SDE+Y  LL+EGEH SP  +    E T T+N  +K+ AM+GWR+G+  GP+ 
Sbjct: 195 IRHDLWLISDEVYSELLFEGEHISPASLPGMAERTATINSLSKSHAMSGWRVGWVIGPQS 254

Query: 252 VIKAMASVS-SQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGLTAL 310
           + + + ++S       PD I   A L      + +   V   RE YR+RRDL+   L   
Sbjct: 255 LCEHLVNLSLCMLFGIPDFIQNAAQLAL----DENLPHVAQMREEYRQRRDLVCASLNLC 310

Query: 311 -GLKAVRPSGAFYVLMDTSPIAPDEVRAAERLLEA-GVAVVPGTDF--AAFGHVRLSYAT 366
            G++A+RP G  +V++D           AERLL+  GV+V+ G  F  +A GH+R+    
Sbjct: 311 PGIQAIRPDGGMFVMVDVRQTGLSAQHFAERLLDGYGVSVLAGEAFGPSAAGHIRIGLVV 370

Query: 367 SEENLRKALER 377
               L  A  R
Sbjct: 371 DRPKLADACRR 381


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: 369
Number of extensions: 11
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: 385
Length of database: 395
Length adjustment: 31
Effective length of query: 354
Effective length of database: 364
Effective search space:   128856
Effective search space used:   128856
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