GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Pseudomonas fluorescens FW300-N1B4

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate Pf1N1B4_4996 Aspartate aminotransferase (EC 2.6.1.1)

Query= BRENDA::Q56232
         (385 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4996
          Length = 395

 Score =  245 bits (626), Expect = 1e-69
 Identities = 143/372 (38%), Positives = 212/372 (56%), Gaps = 9/372 (2%)

Query: 14  SATVAVNAKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAGIPEL 73
           +A   ++ +ALELR QGVD++ L+ G+PDFDTP  +  AA  +L  G T Y+   G   L
Sbjct: 15  AAAWKIHDRALELREQGVDVLLLSIGDPDFDTPLPIIHAAIDSLLAGDTHYSDVRGTRTL 74

Query: 74  REALAEKFRRENGLSVTPEETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPEMVR 133
           R ++A + +R +G  V  +  IV  G + A++++ Q +LDPGDEVIV  P +V+Y  +  
Sbjct: 75  RSSIASRHQRRSGQLVDADHVIVLPGAQCAVYSVAQCLLDPGDEVIVAEPMYVTYEGVFG 134

Query: 134 FAGGVVVEVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALARLA 193
             G  VV V   PE GF  +P  V   IT +T+ +++NSPNNP+GA    +  +ALA L 
Sbjct: 135 ACGASVVPVAVRPENGFRVEPADVAALITSKTRVILLNSPNNPSGASLSLKSWKALAALC 194

Query: 194 VEHDFYLVSDEIYEHLLYEGEHFSPGRV--APEHTLTVNGAAKAFAMTGWRIGYACGPKE 251
           V+HD +L+SDE+Y  LL+EGEH SP  +    E T T+N  +K+ AMTGWR+G+  GPK 
Sbjct: 195 VQHDLWLISDEVYSDLLFEGEHISPASLPGMAERTATINSLSKSHAMTGWRVGWMIGPKP 254

Query: 252 VIKAMASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGLTAL- 310
           + + +  +S           Q A   AL   +     V + RE YR+RRDL+   L+   
Sbjct: 255 LAEHLMHLSLCMLFGLPDFVQNAAQVAL---DKDLPEVALMREEYRQRRDLVCARLSGCP 311

Query: 311 GLKAVRPSGAFYVLMDTSPIAPDEVRAAERLLEA-GVAVVPGTDF--AAFGHVRLSYATS 367
           G++ ++P G  +V++D           AERLLE  GV+V+ G  F  +A GH+R+     
Sbjct: 312 GIRPIKPDGGMFVMVDVRQTGLGAQDFAERLLEGYGVSVLAGEAFGPSAAGHIRIGLVVD 371

Query: 368 EENLRKALERFA 379
           +  L  A +R A
Sbjct: 372 QARLADACQRIA 383


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: 362
Number of extensions: 14
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