GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Caulobacter crescentus NA1000

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate CCNA_02539 CCNA_02539 aspartate aminotransferase

Query= BRENDA::Q56232
         (385 letters)



>FitnessBrowser__Caulo:CCNA_02539
          Length = 381

 Score =  160 bits (406), Expect = 4e-44
 Identities = 114/374 (30%), Positives = 186/374 (49%), Gaps = 17/374 (4%)

Query: 11  MKPSATVAVNAKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAGI 70
           ++P   +A++  A +L+ +G  ++ +  G+P    P      A   L      Y      
Sbjct: 5   IEPFHAIAISRLAHQLKMEGRSIIHMEFGQPSTGAPSKALAKAHDILDAEAMGYWES--- 61

Query: 71  PELREALAEKFRRENGLSVTPEETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPE 130
           P LRE +A++++   G++V PE  I+T G   AL     ++  PGD + +  P +V+Y  
Sbjct: 62  PLLREKIAQRYQTLYGVTVEPERIILTCGASPALVLALSSLFKPGDRIALARPGYVAYRN 121

Query: 131 MVRFAGGVVVEVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALA 190
            ++      VE+   PE+ F    + +   + P    ++V SP NPTG +     LEA+A
Sbjct: 122 TLKALHLEPVEIACGPEDRFQLTAKHL-ADLEPAPVGVIVASPANPTGTIIEPAELEAIA 180

Query: 191 RLAVEHDFYLVSDEIYEHLLYEGEHFSPGRVAPEHTLTVNGAAKAFAMTGWRIGYACGP- 249
           ++       ++SDEIY  L Y G   S    AP+  L VN  +K F+M GWR+G+   P 
Sbjct: 181 KVCAARGIRIISDEIYHGLSYAGRTPSMLEFAPD-ALIVNSFSKYFSMAGWRLGWLLTPP 239

Query: 250 -KEVIKAMASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGLT 308
            +++ +A A V +   T+P ++AQ A L A+   +     +++    YR  R L+L+ L 
Sbjct: 240 GEDLDRARAYVGNLFLTAP-SLAQHAGLAAMDCIDELEGHIDV----YRANRQLMLDALP 294

Query: 309 ALGLKAVR-PSGAFYVLMDTSPIAPDEVRAAERLL-EAGVAVVPGTDF---AAFGHVRLS 363
           ALGLK +  P GAFY+  + + +  D +   E LL + GVA  PG DF        +R S
Sbjct: 295 ALGLKEIAPPDGAFYIWANIAHLTDDSLGFCEDLLRDTGVATAPGVDFDPVEGKRFIRFS 354

Query: 364 YATSEENLRKALER 377
           +A S   + +AL R
Sbjct: 355 FAVSTPEVEEALRR 368


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: 380
Number of extensions: 22
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: 381
Length adjustment: 30
Effective length of query: 355
Effective length of database: 351
Effective search space:   124605
Effective search space used:   124605
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 Jul 25 2024. The underlying query database was built on Jul 25 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