GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Azospirillum brasilense Sp245

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate AZOBR_RS11880 AZOBR_RS11880 1-aminocyclopropane-1-carboxylate deaminase

Query= BRENDA::Q56232
         (385 letters)



>FitnessBrowser__azobra:AZOBR_RS11880
          Length = 384

 Score =  180 bits (457), Expect = 5e-50
 Identities = 126/373 (33%), Positives = 181/373 (48%), Gaps = 11/373 (2%)

Query: 10  AMKPSATVAVNAKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAG 69
           A+ P   + V   A E    G++++ +  G+P    P+ V EAA R L      Y    G
Sbjct: 12  AIPPFFVMEVMRAAAEREAAGLEVLHMEVGQPSTGAPKGVLEAAHRMLDADVLGYTGALG 71

Query: 70  IPELREALAEKFRRENGLSVTPEETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYP 129
           IP LR A+A  +R   G+ V     +VT G   A    F A  DPGD V + SP + +Y 
Sbjct: 72  IPALRAAIAGWYRDRYGIDVPERRVVVTTGSSGAFQLGFLAAFDPGDRVAMASPSYPAYR 131

Query: 130 EMVRFAGGVVVEVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEAL 189
             +   G   VE+ T PE  F P  E + + + P  + L+V SP NPTG +  +E L AL
Sbjct: 132 HTLTAIGVEPVELPTGPEHRFQPTIELLEQ-LDPPIQGLIVASPANPTGTMLSREELTAL 190

Query: 190 ARLAVEHDFYLVSDEIYEHLLYEGEHFSPGRVAPEHTLTVNGAAKAFAMTGWRIGYACGP 249
           A         LVSDEIY  L Y  E  +   V+ E  L VN  +K F+MTGWR+G+   P
Sbjct: 191 AAWCDAKGVRLVSDEIYHGLTYGPEAVTAAEVS-ESALVVNSFSKYFSMTGWRLGWMIVP 249

Query: 250 KEVIKAMASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGLTA 309
            ++I+++  ++     S  +++Q A + A    E     V      Y R R+LLL  L  
Sbjct: 250 DDLIRSVECLAQNLFISAPSLSQAAAVAAFGCTEELDGHV----ARYARNRELLLRELPK 305

Query: 310 LGLKAVRPS-GAFYVLMDTSPIAPDEVRAAERLL-EAGVAVVPGTDF---AAFGHVRLSY 364
            G   + P+ GAFY+  D + +  D     +R+L E G+A  PG DF        VR S+
Sbjct: 306 AGFDKLAPADGAFYIYADVTEMTDDSEAFCKRILAETGIACTPGVDFDPARGLRFVRFSF 365

Query: 365 ATSEENLRKALER 377
           A +EE + +A  R
Sbjct: 366 AGAEETIAEAARR 378


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: 352
Number of extensions: 20
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: 384
Length adjustment: 30
Effective length of query: 355
Effective length of database: 354
Effective search space:   125670
Effective search space used:   125670
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