GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Dinoroseobacter shibae DFL-12

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate 3607759 Dshi_1168 aminotransferase class I and II (RefSeq)

Query= BRENDA::Q56232
         (385 letters)



>FitnessBrowser__Dino:3607759
          Length = 391

 Score =  170 bits (431), Expect = 6e-47
 Identities = 119/378 (31%), Positives = 177/378 (46%), Gaps = 11/378 (2%)

Query: 13  PSATVAVNAKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAGIPE 72
           P   + V   A      G  ++ +  G+P    P   + A    L Q    Y    G+PE
Sbjct: 11  PFIVMDVMEAARRAEAAGRHIIHMEVGQPGTAAPLPARRAVAAQLDQDAMGYTVALGLPE 70

Query: 73  LREALAEKFRRENGLSVTPEETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPEMV 132
           LR A+A  + R  G+ + P   +VT G   A    F    D G  V V  P + SY +++
Sbjct: 71  LRRAIAGLYARWYGVDLDPARVVVTSGSSAAFLLAFTTYFDAGARVGVAEPGYPSYRQIL 130

Query: 133 RFAGGVVVEVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALARL 192
           +      V + T PE G     E + +A        ++ SPNNPTG +  ++ L AL   
Sbjct: 131 KALSLAPVGLPTQPETGHRMTAEALAQA---DIAGAIIASPNNPTGTMLDRDGLGALIAA 187

Query: 193 AVEHDFYLVSDEIYEHLLYEGEHFSPGRVAPEHTLTVNGAAKAFAMTGWRIGYACGPKEV 252
             + D   +SDEIY H L+ G+         +    +N  +K F+MTGWRIG+   P+  
Sbjct: 188 CRDRDRVFISDEIY-HGLHYGDRAVSALEISDDVCVINSFSKYFSMTGWRIGWLVVPEAQ 246

Query: 253 IKAMASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGLTALGL 312
           ++ +  ++         +AQ A L AL   +A+R  +E  R  Y   R L+++GL A GL
Sbjct: 247 VRVVERLAQNMFICAPHVAQIAALGAL--GDAARPELEANRAVYAANRQLVIDGLRAAGL 304

Query: 313 KA-VRPSGAFYVLMDTSPIAPD-EVRAAERLLEAGVAVVPGTDF---AAFGHVRLSYATS 367
            A   P GAFYV +DT  ++ D    AA+ L +AGVAV PG DF      G +RLSYA +
Sbjct: 305 DAFAPPDGAFYVYVDTGALSSDSRTLAADILEKAGVAVTPGLDFDPVRGHGTLRLSYARA 364

Query: 368 EENLRKALERFARVLGRA 385
            E++ + + R       A
Sbjct: 365 TEDIAEGMTRLTNYFAAA 382


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: 365
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: 391
Length adjustment: 30
Effective length of query: 355
Effective length of database: 361
Effective search space:   128155
Effective search space used:   128155
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