GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Desulfovibrio vulgaris Hildenborough

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate 206268 DVU0841 aspartate aminotransferase, putative

Query= BRENDA::Q56232
         (385 letters)



>MicrobesOnline__882:206268
          Length = 393

 Score =  178 bits (451), Expect = 3e-49
 Identities = 126/377 (33%), Positives = 182/377 (48%), Gaps = 33/377 (8%)

Query: 27  RRQGVDLVA-LTAGEPDFDTPEHVKEAAR----RALAQGKTKYAPPAGIPELREALAEKF 81
           ++ G D V   + G PD   P  V +  R    RA       Y P  G    R+ LA   
Sbjct: 30  QQYGEDAVCDFSLGNPDLPAPAAVGDGLRAMADRAGEPFAFGYMPNGGYAWARQKLATHL 89

Query: 82  RRENGLSVTPEETIVTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPEMVRFAGGVVVE 141
             E G+S+T ++ ++T G    L   F+A+LD GDEV+ ++PY+V Y   V   GGV   
Sbjct: 90  SAEQGVSLTGDDVVLTCGAAGGLNAFFRAVLDEGDEVLSMAPYFVEYGFYVENHGGVFRT 149

Query: 142 VETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALARLAVE------ 195
           V+TLP+  F  D + +  A+TPRT+A+++NSPNNPTGAVY +  LE LA +         
Sbjct: 150 VKTLPDT-FGLDLDAIELAMTPRTRAVIINSPNNPTGAVYSRAELEGLADILARASARNG 208

Query: 196 HDFYLVSDEIYEHLLYEGEHFSPGRVAPEHTLTVNGAAKAFAMTGWRIGY-ACGPKEVIK 254
              +L++DE Y  L ++G          +H+L V+  +K  ++ G R+GY A  P+   +
Sbjct: 209 RPVFLIADEPYRFLAFDGAEVPSVLPLYDHSLVVSSFSKNLSLAGERLGYIALSPRMENR 268

Query: 255 AMASVSSQST------TSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGLT 308
              +     T       +P  + Q     AL  Q        +    Y RRRD++ E LT
Sbjct: 269 GKLAAGLLLTNRILGFVNPPVVGQHIMAAALGAQ--------VDASIYARRRDVMAEVLT 320

Query: 309 ALGLKAVRPSGAFYVLMDTSPIAP--DEVRAAERLLEAGVAVVPGTDFAAFGHVRLSYAT 366
             G     P GAFY      P AP  D+V    RL+E  +  VPG+ F   GH RL++  
Sbjct: 321 EAGYDFQMPRGAFYFF----PKAPGGDDVTFVSRLMEERILAVPGSGFGGPGHFRLTFCV 376

Query: 367 SEENLRKALERFARVLG 383
            E  +R+A E F R  G
Sbjct: 377 DETIIRRAAEGFRRARG 393


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: 370
Number of extensions: 15
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: 393
Length adjustment: 30
Effective length of query: 355
Effective length of database: 363
Effective search space:   128865
Effective search space used:   128865
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