GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Halorhodospira halophila SL1

Align LL-diaminopimelate aminotransferase; DAP-AT; DAP-aminotransferase; LL-DAP-aminotransferase; EC 2.6.1.83 (uncharacterized)
to candidate WP_049751641.1 HHAL_RS09970 aminotransferase class I/II-fold pyridoxal phosphate-dependent enzyme

Query= curated2:B1I544
         (392 letters)



>NCBI__GCF_000015585.1:WP_049751641.1
          Length = 399

 Score =  176 bits (447), Expect = 8e-49
 Identities = 111/353 (31%), Positives = 171/353 (48%), Gaps = 5/353 (1%)

Query: 33  DVISLGIGDPDVPTPDHIIEAAEKELKIPANHQYPSSAGMPAYRRAVADWYARRFGVELD 92
           DVI L IG PD P P+H++EA  + L+      Y   AG+P    AVA++Y+ R+   L+
Sbjct: 41  DVIHLSIGQPDFPMPEHVVEAHIQALR-DGKTGYTMDAGLPQMLEAVAEYYSHRYDRPLE 99

Query: 93  PQREVVSLIGSKEGIAHLPWCFVDPGDVVLVPDPGYPVYAGGTILAGGIPHPVPLTAGNG 152
           P+  +++  G+ E +         PG   L+PDP +P+YA    + G    P+P  A +G
Sbjct: 100 PENVLITT-GATEAMYLAIAATAAPGRQFLIPDPTFPLYAPLIRMNGAEVKPIPTRAEHG 158

Query: 153 FLPDLAAIPAETARRAKVMFINYPNNPTGAVASKEFFARVVDFAREYGILVCHDAAYSEI 212
              D   +      R   + +N P+NPTG V  +E    +V  A   G+ V  D  Y  +
Sbjct: 159 HQIDPQEVIDNIGMRTFGIILNSPSNPTGTVYPRETIEAIVQEAAYRGVYVFSDEVYDHL 218

Query: 213 AFDGYRPPSFLEVAGAREVGIEFHSVSKTYNMTGWRAGWAAGNAGAVEALGRLKSNLDSG 272
             D    PS L      +  +   S+SKT++M G R GW   + GA++ L R      + 
Sbjct: 219 LLDEMEYPSVLRCTSDLDHVMAVSSLSKTFSMAGLRIGWLISSQGAIKKLQRFHIFTTTV 278

Query: 273 VFQVVQYAAIAALNGPQDGVQSLCEMYRERRDLVVDTLNDLGWRLT--RPRATFYIWAPV 330
                Q+A +AAL G    V  + E YR+RRD +V+ ++     LT  RP+  FYI+  +
Sbjct: 279 ANTPAQWAGVAALKGGMACVDEMLEAYRQRRDRIVELVSKTP-HLTSYRPQGAFYIFPSL 337

Query: 331 PAGHDASSFAEMVLEKAGVVITPGTGYGTYGEGYFRISLTLPTPRLVEAMERL 383
           P   DA++ A  +L++ GV + PG  +G       RIS       +  A ER+
Sbjct: 338 PPNTDATNLATRMLKETGVCVVPGDAFGDSCPNSLRISYAASMDDIERAFERI 390


Lambda     K      H
   0.321    0.139    0.430 

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: 361
Number of extensions: 23
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: 392
Length of database: 399
Length adjustment: 31
Effective length of query: 361
Effective length of database: 368
Effective search space:   132848
Effective search space used:   132848
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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