GapMind for Amino acid biosynthesis

 

Alignments for a candidate for DAPtransferase in Azorhizobium caulinodans ORS 571

Align LL-diaminopimelate aminotransferase; DAP-AT; DAP-aminotransferase; LL-DAP-aminotransferase; EC 2.6.1.83 (uncharacterized)
to candidate WP_012169089.1 AZC_RS02835 pyridoxal phosphate-dependent aminotransferase

Query= curated2:B1I544
         (392 letters)



>NCBI__GCF_000010525.1:WP_012169089.1
          Length = 394

 Score =  206 bits (523), Expect = 1e-57
 Identities = 132/359 (36%), Positives = 183/359 (50%), Gaps = 6/359 (1%)

Query: 29  AQGVDVISLGIGDPDVPTPDHIIEAAEKELKIPANHQYPSSAGMPAYRRAVADWYARRFG 88
           AQG D+I+LGIG PD  TP+HI+EAA K LK    H Y  S G+   R AVA    +RF 
Sbjct: 28  AQGRDIINLGIGQPDFRTPEHIVEAAVKALK-DGQHGYTPSVGIQPLREAVARDLHKRFD 86

Query: 89  VELDPQREVVSLIGSKEGIAHLPWCFVDPGDVVLVPDPGYPVYAGGTILAGGIPHPVPLT 148
           VE+DP   V+ + G K  +      F +PG  +L PDPG+P+Y       G  P PVP+ 
Sbjct: 87  VEVDPGL-VMIMPGGKVTMYAAILLFGEPGAEILYPDPGFPIYRSMIEYTGATPIPVPIR 145

Query: 149 AGNGFLPDLAAIPAETARRAKVMFINYPNNPTGAVASKEFFARVVDFAREYG-ILVCHDA 207
             NGF        A    + +++ IN P NPTG V  K    ++V    ++  + +  D 
Sbjct: 146 EENGFAFSAEETLALITPKTRLLIINSPANPTGGVTPKAEIDKLVKGLADHPHVALMSDE 205

Query: 208 AYSEIAFDGYRPPSFLEVAGAREVGIEFHSVSKTYNMTGWRAGWAAGNAGAVEALGRLKS 267
            Y +  FDG R  + L     R+  I  +  SKTY MTGWR G++       + + +L  
Sbjct: 206 IYDQFLFDGERHQTLLAYPEIRDRLILLNGWSKTYAMTGWRLGYSIWPQALYDKVRKLSV 265

Query: 268 NLDSGVFQVVQYAAIAALNGPQDGVQSLCEMYRERRDLVVDTLNDL-GWRLTRPRATFYI 326
           N  S V    QYA IAAL GPQ+ V ++   + +RR LVV+ LN L G    +P+  FY 
Sbjct: 266 NAWSCVNAATQYAGIAALEGPQEPVAAMLAEFDKRRRLVVEGLNALPGVTCAKPKGAFYA 325

Query: 327 WAPV--PAGHDASSFAEMVLEKAGVVITPGTGYGTYGEGYFRISLTLPTPRLVEAMERL 383
           +  V       A + A  +LE AGV    G  +G +GEGY R+S       +  A+ER+
Sbjct: 326 FPNVSRTGWTSAKALASALLEDAGVATIGGPDFGVHGEGYIRLSYANSAENIARALERM 384


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: 305
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: 392
Length of database: 394
Length adjustment: 31
Effective length of query: 361
Effective length of database: 363
Effective search space:   131043
Effective search space used:   131043
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 Apr 10 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