GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Allochromatium vinosum DSM 180

Align Phosphoserine aminotransferase; Phosphohydroxythreonine aminotransferase; PSAT; EC 2.6.1.52 (characterized)
to candidate WP_012971153.1 ALVIN_RS09725 phosphoserine transaminase

Query= SwissProt::Q59196
         (362 letters)



>NCBI__GCF_000025485.1:WP_012971153.1
          Length = 372

 Score =  294 bits (753), Expect = 2e-84
 Identities = 158/364 (43%), Positives = 219/364 (60%), Gaps = 4/364 (1%)

Query: 3   KRAYNFNAGPAALPLEVLERAQAEFVDYQHTGMSIMEMSHRGAVYEAVHNEAQARLLALL 62
           + A NF+ GP ALP  VL   +         G+SI+ +SHR   +  +  + +  L ALL
Sbjct: 9   RNALNFSGGPGALPAVVLAETRQAIDAVPEIGLSILGVSHRSDWFAGLIEQTERDLRALL 68

Query: 63  GNPTGYKVLFIQGGASTQFAMIPMNFLK-EGQTANYVMTGSWASKALKEAKLIGDTHVAA 121
             P  + VL +QGGA+ QF+MIPM  L+  G+ A Y+ TG W++K++  A+L GD  V  
Sbjct: 69  DLPDSHAVLMLQGGATLQFSMIPMLLLRGSGRVAEYLRTGYWSAKSIAPARLEGDVRVLW 128

Query: 122 SSE--ASNYMTLPKLQEIQLQDNAAYLHLTSNETIEGAQFKAFPDTGSVPLIGDMSSDIL 179
             E   + +  LP   E++    AAYLH  SNET+EG QF   P    V  + DMSSD L
Sbjct: 129 DGERQGAGFRRLPTADELECSPEAAYLHYVSNETVEGVQFHHIPGLDGVRRVCDMSSDFL 188

Query: 180 SRPFDLNQFGLVYAGAQKNLGPSGVTVVIVREDLVAESPKHLPTMLRYDTYVKNNSLYNT 239
           SRP D  +F LVYA AQKNLGP+GVT+V++R  L+ + P  +P +L Y  +++  S+YNT
Sbjct: 189 SRPCDPERFDLVYAHAQKNLGPAGVTLVVIRRALLDQVPPGIPDILDYRAHLQARSIYNT 248

Query: 240 PPSFGIYMVNEVLKWI-EERGGLEGVQQANRKKASLIYDAIDQSGGFYRGCVDVDSRSDM 298
           PP   IY+V+ VL+W+ E+ GGLE +   NR KA+ +Y+ ID+    Y G      RS M
Sbjct: 249 PPVMAIYVVSRVLRWLREDIGGLERMDALNRHKAACLYEVIDRYPDVYTGWAHPADRSRM 308

Query: 299 NITFRLASEELEKEFVKASEQEGFVGLKGHRSVGGLRASIYNAVPYESCEALVQFMEHFK 358
           N+ FRL + E E +F+  +E  GF GLKGHRS+GG+RASIYN +   + E L +FM  F 
Sbjct: 309 NVVFRLPTPEREADFLHRAESAGFSGLKGHRSLGGIRASIYNGMSLAAVERLAKFMTDFA 368

Query: 359 RSRG 362
           R  G
Sbjct: 369 RHGG 372


Lambda     K      H
   0.316    0.132    0.378 

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: 348
Number of extensions: 20
Number of successful extensions: 4
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: 362
Length of database: 372
Length adjustment: 30
Effective length of query: 332
Effective length of database: 342
Effective search space:   113544
Effective search space used:   113544
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 (21.6 bits)
S2: 49 (23.5 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