GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Sinorhizobium meliloti 1021

Align Aspartate/prephenate aminotransferase; AspAT / PAT; EC 2.6.1.1; EC 2.6.1.79 (characterized)
to candidate SMc02262 SMc02262 aminotransferase

Query= SwissProt::A3PMF8
         (400 letters)



>FitnessBrowser__Smeli:SMc02262
          Length = 396

 Score =  194 bits (493), Expect = 4e-54
 Identities = 129/375 (34%), Positives = 189/375 (50%), Gaps = 16/375 (4%)

Query: 22  KARELAAAGRDVIGLGAGEPDFDTPDNIKAAAKRAIDAGRTKYTAVDGIPELKRAICEKF 81
           +AR+L A+G ++I L  GEPD      +    +RA++AGR +Y+   G P +  A+ EK+
Sbjct: 23  RARQLKASGAELIELTIGEPDLPPDRALLEECQRAMNAGRYRYSNGRGEPAVVAALTEKY 82

Query: 82  ERENGLKYTPAQVTVGTGGKQILYNALVATLNPGDEVIIPAPYWVSYPDMVLLAGGTPVS 141
            R      T   +    G +  L+  + A    GD V++  P + +Y  ++   G  PV 
Sbjct: 83  RRRRAA-VTAENILCFPGTQTALFAVMFALAEAGDGVLVGDPLYATYEGVIRSTGAHPVF 141

Query: 142 VAAGMETGFKLTPEQLEAAITPRTKWFIFNSPSNPTGAAYTRAELAALCEVLMRHPQVWI 201
           V    E GF +  E LE A+TP  +  + N+P NPTGA  T  E+AA+ EV  RH  +WI
Sbjct: 142 VPLNPENGFHMRAEDLEKAVTPECRVLLLNTPHNPTGAVLTAEEIAAIGEVARRH-DLWI 200

Query: 202 MSDDMYEHLVFDDFDFTTPAQIEPGLYDRTLTCNGVSKAYCMTGWRIGYAAGPVELIRAM 261
           + D++YE LVFD   F +P    P L +RT+  + +SK++   G+R G+A GP E    +
Sbjct: 201 VCDEVYEELVFDAL-FASPFD-NPDLAERTVVVSSISKSHAAPGFRSGWAVGPAEFTERL 258

Query: 262 GTIQSQSTSNPCSIAQYAALEALSGPQEFLATNREAFQRRRDLVVSMLNEAKGVTCPNPE 321
             I                  AL+   +     RE++ RR   ++  L  A GV+   PE
Sbjct: 259 LPISETMLFGQQPFIADMTAYALTHDIDTARQMRESYSRRARRIIDGLAGASGVSVLPPE 318

Query: 322 GAFYVYPDISGCIGKTSAGGAKITDDEAFASALLEETGVAVVFGAAFG-LSPNF-RISYA 379
              +   D+SG    T   G      EAFA ALLEE GVAV+ G++FG  + NF R+S  
Sbjct: 319 AGMFALIDVSG----TGLSG------EAFAWALLEEEGVAVMPGSSFGDKARNFLRVSLT 368

Query: 380 TADEVLREACARIQA 394
             D  + EAC RI A
Sbjct: 369 VPDAAIEEACRRIAA 383


Lambda     K      H
   0.318    0.134    0.399 

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: 427
Number of extensions: 34
Number of successful extensions: 7
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: 400
Length of database: 396
Length adjustment: 31
Effective length of query: 369
Effective length of database: 365
Effective search space:   134685
Effective search space used:   134685
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 (21.7 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