GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metX in Azospirillum brasilense Sp245

Align Homoserine O-acetyltransferase; HAT; Homoserine transacetylase; HTA; EC 2.3.1.31 (characterized)
to candidate AZOBR_RS14010 AZOBR_RS14010 homoserine O-succinyltransferase

Query= SwissProt::Q2GAJ2
         (301 letters)



>FitnessBrowser__azobra:AZOBR_RS14010
          Length = 307

 Score =  412 bits (1059), Expect = e-120
 Identities = 193/304 (63%), Positives = 234/304 (76%), Gaps = 4/304 (1%)

Query: 1   MPIRIADNLPARRTLEAEGVIVMSETEAARQDIRPMRIALLNLMPDKITTETQIARLLGA 60
           MPIRI ++LPA   L+ EGV+VM E +A RQDIRP+R  LLNLMPDKI TETQIARLLG 
Sbjct: 1   MPIRIPNDLPAFTALQTEGVMVMQEADAIRQDIRPLRFGLLNLMPDKIRTETQIARLLGN 60

Query: 61  TPLQVDLELVRISDHVSKNTSAGHISAFYRPWDDVRAEKYDGLIVTGAPVETIPYEEVSY 120
           TPLQV+L L+RI++HV +NT+A H+SAFYR W+D R E +DG I+TGAPVET+P+EEVSY
Sbjct: 61  TPLQVELSLIRITNHVPRNTAADHMSAFYRSWEDARRETFDGFIITGAPVETMPFEEVSY 120

Query: 121 WDELRRIFDWSQSNVHRTLSVCWGAMAALYHFHGIEKHGLPTKASGVFRHVNHAPASPWM 180
           WDEL  +FDW+QS+VH  L++CW A AA++HFHG+ KH LP KASGVFRH N APASP++
Sbjct: 121 WDELCSVFDWTQSHVHACLNICWAAQAAVHHFHGVPKHLLPRKASGVFRHRNRAPASPYL 180

Query: 181 RGLPDVFDVPVSRWSEVRREDLPEGRGLSVLADSAETGLCLIDDPAMRTLHMFNHLEYDT 240
            GL D   +PVSRW+EVR +DLP   GL VL DS ETG CL++D A R+LHMFNH+EYDT
Sbjct: 181 CGLSDGVPIPVSRWTEVREDDLPPESGLRVLLDSPETGPCLLEDAAHRSLHMFNHIEYDT 240

Query: 241 LTLAGEYARDEGK----YLPRNYFPGDDPQAMPANTWRGHGHLLYGNWINETYQTTPYDL 296
            TL  EY RD  K     +P  YFP DDP   P N WR H HLL+ NWIN+ YQTTP++L
Sbjct: 241 DTLRNEYVRDVAKDAATPVPHGYFPDDDPSQPPENRWRSHAHLLFANWINQIYQTTPFEL 300

Query: 297 ADIG 300
           + IG
Sbjct: 301 SRIG 304


Lambda     K      H
   0.320    0.137    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: 388
Number of extensions: 12
Number of successful extensions: 2
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: 301
Length of database: 307
Length adjustment: 27
Effective length of query: 274
Effective length of database: 280
Effective search space:    76720
Effective search space used:    76720
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: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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