GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metX in Rhizobium johnstonii 3841

Align Homoserine O-acetyltransferase; HAT; EC 2.3.1.31; Homoserine transacetylase; HTA (uncharacterized)
to candidate WP_011654184.1 RL_RS28060 homoserine O-acetyltransferase

Query= curated2:Q67NS3
         (383 letters)



>NCBI__GCF_000009265.1:WP_011654184.1
          Length = 391

 Score =  226 bits (577), Expect = 6e-64
 Identities = 131/358 (36%), Positives = 199/358 (55%), Gaps = 10/358 (2%)

Query: 26  VLESGQRLTDVTLCYEVFGRLNPAGDNAILVCHALTGDSHVAGRYRPDDPKPGWWDDAVG 85
           V   G+ + ++ L YE +G LN A DNAIL+ H  +G+SH AG+Y+  D   G+WD  +G
Sbjct: 34  VTRGGRTVPEMRLGYETYGTLNDAKDNAILIPHYFSGNSHAAGKYKEADVSAGYWDAIIG 93

Query: 86  PGKALDTDRYCVICSNV---LGGCQGS---TGPSSVNPATGRPYGLDFPLVTVRDMVRAQ 139
            GK +DTD+Y V+  +    LG    +   TGP++ NP TG+P+G+DFP++T+ D V  Q
Sbjct: 94  SGKPVDTDKYFVVSVDTPVNLGANDPNVITTGPATTNPKTGKPWGMDFPIMTIGDFVDTQ 153

Query: 140 ARLLDLLGVRRLLAVIGGSLGAMQALEWAATYPDRMRGIIPIGGAGRFHPQGIAFNEVQR 199
             L++ LG+ +  AV+G S+G +Q+ EWAA YPD++  +IP+  +G      IA+ +V  
Sbjct: 154 KGLMEQLGIGKWHAVMGASMGGLQSYEWAARYPDKLERVIPVISSGWADANLIAWLDVWA 213

Query: 200 QAILNDPGFLGGQYYGTPGPVRGLATARMLGMITYRSDESMWTQ--FGRNPQGEANPLHQ 257
             I  DP + GG YY    P  GLA A  +  +T +++ + WT   FGR+   E     Q
Sbjct: 214 SPIKLDPNWNGGDYYTGQAPNAGLAQA--MKTLTLQANSAEWTDGTFGRDWASEGADPGQ 271

Query: 258 GFAVAYQVESYLHYQGRKLVERFDANSYLYLTRAMDLMDLGRGRGSYEEAHARIQARVLA 317
            +A  Y+V + L+  G   V + DAN +LYL RA  L   G+ + S  +    I   V+ 
Sbjct: 272 SWANDYKVVTKLNEAGAARVAQSDANHFLYLARANQLFVAGQPKDSLYKGLLNIDVPVML 331

Query: 318 VGIRSDLLFPTYLQRETVELVRASGGRAEYVEMDSPWGHDAFLLDFPLIEEPIRRFLQ 375
           +    DL+FP    R T  ++++ G   E+VE++   GH   LL      E IR FL+
Sbjct: 332 IYTDEDLIFPGDAVRGTGTIIKSDGTPVEFVELEGTRGHMDGLLSIAQAGERIRAFLE 389


Lambda     K      H
   0.321    0.140    0.432 

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: 437
Number of extensions: 18
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: 383
Length of database: 391
Length adjustment: 30
Effective length of query: 353
Effective length of database: 361
Effective search space:   127433
Effective search space used:   127433
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 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