GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Mycolicibacterium vanbaalenii PYR-1

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_011778808.1 MVAN_RS07820 homoserine O-acetyltransferase

Query= SwissProt::A9I0E6
         (424 letters)



>NCBI__GCF_000015305.1:WP_011778808.1
          Length = 375

 Score =  238 bits (606), Expect = 3e-67
 Identities = 136/364 (37%), Positives = 195/364 (53%), Gaps = 18/364 (4%)

Query: 39  PLPLASGQSLQSYELAVETYGTLNAGRTNAVLVCHALNASHHVAGLAADDPNDVGWWDNM 98
           PL L +G+ +    +AV+ +G L+A R N V+V HAL    H+ G A  D    GWWD +
Sbjct: 26  PLTLENGEVIDDVSIAVQRWGELSARRDNVVVVLHALTGDSHITGPAGPDHPTPGWWDGV 85

Query: 99  VGPGKPLDTNRFFVIGVNNLGSCFGSTGPASINPATGHPWGAAFPVLTVEDWVHAQARLA 158
            GPG P+DT+R+  I  N LG C GSTGP+S+ P  G  WG+ FP +++ D V A     
Sbjct: 86  AGPGAPIDTDRWCAISTNVLGGCRGSTGPSSLAP-DGKAWGSRFPTISIRDQVAADVAAL 144

Query: 159 DHFGIERFAAVMGGSLGGMQALSWAITCPERVAHCIVIASTPRLSAQNIGFNEVARRAII 218
           + FGI   AAV+GGS+GG +AL W +  P+ V   +V+A   R +A  IG       AI 
Sbjct: 145 ERFGITEVAAVIGGSMGGARALEWMMLHPDSVRAALVLAVGARATADQIGTQCTQVAAIK 204

Query: 219 TDPDFHGGDYYAHNTVPRRGLSVARMIGHITYLSDDDMAEKFGRTQR---EPAEGGAYRY 275
           +DP++ GGDY+     P  GL +AR   H+TY  + ++ E+FG   +   +PA GG Y  
Sbjct: 205 SDPNWRGGDYHGTGRSPDHGLEIARRFAHLTYRGETELDERFGNDAQPGEDPATGGRY-- 262

Query: 276 GYDVEFEVESYLRYQGEKFSRYFDANTYLLITRALDYFDPARGTGGDLARALKPAQADFL 335
                  V+SYL +QG K    FDA TY+ +T AL   D  RG GG +A AL+      +
Sbjct: 263 ------SVQSYLEHQGRKLLARFDAGTYVTLTDALSSHDIGRGRGG-VAAALQSCPVPTV 315

Query: 336 LVSFSTDWRFPPERSREIVRALLK-NGSPVTYAEIDAPHGHDAFLLDDARYHAVVRGYYE 394
           +   ++D  +P     E+   L   +G  V    +D+  GHD FL++      ++R   E
Sbjct: 316 VGGITSDRLYPLRLQAELAELLPGCDGLDV----VDSACGHDGFLVETDAVGKLIRRTLE 371

Query: 395 RIAR 398
             AR
Sbjct: 372 LAAR 375


Lambda     K      H
   0.320    0.137    0.427 

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: 438
Number of extensions: 18
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: 424
Length of database: 375
Length adjustment: 31
Effective length of query: 393
Effective length of database: 344
Effective search space:   135192
Effective search space used:   135192
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