GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Pseudarthrobacter sulfonivorans Ar51

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_058932725.1 AU252_RS03655 homoserine O-acetyltransferase

Query= SwissProt::Q4ZZ78
         (379 letters)



>NCBI__GCF_001484605.1:WP_058932725.1
          Length = 369

 Score =  277 bits (708), Expect = 4e-79
 Identities = 156/344 (45%), Positives = 209/344 (60%), Gaps = 13/344 (3%)

Query: 24  LALACGRSLPAYDLIYETYGQLNAARSNAVLICHALSGHHHAAGFHSADDRKPGWWDSCI 83
           L L  G  LP   L YET+G LNA  SNAVLI HAL+G  H       D  +PGWW+   
Sbjct: 22  LELEAGGYLPEVTLGYETWGTLNADGSNAVLIEHALTGSTHVT---RGDSDEPGWWEQLA 78

Query: 84  GPGKPIDTTKFFVVSLNNLGGCNGSTGPSSIDPDTGKPFGANFPVVTVEDWVNSQARLAD 143
           GPG P+DT +FFVVS+N +GGC GSTGPSS+ PD GKP+G+ FP+VT+ D   ++ARLAD
Sbjct: 79  GPGAPVDTDRFFVVSINIVGGCYGSTGPSSVAPD-GKPWGSRFPLVTLRDTTAAEARLAD 137

Query: 144 LLGIDTWAAVIGGSLGGMQALQWTISYPNRVRHCLAIASAPKLSAQNIAFNEVARQAILT 203
            LGI +W AV+GGS+GG +AL+W ++YP RV+ C  I+     +A+ IAF +    AI  
Sbjct: 138 QLGIPSWYAVLGGSMGGARALEWAVTYPERVQRCAVISIGAASTAEQIAFAQAQTLAIRQ 197

Query: 204 DPEFHGGSFQERGVIPKRGLMLARMVGHITYLSDDSMGEKFGRGLKSEKLNYDFHSV--- 260
           D  F+ G +   G +P+ GL LAR + HITY S +    +FGR  +  +  +   ++   
Sbjct: 198 DSNFNDGDYY-GGPLPEDGLALARRIAHITYRSAEEFHGRFGRSAQHPESPFQAAALGER 256

Query: 261 -EFQVESYLRYQGEEFSGRFDANTYLLMTKALDYFDPAANFNDDLAKTFANATARFCVMS 319
             +QVESYL +QG++   RFDAN+Y+ +T AL   D        L +    ATARF V +
Sbjct: 257 GRYQVESYLDHQGKKLVRRFDANSYIAITDALMSHD-VCRGRGSLNEALGRATARFFVAA 315

Query: 320 FTTDWRFSPARSRELVDALMAARKDVCYLEIDAPQGHDAFLIPI 363
             +D  + P++SREL DAL     DV    I+AP GHD FL  I
Sbjct: 316 VDSDRLYFPSQSRELADALPG---DVDVHVIEAPIGHDGFLTEI 356


Lambda     K      H
   0.321    0.137    0.428 

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: 368
Number of extensions: 25
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: 379
Length of database: 369
Length adjustment: 30
Effective length of query: 349
Effective length of database: 339
Effective search space:   118311
Effective search space used:   118311
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 (21.9 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