GapMind for Amino acid biosynthesis

 

Alignments for a candidate for split_metH_2 in Dinoroseobacter shibae DFL-12

Align Methionine synthase component, methyltransferase domain (EC:2.1.1.13) (characterized)
to candidate 3607665 Dshi_1074 homocysteine S-methyltransferase (RefSeq)

Query= reanno::Phaeo:GFF1321
         (338 letters)



>FitnessBrowser__Dino:3607665
          Length = 341

 Score =  457 bits (1175), Expect = e-133
 Identities = 231/333 (69%), Positives = 261/333 (78%), Gaps = 3/333 (0%)

Query: 6   TTLLETKDALLADGATGTNLFNMGLQSGDAPELWNVDEPKKITALYQGAVDAGSDLFLTN 65
           T LL  +  LL DGATGT LFNMGL SGDAPELWN D P +I ALYQGAVDAGSDLFLTN
Sbjct: 7   TPLLAERGILLTDGATGTTLFNMGLSSGDAPELWNTDHPDRIAALYQGAVDAGSDLFLTN 66

Query: 66  TFGGTAARLKLHDAHRRVRELNVAGAELGRNVADRSERKIAVAGSVGPTGEIMQPVGELS 125
           +FGG A+RLKLH A  RVRELN   AE+GR VAD+++RK+ VAGS+GPTGEIM P+G L+
Sbjct: 67  SFGGNASRLKLHAAQDRVRELNRLAAEIGRGVADKADRKVLVAGSMGPTGEIMAPMGPLT 126

Query: 126 HALAVEMFHEQAEALKEGGVDVLWLETISAPEEYRAAAEAFKLADMPWCGTMSFDTAGRT 185
           H +AVEMFHEQAE LKEGG D+LW+ETISAPEEY AAAEA   ADMPWCGTMSFDTAGRT
Sbjct: 127 HDIAVEMFHEQAEGLKEGGADILWVETISAPEEYAAAAEAAARADMPWCGTMSFDTAGRT 186

Query: 186 MMGVTSADMAQLVEEFDPAPLAFGANCGTGASDILRTVLGFAAQGTTRPIISKGNAGIPK 245
           MMG TSA MA++VE+    P+AFGANCG GASD+LRTVLGFAA GT RPII+KGNAGIPK
Sbjct: 187 MMGTTSATMARMVEKLAHPPVAFGANCGVGASDLLRTVLGFAAAGTERPIIAKGNAGIPK 246

Query: 246 YVDGHIHYDGTPTLMGEYAAMARDCGAKIIGGCCGTMPDHLRAMREALDTRPRG-EQLTL 304
           YVDGHIHYDGTP LM +YA +AR  GA +IGGCCGT  +HLR MR ALD       + +L
Sbjct: 247 YVDGHIHYDGTPDLMAQYAILARASGASVIGGCCGTTFEHLRHMRAALDASAADMPRPSL 306

Query: 305 ERIVEVLGPFTSDSDGT--GEDTAPDRRSRRGR 335
           + I E LG F+S +DGT  G     DR  RR R
Sbjct: 307 DEITEALGGFSSAADGTEAGGPKPADRPRRRRR 339


Lambda     K      H
   0.317    0.134    0.397 

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: 481
Number of extensions: 18
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 338
Length of database: 341
Length adjustment: 28
Effective length of query: 310
Effective length of database: 313
Effective search space:    97030
Effective search space used:    97030
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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