GapMind for Amino acid biosynthesis

 

Alignments for a candidate for split_metH_2 in Trichodesmium erythraeum IMS101

Align Methionine synthase component, methyltransferase domain (EC:2.1.1.13) (characterized)
to candidate WP_044137191.1 TERY_RS05005 methionine synthase

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



>NCBI__GCF_000014265.1:WP_044137191.1
          Length = 1196

 Score =  120 bits (300), Expect = 2e-31
 Identities = 89/302 (29%), Positives = 146/302 (48%), Gaps = 22/302 (7%)

Query: 12  KDALLADGATGTNLFNMGLQSGD--------APELWNVDEPKKITALYQGAVDAGSDLFL 63
           +  ++ DGA GT+L    L + D          E     +P  +  +++  + AG+D+  
Sbjct: 14  RPVIVFDGAMGTSLQVQNLTAEDFGGKEYEGCNEYLVHTKPDAVAKVHRDFLAAGADVIE 73

Query: 64  TNTFGGTAARLKLHDAHRRVRELNVAGAELGRNVA---DRSERKIAVAGSVGPTGEIMQP 120
           T+TFGGT   L  +D   +   LN   AEL ++ A      E+   VAGS+GP G  +  
Sbjct: 74  TDTFGGTKIVLAEYDLADQAYYLNKTAAELAKSAAAEYSTPEKPRFVAGSIGP-GTKLPT 132

Query: 121 VGELSHALAVEMFHEQAEALKEGGVDVLWLETISAPEEYRAAAEAF-----KLADM-PWC 174
           +G +  A   + F EQAE L +GGVD+  +ET     + +AA         K  D  P  
Sbjct: 133 LGHIDFATLKDSFTEQAEGLFDGGVDLFLVETCQDVLQIKAALNGIEEIFAKKGDRRPIM 192

Query: 175 GTMSFDTAGRTMMGVTSADMAQLVEEFDPAPLAFGANCGTGASDILRTVLGFAAQGTTRP 234
            +++ ++ G  ++G        ++E +    L  G NC TG  D+++  + + ++ +   
Sbjct: 193 VSVTMESFGTMLVGSEINAALTILEPYSIDIL--GLNCATGP-DLMKEHIRYLSENSPFI 249

Query: 235 IISKGNAGIPKYVDGHIHYDGTPT-LMGEYAAMARDCGAKIIGGCCGTMPDHLRAMREAL 293
           +    NAG+P+ + G  HY  TP  L         D G ++IGGCCGT PDH++A+ E  
Sbjct: 250 VSCIPNAGLPENIGGQAHYKLTPVELKMALMHFVEDLGVQVIGGCCGTRPDHIKALAEIT 309

Query: 294 DT 295
           +T
Sbjct: 310 ET 311


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: 913
Number of extensions: 54
Number of successful extensions: 6
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: 1196
Length adjustment: 38
Effective length of query: 300
Effective length of database: 1158
Effective search space:   347400
Effective search space used:   347400
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: 54 (25.4 bits)

This GapMind analysis is from Apr 10 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