GapMind for Amino acid biosynthesis

 

Alignments for a candidate for split_metH_2 in Thermomonospora curvata DSM 43183

Align Methionine synthase component, methyltransferase domain (EC:2.1.1.13) (characterized)
to candidate WP_012852642.1 TCUR_RS11345 methionine synthase

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



>NCBI__GCF_000024385.1:WP_012852642.1
          Length = 1157

 Score =  112 bits (281), Expect = 4e-29
 Identities = 93/309 (30%), Positives = 138/309 (44%), Gaps = 28/309 (9%)

Query: 15  LLADGATGTNLFNMGLQSGD------APELWNVDEPKKITALYQGAVDAGSDLFLTNTFG 68
           ++ADGA GT L        D        E+ NV  P  + A++   +DAG D   TNTFG
Sbjct: 17  VVADGAMGTMLQAHNPTLDDFQGYEGCNEILNVTRPDIVRAVHAAYLDAGVDCVETNTFG 76

Query: 69  GTAARLKLHDAHRRVRELNVAGAELGRNVAD---RSERKIAVAGSVGPTGEIMQPVGELS 125
                L  +    R+ EL  AGA + R VAD     ER   V GS+GP G  +  +G +S
Sbjct: 77  ANLGNLGEYGITDRIEELAEAGARIAREVADSYSTPERPRWVIGSIGP-GTKLPTLGHVS 135

Query: 126 HALAVEMFHEQAEALKEGGVDVLWLETISAPEEYRAAAEAFKL------ADMPWCGTMSF 179
           +    E +   A  L  GG   L +ET     + +AA    K       AD+     ++ 
Sbjct: 136 YGELRESYRRTAAGLIAGGAHALLVETCQDLLQVKAALNGAKQAVAEAGADVVLIAQVTI 195

Query: 180 DTAGRTMMGVTSADMAQLVEEFDPAPL-AFGANCGTGASDILRTVLGFAAQGTTRPIISK 238
           +  G  ++G   +++   +   +P  +   G NC TG ++ +   L + ++     +   
Sbjct: 196 EQNGAMLLG---SEIGAALTALEPLGIDLIGLNCATGPAE-MSEHLRYLSRHARVGLSCM 251

Query: 239 GNAGIPKYVDGHIHYDGTP-TLMGEYAAMARDCGAKIIGGCCGTMPDHLRAM------RE 291
            NAG+P+       Y  TP  L   + A  RD G  ++GGCCGT P+HLR +      RE
Sbjct: 252 PNAGLPELTPDGARYPLTPQELADAHDAFTRDYGLSLVGGCCGTTPEHLRLVVERVRGRE 311

Query: 292 ALDTRPRGE 300
               RPR E
Sbjct: 312 LAPRRPRPE 320


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: 953
Number of extensions: 55
Number of successful extensions: 3
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: 338
Length of database: 1157
Length adjustment: 37
Effective length of query: 301
Effective length of database: 1120
Effective search space:   337120
Effective search space used:   337120
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: 53 (25.0 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