GapMind for Amino acid biosynthesis

 

Alignments for a candidate for split_metH_2 in Methylosarcina fibrata AML-C10

Align Methionine synthase component, methyltransferase domain (EC:2.1.1.13) (characterized)
to candidate WP_020562591.1 A3OW_RS0106365 methionine synthase

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



>NCBI__GCF_000372865.1:WP_020562591.1
          Length = 1224

 Score =  109 bits (272), Expect = 4e-28
 Identities = 104/333 (31%), Positives = 151/333 (45%), Gaps = 49/333 (14%)

Query: 6   TTLLETKDA---LLADGATGTNLFNMGLQS----GDAPELWNVD-----------EPKKI 47
           TTLL+ + A   L  DGA GT + +  L      G+    W+ D           +P  I
Sbjct: 4   TTLLKKQLAQRILFLDGAMGTMIQSYKLDEKDYRGERFAAWDSDLKGNNDLLSLTQPAII 63

Query: 48  TALYQGAVDAGSDLFLTNTFGGTAARLKLHDAHRRVRELNVAGAELG-RNVADRSERKIA 106
            A++   +DAG+D+  TNTF  T   +  +       E+N+  A L     AD S R  A
Sbjct: 64  KAIHSAYLDAGADIIETNTFNATRIAMADYRMESLAYEINLESARLACEAAADYSARTPA 123

Query: 107 ----VAGSVGPTGEI--MQP------VGELSHALAVEMFHEQAEALKEGGVDVLWLETIS 154
               VAG +GPT     M P         ++     E + E    L +GG D+L +ET+ 
Sbjct: 124 KPRFVAGVLGPTNRTASMSPDVNDPGFRNITFDELAEAYTESVRGLIDGGADILLIETVF 183

Query: 155 APEEYRAAAEA---------FKLADMPWCGTMSFDTAGRTMMGVTSADMAQLVEEFDPAP 205
                +AA  A         +KL  M   GT++ D +GRT+ G T A     ++  +P  
Sbjct: 184 DTLNAKAAIFAVEQYFDSIGYKLPVMI-SGTIT-DASGRTLSGQTVAAFWHSLKHVEP-- 239

Query: 206 LAFGANCGTGASDILRTVLGFAAQGTTRPIISKGNAGIPKYVDGHIHYDGTPTLMGEYAA 265
           ++FG NC  GA ++ + +   A+   T  + +  NAG+P        YD TP  M E  A
Sbjct: 240 ISFGFNCALGARELRQHIDELASIADTH-VSAHPNAGLPNEFG---EYDETPEAMAEELA 295

Query: 266 -MARDCGAKIIGGCCGTMPDHLRAMREALDTRP 297
             AR     +IGGCCGT PDH+RA+  A+   P
Sbjct: 296 DWARSGYLNVIGGCCGTTPDHIRAIVAAVQKYP 328


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: 888
Number of extensions: 52
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: 338
Length of database: 1224
Length adjustment: 38
Effective length of query: 300
Effective length of database: 1186
Effective search space:   355800
Effective search space used:   355800
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.

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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