GapMind for Amino acid biosynthesis

 

Alignments for a candidate for split_metH_2 in Mesorhizobium ciceri WSM1271

Align Methionine synthase component, methyltransferase domain (EC:2.1.1.13) (characterized)
to candidate YP_004142560.1 Mesci_3387 homocysteine S-methyltransferase

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



>NCBI__GCF_000185905.1:YP_004142560.1
          Length = 345

 Score =  337 bits (864), Expect = 3e-97
 Identities = 179/336 (53%), Positives = 223/336 (66%), Gaps = 2/336 (0%)

Query: 2   TNTFTTLLETKDALLADGATGTNLFNMGLQSGDAPELWNVDEPKKITALYQGAVDAGSDL 61
           TN    LL  K  LLADGATGTNLF MGL++G+APEL N   P  IT+L+Q  VDAG+D+
Sbjct: 9   TNPIDALLAEKGVLLADGATGTNLFAMGLEAGEAPELLNETAPDTITSLHQNFVDAGADI 68

Query: 62  FLTNTFGGTAARLKLHDAHRRVRELNVAGAELGRNVADRSERKIAVAGSVGPTGEIMQPV 121
            LTN+FGGT  RLKLH A  RV  LN   AE+ R VADR+ RK+ VAGSVGPTGE++ P+
Sbjct: 69  ILTNSFGGTRHRLKLHHAQDRVHALNQRAAEIARAVADRAGRKVIVAGSVGPTGELLVPL 128

Query: 122 GELSHALAVEMFHEQAEALKEGGVDVLWLETISAPEEYRAAAEAFKLADMPWCGTMSFDT 181
           G +++  AV+ F EQ E LKEGG +V W+ET+SAP+E RAAAEA     +P+  T SFDT
Sbjct: 129 GAMTYDEAVDAFAEQIEGLKEGGAEVAWIETMSAPDEIRAAAEAAIRVGLPYTYTGSFDT 188

Query: 182 AGRTMMGVTSADMAQLVEEFDPAPLAFGANCGTGASDILRTVLGFAAQGTTRPIISKGNA 241
           AGRTMMG+   D+  + +    APL  GANCG GASDIL ++L          +I KGN 
Sbjct: 189 AGRTMMGLLPRDIHGVTDGLSAAPLGVGANCGVGASDILASLLDMTEAKPEATVIVKGNC 248

Query: 242 GIPKYVDGHIHYDGTPTLMGEYAAMARDCGAKIIGGCCGTMPDHLRAMREALDTRPRGEQ 301
           GIP++    IHY GTP LM +Y  +A D GAKIIGGCCGT   HL AMR+ALD   + ++
Sbjct: 249 GIPEFRGTEIHYSGTPELMADYVRLAVDGGAKIIGGCCGTSFQHLAAMRKALDAHTKADR 308

Query: 302 LTLERIVEVLGPFTSDSDGTGEDTAPDRRSRRGRRR 337
            T+  IVE +GP  +      E+TA    +RR RRR
Sbjct: 309 PTVAAIVERIGPMRNKV--ATENTAETSEARRERRR 342


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: 412
Number of extensions: 16
Number of successful extensions: 1
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: 345
Length adjustment: 29
Effective length of query: 309
Effective length of database: 316
Effective search space:    97644
Effective search space used:    97644
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 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