GapMind for Amino acid biosynthesis

 

Alignments for a candidate for split_metH_3 in Desulfovibrio gracilis DSM 16080

Align Methionine synthase component, pterin-binding domain (EC:2.1.1.13) (characterized)
to candidate WP_078718028.1 B5D49_RS12400 methionine synthase

Query= reanno::Phaeo:GFF1582
         (353 letters)



>NCBI__GCF_900167125.1:WP_078718028.1
          Length = 806

 Score =  160 bits (405), Expect = 1e-43
 Identities = 102/332 (30%), Positives = 162/332 (48%), Gaps = 17/332 (5%)

Query: 5   VVESKTKTAILGFDEPFCVIGERINPTGRKKLAAELEAGDFSTVEKDALAQVMAGANILD 64
           V+ S+ +   LG   P  +IGERINPTG+K+L  EL+ G+ +   + A  QV  GA +LD
Sbjct: 300 VLTSRGEGVPLGKGHPAVLIGERINPTGKKQLIHELQQGEQTEALRLAGEQVDRGAPVLD 359

Query: 65  INAGVVYNSNPNPNETEPPLMTKIVELVQGLTDTPLCIDSSVPGALEAGLQAAEGRPLLN 124
           +N G        P   E   +  +V+ + G   TPLC+DSS PGA+   L A  G PL+N
Sbjct: 360 VNVGA-------PMVDETVTLPALVKALTGRFTTPLCLDSSTPGAVAEALWAYPGSPLVN 412

Query: 125 SVTGEEERLEHVLPLVKKYNVPVVAISNDDTGISEDPDVRFAVAKKIVERAADFGIPAHD 184
           S++G+  R+  + PL  ++  P + +      +      R A+ +++++ A   G+P   
Sbjct: 413 SISGDPGRMAELGPLCARFGAPFILLPIKGKKLPVTAPERIAIIEQLLDEAESLGVPRRL 472

Query: 185 IVVDPLVMPIGAMATAGQQVFALVRRLREELGVNTTCGASNVSFGLPNRHGINNAFLPMA 244
            VVD L + + +   A +     +R   EELG+ TT G SNVSFGLP R  +N+ FL M 
Sbjct: 473 AVVDGLALTVSSKPEAARATLETIRYCTEELGLATTLGLSNVSFGLPARDLLNSTFLSMC 532

Query: 245 MGAGMTSAIMNPVALPITQKKIAEKKAEVEAAGIILPEGMEDEAFVQMFGLGSTKPRAGK 304
           + +G+ S I NP +        A  +  + A+ ++L    +   F+  +     KP  G 
Sbjct: 533 LASGLASFIANPDS--------ARLREALAASEVLLNRDPQATYFINTY--SDWKPTGGT 582

Query: 305 EMEAIRAANLLTNNDPHGGEWIKANKEPAKEG 336
                 +    T  +P       A  +  K+G
Sbjct: 583 GQPGTNSPQQGTGGEPDSHPLFSAVVKGNKDG 614


Lambda     K      H
   0.315    0.134    0.379 

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: 594
Number of extensions: 28
Number of successful extensions: 3
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: 353
Length of database: 806
Length adjustment: 35
Effective length of query: 318
Effective length of database: 771
Effective search space:   245178
Effective search space used:   245178
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: 42 (22.0 bits)
S2: 52 (24.6 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