GapMind for Amino acid biosynthesis

 

Alignments for a candidate for split_metH_3 in Dinoroseobacter shibae DFL-12

Align Methionine synthase component, pterin-binding domain (EC:2.1.1.13) (characterized)
to candidate 3608273 Dshi_1677 Methionine synthase (RefSeq)

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



>FitnessBrowser__Dino:3608273
          Length = 329

 Score =  436 bits (1120), Expect = e-127
 Identities = 241/371 (64%), Positives = 267/371 (71%), Gaps = 64/371 (17%)

Query: 1   MTRTVVESKTKTAILGFDEPFCVIGERINPTGRKKLAAELEAGDFSTVEKDALAQVMAGA 60
           MTRTV+ESKTKT  +GFDEPFCVIGERINPTGRKKLAAELEAGDFSTVEKDAL QV  GA
Sbjct: 1   MTRTVIESKTKTVTIGFDEPFCVIGERINPTGRKKLAAELEAGDFSTVEKDALEQVACGA 60

Query: 61  NILDINAGVVYNSN-------PNPNETEPPLMTKIVELVQGLTDTPLCIDSSVPGALEAG 113
            +LD+N+G V+ +         + N  EP LM ++V  VQ L D PLCIDSSVPGALE G
Sbjct: 61  MVLDVNSGAVFTNKMAEDPRYADNNFVEPMLMKELVARVQALVDIPLCIDSSVPGALENG 120

Query: 114 LQAAEGRPLLNSVTGEEERLEHVLPLVKKYNVPVVAISNDDTGISEDPDVRFAVAKKIVE 173
           L+ AEGRPLLNSVTGEE+RLE +LPLVKKYNVPVVAISNDDTGISEDPDVRFAVAKKIVE
Sbjct: 121 LEMAEGRPLLNSVTGEEDRLETILPLVKKYNVPVVAISNDDTGISEDPDVRFAVAKKIVE 180

Query: 174 RAADFGIPAHDIVVDPLVMPIGAMATAGQQVFALVRRLREELGVNTTCGASNVSFGLPNR 233
           RAADFGIPAHDIVVDPLVMP+GAMATAG+QVF LV RLREELGVNTTCGASNVSFGLPNR
Sbjct: 181 RAADFGIPAHDIVVDPLVMPVGAMATAGRQVFTLVARLREELGVNTTCGASNVSFGLPNR 240

Query: 234 HGINNAFLPMAMGAGMTSAIMNPVALPITQKKIAEKKAEVEAAGIILPEGMEDEAFVQMF 293
           HG+  AFLPMA+ +GMTSAIMNP+                                    
Sbjct: 241 HGLGAAFLPMAIASGMTSAIMNPI------------------------------------ 264

Query: 294 GLGSTKPRAGKEMEAIRAANLLTNNDPHGGEWI------KANK------EPAKEGEE-GR 340
                +P   +EMEA+ AAN L N+DP+G  WI      +A+K      E AK G   G 
Sbjct: 265 -----RP---QEMEAVHAANFLMNHDPNGATWINFARVMEAHKAGMPFPEAAKAGTSGGG 316

Query: 341 GRGGRAGGRRR 351
           GR GR GGRRR
Sbjct: 317 GRSGRRGGRRR 327


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: 405
Number of extensions: 17
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: 353
Length of database: 329
Length adjustment: 28
Effective length of query: 325
Effective length of database: 301
Effective search space:    97825
Effective search space used:    97825
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: 49 (23.5 bits)

This GapMind analysis is from Apr 09 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