GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metY in Methanosarcina barkeri Fusaro

Align O-acetylhomoserine sulfhydrylase (EC:2.5.1.49) (characterized)
to candidate WP_011307957.1 MBAR_RS16035 aminotransferase class V-fold PLP-dependent enzyme

Query= reanno::Korea:Ga0059261_3194
         (402 letters)



>NCBI__GCF_000195895.1:WP_011307957.1
          Length = 394

 Score =  288 bits (736), Expect = 3e-82
 Identities = 156/371 (42%), Positives = 225/371 (60%), Gaps = 5/371 (1%)

Query: 31  WGETSEALFLTSGYAYDCAGDAAARFSGDQQGMTYSRL--QNPTVEMLEQRIALLEGAEA 88
           +G  +  +F TS + ++ A   AARF+G++ G  Y+R+    PT  +L ++ A LEG EA
Sbjct: 22  FGAHTTPIFQTSTFIFENARQGAARFAGEESGYVYARIPPNTPTHAVLAEKFAALEGGEA 81

Query: 89  CRATASGMAAMTAALLCQLSAGDHLIGGRAAFGSCRWLTDTQLPKFGIETTVVDARDPQQ 148
            +  ASGMAA+TA  L  L  GDHLI     +G    L    LP  GIE + VD    + 
Sbjct: 82  GQTFASGMAAVTAIALTALKQGDHLISTDVVYGCTYSLFSQVLPGLGIEVSFVDTSKTEN 141

Query: 149 FIDAIRPNTKVFFFETPANPTMDVVDLKAVCAIARERGIVTVVDNAFATPALQRPMDFGA 208
              A +P TK+ F E+PANPT++V D+  +  IARE   + VVDN FATP  QRP++ GA
Sbjct: 142 VKRAFKPETKMVFLESPANPTLNVCDIPEIARIARENEALCVVDNTFATPYFQRPLELGA 201

Query: 209 DVVAYSATKMMDGQGRVLAGAVCGTEEFINNTLLPFHRNTGPTLSPFNAWVVLKGLETLD 268
           D+   S TK + G   +L G V G  +FI+  +      TG  + P  AW+ ++GL+TL 
Sbjct: 202 DLSLSSCTKYIGGHADLLGGIVAGNNDFIDR-MSEVVGYTGGIMGPHEAWLCIRGLKTLH 260

Query: 269 LRIQRQSENALKVARFLEGR--VPRVNFPGLPSHPQHNLAMSQMAAAGPIFSIELDGGRT 326
           +R++R +ENA+KVA FLE R  V  V +PGLP HPQ+ LA  QM+    + S E+ GG  
Sbjct: 261 IRMERHAENAMKVAEFLESRPEVEWVRYPGLPGHPQYELARKQMSGFSGMLSFEVKGGIE 320

Query: 327 QAHGLLDALGLIDISNNIGDSRSLMTHPASTTHSGVAEDQRLLMGVGEGMLRLNVGLEDP 386
               L+D + L  ++ ++G + +L+ HPAS TH+ V  + R  +G+ +G++RL+VG+EDP
Sbjct: 321 AGRKLMDNVKLCSLAVSLGATDTLIQHPASMTHACVPHEVRKSVGITDGLVRLSVGIEDP 380

Query: 387 EDLIADLDQAL 397
           ED+IADL QAL
Sbjct: 381 EDIIADLKQAL 391


Lambda     K      H
   0.319    0.134    0.396 

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: 393
Number of extensions: 17
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: 402
Length of database: 394
Length adjustment: 31
Effective length of query: 371
Effective length of database: 363
Effective search space:   134673
Effective search space used:   134673
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 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