GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Methanosarcina acetivorans C2A

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_011021821.1 MA_RS09470 pyridoxal phosphate-dependent aminotransferase

Query= BRENDA::Q8YMS6
         (388 letters)



>NCBI__GCF_000007345.1:WP_011021821.1
          Length = 380

 Score =  330 bits (845), Expect = 5e-95
 Identities = 179/381 (46%), Positives = 247/381 (64%), Gaps = 8/381 (2%)

Query: 4   AARVSQVTPSITLAIAAKAKAMKAEGIDVCSFSAGEPDFDTPAHIKAAAAKALDEGKTKY 63
           +AR+ +V  S T+ I+  A  M  EG DV +FS GEPDFDTP +I  AAAKA+ EGKT Y
Sbjct: 3   SARLKRVEESATIRISNIATRMIKEGTDVINFSLGEPDFDTPKNICDAAAKAMYEGKTHY 62

Query: 64  GAAAGEPKLREAIARKLQKDNHLDYKPENVIVTNGGKHSLYNLIVALIDPGDEVIIPAPY 123
             +AG P+LR AIA KL+ +NHL+   ++V+VT G K +++ +++  +D GD  ++  P 
Sbjct: 63  APSAGIPELRAAIAEKLKTENHLEVTEKDVLVTPGAKQAIFEIMMGALDDGDRALLFDPA 122

Query: 124 WLSYPEMVTLVGGKSVIVPTDASTGYKITPEQLRKAITPKTKLFVLNSPSNPTGMVYTPE 183
           W++Y   +   G  +V VPT    G+   P+   + I  KTKL V+NSP NPTG V+  +
Sbjct: 123 WVTYDACIRFSGANTVWVPTVPERGF--LPDNFAEYINDKTKLIVVNSPGNPTGGVFGKK 180

Query: 184 EIKALAQVVVDADIYVVSDEIYEKILYDGAQHISIGSLGKEIFNRTLISNGFAKAYSMTG 243
            ++ +A + +D D+ VVSDEIYEKI+YD  +HISIGS    + +RT+  NGF+KAY+MTG
Sbjct: 181 TLQCIADLAIDHDLLVVSDEIYEKIIYD-REHISIGSF-DGMQDRTITVNGFSKAYAMTG 238

Query: 244 WRLGYLAGPVDIIKAASSIQGHSTSNVCTFAQYGAIAALEDSQDCVEEMRQAFAKRRQVM 303
           WRLGYL  P +I K    IQ HS S+  TF QYG + AL+  QD V+ M   F  RR ++
Sbjct: 239 WRLGYLTAPPEIFKLLQKIQSHSVSSATTFVQYGGLEALQGPQDGVKAMVDRFKMRRDIL 298

Query: 304 LDRLNAIPGLSTAKPDGAFYLFPDISKTGLKSLEFCDALIEEHKVAVIPGIAFGA--DDN 361
           +D LN I G+   KPDGAFY F ++S+ G    E  + L++E  VAV PGIAFGA  +D 
Sbjct: 299 IDGLNKI-GIECKKPDGAFYAFANVSEYG-NGTEVAERLLKEAHVAVTPGIAFGASGEDF 356

Query: 362 IRLSYATDLATIEKGLDRLEK 382
           IR+SYAT +  I + L+RLEK
Sbjct: 357 IRISYATSIDRIREALERLEK 377


Lambda     K      H
   0.317    0.134    0.381 

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: 14
Number of successful extensions: 6
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: 388
Length of database: 380
Length adjustment: 30
Effective length of query: 358
Effective length of database: 350
Effective search space:   125300
Effective search space used:   125300
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 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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