GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Methanobacterium lacus AL-21

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_013644807.1 METBO_RS06075 homoserine O-acetyltransferase

Query= SwissProt::D0L1T6
         (403 letters)



>NCBI__GCF_000191585.1:WP_013644807.1
          Length = 489

 Score =  389 bits (998), Expect = e-112
 Identities = 195/371 (52%), Positives = 263/371 (70%), Gaps = 7/371 (1%)

Query: 14  SRSVGIVEPKTARFSEPLALDCGRSLPSYELVYETYGQLNDEGSNAVLICHALSGDHHAA 73
           + S+GIVE K    S+ L L+ G  L + ++ YETYG+LN E SNA+L+CHAL+GD H A
Sbjct: 3   NESIGIVETKYHSLSDDLILESGEKLKNVQVAYETYGKLNKEKSNAILVCHALTGDAHVA 62

Query: 74  GFHAETDRKPGWWDSAIGPGKPIDTDRFFVVCLNNLGGCKGSTGPLSVDPASGKPYGPDF 133
           G++ E D+KPGWWD  IGPGK +DT+++F++C N +GGCKGSTGP S++P + KPYG DF
Sbjct: 63  GWY-EGDKKPGWWDVIIGPGKCLDTEKYFIICSNVIGGCKGSTGPSSINPETNKPYGLDF 121

Query: 134 PIVTVKDWVHAQYRLMQYLGLSGWAAVIGGSLGGMQVLQWSITYPDAVAHAVVIAAAPRL 193
           PI+T+KD V+AQ +L+  +G++   AVIGGS+GGMQVLQW ++YPD V  A+ IA     
Sbjct: 122 PIITIKDMVNAQKKLVNSMGVTQLFAVIGGSMGGMQVLQWCVSYPDMVRSAIPIATTAFS 181

Query: 194 SAQNIAFNEVARQAIITDPEFYGGRYADHNALPRRGLMLARMLGHITYLSDDAMRAKFGR 253
           S Q IAFNEV R+AII+DP +  G+Y D + +P  GL LARM+ HITYLS+++M  KFGR
Sbjct: 182 SPQQIAFNEVGRRAIISDPNWNNGQYYD-SEVPTEGLALARMIAHITYLSNESMYQKFGR 240

Query: 254 ELRAGQVQYGFDVE--FQVESYLRYQGTSFVDRFDANTYLLMTKALDYFDPAQASNDDLV 311
            L+  +  YGFD E  F+VESYL YQG SF  RFDAN+YL +TKA+DYFD   A    L 
Sbjct: 241 RLQ-DKEDYGFDFETDFEVESYLHYQGNSFTKRFDANSYLYITKAVDYFD--LAGEGSLA 297

Query: 312 AALAEVKAHFLVVSFTSDWRFSPERSREIVRALLASGKQVSYAEIESNHGHDAFLMTIPY 371
                +K  FLV+S  SDW + P  SR+IV  L A+   VSY EI+S++GHDAFL+    
Sbjct: 298 ETFYGLKIKFLVISVDSDWLYPPSLSRDIVMGLNANDINVSYCEIKSSYGHDAFLIEAGQ 357

Query: 372 YHRVLAGYMAN 382
            + ++AG++++
Sbjct: 358 LNYLIAGFLSD 368


Lambda     K      H
   0.320    0.135    0.412 

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: 557
Number of extensions: 27
Number of successful extensions: 5
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: 403
Length of database: 489
Length adjustment: 32
Effective length of query: 371
Effective length of database: 457
Effective search space:   169547
Effective search space used:   169547
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: 51 (24.3 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