GapMind for Amino acid biosynthesis

 

Alignments for a candidate for SST in Hydrogenovibrio kuenenii DSM 12350

Align Serine O-succinyltransferase; SST; Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.-; EC 2.3.1.46 (characterized)
to candidate WP_024850420.1 N745_RS0101730 homoserine O-acetyltransferase

Query= SwissProt::S2KHP1
         (367 letters)



>NCBI__GCF_000526715.1:WP_024850420.1
          Length = 386

 Score =  227 bits (578), Expect = 5e-64
 Identities = 134/360 (37%), Positives = 192/360 (53%), Gaps = 7/360 (1%)

Query: 8   IELPGPVRMYRGGELPSVTIAYETWGELRGQGDNALLLFTGLSPSAHAAS-SMADPSPGW 66
           + +  P+ M  G  LP   +A+ET+GEL     NA+L+   LS   H A     D   GW
Sbjct: 12  LHISTPLNMVCGSVLPEYDLAFETYGELNDDHSNAILICHALSGHQHVAGFHEGDKDAGW 71

Query: 67  WEYMIGPGKPIDTERFFVIAINSLGSCFGSTGPASINPATGQPYRLDFPKLSVEDIVAAA 126
           W+  IGPGK IDT+RFFV+  N+LG C GS+GP SINP TGQ Y  DFP ++ +D V + 
Sbjct: 72  WDSYIGPGKVIDTDRFFVVCSNNLGGCHGSSGPTSINPETGQVYGPDFPIVTCKDWVNSQ 131

Query: 127 RGACRALGIDHVHTVAGASLGGMDALAYAVMYPGTYRDIISISAAAHATPFTIALRSIQR 186
               + L I+    + G S+GGM  + +A+ YP   +  + I++A   +   IA   + R
Sbjct: 132 NELRKYLKIEAWAAIIGGSMGGMQVMQWAIDYPDKIKHAVVIASAPKLSAQNIAFNEVAR 191

Query: 187 EAVRADPAWAGGNY-APGEGPKDGMRVARQLGILTYRSAEEWLQRFDRERLEGSDDSANP 245
            A+  DP +  G +      PK G+ +AR LG LTY S +    +F RE  EG  +    
Sbjct: 192 RAIMTDPDFLDGRFIEKNTTPKRGLALARMLGHLTYLSDDLMGTKFGRELREGKLN--YN 249

Query: 246 FAMAFQVQSYMEANARKFADR--FDANCYLYLSQAMDLFDMAEHGDGSLEAAVRRIDAKR 303
           + + FQV+SY+     KFA +  FDAN YL +++A+D FD A   D  L  A+    AK 
Sbjct: 250 YEVEFQVESYLRYQGEKFATKQNFDANTYLLMTKALDYFDPASEYDNDLTKALSHAKAK- 308

Query: 304 ALVAGVTTDWLFPLWQQRQVAELLEHAGVAVSYHELGSIQGHDAFLVDSERFAPMVAEFL 363
            LV   TTDW F   +  ++ + L      VSY E+ S  GHDAFL+ +  +  +   +L
Sbjct: 309 FLVISFTTDWRFAPERSHEIVKALLDNDADVSYAEIESKHGHDAFLLPNPHYENVFRAYL 368


Lambda     K      H
   0.320    0.135    0.414 

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: 368
Number of extensions: 18
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: 367
Length of database: 386
Length adjustment: 30
Effective length of query: 337
Effective length of database: 356
Effective search space:   119972
Effective search space used:   119972
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 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