GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Hydrogenovibrio marinus DSM 11271

Align Phosphoserine aminotransferase; Phosphohydroxythreonine aminotransferase; PSAT; EC 2.6.1.52 (characterized)
to candidate WP_029907839.1 P166_RS0100985 phosphoserine transaminase

Query= SwissProt::Q9RME2
         (361 letters)



>NCBI__GCF_000711315.1:WP_029907839.1
          Length = 367

 Score =  314 bits (804), Expect = 3e-90
 Identities = 162/356 (45%), Positives = 230/356 (64%), Gaps = 4/356 (1%)

Query: 7   NFNAGPSALPKPALERAQKELLNFNDTQMSVMELSHRSQSYEEVHEQAQNLLRELLQIPN 66
           NF+AGP ALP+  L + Q+ +L   +T MSV+ +SHRS  +  V E+A+  +R+LL I  
Sbjct: 8   NFSAGPGALPETVLNQVQESILTLPETGMSVLGMSHRSDWFSSVLEEAETNIRQLLGIGE 67

Query: 67  DYQILFLQGGASLQFTMLPMNLLTK-GTIGNYVLTGSWSEKALKEAKLLGETHIAASTKA 125
           ++ +LFLQGGA+ QF+M+P+ LL   G    Y+ TG W +KA+ EA+  G+     S +A
Sbjct: 68  EFHVLFLQGGATQQFSMIPITLLRNTGREAEYLQTGYWGKKAIVEAEKEGKVKTLWSGQA 127

Query: 126 NSYQSIPDFSEFQLNENDAYLHITSNNTIYGTQYQNFPEINHAPLIADMSSDILSRPLKV 185
           + Y+ +PD +E   +E  AYLH  SN T+ G Q+      +  P + DMSSD LSRP+  
Sbjct: 128 DGYKRLPDDAELSFSEQAAYLHYASNETVEGLQFHRVLGPDSVPRVCDMSSDFLSRPVDA 187

Query: 186 NQFGMIYAGAQKNLGPSGVTVVIVKKDLLNTKVEQ--VPTMLQYATHIKSDSLYNTPPTF 243
           ++F +IYA AQKN+GP+GVTVV++KK LL++  EQ  +P+ L Y  H+ + S YNTPP F
Sbjct: 188 DRFSIIYAHAQKNIGPAGVTVVLIKKSLLDSAQEQPNLPSFLDYRNHVATHSNYNTPPVF 247

Query: 244 SIYMLRNVLDWIKD-LGGAEAIAKQNEEKAKIIYDTIDESNGFYVGHAEKGSRSLMNVTF 302
           +IY+   V  WIKD +GG E +   N  KA+++Y  ID+S GFY G + K  RS MN TF
Sbjct: 248 AIYVTLLVTRWIKDVVGGLENMENINHRKAELLYQAIDDSQGFYQGWSRKEDRSYMNATF 307

Query: 303 NLRNEELNQQFLAKAKEQGFVGLNGHRSVGGCRASIYNAVPIDACIALRELMIQFK 358
           NL   EL Q+FL +A + GF GL+GHRS+GG RAS+YN + + A   L + M  F+
Sbjct: 308 NLTTPELEQRFLQEAAQAGFSGLDGHRSLGGVRASLYNGLTVPAVEQLLDFMSTFE 363


Lambda     K      H
   0.316    0.132    0.372 

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: 367
Number of extensions: 12
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: 361
Length of database: 367
Length adjustment: 29
Effective length of query: 332
Effective length of database: 338
Effective search space:   112216
Effective search space used:   112216
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: 49 (23.5 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