GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Hydrogenovibrio kuenenii DSM 12350

Align Phosphoserine aminotransferase; Phosphohydroxythreonine aminotransferase; PSAT; EC 2.6.1.52 (characterized)
to candidate WP_024850635.1 N745_RS0102880 phosphoserine transaminase

Query= SwissProt::Q59196
         (362 letters)



>NCBI__GCF_000526715.1:WP_024850635.1
          Length = 367

 Score =  319 bits (817), Expect = 8e-92
 Identities = 169/358 (47%), Positives = 231/358 (64%), Gaps = 4/358 (1%)

Query: 7   NFNAGPAALPLEVLERAQAEFVDYQHTGMSIMEMSHRGAVYEAVHNEAQARLLALLGNPT 66
           NF+AGP ALP  VL++ Q   +    TGMS++ MSHR A + +V  EA+A +  LLG   
Sbjct: 8   NFSAGPGALPQSVLDQVQQSIIALPETGMSVLGMSHRSAWFLSVLEEAEANVRELLGIDD 67

Query: 67  GYKVLFIQGGASTQFAMIPMNFLK-EGQTANYVMTGSWASKALKEAKLIGDTHVAASSEA 125
            + VLF+QGGA+ QF+MIP+  L+  G  A Y+ TG W  KA+ EAK  G   V  S E 
Sbjct: 68  EFHVLFLQGGATQQFSMIPITLLRGSGLEAEYLQTGYWGQKAVAEAKKEGKVKVLWSGED 127

Query: 126 SNYMTLPKLQEIQLQDNAAYLHLTSNETIEGAQFKAFPDTGSVPLIGDMSSDILSRPFDL 185
           + Y  LP  +E+    +AAY H  SNET+EG QF       SVP + DMSSD LSRP + 
Sbjct: 128 AGYHRLPDDEELTFSKDAAYFHYVSNETVEGLQFHRVLGHDSVPRVCDMSSDFLSRPIEA 187

Query: 186 NQFGLVYAGAQKNLGPSGVTVVIVREDLV--AESPKHLPTMLRYDTYVKNNSLYNTPPSF 243
           N+F ++YA AQKN+GP+GVTVV++++ ++  A    +LP+ L Y   V  +S YNTPP F
Sbjct: 188 NRFSIIYAHAQKNIGPAGVTVVLIKKSVLDSAREQGNLPSFLDYRNQVSAHSNYNTPPVF 247

Query: 244 GIYMVNEVLKWI-EERGGLEGVQQANRKKASLIYDAIDQSGGFYRGCVDVDSRSDMNITF 302
            IY+   V +WI +E GGL+ ++  NRKKA L+Y AID S GFY G    + RS MN+ F
Sbjct: 248 AIYVTLLVTRWIKDEVGGLKNMEAINRKKAELLYQAIDGSDGFYTGWARQEDRSLMNVAF 307

Query: 303 RLASEELEKEFVKASEQEGFVGLKGHRSVGGLRASIYNAVPYESCEALVQFMEHFKRS 360
            LA++ELE+ F++A+ + GF GL GHRS+GG+RASIYN +   + E LV FM  F+++
Sbjct: 308 NLATQELEQSFLQAAGEAGFSGLDGHRSLGGVRASIYNGLTISAAEQLVDFMSSFQQA 365


Lambda     K      H
   0.316    0.132    0.378 

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: 339
Number of extensions: 13
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: 362
Length of database: 367
Length adjustment: 29
Effective length of query: 333
Effective length of database: 338
Effective search space:   112554
Effective search space used:   112554
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