GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Methylomonas methanica MC09

Align Phosphoserine aminotransferase; Phosphohydroxythreonine aminotransferase; PSAT; EC 2.6.1.52 (characterized)
to candidate WP_041365930.1 METME_RS20000 phosphoserine transaminase

Query= SwissProt::Q59196
         (362 letters)



>NCBI__GCF_000214665.1:WP_041365930.1
          Length = 367

 Score =  312 bits (800), Expect = 8e-90
 Identities = 166/359 (46%), Positives = 225/359 (62%), Gaps = 2/359 (0%)

Query: 3   KRAYNFNAGPAALPLEVLERAQAEFVDYQHTGMSIMEMSHRGAVYEAVHNEAQARLLALL 62
           + + NF+ GP ALP  VL +   E +     G+SI+ +SHR   +  V +E +  + ALL
Sbjct: 4   QNSLNFSGGPGALPESVLLQLSEELIQVPGLGISILGISHRSEWFAEVISELEDNIRALL 63

Query: 63  GNPTGYKVLFIQGGASTQFAMIPMNFLKEGQTA-NYVMTGSWASKALKEAKLIGDTHVAA 121
           G    Y VL +QGGA+ QF+M+PM  L+   TA  Y+ TG W+ KA+ EAKL G   V  
Sbjct: 64  GLNEKYHVLLLQGGATQQFSMVPMTLLRGKSTAAEYIQTGYWSGKAIPEAKLEGPIRVIW 123

Query: 122 SSEASNYMTLPKLQEIQLQDNAAYLHLTSNETIEGAQFKAFPDTGSVPLIGDMSSDILSR 181
           +  A+ +  LP   E+    +A Y+H  SNET+EG QF+       VP + DMSSD LS+
Sbjct: 124 NGRAAGFNRLPTDDELCFSPDAPYIHYISNETVEGLQFQRVLGRDDVPRVCDMSSDFLSK 183

Query: 182 PFDLNQFGLVYAGAQKNLGPSGVTVVIVREDLVAESPKHLPTMLRYDTYVKNNSLYNTPP 241
           P D  +F L+YA AQKN+GPSG+TVV+VR++L+ +    LP+ L Y T  K +S +NTPP
Sbjct: 184 PGDFERFSLIYAHAQKNIGPSGITVVVVRDELIEQPHAELPSFLDYKTQAKAHSNFNTPP 243

Query: 242 SFGIYMVNEVLKW-IEERGGLEGVQQANRKKASLIYDAIDQSGGFYRGCVDVDSRSDMNI 300
            F IY V  V +W I++ GGL  + + NR+KA L+Y  ID S GFY+G  +   RS MN+
Sbjct: 244 VFAIYAVLLVTRWLIKDIGGLTQMDRINRRKAELLYGLIDDSDGFYQGRAETADRSLMNV 303

Query: 301 TFRLASEELEKEFVKASEQEGFVGLKGHRSVGGLRASIYNAVPYESCEALVQFMEHFKR 359
            F L S ELEK F++ S+  GF GL GHR++GGLRASIYNAV  E+ E LV FM+ F R
Sbjct: 304 VFNLPSLELEKRFIQESQAAGFSGLAGHRAIGGLRASIYNAVTIEAVEELVNFMDAFWR 362


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: 330
Number of extensions: 13
Number of successful extensions: 3
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