GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Persephonella marina EX-H1

Align phosphoserine transaminase (EC 2.6.1.52) (characterized)
to candidate WP_012676496.1 PERMA_RS01695 alanine--glyoxylate aminotransferase family protein

Query= BRENDA::P74281
         (384 letters)



>NCBI__GCF_000021565.1:WP_012676496.1
          Length = 381

 Score =  280 bits (717), Expect = 4e-80
 Identities = 153/379 (40%), Positives = 227/379 (59%), Gaps = 7/379 (1%)

Query: 4   KQMLMIPGPTPVPEKVLLAMAKHPIGHRSGDFSKIIAELTANLKWLHQTENDVLMLTTSG 63
           K+ L  PGP P+P +V+ A+ +  I HR+ +F++I  E   NL+ L +TE DV+M  +SG
Sbjct: 4   KERLFTPGPVPLPPQVIKALGQQIIHHRTPEFTQIFLEARENLQKLLKTERDVIMFASSG 63

Query: 64  TGAMEASIINFLSPGDRVLVGNNGKFGDRWVKVAKTFGLAVEEIKAEWGKALDPNDFKTL 123
           TGAMEAS+ NF   GDRVL+ N GKFG RW ++A  + L + + + EWGK  D      +
Sbjct: 64  TGAMEASVANFFRKGDRVLIINAGKFGQRWKELASVYQLKIVDYEIEWGKTYDKERILQI 123

Query: 124 LEADSDKTIKALIITHSETSTGVLNDLAAINAAAKAHGGALMIVDAVTSLGATPVAIDDL 183
           +    D  IK + + HSETST   +D+  +   AK     L++VD +TS+G   V  ++L
Sbjct: 124 ISEFPD--IKGIFVQHSETSTTTYHDVKYLGDIAKKLDDCLLVVDGITSVGVYQVYPEEL 181

Query: 184 GLDVVASGSQKGYMIPPGLGFVSVSAKAWQAYETATIPRFYLDLKKYKKSTDEDSSPFTP 243
           G+DV+ +GSQK  M+PPGL  +  S KA +    + +PR+Y D+ K  K   +  + +TP
Sbjct: 182 GIDVLVTGSQKALMLPPGLSVLYFSEKAEERASKSDMPRYYFDVLKEAKKQSKGQTAYTP 241

Query: 244 PINLMYGLQASLQMMKAEGLDAIFTRHQRHTNATRGAMKALNLPLFAPDNAASNAITAV- 302
            INL+  L  SL+++  EGLD +  RH+    ATR A+K + L L +   + SN+ T V 
Sbjct: 242 AINLIIALNESLKLILGEGLDNLEERHRIMAEATREAVKEIGLKLLS--ESPSNSATGVY 299

Query: 303 APLGVEAEKIRSTMRKKFDIAMAGGQDHLKGKIFRIGHLGFVCDRDILSCIGALEATLIE 362
           +P G++A+++R  +  K    +AGGQDHLKGKIFRI H+G+    D++  I  LE  L  
Sbjct: 300 SPAGIDADQLRKEL-LKLGFRVAGGQDHLKGKIFRIAHMGYFDFMDVVQVIAGLEMALKR 358

Query: 363 LGYEGVTPGSGVAAAAGVL 381
           +GYE +  G GV  A  V+
Sbjct: 359 IGYE-IEIGKGVRKAQEVI 376


Lambda     K      H
   0.317    0.134    0.386 

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: 341
Number of extensions: 7
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: 384
Length of database: 381
Length adjustment: 30
Effective length of query: 354
Effective length of database: 351
Effective search space:   124254
Effective search space used:   124254
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 (21.7 bits)
S2: 50 (23.9 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