GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Calditerrivibrio nitroreducens DSM 19672

Align phosphoserine transaminase (EC 2.6.1.52) (characterized)
to candidate WP_013450502.1 CALNI_RS01845 alanine--glyoxylate aminotransferase family protein

Query= BRENDA::P74281
         (384 letters)



>NCBI__GCF_000183405.1:WP_013450502.1
          Length = 383

 Score =  298 bits (763), Expect = 2e-85
 Identities = 159/374 (42%), Positives = 234/374 (62%), Gaps = 3/374 (0%)

Query: 4   KQMLMIPGPTPVPEKVLLAMAKHPIGHRSGDFSKIIAELTANLKWLHQTENDVLMLTTSG 63
           K+ L+ PGPTPVPEKVLL MA   I HR+ +FS I  E+   LK +  T  DVL+L  SG
Sbjct: 3   KRYLLSPGPTPVPEKVLLDMAMPMIHHRTSEFSNIFKEVREGLKPIFGTRQDVLILAGSG 62

Query: 64  TGAMEASIINFLSPGDRVLVGNNGKFGDRWVKVAKTFGLAVEEIKAEWGKALDPNDFKTL 123
           T AMEA+++N L+ GD+VLV N GKFG RWV++A T+GL V  I  EWG+++ P+  ++ 
Sbjct: 63  TAAMEAAVVNTLNEGDKVLVVNAGKFGKRWVEIATTYGLDVITIDIEWGRSVKPDQVESK 122

Query: 124 LEADSDKTIKALIITHSETSTGVLNDLAAINAAAKAHGGALMIVDAVTSLGATPVAIDDL 183
           L A  +  IKA+++  SETST   + +  I          L+IVD +TS+G     +D+ 
Sbjct: 123 LIAHPE--IKAVLVQASETSTTAYHPIEEIGKIVSLRDETLLIVDGITSVGVYETKMDEW 180

Query: 184 GLDVVASGSQKGYMIPPGLGFVSVSAKAWQAYETATIPRFYLDLKKYKKSTDEDSSPFTP 243
           G+D++ +GSQK +M+PPGL  +++S KAW+  E + IP+FYL+LKK +KS  E+++ +TP
Sbjct: 181 GIDILITGSQKAFMLPPGLALIALSEKAWKFTEKSRIPKFYLNLKKERKSQLENTTSWTP 240

Query: 244 PINLMYGLQASLQMMKAEGLDAIFTRHQRHTNATRGAMKALNLPLFAPDNAASNAITAVA 303
            ++L+ GL++ L++M  EGL  ++ RH     ATR  + A+   L A D  +++A   V 
Sbjct: 241 AVSLIIGLKSVLEIMNKEGLPNVYKRHALCAEATRKGLMAMGFELLAKDIPSNSATGIVL 300

Query: 304 PLGVEAEKIRSTMRKKFDIAMAGGQDHLKGKIFRIGHLGFVCDRDILSCIGALEATLIEL 363
           P G +  K    MR+K  +  AGGQDHLKGKI R+ HLG+    D +  + +LE    + 
Sbjct: 301 PEGFDGGKFVKLMREKAGLTFAGGQDHLKGKILRVSHLGYHDFFDTIIALSSLEIGFSQF 360

Query: 364 GYEGVTPGSGVAAA 377
           G + V  G+GV  A
Sbjct: 361 GLK-VELGAGVKVA 373


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: 322
Number of extensions: 9
Number of successful extensions: 2
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: 383
Length adjustment: 30
Effective length of query: 354
Effective length of database: 353
Effective search space:   124962
Effective search space used:   124962
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