GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Methylobacterium nodulans ORS 2060

Align phosphoserine transaminase (EC 2.6.1.52) (characterized)
to candidate WP_015933415.1 MNOD_RS33600 aminotransferase class V-fold PLP-dependent enzyme

Query= BRENDA::P74281
         (384 letters)



>NCBI__GCF_000022085.1:WP_015933415.1
          Length = 417

 Score =  251 bits (641), Expect = 3e-71
 Identities = 143/378 (37%), Positives = 218/378 (57%), Gaps = 5/378 (1%)

Query: 4   KQMLMIPGPTPVPEKVLLAMAKHPIGHRSGDFSKIIAELTANLKWLHQTEN-DVLMLTTS 62
           +  L +PGPT VPE+V  AM      HRS  F  +   L  N+K + ++++  V +  +S
Sbjct: 9   RNFLFVPGPTNVPERVQRAMIVPMEDHRSSSFPDLTLPLFENMKKVFKSKDGQVFIFPSS 68

Query: 63  GTGAMEASIINFLSPGDRVLVGNNGKFGDRWVKVAKTFGLAVEEIKAEWGKALDPNDFKT 122
           GTGA EA++ N LSPGDRVL    G+F   W+ +A+  GL V     EWG   +P+  + 
Sbjct: 69  GTGAWEAALTNTLSPGDRVLASRFGQFSTLWIDLAQRVGLDVVIQDEEWGTGANPDRIEE 128

Query: 123 LLEADSDKTIKALIITHSETSTGVLNDLAAINAAAKA-HGGALMIVDAVTSLGATPVAID 181
            L AD D  IKA++I H+ET+TGV +D+ A+  A  A +  A++ VD V+S+G+      
Sbjct: 129 ALRADRDHRIKAVLIVHNETATGVTSDIGAVRRAIDAANHPAMLYVDGVSSIGSIDFRAS 188

Query: 182 DLGLDVVASGSQKGYMIPPGLGFVSVSAKAWQAYETATIPRFYLDLKKYKKSTDEDSSPF 241
           + G+D   +GSQKG M+P GLG V VS KA  AY+TA   R Y D     K+      P+
Sbjct: 189 EWGVDCAITGSQKGLMLPAGLGIVCVSPKALAAYKTAECRRVYFDFGDMSKANATGYFPY 248

Query: 242 TPPINLMYGLQASLQMMKAEGLDAIFTRHQRHTNATRGAMKALNLPLFAPD-NAASNAIT 300
           TP + L+YGL+ S+  +  EGL+ +F RH+   +  R A+KA  L L A +    S+ ++
Sbjct: 249 TPALPLLYGLRESMACLFEEGLERVFERHRVLADGCRAAVKAWGLTLCAKEPKWYSDTVS 308

Query: 301 AV-APLGVEAEKIRSTMRKKFDIAMAGGQDHLKGKIFRIGHLGFVCDRDILSCIGALEAT 359
           A+  P G+    +     +++++A+  G   + GK+FRIGHLG + D  +L  +   E +
Sbjct: 309 AIMVPEGINGADVIDIAFRRYNLALGAGLSKVAGKLFRIGHLGDLNDLMLLGALAGAEMS 368

Query: 360 LIELGYEGVTPGSGVAAA 377
           +++ G + + PGSGVAAA
Sbjct: 369 MLDAGIK-IEPGSGVAAA 385


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: 366
Number of extensions: 27
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: 384
Length of database: 417
Length adjustment: 31
Effective length of query: 353
Effective length of database: 386
Effective search space:   136258
Effective search space used:   136258
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 Jul 25 2024. The underlying query database was built on Jul 25 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