GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Mesorhizobium ciceri WSM1271

Align phosphoserine transaminase (EC 2.6.1.52) (characterized)
to candidate YP_004141244.1 Mesci_2041 class V aminotransferase

Query= BRENDA::P74281
         (384 letters)



>NCBI__GCF_000185905.1:YP_004141244.1
          Length = 401

 Score =  231 bits (590), Expect = 2e-65
 Identities = 140/376 (37%), Positives = 218/376 (57%), Gaps = 7/376 (1%)

Query: 7   LMIPGPTPVPEKVLLAMAKHPIGHRSGDFSKIIAELTANLKWLHQTEN-DVLMLTTSGTG 65
           L IPGPT +P+ V  AM       R+ DF +++  L  +LK + +TE   V +   SGTG
Sbjct: 8   LFIPGPTNIPDAVRRAMNVPMQDMRAPDFPELVLPLFRDLKQIFKTETGSVFIFPGSGTG 67

Query: 66  AMEASIINFLSPGDRVLVGNNGKFGDRWVKVAKTFGLAVEEIKAEWGKALDPNDFKTLLE 125
           A EA+I N L+ GDRVL+   G+F   WV +A+  GL V+ +  EWG+ +  + ++  L 
Sbjct: 68  AWEAAISNTLNRGDRVLMSRFGQFSHLWVDMAERLGLKVDCVDVEWGEGVPLDAYRQRLG 127

Query: 126 ADSDKTIKALIITHSETSTGVLNDLAAINAAAK--AHGGALMIVDAVTSLGATPVAIDDL 183
            D    IKA+  TH+ET+TGV +D+A + AA    AH  AL+ VD V+S+G+    +D+ 
Sbjct: 128 DDKGHEIKAVFATHNETATGVTSDIAGVRAALDETAHD-ALLFVDGVSSIGSIDFRMDEW 186

Query: 184 GLDVVASGSQKGYMIPPGLGFVSVSAKAWQAYETATIPRFYLDLKKYKKSTDEDSSPFTP 243
           G+D+  +GSQKG M+P GLG ++VSAK  +A++ + + R Y   +  + S+     P+TP
Sbjct: 187 GVDLAITGSQKGLMLPAGLGILAVSAKGLEAHKQSHMERCYFSFEDMQASSKTGFFPYTP 246

Query: 244 PINLMYGLQASLQMMKAEGLDAIFTRHQRHTNATRGAMKALNLPLFAPDNA-ASNAITA- 301
           P  L+ GL+ASL ++ AEGL+ IF RH R     R  + A  L L A +    S+ ++A 
Sbjct: 247 PTQLLLGLRASLDLIFAEGLEQIFARHHRLAEGVRRGVHAWGLKLCANEEKWWSDTVSAI 306

Query: 302 VAPLGVEAEKIRSTMRKKFDIAMAGGQDHLKGKIFRIGHLGFVCDRDILSCIGALEATLI 361
           V    V+A ++ +    ++  +   G   + G++FRIGHLG + +   L+ + + E +L 
Sbjct: 307 VVSEDVDARQVIANGYSRYRTSFGAGLSKVAGRVFRIGHLGDLNEVMCLAALASAEMSLR 366

Query: 362 ELGYEGVTPGSGVAAA 377
           + G   +  GSGVAAA
Sbjct: 367 DAGAR-IEAGSGVAAA 381


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: 16
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: 401
Length adjustment: 31
Effective length of query: 353
Effective length of database: 370
Effective search space:   130610
Effective search space used:   130610
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