GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Sulfurihydrogenibium azorense Az-Fu1

Align phosphoserine transaminase (EC 2.6.1.52) (characterized)
to candidate WP_012675016.1 SULAZ_RS02850 alanine--glyoxylate aminotransferase family protein

Query= BRENDA::P74281
         (384 letters)



>NCBI__GCF_000021545.1:WP_012675016.1
          Length = 379

 Score =  277 bits (708), Expect = 4e-79
 Identities = 151/376 (40%), Positives = 226/376 (60%), Gaps = 9/376 (2%)

Query: 4   KQMLMIPGPTPVPEKVLLAMAKHPIGHRSGDFSKIIAELTANLKWLHQTENDVLMLTTSG 63
           K+ L  PGP P+P +V+ A+ +  I HR+ +F+ I  +    L+ L  T+ DVLM  +SG
Sbjct: 3   KERLFTPGPVPLPPQVIKALGQQIIHHRTPEFTNIFLQTREKLQKLFNTDRDVLMFASSG 62

Query: 64  TGAMEASIINFLSPGDRVLVGNNGKFGDRWVKVAKTFGLAVEEIKAEWGKALDPNDFKTL 123
           TGAMEASI+NF S  D+VLV N GKFG+RW  +AKTF L V + + EWG+  D +    +
Sbjct: 63  TGAMEASIVNFFSENDKVLVINAGKFGERWRDLAKTFRLQVIDYQIEWGRTYDKDKVSEI 122

Query: 124 LEADSDKTIKALIITHSETSTGVLNDLAAINAAAKAHGGALMIVDAVTSLGATPVAIDDL 183
           ++ + D  +K +++ HSETST  L+DL  ++  + +    L++VD +TS+G   V   ++
Sbjct: 123 VKNNPD--LKGILVQHSETSTTTLHDLQFLSQISSSLEDCLLVVDGITSVGVYKVFPQEI 180

Query: 184 GLDVVASGSQKGYMIPPGLGFVSVSAKAWQAYETATIPRFYLDLKKYKKSTDEDSSPFTP 243
           G+D++ +GSQK  M+PPGL  +  S KA +  E + +P++Y  +K   K   +  + +TP
Sbjct: 181 GIDILVTGSQKALMLPPGLSILYYSEKAEKRLEKSNLPKYYFSVKAESKKQAKGQTAYTP 240

Query: 244 PINLMYGLQASLQMMKAEGLDAIFTRHQRHTNATRGAMKALNLPLF--APDNAASNAITA 301
            INL+  L  SL ++  EGLD +  RH      TR AMK + L L   +P N+A+   T 
Sbjct: 241 AINLIIALNESLNLILEEGLDNLEKRHSILAQMTREAMKEIGLKLLSESPSNSATGVFT- 299

Query: 302 VAPLGVEAEKIRSTMRKKFDIAMAGGQDHLKGKIFRIGHLGFVCDRDILSCIGALEATLI 361
             P G++A+K R  +  K  I +AGGQDHLKGKI RI H+G+    D++  I A+E  L 
Sbjct: 300 --PEGIDADKFRKDL-LKIGIRVAGGQDHLKGKIIRIAHMGYFDYLDMIEVISAIEIALY 356

Query: 362 ELGYEGVTPGSGVAAA 377
           + GY+ V  G GV  A
Sbjct: 357 KNGYK-VDLGKGVKKA 371


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: 330
Number of extensions: 10
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: 379
Length adjustment: 30
Effective length of query: 354
Effective length of database: 349
Effective search space:   123546
Effective search space used:   123546
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