GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serC in Sulfurimonas denitrificans DSM 1251

Align phosphoserine aminotransferase monomer (EC 2.6.1.1; EC 2.6.1.52) (characterized)
to candidate WP_011371709.1 SUDEN_RS00385 alanine--glyoxylate aminotransferase family protein

Query= metacyc::MONOMER-15919
         (385 letters)



>NCBI__GCF_000012965.1:WP_011371709.1
          Length = 370

 Score =  180 bits (457), Expect = 5e-50
 Identities = 124/362 (34%), Positives = 193/362 (53%), Gaps = 17/362 (4%)

Query: 9   LLMIPGPTMVPPEVLNAMALPVIGHRTKDYSNLLEDTIEKLKKVFITENDTFLITGSGTA 68
           LL  PGPT VP  V NAM+   + HRT ++  +   T E L K+F ++ +  +++ SGT 
Sbjct: 2   LLFTPGPTPVPQNVRNAMSDETMHHRTPEFEAIFFKTREYLFKLFGSD-EVVMLSSSGTG 60

Query: 69  AMDMAISNIIKRGDKVLNIVTGNFGERFANIVKAYKGEAIRLDVEWGDMAEPEAVKEILD 128
           AM+ A+ N+    + +LN+ +G FGERF  I  A+    + +  EW      E V + + 
Sbjct: 61  AMEAAVVNLCH--NTLLNVNSGKFGERFGKIALAHGLGNVEIKNEWDTPVSVEEVIKAIK 118

Query: 129 KYDDIKAVTVVHNETSTGARNPIKEIGEVVKDYDA--LYIVDTVSSLGGDYVNVDKFHID 186
           +  +I A+ V  +E++ G R+P++ I + VK+ +   + I D +++LG +   +D  +ID
Sbjct: 119 ENSNIDAIAVQISESAGGLRHPVEAIAKAVKELNPNIMIIADGITALGVE--KIDIAYID 176

Query: 187 ICVTGSQKCLAAPPGLAAITVSEKAWEVIKKNDDKVGFYLDLLAYKKYYEEKKQTPYTPS 246
             + GSQK L  PPGLA + +S  A E I K     G+Y +L    K  + K  T +T +
Sbjct: 177 CLIAGSQKALMLPPGLAILGLSNAAIEKIGKGR---GYYFNLATEIKS-QRKNTTAWTAA 232

Query: 247 VNLTYALNVALDLVLEEG-IENRVKRHERLAKATRAGLEAMGIELFAKERARSVTVTSAK 305
             LT  L   L+ +   G ++         AKA  A L A+G+ ++ K  A S+T    +
Sbjct: 233 TTLTIGLLEILETIERNGGLDKLYADTASRAKAVMASLVAIGLHVYPKTPALSMTTIDDE 292

Query: 306 YPEGIEDSKFRGILSNKYNIVVAGGQKHLAGKIFRIGHMGICGEKEVLATLACVELALKE 365
                + SK R IL   +++ VAGGQ HL GKIFRI  MGI    E+   +  +ELAL +
Sbjct: 293 -----DASKIRKILKTDFDVNVAGGQDHLDGKIFRINQMGIIAPYEISWVVNSIELALDK 347

Query: 366 LG 367
           LG
Sbjct: 348 LG 349


Lambda     K      H
   0.316    0.135    0.379 

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: 348
Number of extensions: 17
Number of successful extensions: 6
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: 385
Length of database: 370
Length adjustment: 30
Effective length of query: 355
Effective length of database: 340
Effective search space:   120700
Effective search space used:   120700
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 (21.6 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