GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Clostridium kluyveri DSM 555

Align D-3-phosphoglycerate dehydrogenase; PGDH; EC 1.1.1.95 (uncharacterized)
to candidate WP_011989005.1 CKL_RS02155 3-phosphoglycerate dehydrogenase

Query= curated2:O27051
         (525 letters)



>NCBI__GCF_000016505.1:WP_011989005.1
          Length = 320

 Score =  233 bits (593), Expect = 1e-65
 Identities = 127/314 (40%), Positives = 204/314 (64%), Gaps = 5/314 (1%)

Query: 5   KVLIADSINEKGISELEEVA-EVVVNTTITPEELLDAIKDFDAIVVRSRTKVTREVIEAA 63
           K+LI +SI E+G+  L++   E+ +    + + L++ +KD DAI+VR    +T +VI A 
Sbjct: 4   KILITESIEEEGVEYLKKFGYEIKMPRDTSEDVLIEEVKDCDAILVRM-ANITEKVIRAG 62

Query: 64  PRLKIIARAGVGVDNVDVKAATDRGIMVINAPESTSITVAEHSIGLMLALARKIAIADRS 123
            +LK+I+R GVGV+NVD+K A++  I + NAPES   TVAE+++GL++ALA+K  + DR 
Sbjct: 63  KKLKVISRFGVGVNNVDIKTASELSIQITNAPESNKNTVAEYTMGLIIALAKKFFLYDRG 122

Query: 124 VKEGKWEKNRFMGIELNGKTLGIIGMGRIGSQVVVR-TKAFGMDIMVYDPYISKEAAEEM 182
           +++G ++    +GI+L GK LGI+G+G IG  + ++ +K FGM ++ +  +I +E+    
Sbjct: 123 LRKGNFKVRDILGIDLEGKVLGIVGLGSIGKLLALKASKGFGMKVIGFKRHIDEESKSLD 182

Query: 183 GVTVTD-LETLLRESDIVTIHVPLTPETRHLISEDEFKLMKDTAFIVNCARGGIIDEDAL 241
            V +TD L+ +L  SD V+++VPLT  T  +I + E   MK  AF++N ARG ++D DAL
Sbjct: 183 YVELTDSLDYVLENSDFVSLNVPLTKATTKIIGKRELSFMKKDAFLINTARGEVVDNDAL 242

Query: 242 YRALKDGEIAGAALDVFEEE-PPEGSPLLELENVVLTPHIGASTSEAQRDAAIIVANEIK 300
             AL + +IAGAA DVF+ E P + +P+ ++ENV++TPH  A T EA +  ++  A  I 
Sbjct: 243 CNALLNKQIAGAATDVFDGEIPSKDNPIFKMENVIVTPHSAAHTIEAMKRMSVHAAIGIH 302

Query: 301 TVFQGGAPRNVLNM 314
            V  G  P   +N+
Sbjct: 303 EVLSGNKPSWPVNI 316


Lambda     K      H
   0.316    0.135    0.366 

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: 402
Number of extensions: 23
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: 525
Length of database: 320
Length adjustment: 31
Effective length of query: 494
Effective length of database: 289
Effective search space:   142766
Effective search space used:   142766
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.

Links

Downloads

Related tools

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