GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serB in Caulobacter crescentus NA1000

Align fused D-3-phosphoglycerate dehydrogenase / phosphoserine phosphatase (EC 1.1.1.95; EC 3.1.3.3) (characterized)
to candidate CCNA_03322 CCNA_03322 D-3-phosphoglycerate dehydrogenase

Query= reanno::Cola:Echvi_2777
         (630 letters)



>FitnessBrowser__Caulo:CCNA_03322
          Length = 526

 Score =  193 bits (491), Expect = 1e-53
 Identities = 117/320 (36%), Positives = 173/320 (54%), Gaps = 10/320 (3%)

Query: 235 VLLLENVHPIGVEIMKQEGYNVEVVSSAMSEEELCEKIKNVSIIGIRSKTQITKKVLENA 294
           VL+ + + P  VEI K  G   ++  + +S++EL   I +   I IRS  ++ K V+  A
Sbjct: 6   VLIADKLSPAAVEIFKNRGLAFDI-KTGLSKDELIAVIGDYDGIAIRSGAKLDKDVIAAA 64

Query: 295 NRLMAVGAFCIGTNQIDLETCQEKGIAVFNAPFSNTRSVVELAISEIIFLMRNLHDKTLK 354
           N+L  +    IG + +D+     KGI V N PF N+ +  E AI+ +  L R +    + 
Sbjct: 65  NKLRVIARAGIGVDNVDIPAATAKGIVVMNTPFGNSITTAEHAIAMMFALARQIPAADVS 124

Query: 355 MHQGIWNKSASGSFEVRGKKLGIIGYGNIGAQLSVLAENMGMNVFYYD---IVERLALGN 411
              G W K+     E+  K LG+IG GNIG  ++  A  + M V  YD     ER     
Sbjct: 125 TQGGKWEKNRFMGVELYAKTLGLIGAGNIGGIVADRALGLKMKVVAYDPFLSPERAVEMG 184

Query: 412 ATKIDSLDELLETCDIISLHVDGRTENKNILNKEKIFKMKKGAILVNLSRGHVVDVPALR 471
             K++ LDELL   D+I+LH     + +NIL+ E + K KKG ++VN +RG +VD  ALR
Sbjct: 185 VEKVE-LDELLARADVITLHTPLTDKTRNILSAENLAKTKKGVMIVNCARGGLVDEAALR 243

Query: 472 DALESGHLAGAAVDVFPTEPKNNDEPFESELIGCPNTILTPHIGGSTLEAQENIAQFVPG 531
             L+ GH+ GAA DVF  EP       E+ L G    + TPH+G ST EAQEN+A  V  
Sbjct: 244 KLLDEGHVGGAAFDVFTVEPAK-----ENPLFGSDKVVATPHLGASTNEAQENVALQVAE 298

Query: 532 KIIEYINSGNTFNSVNFPNI 551
           ++ +Y+ +G   N++N P+I
Sbjct: 299 QVSDYLLTGAVTNALNSPSI 318


Lambda     K      H
   0.317    0.136    0.377 

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: 641
Number of extensions: 34
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: 630
Length of database: 526
Length adjustment: 36
Effective length of query: 594
Effective length of database: 490
Effective search space:   291060
Effective search space used:   291060
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: 53 (25.0 bits)

This GapMind analysis is from Apr 09 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