GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serB in Bradyrhizobium sp. BTAi1

Align fused D-3-phosphoglycerate dehydrogenase / phosphoserine phosphatase (EC 1.1.1.95; EC 3.1.3.3) (characterized)
to candidate WP_012042059.1 BBTA_RS08500 phosphoglycerate dehydrogenase

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



>NCBI__GCF_000015165.1:WP_012042059.1
          Length = 529

 Score =  198 bits (504), Expect = 4e-55
 Identities = 115/324 (35%), Positives = 180/324 (55%), Gaps = 8/324 (2%)

Query: 231 SRINVLLLENVHPIGVEIMKQEGYNVEVVSS-AMSEEELCEKIKNVSIIGIRSKTQITKK 289
           S+  VL+ + + P  V+I K  G  V+   +    +++L + I +   + IRS T+ T K
Sbjct: 2   SKPKVLISDALSPAAVQIFKDRGVEVDFQPNLGKDKDKLADIIGDYDGLAIRSATKATAK 61

Query: 290 VLENANRLMAVGAFCIGTNQIDLETCQEKGIAVFNAPFSNTRSVVELAISEIIFLMRNLH 349
           ++E A RL  +G   IG + +++     KGI V N PF N+ +  E AI+ ++ L R + 
Sbjct: 62  IIERAKRLKVIGRAGIGVDNVEIPAATAKGIIVMNTPFGNSITTAEHAITMMLSLAREIP 121

Query: 350 DKTLKMHQGIWNKSASGSFEVRGKKLGIIGYGNIGAQLSVLAENMGMNVFYYD--IVERL 407
                   G W K+     E+ GK LG+IG GNIG+ +   A+ + M V  +D  + E  
Sbjct: 122 QADASTQAGKWEKNRFMGVEITGKTLGVIGCGNIGSIVCDRAQGLRMKVIGFDPFLTEER 181

Query: 408 ALGNATKIDSLDELLETCDIISLHVDGRTENKNILNKEKIFKMKKGAILVNLSRGHVVDV 467
           A     +   LDELL+  D I+LH     + +NI++   I KMK+G  ++N +RG ++D 
Sbjct: 182 ARDLGVEKVELDELLKRADFITLHTPLTDKTRNIIDAAAIAKMKQGVRIINCARGGLIDE 241

Query: 468 PALRDALESGHLAGAAVDVFPTEPKNNDEPFESELIGCPNTILTPHIGGSTLEAQENIAQ 527
            AL  AL S H+AGAA+DVF  EP  +     + L G P+ I TPH+G ST EAQEN+A 
Sbjct: 242 QALLAALNSKHVAGAALDVFAEEPATS-----NPLFGHPSVICTPHLGASTTEAQENVAL 296

Query: 528 FVPGKIIEYINSGNTFNSVNFPNI 551
            +  ++ +Y+ +G   N++NFP+I
Sbjct: 297 QIAEQMSDYLLTGAISNAINFPSI 320


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: 653
Number of extensions: 34
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 630
Length of database: 529
Length adjustment: 36
Effective length of query: 594
Effective length of database: 493
Effective search space:   292842
Effective search space used:   292842
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