GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serB in Desulfotalea psychrophila LSv54

Align fused D-3-phosphoglycerate dehydrogenase / phosphoserine phosphatase (EC 1.1.1.95; EC 3.1.3.3) (characterized)
to candidate WP_011188950.1 DP_RS08685 3-phosphoglycerate dehydrogenase

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



>NCBI__GCF_000025945.1:WP_011188950.1
          Length = 393

 Score =  170 bits (431), Expect = 9e-47
 Identities = 113/355 (31%), Positives = 186/355 (52%), Gaps = 37/355 (10%)

Query: 297 LMAVGAFCIGTNQIDLETCQEKGIAVFNAPFSNTRSVVELAISEIIFLMRNLH------- 349
           L+AV     GTN +++E   +KGI VFN P +N  +VV+L    +    RN+        
Sbjct: 51  LLAVARAGAGTNNVNVERATKKGICVFNTPGANANAVVDLVFPMLGVWKRNIFNGINFCK 110

Query: 350 -------DKTLKMHQGIWNKSASGSFEVRGKKLGIIGYGNIGAQLSVLAENMGMNVFYYD 402
                  DK   + +    KSA    E+ GK L ++G G IG +L+       MNV  +D
Sbjct: 111 SLTAVDPDKVDSVVEA--QKSAYKGEEIAGKNLTVVGLGQIGVRLANGGIQRLMNVKGFD 168

Query: 403 IVERLALGNATKID-------SLDELLETCDIISLHVDGRTENKNILNKEKIFKMKKGAI 455
                AL N  ++        +L + +   D+ISLH+      +N++N E + K+K+GAI
Sbjct: 169 PAP--ALENIHQLSPQVRVCRALKDAVSDADVISLHLPLNDRTRNLVNAEFLAKVKRGAI 226

Query: 456 LVNLSRGHVVDVPALRDALESGHLAGAAVDVFPTEPKNNDEPFESELIGCPNTILTPHIG 515
           L+N SR  +VD  A+ DAL+SG L GA +  FPT          ++ IG    + TPH+G
Sbjct: 227 LINYSRAPIVDEQAVLDALDSGQL-GAFLSDFPT----------AKTIGHEKILTTPHLG 275

Query: 516 GSTLEAQENIAQFVPGKIIEYINSGNTFNSVNFPNIQ-LPFLKDAHRLIHIHQNAPGVLA 574
            ST +++ N +     ++  Y+  GN  +SVNFPNI+  P     +RLI I+++ PG++A
Sbjct: 276 ASTSQSEGNCSTMAVKELSSYLKYGNVVHSVNFPNIESTPADTVKNRLIVINKDVPGMIA 335

Query: 575 KINQVLASYKINIVGQYLKTNEKIGYVITDIDKRYSNDVIDALKEIEGTIRFRIL 629
            ++ + + + +NIV    ++N  IGY I D+++    +++  + E+   IR R++
Sbjct: 336 NVSNIFSGFNVNIVSYLNQSNGAIGYNIIDMEETIPEELVAKIVELPDVIRTRVI 390


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: 596
Number of extensions: 34
Number of successful extensions: 5
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: 393
Length adjustment: 34
Effective length of query: 596
Effective length of database: 359
Effective search space:   213964
Effective search space used:   213964
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: 52 (24.6 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