GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serB in Desulfuromusa kysingii DSM 7343

Align fused D-3-phosphoglycerate dehydrogenase / phosphoserine phosphatase (EC 1.1.1.95; EC 3.1.3.3) (characterized)
to candidate WP_092350915.1 BLU87_RS16615 phosphoglycerate dehydrogenase

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



>NCBI__GCF_900107645.1:WP_092350915.1
          Length = 531

 Score =  168 bits (426), Expect = 5e-46
 Identities = 102/329 (31%), Positives = 171/329 (51%), Gaps = 7/329 (2%)

Query: 263 MSEEELCEKIKNVSIIGIRSKTQITKKVLENANRLMAVGAFCIGTNQIDLETCQEKGIAV 322
           +S  EL + I     I  RS T + K +L+ A+ L  V    +G + +D++    KGI V
Sbjct: 31  LSIPELHKIIGGYEAIITRSGTLVDKALLDCADNLKIVARAGVGIDNVDVDAASSKGIIV 90

Query: 323 FNAPFSNTRSVVELAISEIIFLMRNLHDKTLKMHQGIWNKSASGSFEVRGKKLGIIGYGN 382
            NAP+ N  S  E  ++ ++ L RN+      +  G W ++     E++GK +GIIG G 
Sbjct: 91  VNAPYGNVNSAAEHTMAIMLSLFRNVPMANTSLKGGDWKRALFTGCELKGKTVGIIGLGK 150

Query: 383 IGAQLSVLAENMGMNVFYYD--IVERLALGNATKIDSLDELLETCDIISLHVDGRTENKN 440
           +G +++         V  YD  I E+ A     K+  L++++   D+I++H     E +N
Sbjct: 151 VGGRVARRCRAFEAEVITYDPYISEKRADDFGVKLQPLEDIIRFSDVITVHTPLNDETRN 210

Query: 441 ILNKEKIFKMKKGAILVNLSRGHVVDVPALRDALESGHLAGAAVDVFPTEPKNNDEPFES 500
           I++ +    MK G +++N +RG +++  A+ +ALESG  AGAA DV+  EP   D     
Sbjct: 211 IISSDSFKGMKDGVVIINCARGGIINEAAMLEALESGKCAGAAFDVWSQEPPKTD--VLQ 268

Query: 501 ELIGCPNTILTPHIGGSTLEAQENIAQFVPGKIIEYINSGNTFNSVNFPNI---QLPFLK 557
           +LI  P  ++TPH+G +T EAQ+N+A  V  +I+ Y++     N+VN P     Q+  +K
Sbjct: 269 KLIAHPKMLVTPHLGANTFEAQKNVAVDVSKEIVNYVDGRPLENAVNIPRFDPDQMEHMK 328

Query: 558 DAHRLIHIHQNAPGVLAKINQVLASYKIN 586
              +L+ I  +    LA  N    ++  N
Sbjct: 329 PFMQLVSILGDFISQLAPPNPNKVTFTYN 357


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: 656
Number of extensions: 24
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: 531
Length adjustment: 36
Effective length of query: 594
Effective length of database: 495
Effective search space:   294030
Effective search space used:   294030
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 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