GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serB in Rhodospirillum centenum SW; ATCC 51521

Align fused D-3-phosphoglycerate dehydrogenase / phosphoserine phosphatase (EC 1.1.1.95; EC 3.1.3.3) (characterized)
to candidate WP_012566968.1 RC1_RS08565 phosphoglycerate dehydrogenase

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



>NCBI__GCF_000016185.1:WP_012566968.1
          Length = 525

 Score =  198 bits (504), Expect = 4e-55
 Identities = 121/331 (36%), Positives = 184/331 (55%), Gaps = 13/331 (3%)

Query: 235 VLLLENVHPIGVEIMKQEGYNVEVVSSAMSEEELCEKIKNVSIIGIRSKTQITKKVLENA 294
           VL+ +++ P  VEI K+ G  V+V  + +  +EL   I     + IRS T++TK VL  A
Sbjct: 4   VLISDSLSPRAVEIFKERGIEVDV-KTGLKPDELKAIIGGYDGLAIRSSTKVTKDVLAVA 62

Query: 295 NRLMAVGAFCIGTNQIDLETCQEKGIAVFNAPFSNTRSVVELAISEIIFLMRNLHDKTLK 354
             L  VG   IG + +D+     +G+ V N PF N+ +  E AI+ ++ L R++ +    
Sbjct: 63  TNLRVVGRAGIGVDNVDVPAATARGVVVMNTPFGNSITTAEHAIAMMMALARDIPEANAS 122

Query: 355 MHQGIWNKSASGSFEVRGKKLGIIGYGNIGAQLSVLAENMGMNVFYYD---IVERLALGN 411
            H G W K+     E+ GK LG+IG GNIG+ ++  A  + M V  +D     ER     
Sbjct: 123 THAGKWEKNRFMGVELYGKTLGVIGCGNIGSIVADRALGLKMKVVAFDPFLSPERAQDLG 182

Query: 412 ATKIDSLDELLETCDIISLHVDGRTENKNILNKEKIFKMKKGAILVNLSRGHVVDVPALR 471
             K++ LDELL   D I+LH     E + ILN++ + + KKG  ++N +RG ++    L+
Sbjct: 183 VEKVE-LDELLRRADFITLHTPLTNETRAILNRDSLARTKKGVRIINCARGGLIVEEDLK 241

Query: 472 DALESGHLAGAAVDVFPTEPKNNDEPFESELIGCPNTILTPHIGGSTLEAQENIAQFVPG 531
            A+ESGH+AGAA+DVF  EP       ++ L G    I TPH+G ST EAQEN+A  V  
Sbjct: 242 AAIESGHVAGAALDVFAEEPAK-----QNGLFGMERVICTPHLGASTTEAQENVALQVAE 296

Query: 532 KIIEYINSGNTFNSVNFPNIQLPFLKDAHRL 562
           ++ +Y+ SG   N++N P++     +DA RL
Sbjct: 297 QMADYLVSGAVVNALNMPSVS---AEDAPRL 324


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: 609
Number of extensions: 36
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: 525
Length adjustment: 36
Effective length of query: 594
Effective length of database: 489
Effective search space:   290466
Effective search space used:   290466
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