GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serB in Rhodobacter sphaeroides ATCC 17029

Align fused D-3-phosphoglycerate dehydrogenase / phosphoserine phosphatase (EC 1.1.1.95; EC 3.1.3.3) (characterized)
to candidate WP_011338899.1 RSPH17029_RS00105 phosphoglycerate dehydrogenase

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



>NCBI__GCF_000015985.1:WP_011338899.1
          Length = 534

 Score =  207 bits (526), Expect = 1e-57
 Identities = 122/327 (37%), Positives = 179/327 (54%), Gaps = 10/327 (3%)

Query: 229 PKSRINVLLLENVHPIGVEIMKQEGYNVEVVSS-AMSEEELCEKIKNVSIIGIRSKTQIT 287
           P     VL+ + +    V+I +  G  V+ +      +E+L E I     + IRS T++T
Sbjct: 2   PDMAPRVLVSDELSETAVQIFRDRGVEVDYMPKLGKDKEKLAEIIGQYDGLAIRSATKVT 61

Query: 288 KKVLENANRLMAVGAFCIGTNQIDLETCQEKGIAVFNAPFSNTRSVVELAISEIIFLMRN 347
           +K+LE A  L  +G   IG + +D+     KG+ V N PF N+ +  E AI+ +    R 
Sbjct: 62  EKLLEQATNLKVIGRAGIGVDNVDIPAASRKGVIVMNTPFGNSITTAEHAIAMMFACARQ 121

Query: 348 LHDKTLKMHQGIWNKSASGSFEVRGKKLGIIGYGNIGAQLSVLAENMGMNVFYYD---IV 404
           L +     H G W KS     E+  K LG+IG GNIG  +   A  + M V  YD     
Sbjct: 122 LPEANASTHAGKWEKSRFMGVELFNKTLGVIGAGNIGGIVCDRALGLSMKVVAYDPFLSE 181

Query: 405 ERLALGNATKIDSLDELLETCDIISLHVDGRTENKNILNKEKIFKMKKGAILVNLSRGHV 464
           ER      TK++ LD+LL   D I+LHV    + +NIL+ E I K KKG  ++N +RG +
Sbjct: 182 ERAKALGVTKVE-LDDLLARADFITLHVPLTDKTRNILSAEAIAKTKKGVRIINCARGGL 240

Query: 465 VDVPALRDALESGHLAGAAVDVFPTEPKNNDEPFESELIGCPNTILTPHIGGSTLEAQEN 524
           VD  AL +A++SGH+AGAA DVF  EP +     ES L   PN ++TPH+G ST EAQEN
Sbjct: 241 VDEKALAEAIKSGHVAGAAFDVFEVEPAS-----ESPLFNLPNVVVTPHLGASTTEAQEN 295

Query: 525 IAQFVPGKIIEYINSGNTFNSVNFPNI 551
           +A  V  ++ +Y+ +G   N++N P++
Sbjct: 296 VALQVAEQMSDYLLTGAVQNALNMPSV 322


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: 663
Number of extensions: 25
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: 534
Length adjustment: 36
Effective length of query: 594
Effective length of database: 498
Effective search space:   295812
Effective search space used:   295812
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