GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Sinorhizobium medicae WSM419

Align phosphoglycerate dehydrogenase (EC 1.1.1.95) (characterized)
to candidate YP_001328133.1 Smed_2466 NAD-binding D-isomer specific 2-hydroxyacid dehydrogenase

Query= BRENDA::Q972A9
         (313 letters)



>NCBI__GCF_000017145.1:YP_001328133.1
          Length = 310

 Score =  158 bits (400), Expect = 1e-43
 Identities = 105/313 (33%), Positives = 169/313 (53%), Gaps = 16/313 (5%)

Query: 3   IYTVKALITDPIDEILIKTLREKGIQVDY-----MPEISKEELLNIIGNYDIIVVRSRTK 57
           + T ++L  DP  E+  + LR+ G ++ +     MP  S+ EL+ ++    I  +     
Sbjct: 5   LVTPRSLSLDPPPEL--EPLRQAGFELVFPTPGRMP--SEAELIGLVPGC-IGWLAGVEP 59

Query: 58  VTKDVIEKGKKLKIIARAGIGLDNIDTEEAEKRNIKVVYAPGASTDSAVELTIGLMIAAA 117
           V+  VI     L+ I+R G G+DN+     ++R I ++ A GA+     EL++GLM+AA 
Sbjct: 60  VSDKVIAAADSLRAISRNGTGIDNLPLPLLKERGIGILKAEGANAVGVAELSVGLMLAAL 119

Query: 118 RKMYTSMALAKSGIFKKIEGLELAGKTIGIVGFGRIGTKVGIIANAMGMKVLAYDILDIR 177
           R +    A  ++G + +  G E+A +T+GI+G G IG +V    +AM   V+A D    R
Sbjct: 120 RHIPAETAGIRAGGWPRSRGREIAERTVGIIGCGAIGKRVARAVSAMRASVIACD--PFR 177

Query: 178 EKAEKINA-KAVSLEELLKNSDVISLHVTVSKDAKPIIDYPQFELMKDNVIIVNTSRAVA 236
              E     K  SL+E+   +D++SLH     D KPI+D P+   +  + I++NT+RA  
Sbjct: 178 PNVEVYGPFKWASLDEVFAGADIVSLHCPAPADGKPIVDAPRLATVPPHAILINTARATL 237

Query: 237 VNGKALLDYIKKGKVYAYATDVFWNEPPKEEWELELLKHERVIVTTHIGAQTKEAQKRVA 296
           V+  A+   + +G++ AYATDVF  EPP       L  H RVI T+HIG  T E+  +  
Sbjct: 238 VDEDAVRAALDEGRLQAYATDVFTTEPPAPG---SLASHPRVIATSHIGGLTDESVGKAT 294

Query: 297 EMTTQNLLNAMKE 309
           ++   NLL+A+ E
Sbjct: 295 KIAVANLLSALVE 307


Lambda     K      H
   0.317    0.134    0.361 

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: 212
Number of extensions: 14
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: 313
Length of database: 310
Length adjustment: 27
Effective length of query: 286
Effective length of database: 283
Effective search space:    80938
Effective search space used:    80938
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: 48 (23.1 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