GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Methylocella silvestris BL2

Align D-3-phosphoglycerate dehydrogenase; PGDH; EC 1.1.1.95; 2-oxoglutarate reductase; EC 1.1.1.399 (uncharacterized)
to candidate WP_012591482.1 MSIL_RS12680 D-glycerate dehydrogenase

Query= curated2:O33116
         (528 letters)



>NCBI__GCF_000021745.1:WP_012591482.1
          Length = 331

 Score =  171 bits (434), Expect = 3e-47
 Identities = 116/322 (36%), Positives = 171/322 (53%), Gaps = 14/322 (4%)

Query: 4   PVVLIADKL---AQSTVAALGDQVEVRWVDGP-DRTKLLAAVPEADALLVRSATTVDAEV 59
           P+V++  KL    ++ +  L D  ++   D P  R++L AA+  AD L+      +DAE+
Sbjct: 6   PLVIVTRKLPDVVETRMCELFD-AKLNIDDKPMSRSELAAAMAAADVLVPTVTDRIDAEL 64

Query: 60  L-AAAPKLKIVARAGVGLDNVDVDAATARGVLVVNAPTSNIHSAAEHALALLLAASRQIA 118
           +  A  ++K++A  G G+DN+DV  A  RG+ V N P       A+  +AL+LA +R+I 
Sbjct: 65  IRVAGEQMKLIANFGNGVDNIDVGIAAERGITVTNTPGVLTEDTADMTMALILAVARRIV 124

Query: 119 EADASLRAHIWKRSS---FSGTEIFGKTVGVVGLGRIGQLVAARIAAFGAHVIAYDP-YV 174
           E   S+    W   S     G  I GK +G+VG+GRIGQ +A R  AFG  +  ++  +V
Sbjct: 125 EGAKSIPDGAWSGWSPTWMLGRRITGKRLGIVGMGRIGQALARRAKAFGLQIHYHNRRHV 184

Query: 175 APARAAQLGIELM-SFDDLLARADFISVHLPKTPETAGLIDKEALAKTKPGVIIVNAARG 233
           A A   QL      S D +LAR D +SV+ P TP T  L+    L   +P  I+VN ARG
Sbjct: 185 AAAIEEQLEATYWESLDQMLARMDVVSVNCPHTPATYHLLSARRLKYLRPHAILVNTARG 244

Query: 234 GLVDEVALADAVRSGHVRAAGLDVFATEPCTDSPLFELSQ---VVVTPHLGASTAEAQDR 290
            ++DE AL   +  G +  AGLDVF  EP     L  L++   V + PH+G++T E +  
Sbjct: 245 EIIDEAALTRMLELGELGGAGLDVFEHEPAVSKKLLRLAEAGKVTLLPHMGSATTEGRID 304

Query: 291 AGTDVAESVRLALAGEFVPDAV 312
            G  V  +V+  L G   PD V
Sbjct: 305 MGEKVIVNVKTFLDGHRPPDRV 326


Lambda     K      H
   0.317    0.132    0.364 

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: 348
Number of extensions: 19
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: 528
Length of database: 331
Length adjustment: 32
Effective length of query: 496
Effective length of database: 299
Effective search space:   148304
Effective search space used:   148304
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: 50 (23.9 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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