GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Methyloferula stellata AR4T

Align D-3-phosphoglycerate dehydrogenase; PGDH; EC 1.1.1.95 (uncharacterized)
to candidate WP_020174531.1 A3OQ_RS0106350 D-glycerate dehydrogenase

Query= curated2:O27051
         (525 letters)



>NCBI__GCF_000385335.1:WP_020174531.1
          Length = 331

 Score =  179 bits (454), Expect = 1e-49
 Identities = 111/304 (36%), Positives = 171/304 (56%), Gaps = 9/304 (2%)

Query: 14  EKGISELEEVAEVVVNTTITPEELLDAIKDFDAIVVRSRTKVTREVIEAA-PRLKIIARA 72
           E  + EL +    + +  ++  E+++A+K+ D +V     ++   +I AA  ++K+IA  
Sbjct: 19  ETRMCELFDTRLNIDDRPMSAAEIIEAVKNADVLVPTVTDRIDAALIAAAGDKMKLIANF 78

Query: 73  GVGVDNVDVKAATDRGIMVINAPESTSITVAEHSIGLMLALARKIAIADRSVKEGKW--- 129
           G GVDN+DV AA +RG+ V N P   +   A+ ++ L+LA+AR++    + +  G+W   
Sbjct: 79  GNGVDNIDVLAAYERGMTVTNTPGVLTEDTADMTMALILAVARRLVEGAQVIPGGEWGGW 138

Query: 130 EKNRFMGIELNGKTLGIIGMGRIGSQVVVRTKAFGMDIMVYDPY-ISKEAAEEMGVTVTD 188
                +G  + GK LGI+GMGRIG  V  R KAFG+ I  ++   +S    EE+  T  D
Sbjct: 139 SPTWMLGRRITGKRLGIVGMGRIGQAVARRAKAFGLQIHYHNRRRLSATVEEELEATYWD 198

Query: 189 -LETLLRESDIVTIHVPLTPETRHLISEDEFKLMKDTAFIVNCARGGIIDEDALYRALKD 247
            L+ +L   DIV+++ P TP T HL+S    K ++  A +VN ARG +IDE  L + L  
Sbjct: 199 SLDQMLARMDIVSVNCPHTPATYHLLSARRLKYLRPHAILVNTARGEVIDEVTLTKMLDA 258

Query: 248 GEIAGAALDVFEEEPPEGSPLLELE---NVVLTPHIGASTSEAQRDAAIIVANEIKTVFQ 304
           GEIAGA LDVFE EP   + L++L     V L PH+G++T+E + D    V   +K    
Sbjct: 259 GEIAGAGLDVFEHEPAVSTKLVKLAQAGKVTLLPHMGSATTEGRVDMGEKVIINVKAFMD 318

Query: 305 GGAP 308
           G  P
Sbjct: 319 GHRP 322


Lambda     K      H
   0.316    0.135    0.366 

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: 383
Number of extensions: 21
Number of successful extensions: 4
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: 525
Length of database: 331
Length adjustment: 31
Effective length of query: 494
Effective length of database: 300
Effective search space:   148200
Effective search space used:   148200
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.

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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